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2012 KCE REPORT 1 SUPPO PART 1: 85C ORTIVE EXERCISE E TREAT E TREATM TMENT ENT T FOR C CANCER R www.kce.fgo ov.be

SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

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Page 1: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

2012

KCE REPORT 1

SUPPOPART 1:

85C

ORTIVEEXERCISE

E TREATE TREATM

TMENTENT

T FOR CCANCERR

www.kce.fgoov.be

Page 2: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

Belgian He

Executive

ealth Care KTh20th

Board

PrCEprPrEnPrGePrRe Re Re Int Pr

Pr

Ho So Ho

Knowledge Che Belgian Healt002 under the suhat support the p

resident EO - National Instresident) resident of the Fenvironment (vice president of the Feeneral Administraroducts epresentatives of

epresentatives of

epresentatives of

termutualistic Age

rofessional Organ

rofessional Organ

ospital Federation

ocial Partners

ouse of Represen

Centre h Care Knowled

upervision of theolitical decision

titute for Health an

deral Public Servpresident) deral Public Serv

ator of the Federal

the Minister of Pu

the Minister of So

the Council of Mi

ency

nisations - represe

nisations - represe

ns

ntatives

ge Centre (KCE)e Minister of Pubmaking on healt

nd Disability Insur

ice Health, Food C

ice Social Securitl Agency for Medi

ublic Health

ocial Affairs

nisters

entatives of physic

entatives of nurses

) is an organizatiblic Health and Sth care and healt

rance (vice

Chain Safety and

y (vice president)cines and Health

cians

s

ion of public inteSocial Affairs. KCth insurance.

Actual Me

Pierre GilleJo De Coc

Dirk Cuype

Frank VanXavier De

Bernard LaMarco SchOlivier de Ri De RiddJean-NoëlDaniel DevMichiel CaPatrick VeXavier BreMarc MoenJean-PierrMichel FouMyriam HuJohan PauJean-ClauRita ThysPaul PalstLieve Wier

erest, created onCE is in charge

mbers

et ck

ers

n MassenhoveCuyper

ange hetgen Stexhe der Godin vos

allens rertbruggen

enez ns re Baeyens ulon ubinon uwels de Praet

erman rinck

n the 24th of Deceof conducting s

Substitute Membe

Benoît Collin

Chris Decoster

Jan Bertels Greet Musch

François Perl Annick Poncé Karel Vermeyen Lambert StamataFrédéric Lernoux Bart Ooghe Frank De Smet Yolande Husden Geert Messiaen Roland Lemye Rita Cuypers Ludo Meyers Olivier Thonon Katrien KestelootPierre Smiets Leo Neels Celien Van Moerk

ember tudies

ers

akis

t

kerke

Page 3: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

Control Manageme

Contact

ent

Gove

ChiefAssis

Mana

BelgiDoorbBouleB-100Belgi T +32F +32info@http://

ernment commissi

f Executive Officestant Chief Execut

agers Program Ma

an Health Care Kbuilding (10th Flooevard du Jardin B00 Brussels um

2 [0]2 287 33 88 2 [0]2 287 33 85

@kce.fgov.be /www.kce.fgov.be

ioner

r tive Officer

anagement

Knowledge Centreor) otanique, 55

e

Yv

RaJe

ChKr

(KCE)

ves Roger

af Mertens ean-Pierre Closon

hristian Léonard ristel De Gauquierr

Page 4: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

 

Page 5: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

2012

KCE REPORT 1GOOD CLINICA

SUPPOPART 1: KIRSTEN HOL

85C AL PRACTICE

ORTIVEEXERCISE

DT HENNINGSEN

E TREATE TREATM

N, ANJA DESOM

TMENTENT

ER, SOPHIE HAN

T FOR C

NSSENS, JOAN V

CANCER

VLAYEN

R

www.kce.fgoov.be

Page 6: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

COLOPHOTitle:

Authors:

External expert

External validat

Conflict of intere

Layout:

Disclaimer:

Publication date

Domain:

MeSH:

NLM Classificat

Language:

Format:

ON

ts:

tors:

est:

e:

tion:

Supp

Kirste

AhmAnneLeuvDidie

JeroeJean

Fees

Ine V

The comneceSubsa corepoFinaOnlyalso

09 O

Good

Neop

QZ 2

Engli

Adob

portive treatment f

en Holdt Henning

ad Awada (Instituemarie Coolbrandven), Robert Parider Vander Steiche

en Mebis (Limburn-Pierre van den B

s or other compen

Verhulst

external expertments were disc

essarily agree wisequently, a (finansensus or a vo

ort and did not nelly, this report ha

y the KCE is respunder the full re

October 2012

d Clinical Practice

plasms; Chemothe

266

ish

be® PDF™ (A4)

for cancer – Part

sen (KCE), Anja D

ut Bordet), Sabiendt (UZ Leuven), Judaens (UZ Leuvel (Fondation Cont

gs Oncologisch CBerg (Meander Me

nsation for writing

ts were consultcussed during mth its content. al) version was s

oting process beecessarily all thras been approveponsible for erroesponsibility of th

e (GCP)

erapy, Adjuvant; R

1: exercise treatm

Desomer (KCE), S

n Bauwens (UZ Bulie Degée (Instituen), Marc Peeterstre le Cancer)

Centrum), Emmanedisch Centrum, N

a publication or p

ted about a (pmeetings. They

submitted to theetween the validaee agree with its

ed by common asors or omissionshe KCE.

Radiotherapy; Exe

ment

Sophie Hanssens

Brussel), Tom Boteut Bordet), Frédérs (UZA), Ward R

nuel Simons (RugsNederland)

articipating in its d

preliminary) versdid not co-auth

e validators. The ators. The validas content. ssent by the Exe that could pers

ercise Therapy

s (UZ Brussel), Jo

erberg (UGent), Jric Duprez (UGen

Rommel (Vlaamse

school - Ecole du

development: Ann

sion of the sciehor the scientific

validation of theators did not co-

ecutive Board. ist. The policy re

an Vlayen (KCE)

Jan Bourgois (UGnt), Johan Mentene Liga tegen Kan

dos CHU Brugma

nemarie Coolbran

entific report. Tc report and did

e report results f-author the scien

ecommendations

Gent), n (UZ nker),

ann),

ndt

Their d not

from ntific

s are

Page 7: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

Legal depot:

Copyright:

How to refer to

this document?

D/20

KCE http:/

HoldttreatmRepo

This

12/10.273/61

reports are publis//kce.fgov.be/cont

t Henningsen K, ment. Good Cliniort 185C. D/2012/

document is avai

shed under a “by/tent/about-copyrig

Desomer A, Hancal Practice (GCP/10.273/61.

lable on the webs

/nc/nd” Creative Cghts-for-kce-repor

nssens S, VlayenP). Brussels: Belg

site of the Belgian

Commons Licencets.

n J. Supportive trgian Health Care

Health Care Kno

e

reatment for cancKnowledge Cent

owledge Centre.

cer – Part 1: exetre (KCE). 2012.

ercise KCE

Page 8: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

 

Page 9: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

KCE Report 185

FORE

5C

EWORD The KCE recommendradiotherapcancer typeYet, other, importanceno reason interventionThe presensupportive tThese four in a transvecancer in th

Jean-PierreAssistant C

Exercise t

already publishdations are often py and surgery. Ofes.

more supportive for the well-beingat all, even on t

ns are proven to bnt report about etreatment for patiereports do not co

ersal way for all che most human an

e CLOSON Chief Executive Of

treatment for adult

hed many repolimited to diagno

f course, these ar

e interventions ag of the patient duhe contrary, to s

be effective, whenexercise treatmenents undergoing concern just one spcancer types. We nd tolerable way f

fficer

t cancer patients

rts with clinicalostic procedures re the intervention

are also frequenturing the very bur

show no interest , and for which cant introduces a scurative treatmentpecific cancer type

hope that they wfor their patient.

recommendatioand therapeutic

ns that are used to

tly used in daily rdensome treatmein these interven

ancer type. series of four ret for their cancer.e. They evaluate

will be a useful aid

ons about cancinterventions, suo stop or eradicat

practice, and apent for their cance

ntions. The quest

ports that evalua

the use of these d for all professio

Raf MChief E

cer. However, thch as chemotherte the tumour for m

ppear to be of her. Therefore, theion is which of th

ate different type

supportive treatmnals that fight aga

ERTENS Executive Officer

i

hese rapy, most

huge ere is hese

es of

ments ainst

Page 10: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

ii

EXECCUTIVE SSUMMAR

Exercise t

RY

treatment for adult

ITpcmcstroCpgcgScinsw••

••Trecptyin

t cancer patients

NTRODUCThere is a wide bphysical activity iscancer patients dmedical needs, echemotherapy or specific recommerivial, since the deof the Belgian NatCollege of Oncoloprovides scientificguidelines. Until colorectal cancegastrointestinal caSince many guidecare, which are ofnto the question supportive care ofwill be covered: Exercise treat Treatment o

radiotherapy; Psychosocial Treatment of c

The present reporecommendations

chemo- and/or physiotherapy targype, e.g. lymphoen prostate cancer

CTION body of evidence beneficial for hea

deserve to get aspecially during tradiotherapy. Butndations in our cevelopment of gutional Cancer Planogy. KCE collaborc support in the

now guidelines er, testicular cancer and cervicalelines already nowften not cancer typand to develop af cancer patients

tment during chemf adverse even support; cancer-related part aims to formularelative to exerciradiotherapy fo

geted to specific edema in breast patients, are out

and a large conalth. Likewise, eveample support, inthe difficult periot, can we be morcancer guidelinesidelines is one of n 2008-2010 and rates with the Cojoint developmewere develope

cancer, pancre cancer (www.kcew cover different pe specific, it was

a separate series under treatment.

motherapy and/or nts related to

ain. ate, on the basis se treatment for aor cancer. Exesymptoms relate

cancer patients oof the scope of th

KCE Report 1

sensus in societyerybody will agreencluding for theirod when they undre precise and in

s? The question ithe main action pone of the tasks o

ollege of Oncologyent of clinical prad on breast caatic cancer, ue.fgov.be). aspects of supp

s decided to go deof four reports oThe following as

radiotherapy; chemotherapy a

of scientific evidadult patients receercise treatmened to a certain caor urinary incontinhe present report.

185C

y that e that r non dergo clude is not points of the y and actice ancer, upper

ortive eeper

on the spects

and/or

ence, eiving nt or ancer nence

Page 11: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

KCE Report 185

METHODThe following reWhat is the effactive curative The following o1. Quality of

as FACT sSee text bo

2. CardiopulmVO2max, hwalk tests)

3. Fatigue (aPiper Fatigsubscales,

4. Safety of events).

Text box 1: Sc

FACT

WHOQOL-BRE

EQ-5D

SF-36

EORTC-C30

FACIT

5C

DS esearch question ffect of exercise ttreatment? utcomes are conslife (as measured

scales, WHOQOL-ox); monary function heart rate, Metabo; s measured by v

gue Scale, Brief FFACIT-F, Multidiexercise treatme

cales to mesure Q

Function

EF WHO qu

EuroQol

Short Fo

EuropeaTreatme

Function

was addressed intreatment for adu

sidered: d by validated sca-BREF, QOL EQ-

(as measured olic Equivalence o

validated scales Fatigue Inventory, mensional Fatigueent (i.e. frequenc

Quality of Life

nal Assessment of

uality of life assess

-5D instrument

orm Health Survey

an Organisationnt of Cancer- Qua

nal Assessment of

Exercise t

n this review: ult cancer patient

ales or instrumen-5D, SF-36, EORT

by absolute or of Task or 6 or 12

or instruments, FACT-F or FACT

e Inventory); cy and type of

f Cancer Therapy

sment instrument

y

n for Researcality of Life-C30

f Chronic Illness T

treatment for adult

ts during

nts, such TC-C30.

relative 2 minute

such as T fatigue

adverse

ch and

Therapy

AthtrwdincTanth•

Sdo(sSTsuGre

t cancer patients

Active treatment eherapy (for breareatment” period weeks post-surgediagnosis until 3 wntervention had continue after this The literature seaanalyses. Howeveno recent systemhose developed fo to analyse t

systematic rev to perform a

inclusion of alSystematic reviewdatabases: OVID of Systematic ReDARE) and Healt

searched in: OVSearches were runThe AMSTAR inssystematic reviewusing the CochraGRADE system wecommendations

encompassed radast or prostate was defined as t

ery, or one weeweeks after the lto begin within period.

arch initially focuer, after an evalua

matic review had or the present repthe individual RCviews, and full literature se

l relevant studiesws and meta-anaMedline and PreM

eviews, Databaseth Technology As

VID Medline, Prn between Decemstrument was ap

ws. Risk of bias fne Collaboration’

was used to assig.

diotherapy and chcancer) was e

the period from dk after the last ast chemotherapthe period defin

sed on systematation of the reviewused exactly the

port. ConsequentlyCTs from the r

arch for RCTs in. alyses were searMedline, EMBASEe of Abstracts ossessment (HTA) reMedline, EMBAmber 2011 and Fepplied for the crfor the included R’s tool for assess

gn the levels of ev

emotherapy. Horexcluded. The “adiagnosis until eit

radiotherapy or y, cycle. The exe

ned above, but

tic reviews and mws, it was obviouse same definitiony, it was decided: reference lists o

n order to ensur

rched in the folloE, Cochrane Dataof Reviews of E

database. RCTs ASE and CENT

ebruary 2012. itical appraisal oRCTs was determsing risk of biasvidence and grad

iii

mone active ther 3

from ercise could

meta-s that ns as

of the

e the

owing abase ffects were

TRAL.

of the mined . The

des of

Page 12: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

iv

RESULTSEffectivenessA total of 33 Rbeing most copossible to comaerobic exercismuscle strengthcancer types deffectiveness otable below.

Safety In about half treatment was treatment seem

S s

RCTs were identifiommon (12 studimpare institution-bse (e.g. walkinghening). This comdue to a limited of exercise treatm

of the included available. From

ms to be safe in pa

ied with studies oies). For breast based with home, cycling) with r

mparison was not pnumber of trials.

ment are presente

studies, data onthese studies, w

atients undergoing

Exercise t

on breast cancer cancer it was t

e-based interventiresistance exercipossible for the re

The conclusionsed by cancer typ

n the safety of e conclude that g treatment for ca

treatment for adult

patients herefore ons and se (e.g.

emaining s on the pe in the

exercise exercise ncer.

t cancer patients KCE Report 1185C

Page 13: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

KCE Report 185

Cancer type

Breast cancer

Prostate cance

Lung cancer

Colorectal can

Haematologica

Haematopoietictransplantation

Lymphoma

Acute myelogenleukemia

Mixed cancer p

5C

N

1

er 4

1

ncer 2

al cancers

c stem cell 4

1

nous 1

populations 8

N studies Con

2 •

4 •

2 •

4 ••

8 •

Exercise t

nclusions

Conflicting evidenof exercise treatresistance exerciConflicting evideevidence) Evidence suggesfunction (low leveConflicting eviden

Conflicting evidefatigue (very low

A combination ohave an effect on

The evidence su(very low level of There are indicat

Exercise treatmeConflicting evidelevel of evidence

It is plausible thaafter 6 months afIt is plausible th(moderate level o

Exercise treatme

Conflicting evidefatigue (very low

treatment for adult

nce (i.e. a mix ofment on quality se (very low level

ence on the effec

sts that aerobic eel of evidence) nce on the effect o

nce on the effeclevel of evidence)

f preoperative hon quality of life and

ggests that exercevidence)

tions that exercise

nt does not seemnce on the effect )

t exercise treatmefter the end of exehat exercise treatof evidence)

nt seems to have

nce on the effeclevel of evidence)

t cancer patients

studies reporting of life, regardlessl of evidence) ct of exercise tre

exercise is superi

of exercise treatm

ct of exercise trea)

ospital-based andd cardiopulmonary

cise treatment has

e treatment has no

m to have a significof exercise treat

ent has a significaercise treatment (mtment has a sign

a temporary effe

ct of exercise trea)

a positive effect s of it being inst

eatment on cardio

ior to resistance

ment on fatigue (ve

atment on quality

d postoperative hoy function (low lev

s no effect on qu

o effect on fatigue

cant effect on quatment on cardiopu

ant effect on qualimoderate level of nificant effect on

ct on fatigue (very

atment on quality

and studies with nitution- or home-

opulmonary funct

exercise in impro

ery low level of ev

y of life, cardiopu

ome-based exercvel of evidence)

uality of life or car

e (low level of evid

lity of life (very lowulmonary function

ity of life, althoughevidence) cardiopulmonary

y low level of evid

y of life, cardiopu

no effect) on the based, aerobic a

tion (very low lev

oving cardiopulmo

vidence)

ulmonary function

cise does not see

rdiopulmonary fun

dence)

w level of evidencn and fatigue (ver

h the effect disap

y function and fa

ence)

ulmonary function

v

effect and/or

vel of

onary

n and

em to

nction

ce) ry low

pears

atigue

n and

Page 14: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

vi

CONCLUIn this study, wof exercise treaand/or radiotheFor most canceexcept for brmethodologicalheterogeneousdifferent treatmthese scales, th• For most

benefits cardiopulmreporting aexception patients, wincluded ou

• Neither didquality of lsymptoms.safe duringreported on

A generalizatiodue to the abostudies. Moreorecommendationews is that thharmful during c

SIONS we analysed the patment for adult crapy. er types, only a sreast cancer. M limitations. Mor, both in terms of

ment regimens), ahey report conflictcancer types, wof exercise t

monary function ana positive effect awas one single

which reported stautcomes. d we find consislife or cardiopulm. Furthermore, thg adjuvant therapyn exercise-related

on of the results aove-mentioned pover, the available

on in favour of a here is no reasoncancer treatment.

published RCTs ocancer patients u

small number of Most of these reover, the inclustudy populations

and in terms of oing results:

we found no contreatment, inclund fatigue; i.e. thnd of studies repstudy (of moderaatistically significa

stent evidence thmonary function, ohere was some ey for cancer patie

d adverse events. and conclusions opulation differene evidence did nparticular exercisn to fear that phy.

Exercise t

n the benefits anundergoing chemo

RCTs could be instudies suffere

uded studies wes (different canceroutcome scales.

nsistent evidence uding quality oere was a mix oforting no effect. Tate quality) in lymant positive result

hat exercise wouor would increaseevidence that exeents, although not

might not be app

nces across the ot allow us to ex

se intervention. Tysical exercise w

treatment for adult

d harms otherapy

ncluded, ed from ere very r stages, Across

on the of life, f studies The only mphoma ts on all

uld harm e fatigue ercise is all trials

propriate included xpress a he good

would be

t cancer patients KCE Report 1185C

Page 15: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

KCE Report 185

RECO

a These rec

5C

OMMEND

commendations are

DATIONS

under the sole resp

Exercise t

Sa

Clinical rec• In the

treatmundergof a spthat pevideninto ac

• As thecance(weak

Agenda fo• Since

of quafor can

• For ouvalidatspecif

• For fuoutcom

ponsibility of the KC

treatment for adult

commendations absence of co

ment on quality going active treapecific type of ex

physical activity nce). Hence, it is ccount. ere is no consisr patients underrecommendatio

or the research cothere is a lack o

ality of life, cardioncer patients unutcomes such ated scales and tfic instrument to ture studies it isme measures ba

CE

t cancer patients

for the healthcaonsistent eviden

of life, cardiopatment, we cannxercise treatmenis beneficial foadvisable to tak

stent evidence er treatment, they n; very low level

ommunity of consistent andopulmonary funcdergoing active

as quality of lifehe research comrender the resul

s crucial to pre-dased on clinical s

are providers ce on the shortulmonary functiot formulate mo

nt, over and abovor health (weak ke the local conte

either that exercshould not be d

l of evidence).

d high-quality evction and fatiguetreatment, large

e and fatigue, remmunity should alts comparable.

define main outcosignificance.

t-term beneficiaion and fatigue re precise recomve the generally recommendatio

ext and the prefe

cise treatment wdiscouraged to d

idence on the efe) and on safety high-quality RC

esearchers shouagree on a gene

omes and the m

al effects of exefor cancer pat

mmendation in faaccepted couns

on; very low leverences of the pa

would be harmfudo physical activ

ffectiveness (in tof exercise treatTs are needed.

uld use standardric and on a dise

agnitude of effec

vii

ercise tients avour seling vel of atient

ul for vities.

terms tment

dized, ease-

ct for

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Page 17: SUPPORTIVE TREATMENT FOR CANCER · dema in breast patients, are out and a large con lth. Likewise, eve mple support, in he difficult perio, can we be mor ancer guidelines idelines

KCE Report 185

TABL

5

LE OF COONTENTLIST LIST

122.1

2.22.32.42.52.62.72.833.13.244.1

4.2

Exercise t

TS OF TABLES ......OF ABBREVIAT

SCIENTIFIC INTRODUCTMETHODS ...SCOPING ....2.1.1 Meth2.1.2 ReseDEFINITIONSLITERATURESELECTION SELECTION QUALITY APGRADING OFFORMULATIOSEARCH RESYSTEMATICRANDOMIZEEVIDENCE RBREAST CAN4.1.1 Qua4.1.2 Card4.1.3 Fatig4.1.4 SafePROSTATE C4.2.1 Qua

treatment for adult

............................TIONS ...................REPORT .............ION .............................................................................

hodology ..............earch questions aS ..........................E SEARCH ..........CRITERIA ...........PROCESS ..........PRAISAL ............F EVIDENCE .......ON OF RECOMMSULTS ................C REVIEWS ........

ED CONTROLLEDREPORT ..............NCER ..................lity of Life .............

diopulmonary funcgue .......................ety ........................CANCER .............lity of Life .............

t cancer patients

............................

............................

............................

............................

............................

............................

............................and outcomes ..............................................................................................................................................................................

MENDATIONS .............................................................

D TRIALS ................................................................................................ction ....................................................................................................................................

............................

............................

............................

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............................

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.......................... 1

.......................... 1

.......................... 1

.......................... 1

.......................... 1

.......................... 1

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.......................... 2

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.......................... 3

.......................... 3

1

. 4

. 5

. 7

. 7

. 8

. 8

. 8

. 8

. 8

. 9

. 9 10 10 10 12 13 13 14 15 15 15 25 28 30 30 30

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4.3

4.4

4.5

4.6

566.16.277.1

Exercise t

4.2.2 Card4.2.3 Fatig4.2.4 SafeLUNG CANC4.3.1 Qua4.3.2 Card4.3.3 Fatig4.3.4 SafeCOLORECTA4.4.1 Qua4.4.2 Card4.4.3 Fatig4.4.4 SafeHAEMATOLO4.5.1 Qua4.5.2 Card4.5.3 Fatig4.5.4 SafeMIXED CANC4.6.1 Qua4.6.2 Card4.6.3 Fatig4.6.4 SafeDISCUSSIONRECOMMENCLINICAL RERESEARCH AAPPENDICESAPPENDIX 1

treatment for adult

diopulmonary funcgue .......................ety ........................ER .......................lity of life ..............

diopulmonary funcgue .......................ety ........................AL CANCER ........lity of Life .............

diopulmonary funcgue .......................ety ........................OGICAL CANCERlity of life ..............

diopulmonary funcgue .......................ety ........................CER POPULATIOlity of life ..............

diopulmonary funcgue .......................ety ........................N...........................DATIONS ...........

ECOMMENDATIOAGENDA .............S..........................: QUALITY APPR

t cancer patients

ction ....................................................................................................................................ction ....................................................................................................................................ction ............................................................................

RS ....................................................ction ............................................................................

ONS..................................................ction ....................................................................................................................................

ONS .............................................................................

RAISAL INSTRUM

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KCE Report

.......................... 3

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t 185

32 33 35 35 35 35 35 36 36 36 36 36 38 38 38 40 42 44 45 45 47 51 55 55 57 57 57 58 58

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KCE Report 185

5

7.2

7.37.4

Exercise t

7.1.1 AMS7.1.2 CochAPPENDIX 27.2.1 Syst7.2.2 RandAPPENDIX 3APPENDIX 47.4.1 Brea7.4.2 Pros7.4.3 Lung7.4.4 Colo7.4.5 Haem7.4.6 MixeREFERENCE

treatment for adult

STAR ....................hrane Collaboratio: SEARCH SYNTtematic reviews ....domized controlle: GRADE PROFIL: EVIDENCE TAB

ast cancer ............state cancer .........g cancer ...............orectal cancer ......matological cance

ed cancers ...........ES ........................

t cancer patients

............................on’s tool for asses

TAX BY DATABAS............................

ed trials ................LES BY INTERVEBLES ...................................................................................................................................ers ...............................................................................

............................ssing risk of bias .SE ................................................................................

ENTION AND OU................................................................................................................................................................................................................................

............................

............................

............................

............................

............................TCOME ..............................................................................................................................................................................................................................................

.......................... 5

.......................... 6

.......................... 6

.......................... 6

.......................... 6

.......................... 7

.......................... 7

.......................... 7

.......................... 8

.......................... 9

.......................... 9

.......................... 9

........................ 10

........................ 11

3

58 60 62 62 65 70 74 74 88 93 94 96 06 17

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LIST OF TTABLES TableTableTableTableTableTablein patTablein patTablein patTablein patTableand pTableTableTableTableTableTableTablehaemTablehaemTablecell trTableTableTable

Exercise t

e 1 – In- and exclue 2 – Levels of evie 3 – Down- or upe 4 – Strength of re 5 – Factors that e 6 – Effect of insttients with breast e 7 – Effect of homtients with breast e 8 – Effect of aertients with breast e 9 – Effect of resitients with breast e 10 – Effect of cophysical subscalese 11 – Effect of exe 12 – Effect of exe 13 – Effect of exe 14 – Effect of exe 15 – Effect of exe 16 – Effect of exe 17 – Effect of exmatopoietic stem ce 18 – Effect of exmatopoietic stem ce 19 – Effect of exransplantation .....e 20 – Effect of exe 21 – Effect of exe 22 – Effect of ex

treatment for adult

usion criteria ........idence according grading the eviderecommendationsinfluence the stre

titution-based execancer.................

me-based exercisecancer.................obic interventionscancer.................istance interventiocancer.................

ombined aerobic as of QOL in patien

xercise treatment xercise treatment xercise treatment xercise treatment xercise treatment xercise treatment xercise treatment cell transplantationxercise treatment cell transplantationxercise treatment ............................

xercise treatment xercise treatment xercise treatment

t cancer patients

............................to the GRADE sy

ence according to s according to the ength of a recommercise on quality of............................e on quality of life............................s on quality of life ............................ons on quality of l............................and resistance intents with breast caon cardiopulmonaon fatigue in patieon quality of life inon cardiopulmonaon fatigue in proson fatigue in patieon quality of life inn ..........................on cardiopulmonan ..........................on fatigue in patie............................on quality of life inon cardiopulmonaon fatigue in mixe

............................ystem ...................the GRADE systeGRADE system ..

mendation.............f life (QOL) and p............................

e (QOL) and physi............................(QOL) and physic............................ife (QOL) and phy............................erventions on quancer .....................ary function in patents with breast can prostate cancer ary function in prostate cancer patienents with colorectan patients undergo............................ary function in pat............................

ents undergoing h............................n mixed cancer poary function in mixed cancer populat

............................

............................em ...............................................................................

physical subscales............................ical subscales of Q............................cal subscales of Q............................ysical subscales o............................ality of life (QOL) ............................tients with breast cancer ..................patients..............

ostate cancer patients .......................al cancer .............oing ............................tients undergoing ............................

haematopoietic ste............................opulations ...........xed cancer populaions ....................

KCE Report

............................

.......................... 1

.......................... 1

.......................... 1

.......................... 1s of QOL .......................... 1QOL .......................... 1

QOL .......................... 2of QOL .......................... 2

.......................... 2cancer ............... 2.......................... 2.......................... 3ents ................... 3.......................... 3.......................... 3

.......................... 3 .......................... 4em .......................... 4.......................... 4ations ................. 4.......................... 5

t 185

. 9 11 11 12 12

16

18

21

23

24 26 29 31 32 34 37

39

41

43 46 49 52

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KCE Report 185

LIST OF A

5

ABBREVIAATIONS

Exercise t

ABBREVIATION95%CI ADL ADT AMSTAR BFI bpm CG EORTC-QLQ-C3EQ-5D FACIT FACIT-F FACT FACT-AN FACT-B FACT-C FACT-F FACT-G FACT-GP FACT-P GRADE HR HSCT HTA IG ITT KCE LASA

treatment for adult

N DEFINITI95% confActivities AndrogenQuality aBrief FatiBeats peControl g

30 EuropeanEuroQol-FunctionaFunctionaFunctionaFunctionaFunctionaFunctionaFunctionaFunctionaFunctionaFunctionaGrading oHeart rateHaematoHealth teInterventiIntention Belgian HLinear An

t cancer patients

ION fidence interval of daily living

n depression therappraisal tool to asgue Inventory r minute

group n Organisation for-5D instrument al Assessment of al Assessment of al Assessment of al Assessment of al Assessment of al Assessment of al Assessment of al Assessment of al Assessment of al Assessment of of Recommendatie

opoietic stem cell tchnology assessmion group to treat

Healthcare Knowlenalogue Scales of

apy ssess systematic r

r Research and T

Chronic Illness TChronic Illness TCancer TherapyCancer Therapy Cancer Therapy Cancer Therapy Cancer Therapy Cancer Therapy Cancer Therapy Cancer Therapy ions Assessment,

transplantation ment

edge Centre f Assessment

reviews

reatment of Canc

herapy herapy-Fatigue

- Anemia scale - Breast Cancer - Colorectal Canc- Fatigue - General - General Populat- Prostate Cancer, Development an

er- Quality of Life

cer

tion r d Evaluation

5

-C30

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6

Exercise t

MD MET min MOS NSCLC POMS QOL RCT SD SDS SF-36 SR STAI TOI-AN VAS VO2max WHOQOL-BREF

treatment for adult

Mean diffMetabolicMinutesMedical ONon-smaProfile of Quality ofRandomiStandardSymptomShort ForSystematSpielbergTrial OutcVisual anMaximal

F WHO qua

t cancer patients

ference c Equivalent of Ta

Outcome Study all cell lung cancerf Mood States f life zed controlled tria

d deviation m distress scale rm Health Surveytic review ger’s state-trait ancome Index-Anemnalogue scale Oxygen Consumpality of life assess

ask

r

al

nxiety inventory mia

ption sment instrument

KCE Reportt 185

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KCE Report 185

SCIE

5

NTIFIC RREPORT

Exercise t

T

treatment for adult

1TBCpgcgSctocatosTrerecsinpTth

t cancer patients

1 INTRODThe development Belgian National College of Oncoloprovides scientifiguidelines. Up to cancer, colorectagastrointestinal caSince many canccare, which are ofo develop a sepacancer patients reaspects will be coo chemotherapy support, and treatmThe present reporecommendations eceiving active c

cancer. Exercise symptoms, e.g. ncontinence in ppresent report. This report is intenhe supportive car

DUCTION of care pathway

Cancer Plan 20ogy. KCE collaborc support in tthis date guidel

l cancer, testicuancer and cervicalcer-specific guideften not specific trate series of fou

eceiving active trevered by this seriand/or radiother

ment of cancer-rert aims to formularelative to exerc

urative treatmenttreatment or phylymphoedema in

prostate cancer p

nded to be used be of cancer patien

ys is one of the 08-2010 and onerates with the Cohe developmentines were jointly

ular cancer, panc cancer (www.kcelines also cover to a certain cancer reports on the seatment for their ies: treatment of arapy, exercise treelated pain. ate, on the basiscise treatment fort (chemo- and/or ysiotherapy for sn breast cancerpatients, are out

by health care pronts during active t

main items withie of the tasks o

ollege of Oncologyt of clinical pra developed on bcreatic cancer, ue.fgov.be). aspects of supp

er type, it was desupportive care of

cancer. The folloadverse events reeatment, psychos

of scientific evidr adult cancer paradiotherapy) for

specific cancer-rer patients or ur

of the scope o

ofessionals involvreatment.

7

n the of the y and actice breast upper

ortive cided adult

owing elated social

ence, tients

r their elated rinary

of the

ved in

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8

2 METH2.1 Scopin2.1.1 MethoOn 8 Novembethe basis of a wresearch quespresented to aclinical practiceby the KCE in validated by the

2.1.2 ReseaFor exercise trbeing of primary• Which evid

during activThe reason forguidelines deveAdditionally, thduring the perireferred to as tthis period was of these RCTscollaboration wfocus on canceExercise treatmpsychosocial multidisciplinarypsychosocial su

ODS g

odology er 2011, a stakehweb-survey condutions and outco

an expert group ie. A final selectioncollaboration with

e experts via ema

arch questions areatment the folloy interest:

dence exists on eve curative treatmfocusing on the a

eloped by the KCEe experts expresod immediately fthe “rehabilitation found1. This revie

s measured outcoith the content exr patients during a

ment as part of asupport was cy programs will upport.

holder meeting toucted prior to the mmes related to in order to discun and prioritizationh a content experil.

and outcomes owing research q

xercise programsment? active treatment pE focus on this pessed an interest following treatmenn” period. One syew included four omes within the

xpert, it was conseactive treatment. a multidisciplinaryonsidered to bbe discussed in

Exercise t

ok place at the Kmeeting, a list of pexercise treatme

uss themes of intn of outcomes wart (Sophie Hansse

question was def

s for adult cancer

period is that moseriod.

in the effect of nt – a period som

ystematic review cRCTs. However, scope of our pro

equently decided

y program also ibe out-of-scope. n a separate re

treatment for adult

KCE. On potential ent was terest to as made ens) and

fined as

patients

st cancer

exercise metimes covering only two oject. In to solely

nvolving These

eport on

Tw•

2Dfrcaduwc(wthwpEsTmc

t cancer patients

The list of outcomwith the content ex Quality of Lif

EQ-5D, SF-36 Cardiopulmon

heart rate, ME Fatigue (Pipe

FACT fatigue or similar instr

Safety (expreintervention o

2.2 DefinitionDefinitions for the rom the literatureclose collaborationaligned with the cudefined as being funtil one week aftweeks after the cancer type or tincluding breast c

were not considerhe definitions dewithin the period dperiod. Exercise treatmensetting and measuThe results in chamixed cancer popcancer types.

mes to be studiedxpert and ranked fe (measured by 6, EORTC-C30, Fnary function (meaET or 6 or 12 minuer Fatigue Scalesubscales, FACIT

rument); essed as adverr relapse).

ns “active treatment

e, including a ren with the contenurrent Belgian conrom diagnosis unter the last radiatlast chemotheraptreatment form. cancer patients anred to be on activscribed above. T

defined and descr

nt included all exured by the defineapter 4 are descpulations contains

d was similarly daccording to impoFACT scales, W

FACIT scale or simasured by absoluute walk tests); e, Brief Fatigue T-F, Multidimensi

rse events relat

” phase were devcent Dutch syste

nt expert to ensurntext. The “active til 3 weeks post-stion treatment or py treatment. ThPatients being

nd patients on ADve treatment unleThe exercise inteibed above, but co

xercise interventiod outcomes.

cribed per cancers the RCTs with

KCE Report

efined in collaborortance: WHOQOL-BREF, milar instrument); ute or relative VO2

Inventory, FACTonal Fatigue Inve

ted to the exe

veloped with inspirematic review2 are our definitions treatment” period

surgery, from diagfrom diagnosis u

his was regardleon hormone the

DT for prostate cass they also fell w

ervention had to ould continue afte

ons performed in

r type. The sectioat least two diff

t 185

ration

QOL

2max,

-F or entory

rcise-

ration nd in were

d was gnosis until 3 ss of erapy

ancer) within begin er this

n any

on on ferent

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KCE Report 185

2.3 LiteratuFor all researchmeta-analyses.systematic revisystematic revie• OVID Med• EMBASE (• Cochrane D• DARE (Wil• HTA datab• National GDepending on additional searcfollowing source• OVID Med• EMBASE (• CENTRAL Medline and EMwere run on 13run on 27 Febsearched on 2was run in 16 January 201

5

ure search h topics, the searc If guidelines weiew of the literatuew. The followingline and PreMedli(Embase.com) Database of Systeey)

base (Wiley) uideline Clearinghthe quality and

ch for randomizees were used: line and PreMedli(Embase.com) (Wiley)

MBASE searches 3 December 2011bruary 2012. The9 February 2012Medline on 12 2. Detailed searc

ch first focused ore identified that ure, they were in sources were usne

ematic Reviews (W

house. d currency of thed controlled trials

ne

for systematic re. The search in te National Guide

2. The search forJanuary 2012

ch strategies can b

Exercise t

n systematic reviewere clearly bas

ncluded and treated:

Wiley)

e identified revies (RCTs) was do

views and meta-ahe Cochrane Libreline Clearinghour primary studies

and in EMBAbe found in appen

treatment for adult

ews and sed on a ted as a

ews, an one. The

analyses rary was use was

(RCTs) ASE on ndix 2.

2T

T

Sc

P

InO

D

L

t cancer patients

2.4 SelectionThe selection crite

Table 1 – In- and

Selection criteria

In

Population Atrwtrrc

ntervention EOutcome Q

sDesign M

gLanguage E

criteria eria are summariz

exclusion criteri

nclusion criteria

Adult cancer patiereatment is defineweeks post-surgerreatment) or fromadiation treatmen

chemotherapy treaExercise-programsQuality of life, cardsafety Meta-analysis, sysguideline, HTA, RCEnglish, Dutch, Fr

ed in Table 1.

ia

a

nts during active ed as being from dry (regardless of c diagnosis until on

nt or from diagnosatment s performed in andiopulmonary func

stematic review, eCT ench

treatment. Active diagnosis until 3 cancer type and ne week of last is until 3 weeks o

ny setting ction, fatigue and

evidence-based

9

f last

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10

2.5 SelectiFor the selectHenningsen) pDoubtful casesand consensusfirst selection, tBefore assessinappraisal was appraisal were:• Searched i• Data of sea• Quality ap

looking at tReviews not meAfter a review ono recent systewas completelConsequently, primary studiesperform an addinclusion of all rto that of systeabstract (AD), abstracts (AD), Doubtful cases

on process tion of systematperformed a firsts were discussed was achieved withe full-text of the ng the methodolo

performed of e n Medline and at arch mentioned ppraisal of includthe quality of appreeting these criterof the finally selecematic review hadly comparable tit was decided t

s from the refereditional literature relevant studies. Tematic reviews. Ta second selectiowhich was also dwere discussed w

ic reviews, one t selection based with a second rth a third revieweselected abstractsgical quality of ea

each full-text. Th

least one other d

ded primary studraisal and the useria were excludedcted systematic re defined the studyto the definitionto select relevantnce lists of the ssearch for RCT

The selection proThe first selectionon was based ondiscussed with thewith the third revie

Exercise t

reviewer (Kirsted on title and areviewer (Anja Dr (Joan Vlayen). As was retrieved.

ach review, a quice criteria of the

atabase

dies performed ed tool) d from further revieeviews it was evidy population in a w used for this t and potentially systematic reviews in order to enscess of RCTs wa

n was based on n the full-text of se second revieweewer (JV).

treatment for adult

en Holdt abstract. esomer)

After this

ck critical e critical

(not yet

ew. dent that way that

review. relevant

w and to sure the s similar title and selected r (KHH).

2Fwk••

Fait‘uCreowaina

2DteFincw

t cancer patients

2.6 Quality apFor the quality apwas used (see apkey for labelling a Item 3: Was a Item 7: Was t

documented? Item 9: Were

appropriate?For the quality apassessing risk of tem includes threunclear risk of biaCochrane Handboegarding detectio

outcomes (e.g. suwas labelled as loaccording to the cndividual study, tappendix 4).

2.7 Grading oData extraction wemplate for evideFor each clinical ndividual treatmeconclusion using twas down- or upgr

ppraisal ppraisal of systemppendix 1). Three

review as high qua comprehensive lhe scientific quali

? e the methods us

ppraisal of RCTsbias3 was used

ee categories: ‘lowas’. For each criteook3 were used. on bias and attribjective and objeow risk of bias, ucriteria described the risk of bias is

of evidence was done by onnce tables (see aquestion, conclu

nt outcomes. A lethe GRADE systeraded based on p

matic reviews, theitems of this che

uality: literature search pty of the included

sed to combine t

, the Cochrane C(see appendix 1w risk of bias’, ‘herion the definitioIf applicable, risktion bias were active outcomes). Aunclear risk of bia

in the Cochrane s reported in the

ne reviewer usinppendix 4).

usions were formevel of evidence em4 (Table 2). T

predefined criteria

KCE Report

e AMSTAR instruecklist were consid

performed? studies assessed

the findings of st

Collaboration’s to). Judgement of high risk of bias’ns as described ik of bias for the assessed per claAt the end, each as or high risk ofHandbook3. For

evidence tables

ng the standard

mulated at the levwas assigned to he quality of evid(Table 3).

t 185

ument dered

d and

tudies

ol for each , and in the items

ass of study f bias each (see

KCE

vel of each

dence

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KCE Report 185

Table 2 – Leve

Quality level High

Moderate

Low

Very low

Table 3 – DowStudy designRCT

Observational

5

els of evidence ac

Definition We are very conestimate of the We are moderalikely to be closthat it is substanOur confidence substantially difWe have very lilikely to be subs

n- or upgrading QualityHigh Modera

study Low Very lo

ccording to the G

nfident that the trueffect

ately confident in te to the estimate ntially different in the effect estim

fferent from the esttle confidence in stantially different

the evidence accy of evidence

ate

ow

Exercise t

GRADE system

ue effect lies close

he effect estimateof the effect, but t

mate is limited: thestimate of the effethe effect estimatfrom the estimate

cording to the GLower if Risk of bias: -1 Serious -2 Very serious Inconsistency: -1 Serious -2 Very serious Indirectness: -1 Serious -2 Very serious Imprecision: -1 Serious -2 Very serious Publication bias:-1 Likely -2 Very likely

treatment for adult

e to that of the

e: the true effect isthere is a possibil

e true effect may bect te: the true effect e of the effect

RADE system Higher if Large effect: +1 Large +2 Very large Dose respons+1 Evidence o All plausible co+1 Would redu+1 Would sugg

t cancer patients

MethodologRCTs withouobservationa

s ity

RCTs with imflaws, indirecobservationa

be RCTs with veseries is

e: of a gradient

onfounding: uce a demonstrategest a spurious ef

gical quality of suut important limitaal studies mportant limitationct, or imprecise) oal studies

ery important limit

ed effect ffect when results

upporting evidentions or overwhel

ns (inconsistent reor exceptionally st

tations or observa

s show no effect

nce ming evidence fro

esults, methodologtrong evidence fro

ational studies or c

11

om

gical om

case

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12

2.8 FormulBased on the rewas prepared btogether with th2 weeks prior toccasion (22 Mchanged if imdiscussion meegrade of recomthe GRADE symore circulated

Table 4 – Strsystem

Grade Defin

Strong The dunde

Weak The dunde

lation of recometrieved evidenceby a small workinhe evidence tableto the face-to-fac

May 2012) to discuportant evidenceetings a second dmmendation was ystem (Table 4 ad to the guideline d

rength of recom

nition

desirable effects oesirable effects, or

desirable effects oesirable effects, or

mmendations e, a first draft of ung group (KH, ADs was circulated t

ce meeting. The euss the first draft.e supported this draft of recommen

assigned to eacnd Table 5). Thedevelopment grou

mmendations acc

of an intervention r clearly do not

of an intervention r probably do not

Exercise t

pdated recommenD, SH, JV). This fto the expert grouexpert group met. Recommendatio

change. Based ndations was preph recommendatioe second draft wup for final approv

cording to the

clearly outweigh

probably outweig

treatment for adult

ndations first draft up about t on one ons were

on the pared. A on using

was once val.

GRADE

the

gh the

T

F

Bdue

Qe

Vp

Ca

t cancer patients

Table 5 – Factors

Factor

Balance betweendesirable and undesirable effects

Quality of evidence

Values and preferences

Costs (resource allocation)

s that influence t

Comment

n The larger theundesirable estrong recommthe gradient, trecommendat

The higher thelikelihood that

The more valugreater the unthe higher therecommendat

The higher thegreater the relikelihood that

he strength of a

e difference betweffects, the higher mendation is warrthe higher the liketion is warranted

e quality of evident a strong recomm

ues and preferencncertainty in valuee likelihood that a tion is warranted

e costs of an intersources consumet a strong recomm

KCE Report

recommendatio

een the desirable the likelihood tha

ranted. The narrowelihood that a wea

nce, the higher themendation is warra

ces vary, or the es and preferenceweak

rvention – that is, ed – the lower themendation is warra

t 185

n

and t a wer

ak

e anted

es,

the e anted

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KCE Report 185

3 SEARC3.1 SystemThe searches y

Database Cochrane DataMedline PreMedline EMBASE DARE HTA databaseNational GuideAfter a review ofull-text review.papers fulfilled systematic reviecomprised a cConsequently ireference lists search on priminclusion of all r

5

CH RESULmatic reviews yielded the followin

abase of System

eline Clearinghoof title and abstra Based on the futhe inclusion cri

ews it became evcomparably defint was decided toof the systemat

mary studies durirelevant studies.

LTS

ng number of hits

matic Reviews

use ct (2 931 hits) 68

ull-text (and the qteria1,2,5-25. After

vident that no recened study populo select relevant tic reviews and tng the full period

Exercise t

per database:

Number of hits89

1 68523

1 0666161

papers were seleuick critical appraa review of the

ent systematic revation for this gprimary studies fto perform an add in order to ens

treatment for adult

9536

6

ected for aisal) 24 selected

view fully uideline. from the dditional sure the

t cancer patients 13

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14

3.2 RandoThe search for 44 primary studThe additional fulfilled the incselected for the

Database CENTRAL Medline PreMedline EMBASE

mized controlleprimary studies t

dies of which 25 fusearch for primaclusion criteria.

e report26-59.

ed trials hrough the refereulfilled inclusion crry studies revealeThus, in total 3

Exercise t

ence lists initially rriteria. ed 67 studies of

33 primary studie

Number of hits132191

22 088

treatment for adult

revealed

which 8 es were

2

28

t cancer patients KCE Reportt 185

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KCE Report 185

4 EVIDE4.1 Breast A total of 12 stour predefined 242, with a meintensity seatedexercise progra

4.1.1 Qualit

4.1.1.1 InstFive RCTs repinterventions44,4

remaining had measurement sWHOQOL-BREEstimates of thephysical subscaTwo small studoverall QOL. Oand the other found no signifiOne small stud(p<0.001, WHOeffect on physsubscale45.

5

ENCE REPOcancer

tudies on breast coutcomes were

ean of 92 womed exercise prograams at targeted he

ty of Life

titution-based inported quality of 45,49,53,56. One stuan either moderascales varied an

EF and SF-36 withe effect of institutiales of QOL differdies reported a

One study found tstudy at 12 weecant effect on ovedy found a positiOQOL-BREF subsical subscales44,5

ORT

cancer patients aincluded. Samplen. Interventions am48 to progresseart rate or maxim

terventions life (QOL) measuudy had a low ate44,45,49,53,56 or hd included FACT

h some studies usion-based exercisred widely across positive effect ofthe effect at 5 weeks (FACT-G)44. erall QOL at any mve effect on a pscale “physical”)49

53,56. One study d

Exercise t

assessing one or e size ranged froranged from a mive aerobic or re

mal repetitions45.

ures for institutiorisk of bias53, w

high risk of bias44

T-G, FACT-B, FAsing more than onse on quality of lifethe studies (Table

f supervised exereeks (WHOQOL-The three larger

measure point45,53

hysical subscale 9. Three studies fdid not report a

treatment for adult

more of om 22 to moderate

sistance

on-based while the

,49. QOL ACT-AN, e scale. e and on e 6). rcise on BREF)49 r studies 3,56.

of QOL found no physical

C•

t cancer patients

Conclusions Conflicting e

exercise treapatients (ver2007, Mutrie

Conflicting eexercise treabreast cance2005, Hwang

evidence is availaatment on overry low level of e2007, Hwang 200

evidence is availaatment on physer patients (ver

g 2008, Mutrie 200

able on the effecrall quality of lievidence; Camp08, Segal 2001).able on the effecsical subscales ry low level of 07, Segal 2001).

ct of institution-bife in breast ca

pbell 2005, Cour

ct of institution-bof quality of lievidence; Cam

15

based ancer rneya

based fe in

mpbell

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16

Table 6 – Effec

Study N

Courneya 200745

N=

Mutrie 200753

N=

Segal 200156

N=

Hwang 200849

N=

Campbell 200544

N=

* Data on the 83

ct of institution-b

Overall

=242 No effec(measurfor any ointerventest (meand at 6

=203 No effecany meaEffect foweeks (months

=123* No effecFACT-B

=40 PositiveWHOQO

=22 Positive(p=0.46)No effec

women receiving ch

based exercise o

QOL

ct on overall QOLred by FACT-AN) of the two

ntion arms at post-edian 17 weeks) 6-months follow-up

ct for FAGT-G at asure point or FACT-B at 12 p=0.0007) and 6 (p=0.039)

ct for FACT-G andB

effect for OL-BREF (p<0.00

effect FACT-G ) ct for FACT-B

hemotherapy are re

Exercise t

on quality of life (

Physical su

-

p

No physical reporting

No effect for “Physical” (Fmeasure poi

d No effect for functioning” institution-bafor patients rchemotherapoutcome)

01)Positive effe(WHOQOL-B“physical”)

No effect for being” subsc

eported.

treatment for adult

(QOL) and physi

bscale

subscale

subscale FACT-G) at any nt

“physical (SF-36) in

ased study arm receiving py (primary

ct, p<0.001 BREF subscale

“physical well-cale (FACT-B)

t cancer patients

cal subscales of

Measure point

Baseline Post-test (med17 weeks) 6-months followup

Baseline 12 weeks 6 months (folloup)

Baseline 26 weeks

Baseline 5 weeks

Baseline 12 weeks

f QOL in patients

t(s) Interventio

ian

w-

RET (resistrepetitions amaximum AET (aerobergometer, VO2max Control groasked not to

w-

45 min of mweekly + anControl gro

Supervisedexercise at 2 other weeTwo controdirected execare i.e. ge

Exercise 3 xaerobic exeadjusted maControl grocould contin

Supervisedadjusted heControl gro

s with breast can

on characteristics

tance arm): 3 x weat 60-70% of one

bic arm): 3 x weektreadmill or ellipti

up received usuao initiate exercise

moderate level gron additional exercup received usua

arm: exercise 3 xprescribed pace)

ekdays l groups, one grouercise and one grneral advice

x weekly for 50 mercise). Heart rateaximum up performed shonue their normal a

exercise 2 x weeeart rate maximumup received usua

KCE Report

ncer

s

eekly 2 sets of repetition

kly on cycle cal at 60% of

l care and were e program

oup exercise 2 x cise session at homl care

x weekly (walking + exercise at hom

up performed selfroup received usu

min (stretching and: 50-70% of age

oulder exercises aactivities

ekly at 60-75% agm l care

t 185

me

me

f-al

d

and

e

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KCE Report 185

4.1.1.2 HomSix RCTs (inclhome-based inlimitations. Foustudies had a h5D, EORTC Cstudies using mEstimates of thsubscales of QOOne study founlinear growth rquadratic growtOne 3-arm stusupervised inte(FACT-B, FACThome-based intOne study founat 3 months (pmonths (p=0.02Three studies measures for Qmeasured as le48 and one studstudy it was noon the SF-36 su

5

me-based intervuding a total of 4nterventions43,47,48

ur studies had ahigh risk of bias48,5

C30, FACT-G, FAmore than one scahe effect of homeOL differed acrossnd a positive effecrate difference bth rate difference udy compared a ervention or usualT-G), but an effetervention arm annd a positive effecp=0.006) and on 2). Neither of theshad an unclear

QOL43,48,51. One ofess decline in ovedy suggested no eot possible to asseubscale “Physical

ventions 453 patients) rep8,51,56,58. All studa moderate risk 58. QOL measuremACT-B, SF-36 a

ale. e-based exercise s the studies (Tabct on overall QOLbetween groups between groups (home-based exel care and found ect on SF-36 “phnd not in the supect on generic heaEORTC C30 “ph

se effects remaineor limited reportif these studies su

erall QOL (p=0.02effect for exerciseess whether there Functioning“ or n

Exercise t

ported QOL measdies had method

of bias43,47,51,56 ament scales includand FACIT-F wit

on QOL and on ble 7). L (FACT-G), meas(t70=3.76, p<0.0(t70=2.64, p=0.01ercise interventionno effect on over

hysical functioningervised interventioalth-related QOL hysical functionin

ed after 6-months4

ing of group comuggested a positiv254) in the exercise on overall QOL43

e was a suggestenot51.

treatment for adult

sures for dological and two ded EQ-th some

physical

sured as 01) and 1)58.

n with a rall QOL g” in the on arm56. (EQ-5D)

ng” at 3-47. mparison ve effect se group 3. In one ed effect

C•

t cancer patients

Conclusions Conflicting e

exercise treapatients (verHeadley 2004

Conflicting eexercise treabreast canceHaines 2010,

evidence is avaatment on overry low level of ev4, Segal 2001, Waevidence is avaatment on physer patients (very Headley 2004, M

ailable on the efrall quality of lividence; Cadmuang 2011).

ailable on the efsical subscales low level of evid

Mock 2005, Sega

ffect of home-bife of breast ca

us 2009, Haines 2

ffect of home-bof quality of li

dence; Cadmus 2l 2001).

17

based ancer 2010,

based fe of 2009,

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18

Table 7 – Effec

Study N

Segal 200156

N=

Mock 200551

N=

Haines 201047

N=

ct of home-based

Overall Q

=123* No effectFACT-B

=119 No repor

=89 Positive ehealth-re5D) at 3 No effect(EQ-5D)

d exercise on qu

QOL

t for FACT-G and

rting of overall QO

effect on generic elated QOL (EQ-months (p=0.006)t on generic QOLat 6 months

Exercise t

uality of life (QOL

Physical sub

Effect on SF-functioning” (patient receivchemotherapoutcome)

OL Unclear repocomparison m36 “Physical subscale)

)

Positive effecC30 physicalsubscale (p=months No effect on physical funcat 6-months

treatment for adult

L) and physical s

bscale

-36 “Physical (p=0.03) for ving py (primary

orting of group measures (SF-Functioning”

ct on EORTC l functioning

=0.02) at 3-

EORTC C30 ctioning subscale

t cancer patients

subscales of QOL

Measure point

Baseline 26 weeks

Baseline After interventioIntervention lendependent on leadjuvant therapweeks of radiot3-6 months of chemotherapy)

Baseline, 3, 6 amonths follow-u

L in patients with

t Inte

SelfweeprogTwosuprece

on ngth was ength of py (either 6 therapy or

Pre50-7with30 mConmaiPos39%28%

and 12-up

HommobprogexeConandPar3 m

h breast cancer

ervention charac

f-directed arm: Exekly performing a gram o control groups: opervised exercise eived usual care i

escription to exerc70% of maximumh 15 minutes walkmin as training prontrol group was enintain usual activitssible dilution of tr% of usual care gr% of the exercise g

me-based strengtbility and cardiovagram; recommend

ercises harder eventrol group participd flexibility activitierticipant adherenc

months than in the

KCE Report

cteristics

xercise at home 5progressive walk

one group performand one group .e. general advice

ise 5-6 x weekly a heart rate, startin

k that increased toogressed ncouraged to ty level reatment effect asroup exercised angroup did not

h, balance, shouldascular enduranceded to make ery 2-4 weeks pated in relaxationes ce higher in the firs

second 3 months

t 185

x ing

med

e

at ng o

s nd

der e

n

st s

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KCE Report 185

Wang 201158

N=

Cadmus 200943

N=

Headley 200448

N=

* Data on the 83 **Results provide*** Only data from**** The mean debin/discuss/msg.c

5

=72 FACT-G the 2 grodifferent rate (t70=and quad(t70 = 2.6

=50*** Unclear r(FACT-Bgroup comeasureAuthors ssignifican

=32 StatisticsendpointOverall Qdeclined Exercise slower ragroup (p=graphicaresults)

women receiving ched in text and graphm IMPACT study arecrease of -1.5 poincgi?msg=1592).

change between oups significantly at linear growth =3.76, p <0.001) dratic growth rate 64, p=0.011)**

reporting of QOL B and FACT-G)

mparison s suggest no nce

s between s not provided

QOL (FACIT-F) for both groups group declining a

ate than control =0.0254, only l presentation of

hemotherapy are rehs only. re retrieved. nts in the exercise g

Exercise t

No reporting subscales

Unclear repocomparison mSF-36 subscAuthors sugg(p<0.05) favogroup****

at

Insufficient dStatistics betnot providedPhysical wellsubscale): exdeclining at athan control, graphical preresults)

eported.

roup did not reach c

treatment for adult

of physical

orting of group measures on ale “physical” gest significance ouring usual care

ata reporting tween endpoints

l-being (FACIT-F xercise group a slower rate (p=0.0252, only

esentation of

clinical significance

t cancer patients

4 measure poinsurgery baselin24 hours prior tof chemotherapday of expectedwhich is 7-10 dchemotherapy and end of 6-weintervention (tim

Baseline 6 months

Baseline At the beginnincourse of chemfor 12 weeks (afour measurem

(information retriev

nts; Pre-ne (time 1), to first day py (time 2), d nadir, ays after (time 3) eeks

me 4)

6-w3 to

Lowhea60%

Con

30 mInstof ppartConbut to th64%exe

g of each motherapy a total of

ments)

30 musinProinteConexeany

ved from http://www

weeks, home-baseo 5 sessions per w

w to moderate inteart rate maximum %

ntrol group receive

min of activity 5 dtructed to maintainpredicted maximumticipant received wntrol group could ethe study program

hese patients % of participants mercising 150 min p

min of seated exeng a commercially

ogram consisted oensity repetitive mntrol group receiveercises but were py usual physical ac

w.sf-36.org/cgi-

ed, walking prograweek

ensity measured b(HR max) from 40

ed usual care

ays weekly. n activity at 60-80m heart rate. Eacweekly phone callexercise if they chm was not availab

met the goal of per week

ercise 3 x weekly y available video of 20 min moderateotion exercise ed no specific

permitted to continctivity

19

am,

by a 0 to

0% h ls hose ble

e-

nue

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20

4.1.1.3 AerNine RCTs rinterventions43-4

remaining had aQOL measureWHOQOL-BREone scale. Estimates of thesubscales of QO

Overall qualityTwo studies foOne of these stas linear growtgrowth rate d(N=40) found aBREF (p<0.001One small studoverall QOL melarger study (N(p=0.0007) andTwo studies fouby FACT-AN anTwo other studmeasures for Qmeasured as lesuggested no e

robic interventionreported quality 45,48,49,51,53,56,58. Onan either moderatement scales inEF, FACIT-F and

e effect of aerobicOL differed widely

y of life ound a positive etudies (N=72) fouth rate difference ifference betweea positive effect 1)49. dy (N=22) found easured by FACTN=203) found a d 6 months (p=0.0und no effect of and (FACT-G + FAies had an unclea

QOL43,48. One of ess decline in QOeffect for exercise

ns of life (QOL)

ne study had a lote43,45,51,56 or high ncluded FACT-GSF-36 with some

c exercise on quay across the studi

ffect of aerobic end a positive effebetween groups

en groups (p=0.0on overall QOL

a positive effecT-G (p=0.46), but

positive effect fo39) and no effect

aerobic exercise oACT-B), respectivear or limited reporthese studies su

OL in the exercison overall QOL43

Exercise t

measures for w risk of bias53, wrisk of bias44,48,49,

G, FACT-B, FAe studies using mo

lity of life and on pes (Table 8).

exercise on overact for FACT-G, m(p<0.001) and q

011)58. The othemeasured by WH

t of aerobic exeno effect for FACor FACT-B at 12for FACT-G53.

on overall QOL mely45,56. rting of group comggested a positiv

se group48 and on.

treatment for adult

aerobic while the 58.

ACT-AN, ore than

physical

all QOL. measured quadratic er study HOQOL-

rcise on CT-B44. A 2 weeks

measured

mparison ve effect ne study

POmO(bTbTmpoSwOm

t cancer patients

Physical subscalOne small study (Nmeasured by WHOOne study found SF-36) for patien

but not for patientsTwo studies did nby “physical” (FACTwo studies had measures for physpositive effect on other study suggeSF-36 subscale “pwhether there wasOne study did nmeasure45.

le of quality of lifN=40) found a poOQOL-BREF subsan effect of aero

nts in a self-direcs in a supervised not find an effect CT-GP)53 and by “

an unclear or lsical QOL subscaphysical well-bei

ested an effect (p<physical”. In anoths a suggested effeot include a phy

fe ositive effect of aescale physical (p<obic exercise on

cted (home-based(institution-basedfor physical QOLphysical well-beinlimited reporting ales. One of thesng (FACIT-F sub<0.05) in favour oher study it was nect or not51. ysical QOL subs

KCE Report

robic exercise on<0.001)49.

“physical functiod) study arm (p=0) study arm56.

L subscales, measng” (FACT-B)44.

of group compae studies sugges

bscale; p=0.0252)of the control grounot possible to as

scale as an out

t 185

QOL

oning” 0.03),

sured

arison sted a . The up on ssess

come

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KCE Report 185

Table 8 – Effec

Study NCourneya 200745

N=

Mutrie 200753

N=

Mock 200551

N=

Segal 200156

N=

Wang 201158

N=

5

ct of aerobic inte

Overall =242 No effec

measure

=203 No effecmeasureEffect fo(p=0.000(p=0.039

=119 No repor

=123* No effecFACT-B

=72 FACT-G2 groupsat linear

erventions on qu

QOL ct (FACT-AN) at ae point

ct for FAGT-G at ae point r FACT-B at 12 w07) and 6 months 9) rting of overall QO

ct for FACT-G and

change betweens significantly diffegrowth rate (t70=

Exercise t

ality of life (QOL

Physical ny No physic

any

weeks

No effect G) at any

OL Unclear r36 “Physisubscale measures

d No effect functionininstitutionpatients rchemothePositive e“Physicalfor patienreceiving

the erent =3.76,

No reportsubscales

treatment for adult

L) and physical s

subscale cal subscale repo

for Physical (FACy measure point

reporting of MOS Sical Functioning” group compariso

s

for “physical ng” (SF-36) in n-based study armreceiving erapy effect on SF-36 functioning” (p=0

nt in self-directed achemotherapy

ting of physical s

t cancer patients

ubscales of QOL

Measure prting Baseline

Post-test (weeks) 6-months

CT- Baseline 12 weeks6 months

SF-

n

Baseline After intervInterventiodependenadjuvant th6 weeks oor 3-6 monchemothe

m for

0.03) arm

Baseline a

4 measuresurgery ba1), 24 hou

L in patients with

point

(median 17

follow-up

A

(follow-up)

vention on length was t on length of herapy (either

of radiotherapy nths of rapy) and 26 weeks

e points; Pre-aseline (time rs prior to first

h breast cancer

Intervention chaAET (aerobic armcycle ergometer, beginning at 60%

See Table 6

See Table 7

Supervised arm: e(walking exercise+ expected to exeother weekdays Self-directed arm5 x weekly. Particprogressive walki60% of maximal oControl group recgeneral advice See Table 7

aracteristics m): 3 x weekly on

treadmill or elliptic% of VO2max

exercise 3 x weeke at prescribed pacercise at home 2

: Exercise at homcipants performedng program at 50

oxygen uptake ceived usual care

21

cal

kly ce)

me a

0-

i.e.

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22

Study N

Cadmus 200943

N=

Hwang 200849

N=

Headley 200448

N=

Campbell 200544

N=

* Data on the 83 ** Results provide*** Only data from**** The mean debin/discuss/msg.c

Overall p<0.001rate (t70

=50*** Unclear (FACT-BcomparisAuthors significa

=40 Positive BREF (p

=32 Statisticsnot provOverall Qdecline fExerciseslower ra(p=0.025presenta

=22 Positive (p=0.46)No effec

women receiving ched in text and graphm IMPACT study arecrease of -1.5 poincgi?msg=1592)

QOL ) and quadratic gr

0=2.64, p=0.011)**

reporting of QOLB and FACT-G) grson measures. suggest no nce

effect for WHOQOp<0.001)

s between endpoiided QOL (FACIT-F) for both groups e group declining aate than control g54, only graphical ation of results)

effect FACT-G ) ct for FACT-B hemotherapy are rehs only. re retrieved. nts in the exercise g

Exercise t

Physical rowth *.

roup Unclear rcomparis36 subscaAuthors s(p<0.05) fgroup****

OL- Positive e(WHOQO“physical”

nts

at roup

InsufficienStatistics not providPhysical wsubscale)declining control (pgraphicalresults) No effect being” su

eported.

roup did not reach c

treatment for adult

subscale

reporting of group on measures on Sale “physical”

suggest significanfavoring usual car

* effect, p<0.001 OL-BREF subscale”) nt data reporting. between endpoin

ded well-being (FACIT): Exercise group at a slower rate t

p=0.0252, only presentation of

for “physical wellbscale (FACT-B)

clinical significance

t cancer patients

Measure pday of che(time 2), dexpected n7-10 days chemotheand end ointerventio

SF-

ce re

Baseline 6 months

e Baseline 5 weeks

nts

T-F

han

Baseline At the begcourse of cfor 12 weefour meas

- Baseline 12 weeks

(information retriev

point emotherapy ay of nadir, which is after

rapy (time 3) f 6-weeks

on (time 4)

ginning of each chemotherapy eks (a total of urements)

ved from http://www

Intervention cha

See Table 7

See Table 6

See Table 7

See Table 6

w.sf-36.org/cgi-

KCE Report

aracteristics

t 185

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KCE Report 185

Conclusions • Conflicting

on overallof evidenHeadley 22001,Wang

• Conflictingon physic(very lowCourneya2001, Mutr

4.1.1.4 ResOne three-arme(FACT-AN) for observed no eintervention or reported45.

Table 9 – Effec

Study

Courneya 200745

5

g evidence is av quality of life fo

nce; Cadmus 202004, Hwang 2g, 2011). g evidence is aval subscales of

w level of evide2007, Headley

rie 2007).

sistance intervened RCT, with a mr a resistance exeffect on overal

at 6-months fol

ct of resistance i

N O

N=242 Npwfo

vailable on the efor breast cancer 009, Campbell

2008, Mock 200

vailable on the efquality of life forence; Cadmus 2004, Hwang 2

ntions moderate risk of bxercise interventiol QOL for resisllow-up. No phys

nterventions on

Overall QOL

No effect (FACT-Apost-test (median weeks) or at 6-moollow-up

Exercise t

ffect of aerobic epatients (very lo2005, Courneya

05, Mutrie 2007

ffect of aerobic er breast cancer p2009, Campbel

008, Mock 2005

ias, reported overon (Table 9). Thtance exercise asical QOL subsc

quality of life (Q

Phys

AN) at 17

onths

No p

treatment for adult

exercise ow level a 2007, 7 Segal

exercise patients ll 2005, 5, Segal

rall QOL he study at post-ale was

QOL) and physica

sical subscale

hysical subscale

t cancer patients

al subscales of Q

Meas

reporting BaselPost-tweeks6-mon

QOL in patients w

sure point

line test (median 17 s) nths follow-up

with breast cance

Intervention c

RET (resistancsets of repetitioestimated one Control group and were askeexercise progra

er

characteristics

ce arm): 3 x weekons at 60-70% of repetition maximureceived usual ca

ed not to initiate am

23

kly,

um are

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24

Conclusion • Very little

overall quevidence;

4.1.1.5 ComOne RCT, with resistance exeoverall effect osubscale “physpersist at the 6

Table 10 – Effecancer

Study

Haines 201047

evidence existsality of life for bCourneya 2007)

mbined aerobic a moderate risk

ercise interventionn QOL (EQ-5D) a

sical functioning” months assessm

ect of combined

N O

N=89 Ph5N(

s on the effect obreast cancer pa.

and resistance eof bias, deployedn (Table 10). That 3 months (p=0at 3 months (p=ent47.

aerobic and res

Overall QOL

Positive effect on ghealth-related QO5D) at 3 months (pNo effect on geneEQ-5D) at 6 mont

Exercise t

f resistance traiatients (very low

exercise intervend a combined aerohe authors obse.006) and on the 0.02). The effect

sistance interven

Phys

generic L (EQ-p=0.006) ric QOL ths

Positphys(p=0No ephysat 6-m

treatment for adult

ning on level of

ntions obic and rved an EORTC

t did not

ntions on quality

sical subscale

tive effect on EORical functioning su.02) at 3-monthsffect on EORTC Cical functioning sumonths

t cancer patients

y of life (QOL) an

Meas

RTC C30 ubscale

C30 ubscale

Baselmonth

nd physical subs

sure point

line, 3 and 6 hs

scales of QOL in

Intervention c

See Table 2

KCE Report

n patients with b

characteristics

t 185

breast

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KCE Report 185

Conclusion • Very little

and resistsubscaleslevel of ev

4.1.2 CardioFour RCTs repVO2max, heart institution-basepatients undermoderate risk VO2max measurelative VO2maxand maximum the 12-minute wEstimates of thefunction differedFour RCTs repcapacity measucancer patientreported an efexercise compap=0.004; VO2 mexercise compa0.01-0.18], p=0Similarly, one measured by thhad covered a the usual care gRCT found no Vcontrol or for aonly patients un

5

evidence existstance exercise

s of quality of lifvidence; Haines 2

opulmonary funcported changes rate [HR] or aerobd or home-basedrgoing adjuvant of bias45,56 and

ures included abx (ml/kg/min)45,56. HR (beats/min)50

walk test55. e effect of exercisd across the studi

ported changes inured by a walk tes undergoing adffect on both abared with usual caml/kg/min: MD 1.8ared with resistan0.035; VO2 ml/kg/RCT found an ehe 12-minute walgreater distance

group (p=0.002 foVO2 effect for a sea supervised interndergoing adjuvan

s on the effect intervention on fe for breast ca2010).

ction in cardiopulmonabic capacity measd exercise intervetherapy. Two otwo studies had

bsolute VO2max (Heart rates were

. One RCT meas

se interventions onies (Table 11).

n VO2max, heart rest after exercisedjuvant therapy. bsolute and relatare (VO2 l/min: MD8 [95%CI 0.5-3.2], nce exercise (VO/min: MD 1.6 [95%effect for an aerolk test. After 6 min the test than t

or difference betwelf-directed intervervention arm comnt therapy were co

Exercise t

of a combined quality of life

ncer patients (v

ary function (chasured by a walk teentions for breastof these studies a high risk of (ml/min or l/min)4

e measured as ressured aerobic cap

n cardiopulmonary

rate measures ore interventions fo

One three-armetive VO2max for D 0.13 [95%CI 0.0

p=0.006) and forO2 l/min: MD 0.09 %CI 0.3-2.9), p=0

obic exercise inteonths the exercisthe resistance gro

ween groups)55. Oention arm compa

mpared with contronsidered56.

treatment for adult

aerobic and on

very low

anges in est) after t cancer

had a bias50,55. 45,50 and sting HR pacity by

y

r aerobic or breast ed RCT

aerobic 04-0.22], r aerobic

[95%CI 0.014)45.

ervention se group oup and ne other

ared with rol when

SV

C•

t cancer patients

Similarly, one smaVO2max or heart r

Conclusions Conflicting e

on cardiopulbreast cance2007, Segal 2

Evidence sugexercise in im(low level of

all RCT (N=41) foate measures afte

evidence exists omonary functioner patients (ver2001, Schwartz 2ggests that aeromproving aerobevidence; Courn

ound no significaner an exercise inte

on the effect of en (VO2max, heartry low level of 2007, Kim 2006).bic exercise is sic capacity in br

neya 2007, Schw

nt group differencervention50.

exercise intervet rate or walk tesevidence; Cour

superior to resistreast cancer patartz 2007).

25

ce for

ntion st) for rneya

tance tients

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26

Table 11 – EffeStudy N

Courneya 200745

N

Segal 200156

N

ect of exercise trN Absolu

(ml/mi

N=242 Effect fexercisusual cin l/minMD 0.10.04-0 Effect fexercisresistameasuunadju(95%Cp=0.03 No efferesistaversus

N=123* Not rep

reatment on cardute VO2max n or l/min)

for aerobic se versus care measured n; unadjusted 13 (95%CI .22, p=0.004)

for aerobic se versus ance exercise ured in l/min; usted MD 0.09 CI 0.01-0.18, 35)

ect for ance exercise s usual care ported

Exercise t

diopulmonary funRelative VO2max(ml/kg/min)

Effect for aerobicexercise versus ucare; unadjusted (95%CI 0.5-3.2, p=0.006) Effect for aerobicexercise versus resistance exerciunadjusted MD 1(95%CI 0.3-2.9, p=0.014)

No effect for self-directed interventarm compared wcontrol* No effect for supeintervention arm compared with co

treatment for adult

nction in patientsx Other

cardiofunctiomeasu

c usual MD 1.8

c

ise; .6

Not rep

-tion

with

ervised

ontrol*

Not rep

t cancer patients

s with breast can

pulmonary on ures

Me

ported BaPo17 6-m

ported Ba26

ncer easure point

seline st-test (median weeks)

months follow-up

seline weeks

Intervention c

See Table 6

See Table 8

KCE Report

characteristics

t 185

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KCE Report 185

Schwartz 200755

N

Kim 200650 N

* Data on the 83 ** The p-value re*** 11 of 74 randothrombophlebetisof these 33 wome**** Only interven

5

N=66 Not rep

N=41*** No sigdifferen(ml/min

women receiving cheflects the significanomized women withs (n=2), non-exercisen participated or pntion group showed

ported

nificant group nce in VO2max n)****

hemotherapy are rent difference betweehdrew from the studse related injuries (nartly participated in

d significant positive

Exercise t

Not reported

Not reported

eported. n the three groups.

dy for reasons includn=1) or death (n=1).

the exercise intervechanges in VO2 pe

treatment for adult

After 6 aerobicgroup hcoveredistanc-minute(p=0.02

No signgroup dresting maximurate (beats/

ding personal proble Another 22 womenention. Study reportak and resting HR o

t cancer patients

months the c exercise had d greater

ce on the 12 e walk test 2)**

Ba

6 minte

nificant difference in or

um heart

/min)****

Ba8 winte

ems (n=2), problemn did not complete ets on 41 women. over time but measu

seline

months (post-ervention)

seline weeks (post-ervention)

s at home (n=2), preither pre- or post-in

ures did not reach s

Aerobic arm: hinstructed to cactivity they enor jogging) and30 min four da

Resistance armexercise at howeek using Thband and tubinwere instructedusual activities

Institution baseindividually preexercise 3 dayIntensity correof individuals hControl group including genebenefits of exe

roblems related to cntervention exercise

significance in group

home-based, hoose an aerobicnjoyed (e.g. walkind exercise for 15-ays per week

m: instructed to me four days per

hera-Band resistanng. Control group d to continue withs

ed, supervised anescribed aerobic ys weekly for 30 msponding to 60-70heart rate reservereceived usual ca

eral information onercise

chemotherapy (n=3)e tests. It is unclear

p difference.

27

c ng

nce

h

nd

min 0%

e are n

, if any

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28

4.1.3 FatiguEight RCTs onoutcome measuremaining hadFatigue measuMulti-dimensionF, FACIT-F subSix of the studdeployed a comother RCT waresistance trainwere institution-Estimates of thstudies and didinstitution- or hexercise type cStudies are sumreporting, suggpatients. One control group hdecrease in fatifatigue level ((p<0.05)49. Onegroup had lessgroup (p=0.007aerobic, home-F at two out ochemotherapy days after cheobserved (p<0.point 4) the stud

ue n exercise treatmures on fatigue. O an either modrement scales vanal fatigue inventobscale “Fatigue”, Bdies were on aembined aerobic as a three-arm st

ning intervention a-based44,45,49,53 ane effect of exercis not seem to be dome-based. Neithchosen for the trimmarized in Tablgested an effect

aerobic and inshad an increase igue and that ther(measured by Be small home-bass decline in fatig78), measured bybased RCT found

of three measure (measure point 2

emotherapy (mea001) and, similardy suggested an e

ment for breast cOne study had a lo

erate45,47,51 or hried and includedory, FACT-AN suBrief Fatigue Inverobic interventionnd resistance exetudy with an aer

arm and a control nd four were homese treatment on fadependent on wheher did the resultsial (aerobic, resise 7. Two RCTs, bof exercise on f

stitution-based stin fatigue, that thre was a significa

Brief Fatigue Invesed study sugges

gue over time coy the FACIT-F sd an effect on fati

points: 24 hours2) no effect was oasure point 3) aly, at the end of teffect on fatigue (

Exercise t

cancer patients ow risk of bias53, wigh risk of bias4

d the Piper Fatiguubscale “Fatigue”,ntory and FACT-Fns44,48,49,51,53,58. Oercise interventionrobic interventiongroup45. Four of t

e-based47,48,51,58.atigue differed acether the intervens seem to depend

stance or a combboth with insufficifatigue for breasttudy suggested the exercise grou

ant difference in thentory) between sted that the inte

ompared with theubscale “Fatiguegue measured bys prior to the firsobserved for fatigun effect for fatigthe intervention (mp<0.001).

treatment for adult

reported while the 44,48,49,58. e Scale, FACIT-

F. ne RCT n47. One arm, a the trials

cross the tion was d on the

bination). ent data t cancer that the p had a he mean

groups ervention e control ”48. One

y FACIT-st day of ue, 7-10 gue was measure

Fpbaa

C•

t cancer patients

Five RCTs foundpatients44,45,47,51,53.based44,45,53 and haerobic interventioan intervention wit

Conclusions Conflicting e

fatigue for bMutrie 2007, 2005, Headle

The evidencewas superiorversa.

The evidencsuperior to re

d no effect of e. These RCTs home-based interons44,51,53, aerobicth both aerobic an

evidence exists obreast cancer pa

Courneya 2007ey 2004, Hwang 2e did not indicatr to home-based

ce did not indicesistance exerci

exercise on fatigwere a combi

rventions47,51, andc versus resistannd resistance elem

on the effect of eatients (very low, Mock 2005, Ha

2008, Wang 2011te whether institd exercise in red

cate whether aese in reducing fa

KCE Report

ue for breast caination of institud additionally a mce interventions45

ments combined47

exercise treatmew level of evideaines 2010, Cam).

tution-based exeducing fatigue or

erobic exercise atigue or vice ve

t 185

ancer ution-

mix of 5 and

7.

nt on ence;

mpbell

ercise r vice

was rsa.

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KCE Report 185

Table 12 – Effe

Study

Courneya 2007

Mutrie 200753

Mock 200551

Haines 201047

Wang, 201158

Hwang 200849

Headley 20044

5

ect of exercise tr

N F

745 N=242 N“(

N=203 N(

N=119 Np

N=89 NFt“

N=72 FStp

N=40 IgddF

8 N=32 Ip

reatment on fatig

Fatigue

No effect for fa“Fatigue”) for any(median 17 weeks

No effect for fati(post-intervention)

No effect for fatigpost-intervention*

No effect for any mFatigue was measthat includes sca“reduced activity”,FACIT-F: Significant differenthe “nadir”, (time 3program (time 4: p

nsufficient data isgroup had a incredecrease in fatigdifference in theFatigue Inventory)nsufficient data rprovided

Exercise t

gue in patients w

atigue (measuredy of the two intes) and at 6-month

igue (measured ) and at 6-months

gue (measured b

measures of fatigusured by “Multidimles on “general f “reduced motivat

nces between the3: p<.001) and at p<.001)**

s provided. Figurease in fatigue, tha

gue and that thee mean fatigue ) between groupsreporting. Statisti

treatment for adult

with breast cance

d by FACT-AN ervention arms ats follow-up

by FACT-F) at s follow-up

by Piper Fatigue

ue at 3 and 6 monmensional fatigue fatigue”, “physication” and mental f

e 2 groups detectthe end of the

e suggests that that the exercise groere was a signiflevel (measured (p<0.05) cs between endp

t cancer patients

er

Meas

subscale t post-test

BasePost-6-mo

12 weeks Base12 w6 mo

Scale) at BaseAfterIntervlengtweekof ch

nths inventory”

al fatigue”, fatigue”

Base3 mo6 mo

ed only at 4 baseday oexpeafter 6-we

he control oup had a ficance in

by Brief

Base5 we

points not BaseAt th

sure point

eline -test (median 17 wonths follow-up eline

weeks onths (follow-up) eline r intervention vention length wath of adjuvant thks of radiotherapemotherapy)

eline onths onths

measure pointeline (time 1), 24 hof chemotherapy

ected nadir, whicchemotherapy (ti

eeks intervention (eline eks

eline he beginning of

weeks)

as dependent on herapy (either 6 y or 3-6 months

ts; Pre-surgery hours prior to first

(time 2), day of ch is 7-10 days me 3) and end of

(time 4)

each course of

Intervention characteristics

See Table 6

See Table 6

See Table 7

See Table 7

f

f

See Table 7

See Table 6

fSee Table 7

29

s

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30

Campbell 2005

* Possible dilution** Results provide

4.1.4 SafetyAdverse eventscancer patientsobserved duringreporting of advof the included

Conclusion • There is

treatment Hwang 200

4.2 ProstatA total of four sof our predefine121 with a memoderate intenprogressive aeand maximal re

4.2.1 QualitThree RCTs recancer patientsmoderate risk measurement sFACT-P with so

Gfm

544 N=22 N

n of treatment effeced in text and graph

y s were reported is. All five RCTs rg the trial43,45,48,49

verse events44, 50,

studies.

evidence that e(low level of ev

08, Mutrie 2007,

te Cancer studies on prostaed outcomes wereean of 66 men. nsity, continuous robic or resistanc

epetitions57.

ty of Life ported QOL meass undergoing adj

of bias46,57 andscales varied andome studies using

Graph suggests tfatigue over timemeasured by FACNo effect for fatigu

ct as 39% of usual chs only.

n five of the 12 Rreported that no a,53.The remaining,51,55,56,58. Relapse

exercise is safevidence; CourneHaines 2010).

ate cancer patiente included. SampInterventions ranwalking exercise

ce exercise progra

sures for exercisejuvant therapy46,5

d one study a d included SF-36,g more than one s

Exercise t

that intervention e compared with CIT-F subscale “Faue measured by P

care group exercised

RCTs included oadverse events h

six RCTs did note was not reporte

e during breast eya 2007, Headle

ts assessing one ple size ranged froged from a hom59 to an institutioam at targeted he

e interventions in 52,57. Two studies

high bias risk5

, QLQ-C30, FACTscale.

treatment for adult

group had less control group (p

atigue” Piper Fatigue Sca

d and 28% of the ex

n breast ad been t include d in any

cancer ey 2004,

or more om 21 to

me-based on-based eart rate

prostate s had a 52. QOL T-G and

EQOoc2foOa(oOeQop

C•

t cancer patients

decline in p=0.0078),

chemfour m

le Base12 w

xercise group did no

Estimates of the eQOL differed acrosOne three-armed of aerobic exerciscancer patients57. 24 weeks (p=0.01or neither resistaOne other RCT wian effect for exep=0.022) 46. Fina

overall QOL, measOne RCT suggeexercise on SF-36QLQ-C30 “physicaon FACT-P “physiphysical subscale

Conclusions Conflicting e

quality of lievidence; Se

Conflicting ephysical sub(very low lev

motherapy for 12 measurements)

eline weeks

ot.

ffect of exercise oss the studies (TaRCT suggested a

se on overall QOThis effect was

5). The same stuance nor aerobic ith a combined reercise on QOLally, one RCT fosured by FACT-P

ested an effect 6 “physical healthal”46. One RCT sucal well-being” (pmeasures 57.

evidence exists ofe in prostate

egal 2009, Galvaoevidence exists obscales of quality

el of evidence; G

weeks (a total of

on QOL and on phable 13). an effect of resist

OL (measured byfound both at 12dy did not find anexercise when m

esistance and aeromeasured by Sund an effect fo(p=0.006)52. of combined ae

h composite” (p=0uggested an effec

p<0.001). One RC

on the effect of ecancer patients

o 2010, Monga 20on the effect of exy of life in prostaGalvao 2010, Mon

KCE Report

f

See Table 6

hysical subscales

tance exercise buy FACT-G) in pro weeks (p=0.017

n effect on overallmeasured by FACobic intervention fF-36 “general her aerobic exercis

erobic and resis0.02), but no effect for aerobic exe

CT did not include

exercise treatmes (very low lev007). xercise treatmen

ate cancer patiennga 2007).

t 185

of

ut not ostate ) and QOL CT-P. found ealth” se on

tance ect on ercise QOL

nt on el of

nt on nts

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S

S2

G2

M2

KCE Report 185

Table 13 – Effe

Study N

Segal 200957

N=12

Galvao 201046

N=57

Monga 200752

N=2

* 37.9% of exerci** Results provide

5

ect of exercise tr

QOL

21 Positive effecare at 12-wG; MD 4.76Positive effecare at 24-wFACT-G; MNo effect fomeasured bNo effect foany measur

7* Positive effemeasured b(95%CI 1.9

1 Positive effemeasured bp=0.006

ise group and 39.3%ed in text only.

reatment on qual

ect of resistance iweeks (midpoint) 6 (95%CI 0.86-8.6ect of resistance iweeks (post-interv

MD 4.34 (95%CI 0or aerobic intervenby FACT-G at anyor FACT-P in anyre point

ect for exercise vsby SF-36 “genera

9-23.9), p=0.022

ect for exercise vsby FACT-P; MD 1

% of control group w

Exercise t

lity of life in pros

intervention vs. usmeasured by FAC

65), p=0.017 intervention vs. usvention) measured.88-7.80), p=0.01ntion vs. usual cary measure point y intervention arm

s. usual care l health”; MD 12.9

s. usual care 3.8 (SD ±10.1),

were on radiation be

treatment for adult

state cancer pati

Physical s

sual CT-

sual d by 5 re

m at

Not reporte

9 Positive effexercise veusual care measured “physical hcomposite”(95%CI 0.8p=0.02 No effect foC30 “physi(p=0.062)*

Positive effFACT-P “pwell-being”(SD ± 2.0),

efore trial. 27.6% of

t cancer patients

ents

subscale Meas

ed BaseMidpoweekPost-(24 w

fect for ersus

by SF-36 health ”; MD 5.0 81-9.2),

or QLQ-ical” *

BasePost-(12 w

fect for physical ”; MD 3.6 , p<0.001

BasePost-week

f exercise group and

sure point(s) I

line oint (12

ks) intervention

weeks)

RerrA3t5Ut

line intervention

weeks)

ICaTm8C

line intervention (8

ks)

SwaaC

d 21.4% of control g

Intervention cha

Resistance exerciexercising 3 x perrepetitions at 60-7repetition) Aerobic training g3 x per week on atreadmill, or ellipti50-60% of VO2 peUsual care group to initiate exercise

Institution-basedCombined progresaerobic exercise 2The aerobic compmin of cardiovasc85% maximum heControl group: usu

Supervised aerobweekly for 8 weekaerobic exercise (at targeted heart rControl group: sta

group were on radia

racteristics

ise training group r week (2 x 8-12 70% of 1 maximum

roup (AET) exerca cyclo-ergometercal trainer beginn

eak (UC); UC was as

e

ssive resistance a2 x weekly for 12 wponent included 1cular exercise at 6eart rate ual care

bic exercise prograks consisting of 40(walking on a trearate andard care

tion during trial.

31

(RET)

m

cising ,

ning at

ked not

and weeks. 5-20 5% to

am 3 x 0 min admill)

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32

4.2.2 CardioThree RCTS refunction measucancer patientstwo had a high VO2max measumetabolic equivheart rate as rperformed a moEstimates of tfunction differed

Table 14 – Effe

Study

Segal 200957

Windsor 20045

Monga 200752

*No significant di

opulmonary funceported changes ured by a walk tes. One of these stbias risk52,59.

ures included relavalents (MET 3.5 resting HR and eodified shuttle testthe effect of exd across the studi

ect of exercise tr

N N=121

59 N=66

N=21

ifference between g

ction in VO2max, heartst after exercise tudies had a mod

ative VO2max (mlml O2·kg−1·min−1

exercise HR (beat pre- and post int

xercise interventioies (Table 14).

reatment on card

CardiopulmonPositive effect ointervention ver(post-interventioVO2max: MD 1p=0.041 No effect of theversus usual caNo effect of exeNo effect of exerate Significant diffeshuttle-test distintervention (p=

Effect of exercisfunction measuO2·kg−1·min−1p=0.006

groups were observe

Exercise t

t rate or cardiopuinterventions for

derate risk of bias

/kg/min)57 and re)52. One study m

ats/min) and, addtervention59. ons on cardiopu

diopulmonary fun

ary function of the resistance rsus usual care aton) measured by .5 (95%CI 0.06-3.

e aerobic interventare (p=0.052) ercise on resting hercise on exercise

erence between grtance at the end o=0.0025)*

se on cardiopulmored by MET (MET

1) ; MD 2.8 (SD ±1

ed at baseline.

treatment for adult

ulmonary prostate

s57, while

spective measured ditionally,

ulmonary

Oc0eoeHc

C•

nction in prostat

Mea

t 24-weeks relative .0),

tion

BasePostwee

heart rate e heart

roups in of

BasePostwee

onary T=3.5 ml 1.8),

BasePostwee

t cancer patients

One three-armed Rcardiopulmonary f0.06-3.0; p=0.041)exercise57. One oton MET (mean 2.8effect of exercise oHowever, the samcovered in a shuttl

Conclusion Conflicting e

cardiopulmolevel of evide

te cancer patient

asure point eline t-intervention(24 ks)

eline t-intervention (4 ks)

eline t-intervention (8 ks)

RCT observed anfunction in men wi). The same studyther RCT observe8; SD ± 1.8; p=0.0on neither resting

me study did obserle-test post-interv

evidence exists onary function inence; Segal 2009

ts

Intervention See Table 13

Home-basedwalking 3 dayradiotherapy.rate Control groupactivities but fatigue See Table 13

n effect for resistanith prostate cancey did not find an ed an effect after a

006)52. Finally, onenor exercise hea

rve a between-groention (p=0.0025)

on the effect of en prostate cance9, Windsor 2004,

characteristics3

, moderate-intensys weekly for 30 m Heart rate 60-70

p were not discouwere advised to r

3

KCE Report

nce exercise on er (MD 1.5; 95%Ceffect for aerobic an aerobic intervee RCT observed nrt rate measures.

oup effect on dista)59.

exercise treatmeer patients (veryMonga 2007).

sity, continuous min during % of maximum he

raged to perform rest if they becam

t 185

I

ntion no

ance

nt on y low

eart

e

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KCE Report 185

4.2.3 FatiguFour RCTs repocancer patientsmoderate risk Fatigue measuInventory (BFI)subscale “fatiguEstimates of the(Table 15). One three-arme(MD 4.64, 95%95%CI 0.87-7.measured by Fresistance exer24 weeks (MDpositive effect opositive effect wthe other studySD ± 2.1, p<0.any measure po

5

ue orted fatigue meas undergoing adjuof bias46,57 and rement scales va, revised Piper Fue”. e effect of exercis

ed RCT observedCI 1.47-7.80, p=035, p=0 .010) oACT-F after 12 wrcise maintained aD 4.78, 95%CI:1of exercise treatmwas measured by y the effect was m001)52. One RCToint (Brief Fatigue

asures for exerciseuvant therapy46,52

two studies hadaried and includeatigue Scale (PF

se on fatigue differ

d a positive effect 0.004) and resistan fatigue in me

weeks (mid-point)5

a significant effec.77-7.78, p=0.00

ment on fatigue. InQLQ-C30 subsca

measured by PipeT found no effect e Inventory)59.

Exercise t

e interventions in 2,57,59. Two studie a high risk of

ed FACT-F, Brief S-revised) and Q

red across the stu

for both aerobic ence exercise (me

en with prostate 57. In the same stuct after the interve02). Two RCTs n one of these stuale “fatigue” (p=0.r Fatigue Scale (Mof exercise on fa

treatment for adult

prostate es had a bias52,59. Fatigue

QLQ-C30

udies

exercise ean 4.11,

cancer, udy only

ention, at found a

udies the .21)46. In MD -4.3, atigue at

C•

t cancer patients

Conclusion Conflicting e

fatigue in prSegal 2009, W

evidence exists orostate cancer pWindsor 2004, Ga

on the effect of epatients (very loalvao 2010, Mon

exercise treatmeow level of evide

ga 2007).

33

nt on ence;

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34

Table 15 – EffeStudy N

Segal 200957

N

Windsor 200459

N

Galvao 201046

N

Monga 200752

N

* 37.9% of exerci** Results provide

ect of exercise trN Fatigue

N=121 Positive (midpoinPositive intervenPositive (midpoinNo effecinterven

N=66 No effec

N=57* Positive

N=21 Positive

ise group and 39.3%ed in text only.

reatment on fatige

effect of the resisnt) measured by F effect of the resistion) measured by effect of the aeront) measured by Fct of the aerobic intion)

ct of exercise on B

effect on QLQ-C

effect of exercise

% of control group w

Exercise t

gue in prostate c

stance interventioFACT-F; MD 4.11 stance interventioy FACT-F; MD 4.7

obic intervention vFACT-F; MD 4.64ntervention versus

Brief Fatigue Inven

30 subscale “fatig

e on Piper Fatigue

were on radiation be

treatment for adult

ancer patients

n versus usual ca(95%CI 0.87-7.35n versus usual ca78 (95%CI 1.77-7

versus usual care , (95%CI 1.47-7.8s usual care at 24

ntory at any meas

gue”, p=0.21**

e Scale : MD -4.3

efore trial. 27.6% of

t cancer patients

are at 12-weeks 5), p=0.010 are at 24-weeks (p7.78), p=0.002 at 12-weeks

80), p=0.004 4-weeks (post-

sure point

(SD ± 2.1), p<0.0

f exercise group and

Measure

post-

Baseline12 weeks 24 weeks interventio

BaselinePost-interv4 weeks aradiotheraBaselinePost-intervweeks)

001 BaselinePost-interv

d 21.4% of control g

point

(midpoint) (post-

on)

vention (week 4)after ended apy (week 8)

vention (12

vention (8 weeks)

group were on radia

KCE Report

Intervention characteristicSee Table 13

See Table 14

See Table 13

) See Table 13

tion during trial.

t 185

cs

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KCE Report 185

4.2.4 SafetyAdverse eventscancer patientparticipants exdeemed serioureported that noThe remaining Relapse was no

Conclusion • Limited ev

cancer pa2010).

4.3 Lung cThe evidence overy limited. Twsame single RC

4.3.1 QualitArbane et al.2(NSCLC) underpreoperative howas continued was measured measured preohad a moderateThere were no preoperative asbased programintervention grcomponents of between the twin exercise grocomponent: MDhealth: MD 6.5 time.

5

y s were reported ints. One of thesxperienced adverss (i.e. resulting ino adverse eventstwo RCTs did no

ot reported in any

vidence exists atients (very low

ancer on the effects of exwo systematic revCT27. No additiona

ty of life 27 included 53 prgoing lung resectospital-based exeafter discharge iusing the EORT

operatively and afte risk of bias. significant chang

ssessment and tm) and no significroup (p-values the questionnaire

wo groups (functionup vs. 2.7 [95%C

D -2.5 [95%CI -7.8[95%CI -7.7 to 2

n two of the four Rse RCTs (N=12se events relaten hospitalization had occurred duot include reportiny of the included st

on the safety ow level of eviden

xercise treatmentviews10, 23 were idal RCTs were foun

patients with nontion. The exerciseercise (strength ain a 12-week homTC-QLQ-C30 queter the 12-week h

ges in overall QOhe assessment acant differences not provided).

e no significant dnal component: MCI -4.7 to 10.0] in8 to 2.9] vs. -3.2 [20.7] vs. 2.2 [95%

Exercise t

RCTs included on 21) reported thaed to exercise; oor disability)57. O

uring testing or exng of adverse evetudies.

of exercise in pce; Segal 2009,

in lung cancer padentified that inclund.

n-small cell lunge intervention consand mobility trainime-based progra

estionnaire, and whome program. Th

L over time (betwafter the 12-weekbetween the conAlso, for the

ifferences could bMD 2.0 [95%CI -5.n control group; s95%CI -8.3 to 2.1

%CI -5.2 to 9.6]) a

treatment for adult

prostate at three one was

One RCT xercise46. ents52,59.

prostate Galvao

atients is uded the

cancer sisted of ing) and m. QOL

was only he study

ween the k home-

ntrol and different

be found 5 to 9.3]

symptom ]; global

and over

Indb

C•

4Incindgincp

C•

4Fre

t cancer patients

n the absence distinguish the pobased program.

Conclusions A combinatio

home-based of life in pati2011).

4.3.2 Cardiopun the same studycapacity and meantervention and cday postoperativegroup returned tontervention groupcapacity was foupostoperatively).

Conclusions A combinatio

home-based capacity in Arbane 2011)

4.3.3 FatigueFatigue is one of eported separatel

of an assessmeossible effects of

on of preoperatiexercise does nents with lung c

ulmonary functioy27 cardiopulmonaasured with the control group a sely (p<0.05). At o the preoperatip a slightly (non-nd (from 466.6m

on of preoperatiexercise does npatients with lu).

the subdomains ly by Arbane et al

ent at dischargef the hospital-bas

ve hospital-basenot seem to havecancer (low level

on ary function was six minute walk

ignificant decline 12 weeks postoive level of aer-significant) incre

m at baseline to

ve hospital-basenot seem to haveung cancer (low

of the EORTC-Q.27.

e it is impossibsed versus the h

ed and postopere an effect on qu of evidence; Ar

expressed by aeking test. In bothwas found at the

operatively the coobic capacity. In

eased level of ae480.2m at 12 w

ed and postopere an effect on aew level of evide

QLQ-C30, but wa

35

ble to home-

rative uality rbane

erobic h the e fifth ontrol n the erobic weeks

rative robic ence;

as not

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36

4.3.4 SafetyTwo a priorichanges reportrequiring additiodependency cacomplications iexercise interve

Conclusions • The evide

cancer pat

4.4 Colorec4.4.1 QualitOnly one study QOL in colorepatients with cogroup (n=33). Aa considerable (67.7% in the cit is unclear hbaseline. The eexercise progexercises. QOLhigh risk of biasNo differences were there diffeanalysis compa(measured at performance stdecreased treaa significant d(p=0.038) and Tcould indicate QOL.

y defined postope

ted by radiologistonal ventilator suare) were reportin the control grention. Relapse w

ence suggests thtients (low level

ctal cancer ty of Life was found report

ectal cancer patieolorectal cancer tAll patients underwamount was pote

control group vs. 6how many patienexercise intervenram with indiv

L was measured s. in QOL were fou

erences in changearing a group of pa

baseline and ptatus) and a grodmill time showeddifference at poTrial outcome indean association b

erative complicatt as pneumonia, pport and or neceted in the activeroup, but these

was not reported in

hat exercise treaof evidence; Arb

ting on the effectsents. Courneya to an exercise growent surgery with

entially receiving c63.9% in the internts actually weretion consisted of

vidualized cardiousing the FACT-C

und between bothe in QOL over timarticipants with anost-intervention tup of participantd no significant diost-intervention aex (p=0.044). The

between change

Exercise t

tions (defined arespiratory compessitating a returne group comparewere not related

n the study.

atment is safe fbane 2011).

s of exercise treatet al.32 randomizoup (n=69) and a

hin the past 3 monchemotherapy at irvention group). He on active treatf a 16-week homovascular and fC scale. The stud

h groups at baseme. However, an n increased treadto indicate the ts with an unchafferences at base

assessment for ese significant diffin fitness and ch

treatment for adult

s X-ray plications n to high ed to 3 d to the

for lung

tment on zed 102 a control nths and nclusion

However, tment at

me-based flexibility dy had a

line, nor ancillary mill time physical

anged or eline, but FACT-C ferences hange in

C•

4CcTtrusrainb

C•

4TcpgeoFpbAggs

t cancer patients

Conclusions The evidenc

cancer patieevidence; Co

4.4.2 CardiopuCourneya et al.32

cardiopulmonary fTest) in colorectareadmill until 70%until voluntarily indseconds to reach ate was found ntervention assesbpm [95%CI 3.2 to

Conclusions The evidenc

cancer patienlow level of e

4.4.3 FatigueTwo RCTs evaluatcolorectal cancer ppatients with colorgroup (n=59). All pelective abdominaof a mix of aerobicFatigue was measpostoperatively onbias. At baseline alreadgroups was foundgroup 2.7 cm [95%score of the cont

ce suggests thants has no effec

ourneya 2003).

ulmonary functioalso reported on

function (measural cancer patients% of the age-preddicated by the parthis maximum. Nbetween the cossment (differenco -8.6], p=0.361).

ce suggests thants has no effecevidence; Courne

ted the effect of epatients (Table 16rectal cancer to anpatients were ageal colorectal surgec and strength traisured preoperativen a visual analogu

dy a significant did (intervention gro%CI 1.5-4.2], p=0.rol group increas

at exercise treact on quality of l

on n the effects of red with the Mods. The test consiicted maximum hrticipant, and is scNo significant diffentrol and intervee in mean chang

at exercise treact on cardiopulmeya 2003).

exercise treatment6). Houborg et al.3n intervention groud at least 60 yearry. The exercise iining of upper andely and on day 7, e scale. The stud

ifference in fatiguoup 3.8 cm [95%03). Postoperativ

sed 2.3 cm more

KCE Report

atment in colorlife (very low lev

exercise treatmedified Balke Treaists of walking oeart rate is reach

cored by the numberence in resting ention group at ge from baseline

atment in colormonary function

t on fatigue in 38 randomized 119up (n=60) or contrrs and underwent ntervention consi

d lower extremities30 and 90 y had a low risk o

ue score between%CI 2.5-5.1] vs. co

ely at day 7 the fae than the interve

t 185

rectal vel of

nt on admill n the

hed or ber of heart post-: -2.7

rectal (very

9 rol

sted s.

of

n both ontrol atigue ention

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KCE Report 185

group (p=0.000change in fatiguCourneya et alFACT instrumeintervention anintervention ass

Conclusions • There are

patients h2006, Cou

Table 16 – Effe

Study

Houborg 200638

Courneya 200332

5

07). At day 30 aue were found bet.32 assessed fatigent. They found nd control group sessment (p=0.81

indications that as no effect on rneya 2003).

ect of exercise tr

N Fatig

N=119 VisuaPostoincrea(p=0.0Postono sigbetwefatigu

N=102 FACTPost-ichangintervdiffere(p=0.8

and day 90 no tween both group

gue using the 13-no significant dat baseline (p=0).

exercise treatmfatigue (low leve

reatment on fatig

ue

al Analogue Scaleoperative day 7: mase in control grou0007)

operative day 30 agnificant differenceeen groups in chae score

T-C intervention (diffege from baseline tention): no significence between gro810)

Exercise t

significant differes. item Fatigue Scadifferences betw0.579) and at th

ent in colorectalel of evidence; H

gue in patients w

Measu

more up

and 90: es nge in

Pre-opoperatand da

rence in to post-cant

oups

At basinterveweeks

treatment for adult

ences in

le of the een the he post-

l cancer Houborg

with colorectal ca

ure point

perative, post-tive day 7, day 30ay 90

seline, post-ention (after 16 s)

t cancer patients

ancer

Intervention

Control group(45 min/sessioIntervention gmobilizations,50-80% of ononce a week t

Control groupintervention Intervention gflexibility exerpredicted headirector

characteristics

p: stretching and tion)

group: Institution-b, strength and aere repetition maximthe physiotherapis

p: asked not to init

group: a home-basrcises (3-5 times part rate maximum)

ightening and rela

based + continuedrobic training, 45 mmum 6 times a west home visit

tiate any structure

sed, personalizedper week for 20-30) + weekly telepho

axation exercises

d at home mix of min/session, load eek (+ filling in dia

ed exercise during

d cardiovascular a0 min, 65-75% of one call by project

37

of ary),

g

nd

t

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38

4.4.4 SafetyHouborg et al.38

were related tosafety data32. R

Conclusions • The evide

colorectal

4.5 Haema4.5.1 Qualit

4.5.1.1 Pattran

Two RCTs evalundergoing allo(Table 17). Baumann et cancers) undercontrol group). training duringassessments, questionnaire abias.

y 8 reported on advo the exercise intRelapse was not re

ence suggests patients (low lev

atological cancety of life

tients undergoingnsplantation luated the effect o

ogeneic haematop

al.28 included 4rgoing allogeneic The exercise inte

g hospitalization. QOL was m

at admission and

verse events, but ntervention. Courneported in the incl

that exercise vel of evidence;

ers

g haematopoieti

of exercise treatmpoietic stem cell tr

7 patients (maiHSCT (n=17 in

ervention includedNext to physi

measured with at discharge. The

Exercise t

none of the compneya et al. did noluded studies.

treatment is sHouborg 2006).

ic stem cell

ent on QOL in paransplantation (HS

nly with haemaexercise group,

d strength and encal and anthropthe EORTC-Q

e study had a hig

treatment for adult

plications ot report

safe for

tients SCT)

tological n=16 in

ndurance pometric

QLQ-C30 h risk of

Othinre6cfugeJugaaCNhdapg

C•

t cancer patients

Of the 47 initially heir exercise progn both groups delated complicatio

68.6; change: 7.7change: -9.9%) unctioning decregroup p=0.005 aneffects were foundJarden et al.39 incundergoing allogegroup). The exercadjuvant multimodand psycho-educaC30 questionnaireNo significant diffhealth status, nor discharge: physicaat follow-up (3-p=0.325, global hglobal health statu

Conclusions In patients

transplantatisignificant efunctioning (2009).

randomized patiegram until the da

deceased during ons. QOL increas

7%) and decreasewithout reachi

ased significantlynd control group d (no p-value mencluded 42 patientseneic HSCT (n=21cise intervention dal program of phation. QOL was e. The study had afference was fouduring hospitalisaal functioning p=0

and 6-months ealth status p=0.

us p=0.603 respec

undergoing allon, exercise treeffect on overa(very low level o

ents, 33 patients wy of hospital dischospitalization bsed in the interveed in the control ng statistical sy over time in bp=0.002). No sig

ntioned). s (mainly with ha1 in intervention gincluded a struc

hysical exercise, also measured w

a high risk of bias.nd in physical f

ation (difference b0.089, global healt

after discharge:.841 and physicactively).

logeneic haemaeatment does n

all quality of lifof evidence; Ba

KCE Report

were able to comcharge. Seven pabecause of transention group (63.group (62.5 vs.

significance. Phyboth groups (exegnificant time by g

aematological cangroup, n=21 in coctured and superprogressive relax

with the EORTC-. functioning and gbetween admissionth status p=0.817 physical functi

al functioning p=0

atopoietic stem not seem to hafe and on phy

aumann 2011, Ja

t 185

mplete atients plant-.7 vs. 56.3;

ysical ercise group

ncers) ontrol rvised xation QLQ-

global n and

7), nor oning

0.131,

cell ave a ysical arden

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KCE Report 185

Table 17 – Effe

Study

Baumann 201128

Jarden 200939

5

ect of exercise tr

N Quality o

N=47 Quality ofdifference68.6±11.2(62.5±23.mentionePhysical fin the exe20.7%, p=vs. 59.6±2

N=42 Physical fsignificandischargefollow-up months foFACT-G: and dischmonths foand 6-moFACT-ANand dischmonths foand 6-mo

reatment on qual

of life

f life (EORTC-QLQe over time in exe2, +7.7%) nor in th.9 vs. 56.3±17.6, -d) functioning: a signercise group (83.1=0.005) and in the22.9, -25.1%, p=0

functioning (EORTnt differences betwe (p=0.089), betwe(p=0.325) and be

ollow-up (p=0.131no significant diff

harge (p=0.298), bollow-up (p=0.241onths follow-up (p=N: no significant diharge (p=0.225), bollow-up (p=0.167onths follow-up (p=

Exercise t

lity of life in patie

Q-C30): no signifircise group (63.7±he control group -9.9%) (no p-value

nificant decrease ±16.9 vs. 65.9±16

e control group (70.002)

TC-QLQ-C30): noween baseline andeen baseline and etween baseline a)

ference between bbetween baseline ) and between ba=0.620) ifference betweenbetween baseline 7) and between ba=0.395)

treatment for adult

ents undergoing

Meas

cant ±19.7 vs.

es

over time 6.5, -9.6±19.2

Basefirst 2admiday bhospdisch

o d 3-months

and 6-

baseline and 3-

aseline

n baseline and 3-

aseline

Baseday aadmipost-(at di3- anfollow

t cancer patients

g haematopoietic

sure point Int

eline (during 2 days after ssion) and

before pital harge

Co(ac20staInteerg20wacontra

eline (first after ssion), -intervention ischarge), nd 6-months w-up

ComaIntecon30stretra(20

c stem cell transp

ervention charac

ontrol group: clinicctive and passive min/session, 5 da

art one day after trervention group: agometer, training imin) and ADL-tra

alking and stair climnducted by profesnsplantation until

ontrol group: usuaassage) ervention group: unsisting of 4 min wmin,<75% of maxetching exercisesining (15-20 min, 0 min, 2 days/wee

plantation

cteristics

’s standard physiomobilizations withays/week, conducransplantation untaerobic endurancentensity achieved

aining (strength, combing, 20-30 min/ssional therapist, sdischarge

l care (range of m

usual care plus mwarm-up, stationax heart rate, 5 day (15-20 min, 5 day3 days/week), pro

ek) and psycho-ed

otherapy programh low intensities cted by physiothertil day before disce training (cycle

d watt load -20%, oordination, stretc/day), twice a daystart 6 days prior t

motion, resistance

ultimodal intervenary cycling (15-ys/week), dynamicys/week), resistanogressive relaxatioducation

39

m

rapist, charge

10-ching, y, to

and

ntion,

c and nce on

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40

4.5.1.2 LymOnly one studyof lymphoma patients to an patients, 44.3%consisted of abegan at 60% o15-20 to 40-45mThe study had aAt post-intervenexercise groupp=0.021; adjusPhysical functiowas significan(unadjusted grogroup differencreceived usual remained stableAt six months group was foun(p=0.121 for ph

Conclusions • In lympho

on overalleffect disaCourneya

mphoma patientsy was retrieved onpatients. Courneexercise group

% were on active aerobic exercise of peak power oumin/session). QOa low risk of bias. ntion assessment,p (unadjusted grsted group differoning, a sub-domntly better in thoup difference ine in mean changecare, the scores

e over time. follow-up a trend

nd, but the differehysical functioning

ma patients, exel quality of life aappears after 6 2009).

s n the effects of exeya et al.34 rand(n=60) or a conchemotherapy. Ttraining on a cy

utput, increased bOL was measured

, overall QOL wasroup difference rence in mean c

main of the FACThe exercise gron mean change: e: +7.2, p=0.017).s on overall QOL

d towards improvences did not reag, p=0.054 for ove

ercise seems to hand physical fun

months (mode

Exercise t

xercise treatment domized 122 lymtrol group (n=62The exercise inteycle ergometer (by 5% each week

with the FACT-A

s significantly bettin mean changechange: +7.2, p-AN scale (TOI-A

oup at post-inte+9.0, p=0.012; a

. In the control groand physical fun

ved QOL in the ach statistical signrall QOL).

have a significannctioning, althou

erate level of ev

treatment for adult

on QOL mphoma ). Of all

ervention intensity to 75%,

AN scale.

ter in the e: +9.5, =0.039).

An), also ervention adjusted oup, that nctioning

exercise nificance

nt effect ugh the

vidence;

4

4

TfurJugaacaadbDc(pdgh

C•

t cancer patients

4.5.2 Cardiopu

4.5.2.1 Patientransp

Two RCTs reporteunction in patientisk of bias.

Jarden et al.39 incundergoing allogegroup). The exercadjuvant multimodand psycho-educcapacity was meaafter admission, nand the control grdecreased in the cboth groups (p<0.0Dimeo et al.35

chemotherapy ann=33) or a contro

program of aerobdifference in maxigroups at baselinehigh risk of bias.

Conclusions Conflicting

treatment onallogeneic haimprovementrate (very low

ulmonary functio

nts undergoing hplantation ed on the effect ofts undergoing allo

cluded 42 patientseneic HSCT (n=21cise intervention dal program of phcation. The effecasured with the Vno significant differoup (p-value not control group, resu0001).

randomized nd autologous pel group (n=37). Th

bic exercise on amal heart rate in e (p=0.58) and a

evidence is avn cardiopulmonaaematopoietic stt in VO2max, wiw level of eviden

on

haematopoietic s

f exercise treatmeogeneic HSCT. Bo

s (mainly with ha1 in intervention gincluded a struc

hysical exercise, ct of exercise tVO2max. At base

erence was foundmentioned). At d

ulting in a significa

70 patients ueripheral HSCT the exercise interva bed cycle ergothe stress test wa

at discharge (p=0

vailable on theary function in tem cell transplaithout a difference; Jarden 2009,

KCE Report

stem cell

ent on cardiopulmooth studies had a

aematological cangroup, n=21 in coctured and superprogressive relaxtreatment on aeeline, i.e. the firs between the exe

discharge, the VOant difference bet

ndergoing high-to an exercise g

vention included aometer. No signias found between.84). This study h

e effect of exepatients underg

antation: a signifnce in maximal , Dimeo 1997).

t 185

onary a high

ncers) ontrol rvised xation erobic st day ercise

O2max tween

-dose group

a daily ficant

n both has a

ercise going ficant heart

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KCE Report 185

Table 18 – Effe

Study

Jarden 200939

Dimeo 199735

5

ect of exercise tr

N Card

N=42 At bin VAt psign(p<0

N=70 Maxsigngrousign(p=0% ofsigngrousign(p=0

reatment on card

diopulmonary fu

baseline: no signifiO2max between b

post-intervention (anificant difference 0.001)

ximal heart rate in nificant difference ups at admission (nificant difference 0.84) f estimated maxim

nificant difference ups at admission (nificant difference 0.69)

Exercise t

diopulmonary fun

unction

icant difference both groups at discharge): between groups

stress-test: no between both (p=0.58) and no at discharge

mal heart rate: no between both (p=0.89) and no at discharge

treatment for adult

nction in patients

Measure point

Baseline (first dadmission), posintervention (at A single stage 6submaximal ex(Aastrand-Rhymergometer test)VO2max (l/min)

Baseline (befortransplantationdischarge Treadmill stressstarting at 3 kmelevation, accekm/h every third

t cancer patients

s undergoing ha

t Int

day after st-discharge)

6-min xercise test ming cycle ) to define )

ComaIntco<7strtra(20

re ), at

s-test m/h and 1.5% eleration of 1 d minute

CoIntwit50

aematopoietic ste

tervention chara

ontrol group: usuaassage) tervention group:

onsisting of 4 min w75% of max heart retching exercisesaining (15-20 min,0 min, 2 days/wee

ontrol group: not intervention group: th bed ergometer

0%, 15 repetitions

em cell transplan

acteristics

al care (range of m

usual care plus mwarm-up, stationarate, 5 days/week

s (15-20 min, 5 da 3 days/week), prek) and psycho-ed

n detail describeddaily program of a), 1 min with hear, total of 30 min p

ntation

motion, resistance

multimodal interveary cycling (15-30k), dynamic and ays/week), resistarogressive relaxatducation

d aerobic exercise (rt rate equivalent tper day

41

e and

ntion, 0 min,

ance tion

(biking to

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42

4.5.2.2 LymOne study evafunction in lylymphoma patieOf all patientsintervention co(intensity beganto 75%, 15-20 program a siggroups (VO2machange: +0.43group difference

Conclusions • In lympho

on cardiolevel of ev

4.5.3 Fatigu

4.5.3.1 AcuChang et al.30

undergoing checontrol group Inventory (BFI).Patients in the eworst fatigue in7 average fatig± 2.4 in contrexercise group interference megroup (p=0.04),group versus mmean 5.6 ± 3.1(p=0.01) and fa5.6 ± 2.7 in consignificant at d

mphoma patientsluated the effect mphoma patientents to an exerciss, 44.3% were nsisted of aerobin at 60% of peak to 40-45min/sess

gnificant differencax, l/min: unadjust, p<0.001; VO2me in mean change

ma patients, exeopulmonary funcvidence; Courney

ue

ute myelogenousrandomized 22 pemotherapy to a(n=11). Fatigue . The study had aexercise group ha

ntensity and fatiguue score mean 4.ol group (p=0.02versus mean 7.5

ean 3.6 ± 2.5 in e, at day 14 averag

mean 5.8 ± 3.1 in c1 in exercise grouatigue interferencentrol group (p=0.0day 21 for avera

s of exercise treatmts. Courneya etse group (n=60) oon active chem

ic exercise traininpower output, incsion). After the 1

ce was found inted and adjusted

max, ml/kg/min: ue: +5.2, p<0.001).

ercise seems to hction measured ya 2009).

s leukemia patients with acuta walking exercis

was measured high risk of bias.ad significantly lowue interference at .1 ± 2.3 in exercis2), worst fatigue ± 2.4 in control g

exercise group vege fatigue score mcontrol group (p=up versus mean 7e mean 4.3 ± 2.8

04). However, the age and worst fa

Exercise t

ment on cardioput al.34 randomizor a control group

motherapy. The ng on a cycle ercreased by 5% ea12-week aerobic VO2max betwegroup difference

unadjusted and a

have a significanas VO2max (m

e myelogenous lese program (n=1using the Brief

wer levels of averday 7 and day 14

se group versus mscore mean 5.6

roup (p=0.02) andersus 4.6 ± 2.2 inmean 4.4 ± 2.4 in 0.01), worst fatigu7.1 ± 2.7 in contrin exercise groupdifferences beca

atigue intensity.:

treatment for adult

ulmonary zed 122 p (n=62). exercise rgometer ch week exercise en both in mean adjusted

nt effect moderate

eukemia 1) or a Fatigue

rage and 4: at day mean 5.5 6±2.7 in d fatigue n control exercise ue score ol group p versus me non-average

facg

C•

4

TpbBcctrCoemwpJugaasbCtamtro

t cancer patients

atigue score meacontrol group (p=0group versus 6.3 ±

Conclusions In patients w

seems to haevidence; Ch

4.5.3.2 Patientransp

Three RCTs repopatients undergoinbias. Baumann et al.2cancers) undergocontrol group). Thraining during hosC30 questionnaireof the EORTC-QLexercise group nomentioned) in conwas noticed (p=0.0p-value mentionedJarden et al.39 incundergoing allogegroup). The exercadjuvant multimodand psycho-educascores (EORTC-between the controColeman et al.31 randem transplanmelphalan and preatment (n=14) oof a home-based

an 4.6 ± 3.0 in ex0.1), worst fatigu± 3.8 in control gro

with acute myelogave a temporaryhang 2008).

nts undergoing hplantation orted on the effeng allogeneic HSC

28 included 47 ing allogeneic HSe exercise intervespitalization. QOLe at admission andLQ-C30 is the pao significant differentrast to the cont046). No significad). cluded 42 patientseneic HSCT (n=21cise intervention dal program of phation. They also fo-QCQ-C30), FACol and exercise grrandomized 24 pantation (chemotheperipheral blood or usual care (n=1exercise program

xercise group verse intensity meanoup (p=0.05).

genous leukemiy effect on fatigu

haematopoietic s

ect of exercise trCT. All three stud

patients (mainly SCT (n=17 in exention included stL was measured wd at discharge. Otient’s perceptionences over time wtrol group, where ant time by group

s (mainly with ha1 in intervention gincluded a struc

hysical exercise, ound no significaCT-G scores anroup. atients with multiperapy, stem cell stem cell transp10). The exercise

m with resistance a

KCE Report

sus mean 4.8 ± 3 5.7 ± 3.8 in exe

a, exercise treatue (very low lev

stem cell

eatment on fatigdies had a high r

with haematoloxercise group, n=trength and enduwith the EORTC-

One of the sub-domn on his fatigue. Iwere found (no p-

a significant increffects were foun

aematological cangroup, n=21 in coctured and superprogressive relaxnt difference in fand FACT-AN s

ple myeloma rececollection, high-

plantation) to exe intervention consand aerobic exerc

t 185

3.5 in ercise

tment vel of

ue in risk of

ogical =16 in rance QLQ-mains n the

-value rease

nd (no

ncers) ontrol rvised xation atigue cores

eiving -dose ercise sisted cises.

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KCE Report 185

Fatigue was minertia adjectivetreatment on fathe analysis bedecrease in fatHowever, no p-

Conclusions • Conflicting

treatment haematopevidence;

Table 19 – Effe

Study

Baumann 201128

Jarden 200939

5

measured with thee rating scale. Fo

atigue, 14 patientsecause of its effectigue (-1.2), wher-values were prov

g evidence is on fatigue

oietic stem ceBaumann 2011,

ect of exercise tr

N F

N=47 EEd2nCin2p

N=42 FnbdbubuF

e Profile of Moodor the evaluation s receiving thalidoct on sleep. The ereas the usual ca

vided.

available on tin patients ull transplantatioJarden 2009, Co

reatment on fatig

Fatigue

EORTC-QLQ-C30Exercise group: nodifference over tim25.3 vs. 43.8 ± 22no p-value mentioControl group: signncrease over time24.5 vs. 52.8 ± 27p=0.046)

Fatigue (EORTC-Qno significant diffebetween baseline discharge (p=0.40baseline and 3-moup (p=0.302) and baseline and 6-moup (p=0.097) FACT-G: no signif

Exercise t

d States (POMS) of the effect of

omide were excludexercise group share group did no

the effect of eundergoing alloon (very low loleman 2003).

gue in patients un

Me

0 o significant

me (41.8 ± .7, +4.8%, ned) nificant

e (36.1 ± .1, +46.3%,

Badadadis

QLQ-C30): rences and 5), between

onths follow-between onths follow-

ficant

Baadint3-

treatment for adult

fatigue-exercise ded from howed a

ot (+0.3).

exercise ogeneic evel of

ndergoing haem

easure point

aseline (during firsays after admissioay before hospital scharge

aseline (first day admission), post-tervention (at disc and 6-months fol

t cancer patients

matopoietic stem

Interv

st 2 on) and

Contro(active20 minphysiobeforeInterveergom20 mincoordi30 mintherap

after

charge), llow-up

ContromassaInterveconsis30 minstretchtrainin(20 mi

cell transplantat

vention character

ol group: clinic’s se and passive mobn/session, 5 days otherapist, start one discharge ention group: aero

meter, training inten without interruptnation, stretching

n/day), twice a dapist, start 6 days p

ol group: usual caage) ention group: usuasting of 4 min warmn,<75% of max hehing exercises (15g (15-20 min, 3 din, 2 days/week) a

tion

ristics

standard physiothebilizations with lowper week, conduc

ne day after trans

obic endurance transity achieved wation) and ADL-trai, walking and staiy, conducted by p

prior to transplanta

are (range of motio

al care plus multimm-up, stationary ceart rate, 5 days/w5-20 min, 5 days/ways/week), progreand psycho-educa

erapy program, w intensities), cted by plantation until da

aining ( cycle att load -20%, 10-ning (strength, ir climbing, 20-professional ation until discharg

on, resistance and

modal interventioncycling (15-week), dynamic anweek), resistance essive relaxation ation

43

ay

ge

d

n,

nd

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44

Study

Coleman 2003

4.5.3.3 LymOne study evlymphoma patieto an exercise 44.3% were onof aerobic exerof peak power 45min/session)AN scale. At poin the exercise p=0.013; adjust

N FdabmamFdabmam

31 N=24 Deg

mphoma patientsvaluated the effeents. Courneya e

group (n=60) orn active chemothercise training on aoutput, increased. Fatigue was meost-intervention asgroup (unadjuste

ted group differen

Fatigue difference betweenand discharge (p=between baseline months follow-up (and between basemonths follow-up (FACT-AN: no signdifference betweenand discharge (p=between baseline months follow-up (and between basemonths follow-up (

Decrease in fatiguexercise group, nogroup (no p-values

s ect of exercise et al.34 randomizedr a control grouperapy. The exercia cycle ergometerd by 5% each weeasured using a sssessment, fatigu

ed group differencnce in mean chang

Exercise t

Men baseline 0.298), and 3-(p=0.241) eline and 6-(p=0.620)

nificant n baseline 0.225), and 3-(p=0.167) eline and 6-(p=0.395)

ue in ot in control s mentioned)

BabeaftmotraPO

treatment on fad 122 lymphoma p (n=62). Of all pise intervention cor (intensity beganeek to 75%, 15-2sub-domain of theue was significantce in mean changge: +4.0, p=0.012

treatment for adult

easure point

aseline (app. 3 moefore transplantatiter transplantationonths after ansplantation OMS

tigue in patients patients, onsisted

n at 60% 20 to 40-e FACT-tly better ge: +4.6, 2).

C•

4Inbto(wcds

t cancer patients

Interv

onths ion), n, 3

IndividstrengControleast 3Weekl

Conclusions In lymphoma

on fatigue (m

4.5.4 Safety n the study of Cobut three adverse o a modification owith knee pain)

complications reladifferentiating the severity of pain w

vention character

dualized home-bagth resistance trainol group: usual ca3 times a week) ly phone calls for

a patients, exercimoderate level of

urneya et al.34 noevents (back, hip

of the exercise prowithdrew from th

ated to the toxiciadverse events

was for patients i

ristics

sed exercise progning and an aerob

are (remain active

both groups + we

ise seems to havf evidence; Courn

o serious adverse p and knee pain) rogram in two patihe study. Dimeoty of high-dosis related to the exn exercise group

KCE Report

gram combining bic component and walk 20 min

eekly activity log

ve a significant eneya 2009).

events were reporelated to exerciseents, while one p

o et al.35 reportedchemotherapy w

xercise treatmentp lower than in co

t 185

at

effect

orted, e lead atient d the ithout . The ontrol

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KCE Report 185

group (p=0.01)cancers did not

Conclusions • Exercise

haematoloadverse ev

4.6 Mixed cSeven additiontreatment in mix

4.6.1 QualitFour RCTs repstudies had a lbias33 and the scales varied aof AssessmentFACT-AN scaleEstimates of thephysical subscaA structured ingroup), consistiseveral domainfunctioning), rebetween both gbetween both g(p=0.4229)and Adamsen et awomen with brecare (n=134). Afor advanced dactive treatmenprogram, combon QOL (mea

5

. The other studit report on advers

treatment seeogical cancers, avents (low level o

cancer populatal RCTs were incxed cancer popula

ty of life ported on the effow risk of bias26,4

fourth study hadand included Spitzt (LASA), EORTe, with some studie effect of institutiales of QOL differtervention (n=49 ing of conditionings of QOL (cognitivsulted in an overgroups41. Only atgroups (p=0.469) at week 27 (p=0.9

al.26 randomized east cancer) to e

All patients had redisease or as adnt. The exercise inbining high and loasured by EOR

ies including patie events.

ems to be saalthough many tof evidence; Cou

tions cluded reporting oations.

ffect of exercise 40, while one stud a high risk of b

zer QOL UniscaleTC-QLQ-C30, MOies using more thaion-based exercisred widely across in intervention g

g exercises with eve, physical, emo

rall lack of different week 4 a signifbut this differenc

9922). This study 269 patients wit

exercise treatmenteceived at least ondjuvant treatment,ntervention consisw intensity exerc

RTC-QLQ-C30) w

Exercise t

ents with haema

ave in patienttrials omit to reurneya 2009).

on the effects of

treatment on QOdy had a moderatias41. QOL meas

e, Linear AnalogueOS SF-36, FACITan one scale. se on quality of lifethe studies (Tableroup and n=54 ineducational instru

otional, spiritual annce in overall QOficant difference

ce disappeared athad a high risk of

th cancer (includt (n=135) or convne cycle of chemo, and were still rsted of a 6-week ises. No significa

was found for

treatment for adult

tological

ts with eport on

exercise

OL. Two te risk of urement e Scales T-F and

e and on e 20). n control uction on nd social OL score is found t week 8 f bias.

ding 119 ventional otherapy receiving exercise

ant effect exercise

caMos(S3Tpth(w0Hin(Csamgafo+Sthmn

C•

t cancer patients

compared with tassessed with twoMOS SF-36. For over time betweenshowed a signifip=0.01).

Slightly different re38 cancer patientsThe exercise inteprogram during 4 whe FACIT-F, weCohen’s d=0.26)

with a small declin0.02) and a smalHowever, the interntervention and aboth p<0.05).

Courneya et al.33 rsolid tumours to daaerobic exercise measured with thegroups (p=0.363 adjusted group dior each group se+13.4 in the exercStratification for she outcome, agemetastatic diseasenot alter the findin

Conclusions Conflicting

treatment onlevel of evideRummans 20

the control grouo different instrum

the EORTC-QLQn groups was fouicant increase i

esults were reports to exercise treaervention consisteweeks. Only sma

ere found in theand at 3-months

ne in the control gl improvement atrvention group shat 3-months follow

randomized 55 marbepoetin alfa altraining (n=26).

e FACT-AN scale,for unadjusted

fferences). Howeparately was founcise group, no p-vome baseline cha

e, sex, marital ste, current chemotgs.

evidence is avn quality of life inence; Adamsen 006).

up (p=0.4). Physments, i.e. the EOR

Q-C30 scale, nound (p=0.09), when physical func

ted by Mustian et tment (n=19) or aed of a walking ll improvements i

e exercise groups follow-up (Cohegroup at post-intet 3-months followowed a significanw-up compared w

mild-to-moderately one (n=29) or com

The mean cha, did not differ sign

group differencever, a significantnd (+20.3 for darbvalues mentionedaracteristics, suchtatus, education, therapy and prior

vailable on then mixed cancer p

2009, Mustian 2

sical functioning RTC-QLQ-C30 ano significant differereas the MOS S

ctioning with exe

t al.40, who randoma control group (n

and resistance n QOL, measuredp at post-interve

en’s d=0.41) compervention (Cohen’

w-up (Cohen’s d=0ntly better QOL at with the control g

anaemic patientsmbined with a 12-ange in QOL scnificantly betweences and p=0.637t improvement in bepoetin alfa alond in the primary sth as baseline valprimary tumour

r blood transfusion

e effect of exepopulations (very2009, Courneya 2

45

was nd the rence SF-36 ercise

mized n=19).

band d with ention pared ’s d=-0.28). post-

group

s with -week cores, n both 7 for QOL

ne vs. tudy). lue of type,

n, did

ercise y low 2008,

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46

Table 20 – Effe

Study N

Rummans 200641

N

Adamsen 200926

N

ect of exercise tr

N Quality o

N=103 Baselineboth grouAt week 4both grouAt week both grouAt week both grou

N=269 Global hesignificangroups (e-2.7 to 7.Physical significangroups (e-0.4 to 5.Physical differenc(estimate7.7, p=0.

reatment on qual

of Life

: no significant difups (p=0.4829) 4: a significant difups (p=0.469) 8: no significant dups (p=0.4229) 27: no significant ups (p=0.9922)

ealth status (EORnt differences oveestimated mean d.1, p=0.4) functioning (EOR

nt differences oveestimated mean d.1, p=0.09) functioning (MOSes over time betw

ed mean differenc01)

Exercise t

lity of life in mixe

fference between

fference between

difference between

difference betwee

RTC-QLQ-C30): nor time between bo

difference 2.2, 95%

RTC-QLQ-C30): nor time between bo

difference 2.4, 95%

S SF-36): significaween both groups ce 4.4, 95%CI 1.1

treatment for adult

ed cancer popula

Measure p

n

en

Baseline, w Spitzer QOLinear Anaof AssessmQOL Assessmeconverted scale

o oth %CI

o oth %CI

ant

to

Baseline ainterventio EORTC-Qsubdomainstatus/quaphysical fuMOS SF-3physical fu

t cancer patients

ations

point

week 4, 8, 27

OL Uniscale alogue Scales ment (LASA) of

nt scores were to a 0-100

nd after n (6 weeks)

LQ-C30, n global health lity of life and nctioning

36: subdomain nctioning

Intervention ch

Control group: uIntervention groubasis, completedpsychiatrist or psphysical therapisconditioning exe20 min relaxation

Control group: a+ exercise progrIntervention grouphysical traininghours, 45 min rerepetition maximsession, 15 min bicycles, 70-2503.75 MET hoursrelaxation traininintensity sessionbody awarenessweek), massage

aracteristics

sual care up: eight 90 min-sd within 4 weeks asychologist co facst, chaplain or soc

ercises, educationn exercises

llowed freely to inram after the six wup: 6-week (9 h/w (30 min dynamic

esistance training mum test at 4 MET

cardiovascular tra0W, 85-95% maxim) for 90 min follow

ng + 2 times per wns: relaxation (30 s and restorative te (30 min twice a w

KCE Report

sessions on ambuafter enrollment, lecilitated by nurse, cial worker, 20 mial instruction and

ncrease physical aweek assessment week) high intensitc exercises at 4.5 at 70-100% of on

T hours per traininaining (stationary mum heart rate atwed by 30 min week massage. Lomin, 4 times per wraining (90 min onweek)

t 185

ulatory ed by

n

activity

ty MET e

ng

t

ow week, nce a

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KCE Report 185

Mustian 200940

N

Courneya, 200833

N

4.6.2 CardioFive studies cardiopulmonarreported chancardiopulmonarrisk of bias26,40

bias37,42. Estimates of thefunction differedGriffith et al. 37

chemotherapy (n=68) or usuahome-based wa

5

N=38 Exercise baseline d=0.26) afrom basd=0.41)

Control gbaseline 0.02) butbaseline d=0.28)

Significancompareand at 3-

N=55 No signif(p=0.363p=0.637 Both grou

opulmonary funcreported on t

ry function in mnges in VO2mry function with a0, while 3 studies

e effect of exercisd across the studirandomized 126

and/or radiotheraal care (n=58). Talking intervention

group: small impand post-interven

and continued moeline to 3-months

group: small decreand post-interven

t small improvemeand 3-months fol

nt higher QOL in ed to control group-months follow-up

ficant differences 3 for unadjusted gfor adjusted grouups improved QO

ction the effect of

mixed cancer popax26,33,37, while

a walking test40,42

s had either a m

se interventions onies (Table 21). patients undergo

apy for solid tumoThe exercise inten.

Exercise t

rovements betwention (Cohen’s odest improvemens follow-up (Cohen

ease between ntion (Cohen’s d=-ents between low-up (Cohen’s

exercise group, p, at post-intervenp (all p<0.05)

between groups roup differences, p differences)

OL over time

exercise treatmpulations. Three

2 studies ev2. Two studies ha

moderate33 or high

n cardiopulmonary

oing active treatmours to exercise trervention consist

treatment for adult

en

nts n’s

-

tion

Baseline, ainterventioat 3-month

FACIT-F

Baseline (wprior to stadarbepoetipost-intervweeks afteexercise prFACT-AN s

ment on studies

valuated ad a low h risk of

y

ment with reatment ted of a

NbingdpvTtrara

t cancer patients

after n (4weeks) and

hs follow-up

within 10 days arting in alfa) and at

vention (1-2 er the 12-week rogram) scale

No significant diffebe found for the Vn post-pre changegroup. Sub-analydifference betweepatients, with a nevs. a > 9% decreaThis difference wareatment of prosandrogen deprivatadiotherapy).

Control group: ctherapy)

Intervention groutailored home-baheart rate, 7 dayresistance band progressive resis4 weeks, focuse

Control group: aprogram during iIntervention grouergometry sessiobaseline exercisbasis

erence in changeVO2max. Surprisine in the exercise gysis according toen prostate cancearly 8% increasease in VO2max in as explained by thstate cancer patietion therapy) in co

onventional medic

up: radiation theraased, progressiveys a week for 4 weprogram (modera

stance exercise, 7d on upper body)

sked not to initiateintervention perioup: aerobic exercions) 3 times per w

se capacity, for 12

e over time betwegly, the authors fogroup vs. a 5.6% o cancer type cer patients ande in VO2max in prnon-prostate canche authors by theents (radiotherapontrast to chemoth

cal care (radiation

apy + individually e walking (60-70%eeks) and therapeately intense 7 days a week for

e a structured exed ise training (cycleweek at 60-100% weeks on ambula

een both groups ound a 2.9% decrincrease in the coshowed a signi

d non-prostate carostate cancer pacer patients (p=0.e more easily toley in combinationherapy (with or w

47

n

% of eutic

r

ercise

of atory

could rease ontrol ficant ancer tients .008).

erated n with ithout

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48

Adamsen et awomen with brecare (n=134). Afor advanced dactive treatmenprogram, combdifference overcontrol group group (at baseVO2max of 1.8baseline mean 1.96l/min). The more cleacomponents ofintensities trainCourneya et al.solid tumours toaerobic exercisVO2max (exprein mean chanrespectively, bcovariates, theremained signadjusted group(p=0.003) and +Mustian et al.4capacity, assesbreast and prointervention the

al.26 randomized east cancer) to e

All patients had redisease or as adnt. The exercise inbining high and lor time in VO2max(p<0.0001). The

eline mean VO2m8l/min), whereas VO2max of 1.82l

ar differences in f the exercise inings). .33 randomized 55o darbepoetin alfase training (n=26essed as ml/kg/mige +3.0 (95%CI

both p=0.001) bee mean change nificantly differenp differences in+0.22 (95%CI 0.040 evaluated the ssed with the 6-mostate cancer pae exercise group

269 patients witexercise treatmenteceived at least ondjuvant treatment,ntervention consisow intensity exercx was found betw

VO2max remainmax of 1.90 l/min

it increased in tl/min and after 6

effect can be exntervention (comb

5 mild-to-moderata alone (n=29) or 6). They found ain and l/min, unadI 1.2-4.7) and +etween both gro

over time in Vt (expressed as

n mean change8-0.37) (p=0.004)effect of exercis

inute walking testatients during radp showed small i

Exercise t

th cancer (includt (n=135) or convne cycle of chemo, and were still rsted of a 6-week cises. A significa

ween the intervented stable in theand after 6week

he intervention gweeks mean VO

xplained by the bination of high a

ely anaemic patiecombined with a

a significant differdjusted group diff

+0.21 (95%CI 0.0oups. After adjusVO2max between s ml/kg/min and +3.0 (95%CI ) respectively) . se treatment on t, in a mixed popudiation therapy. Aimprovements in

treatment for adult

ding 119 ventional otherapy receiving exercise nt mean tion and

e control ks mean group (at O2max of

different and low

ents with 12-week rence in ferences 08-0.34) sting for

groups d l/min, 1.1-5.0)

aerobic ulation of At post-aerobic

c±o-2imdnbSebca((gm1sthind

C•

t cancer patients

capacity (differen±227.84 ft, Cohenof the aerobic cap28.44 ±303.75 mprovement in thdifferent from basnon-significant incbaseline (Cohen’sSchwartz et al.42

exercise program breast cancer, pcapacity, measureat 6 and 12 monthboth p<0.05): at SD178), in resista

group mean 911.mean 1201 m (SD

85), in control grshowed the highehe resistance exen aerobic capacitdecreased to 5% f

Conclusions Conflicting

treatment opopulations 2009, Courne

ce between basn’s d=0.16), wherepacity (difference b

ft, Cohen’s d=he exercise grou

seline anymore (Ccrease in aerobi d=0.28). compared the efand versus usuarostate cancer a

ed with the 12-minhs in both exercise

6 months in aeance exercise gro1 m (SD 194), atD183), in resistanroup mean 983m est improvement ercise group (11%ty of 12% at 6 mfrom baseline valu

evidence is avon cardiopulmo(very low level

eya 2008, Mustia

seline and post-eas the control grbetween baseline

=-0.13). At 3 mup continued, butCohen’s d=0.37). c capacity was

ffects of an aeroal care in a mixedand lymphoma pnute walking test,e groups compareerobic exercise goup mean 1174.7t 12 months in ance exercise gro(SD 193). The a

(16%) in aerobic%). The control grmonths, but at 1ue.

vailable on theonary function of evidence; Grn 2009, Schwartz

KCE Report

-intervention: + 4roup showed a de

e and post-intervemonths follow-upt was not significIn the control grofound compared

obic versus a stred sample consistipatients. The ae significantly impred to the control ggroup mean 1219m (SD 191), in co

aerobic exercise gup mean 1144 maerobic exercise gc capacity, followeroup showed a de2 months the de

e effect of exein mixed ca

riffith 2009, Adamz 2009).

t 185

43.58 ecline ntion:

p the cantly oup a with

ength ing of erobic roved group 9.2 m ontrol group

m (SD group ed by ecline ecline

ercise ancer msen

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KCE Report 185

Table 21 – Effe

Study N

Griffith 200937

N

Adamsen 200926

N

Courneya 200833

N

5

ect of exercise tr

N Cardiopu

N=126 ITT-analychange ((p=0.26) change inincrease Dose-resdifferencprostate (p=0.008

N=269 Significangroups (0p<0.0001control gintervent

N=55 SignificanVO2max groups (up=0.001,p=0.003)SignificanVO2max

reatment on card

ulmonary functio

ysis: no significan-8.4%) between bwith a 2.9% decren exercise group in control group

sponse analysis: se in% change preand non prostate

8, 17.45%)

nt mean differenc0.16l:min, 95%CI 1): no difference oroup, increase ovion group

nt difference in m(ml/kg/min) over tunadjusted group adjusted group d) nt difference in m(l/min) over time b

Exercise t

diopulmonary fun

on

nt difference in both groups ease in pre-post and 5.6%

significant e-post between

patients

ce between both 0.1-0.2,

over time in ver time in

ean change in time between differences

differences

ean change in between groups

treatment for adult

nction in mixed c

Measure poin

Baseline (befochemotherapypost-test (aftercancer treatmePeak oxygen udirectly measutesting (modifieincrease by 2.5min) or estimamin walk test

Baseline and a(6weeks) Peak oxygen uindirectely estistepwise work stationary exerwith workload min, increasedconsecutive m

Baseline (withistarting darbeppost-interventithe 12-week exVO2max on elecycle ergometebreath expired

t cancer patients

cancer populatio

nt

ore start y/radiotherapy), r completion of ent) uptake (VO2max) ured by treadmill ed Balke Protocol5% grade each 3 ted from the 12-

after intervention

uptake (VO2max) mated by use of capacity on

rcise cycle (starteof 67W over 8

d by 20W with eacmin)

in 10days prior to poetin alfa) and aton (1-2weeks aftexercise program)ectronically brakeder with breath-by-

d gas analysis on a

ons

Intervention

l,

Control group+ patients wecurrent level oIntervention gintervention, 20-30 min wa(cool down), telephone ca

ed

ch

Control groupactivity + exeassessmentIntervention gintensity physexercises at 4training at 70at 4 MET houcardiovascula250W, 85-95hours) for 90mtraining + 2 tisessions: relabody awarenonce a week)

t er

d -a

Control groupexercise progIntervention gergometry seof baseline exambulatory b

characteristics

p: biweekly phoneere encouraged toof activity group: home-base50-70% of maximalk followed by 5 m5 times per week ll by study nurse

p: allowed freely toercise program afte

group: 6-week (9 hsical training (30 m4.5 MET hours, 45-100% of one rep

urs per training sear training (station% maximum hearmin followed by 3mes per week maaxation (30 min, 4ess and restorativ), massage (30 m

p: asked not to initgram during intervgroup: aerobic exeessions) 3 times pxercise capacity, fasis

e calls by study nuo maintain their

ed walking mum heart rate, brmin slower walkin+ biweekly

o increase physicer the six week

h/week) high min dynamic 5 min resistance

petition maximum ession, 15 min nary bicycles, 70-rt rate at 3.75 MET0 min relaxation

assage. Low inten4 times per week, ve training (90 minin twice a week)

tiate a structured vention period ercise training (cyer week at 60-100for 12 weeks, on

49

urse

isk g

cal

test

T

nsity

n

ycle 0%

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50

Study N

Mustian, 200940

N

Schwartz,200942

N

N Cardiopu(unadjustadjusted

N=38 Control g401.02, p438.27, a468.86. Mbetween mean chpost-inteExercise interventfollow-upof 43.58 post-inte396.79 bfollow-up

N=101 Aerobic e± 210, atmonths 1Resistan1021.7 ±12 monthAerobic e± 200, atmonths 9

ulmonary functioted group differengroup differences

group: at baseline post-intervention 1at 3months follow-Mean change of -2baseline and posange of 78.73 ± 4rvention and followgroup: 1894.37 ±ion 1937.95 ± 261

p 2020.59 ± 386.3± 227.84 betweenrvention, mean chetween post-inter

p

exercise group: att 6-months 1219.21201 ± 183 ce exercise group 186, at 6-monthshs 1144 ± 185 exercise group: att 6-months 911.1 ±983 ± 193

Exercise t

on nces p=0.001, s p=0.004)

1478.21 ± 1 425.28 ± -up 1 600.33 ± 28.44 ± 303.75

st-intervention, 484.12 between w-up

± 296.78, post-1.99, at 3 months 6. Mean change n baseline and hange of 133.53 ±rvention and

t baseline 1017.32 ± 178, at 12

p: at baseline s 1174.7 ± 191, at

t baseline 1035.4± 194, at 12

treatment for adult

Measure poincalibrated metmeasurement increased 5-20exhaustion

±

At baseline, poand at 3-monthAerobic capac6-min walk tes

t

At baseline, 6 months Aerobic capac12-minute walk

t cancer patients

nt abolic system, workload

0 watts/minute un

ost-intervention hs follow-up

city measured withst

months and 12

city measured withk test (m)

Intervention

ds til

h

Control groupphysical exerIntervention gprogressive rof walking prereserve and tprescription

h

Control groupAerobic exercactivities at mResistance ethera-bands o

characteristics

p: instructed not torcise program group: home-baseresistance exercisescription at 60-70therapeutic resista

p: usual care cise group: weigh

moderate intensitiexercise group: spof weight equipme

KCE Report

o initiated any new

ed aerobic and se program consis0% of heart rate ance ban exercise

t-bearing aerobic es ecific exercises went

t 185

w

sting

e

with

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KCE Report 185

4.6.3 FatiguFive studies remixed cancer pwhile 3 studies Estimates of ththe studies (TabBrown et al.2intervention (n=patients receiviwith 20 minutexercises of upwith elastic banto increase enprogram), follostrategies, discafter the intervPOMS Fatiguedifference was in the analysis components of Dodd et al.36 rcancer beginnexercise duringchemotherapy consisted of anphone calls). significant differ

5

ue eported on the epopulations26,29,33,3

had either a mode effect of exercible 22). 29 compared an=49) with usual ing radiotherapy. tes of exercise

pper and lower extnd, stretching exerndurance, relaxatiowed by educacussion and suppvention (week 4) e-Inertia subscalfound between thno difference wasthe intervention.

randomized 119 wing their first chg and after chem(n=36) or usual

n individualized hoFatigue was merence in fatigue sc

effect of exercise36,40. Two studies erate33,36 or high rse interventions o

n 8-session strcare (n=54) in The multidiscipl(consisting of s

tremities progressrcises, functional ion exercises an

ational informatioport. Fatigue wasand at follow-upe, SDS Fatigue

he exercise and cs made between t

women with breahemotherapy tre

motherapy (n=44)l care (n=39). Tome-based exerceasured using Pcores was found (

Exercise t

e treatment on fahad a low risk of risk of bias29. on fatigue differed

uctured multidisnewly diagnosedinary interventionseated range of sing to resistive elower extremity ed a individualize

on, cognitive-behs measured at b

p (week 8 and 27e, LASA. No sigcontrol group. Impthe effects of the

ast, colorectal or atment to indivi, after having co

The exercise intecise program (withPiper Fatigue Sc(p=0.084).

treatment for adult

atigue in bias26,40,

d across

ciplinary d cancer n started f motion xercises xercises

ed home havioural baseline, 7) using gnificant

portantly, different

ovarian dualized

ompleted ervention h weekly cale. No

AwcfoapmdcwMmthreBthCsasfob+

C•

t cancer patients

Adamsen et al.26

women with breascare (n=134). All por advanced diseactive treatment. Tprogram, combinmeasured using fdifference in fatigcontrol group (p=0weeks. Mustian et al.40 evmixed population herapy. The exeresistance training

BFI and FACIT-Ghe exercise groupCourneya et al.33 rsolid tumours to daaerobic exercise tscale. No significaor unadjusted grobut an improveme+9.1 for darbepoet

Conclusions Conflicting

treatment onof evidence;2009, Courne

randomized 269st cancer) to exerpatients had receiease or as adjuvThe exercise intering high and lofatigue subscale ue over time wa0.02) (estimated

valuated the effecof breast and pr

rcise intervention g. Fatigue was m. Both scales shop. randomized 55 marbepoetin alfa altraining (n=26). F

ant differences weoup differences, pent over time wastin alfa alone vs. +

evidence is avn fatigue in mixe Brown 2006, D

eya 2008).

9 patients with crcise treatment (nived at least one

vant treatment, anrvention consistedow intensity exeof the EORTC Q

as found betweenMD -6.6, 95%CI

ct of exercise trearostate cancer pa

consisted of a cmeasured with twowed an improvem

mild-to-moderately one (n=29) or com

Fatigue was measere found betweenp=0.388 for adjusts noticed (mean +7.8 for the exerc

vailable on theed cancer populaDodd 2010, Ada

cancer (includingn=135) or convencycle of chemothend were still reced of a 6-week exeercises. Fatigue QLQ-C30 A signin the intervention -12.3 to -0.9) af

atment on fatigueatients during radcombined walking

wo different scalesment in fatigue le

anaemic patientsmbined with a 12-sured using FAC

n both groups (p=0ted group differenchange from bas

cise group).

e effect of exeations (very low amsen 2009, Mu

51

g 119 tional erapy eiving ercise

was ficant

n and fter 6

e in a iation g and s, i.e. vel in

s with -week

CT-AN 0.694 nces), seline

ercise level

ustian

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52

Table 22 – Effe

Study N

Brown 200629

N

Dodd 201036

N

ect of exercise tr

N Fatigue

N=103 At basebetweeactivity At weekscores overall both gromentionAt weektrend tocontrol p=0.065

N=119 No signchangin

reatment on fatig

e

eline: no significanen groups, except

(p=0.0445) k 4: overall higher(p=0.047) in exerno significant diffeoups at any weekned) k 8: no significantowards better fatiggroup (POMS Fa5 and SDS Fatigu

nificant group diffeng scores over tim

Exercise t

gue in mixed can

nt difference for POMS vigor

r fatigue QOL-rcise group, but erence between k (p-values not

t differences, but gue-score in atigue-inertia ue p=0.098)

erences in the me (p=0.084)

treatment for adult

ncer populations

Measure poin

Baseline (beforadiotherapy), week 8, week POMS (profile states) fatigue-POMS (profile states) vigor-aSDS (symptomscale) FatigueLASA (linear aself assessmelevel of fatigueSTAI (spielbertrait anxiety invfeel rested (onat baseline) Each score watransformed topoint scale, a 1difference is coas clinically sig

Baseline: weeksecond chemoT2: end of cantreatment (4-6 after baseline)study (approxiyear after basePiper Fatigue S

t cancer patients

nt Int

ore week 4, 27

of mood -inertia of mood ctivity

m distress

analogue nt) average

e rger’s state-ventory) I

nly assessed

as o a 0-100 10 point onsidered gnificant

CodeIntonupexfunenho

k before otherapy, ncer

months , T3: end of mately 1 eline) Scale

CoweIntphindpeco

tervention chara

ontrol group: standescribed) tervention group: ambulatory basis

pper and lower extxercises with elastnctional lower extrdurance, relaxatio

ome program

ontrol group: usuaeekly phone calls tervention group: one calls from ex

dividualized cardioer week, heart ratentinuous exercise

cteristics

dard medical care

eight 90-min sesss, seated range oftremities progresstic band, stretchinremity exercises ton exercises and

al care (no exercisby research nurseexercise prescript

xercise trainers, coovascular/aerobice at 60-80% VO2mes

KCE Report

e (not further

sions over 4 weekf motion exercisessing to resistive g exercises, to increase a individualized

se prescription) + e tion with weekly onsisting of c exercises, 3-5 timmax, 20-30 min of

t 185

ks s of

mes

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Study N

Adamsen 200926

N

Mustian 200940

N

5

N Fatigue

N=269 Significgroups 95%CI

N=38 Exercisimprovepost-intcontinubaselind=-0.58Controlbetwee(Cohenbaselin(CohenNon-siggroup, cpost-intat 3-moExercisimprovepost-intcontinubaselin

e

cant difference ove(estimated mean-12.3 to -0.9, p=0

se group (BFI): smements between btervention (Cohened modest improve to 3-months foll

8) l group (BFI): sma

en baseline and pon’s d=-0.08) but woe and 3-months fo

n’s d=0.04) gnificant lower faticompared to conttervention (p=0.07onths follow-up (pse group (FACIT-Fements between btervention (Cohened modest improve to 3-months foll

Exercise t

er time between difference -6.6,

0.02)

mall baseline and n’s d=-0.15) and vements from low-up (Cohen’s

aller improvementost-intervention orsened between ollow-up

igue in exercise trol group, at 7) but significant <0.05) (BFI) F): small baseline and n’s d=0.29) and vements from low-up (Cohen’s

treatment for adult

Measure poin

Baseline and aintervention (6 EORTC-QLQ-subdomain fat

t

Baseline, afterintervention (4at 3-months fo FACIT-F BFI

t cancer patients

nt Int

after weeks)

C30, igue

Co+ eIntphhorepsebic3.7traseawma

r weeks) and

ollow-up

CotheIntho7 dbaexbo

tervention chara

ontrol group: allowexercise program tervention group: ysical training (30

ours, 45 min resistpetition maximumssion, 15 min cardcycles, 70-250W, 75 MET hours) foraining + 2 times pessions: relaxation

wareness and restassage (30 min tw

ontrol group: converapy) tervention group: ome-based, progredays a week for 4and program (modxercise, 7 days a wody)

cteristics

wed freely to increafter the six week6-week (9 h/week0 min dynamic exetance training at 7

m test at 4 MET hodiovascular trainin85-95% maximumr 90 min followed er week massagen (30 min, 4 times torative training (9wice a week)

ventional medical

radiation therapy+essive walking (60 weeks) and thera

derately intense prweek for 4 weeks,

ase physical activk assessment k) high intensity ercises at 4.5 ME

70-100% of one ours per training ng (stationary m heart rate at by 30 min relaxat

e. Low intensity per week, body

90 min once a wee

care (radiation

+ individually tailo0-70% of heart ratapeutic resistancerogressive resista focused on uppe

53

vity

T

tion

ek),

ored te, e ance er

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Study N

Courneya 200833

N

N Fatigued=0.45)Controlbetwee(Cohenbaselin(CohenSignificgroup, cpost-intup (p<0

N=55 No sign(p=0.69p=0.388 Both gr

e ) l group (FACIT-F)

en baseline and pon’s d=-0.09) but ime and 3-months fo

n’s d=0.29) cant lower fatigue compared to conttervention and at 0.05) (FACIT-F)

nificant differences94 in unadjusted g8 for adjusted gro

roups improved fa

Exercise t

): a decline ost-intervention

mproved between ollow-up

in exercise trol group, at 3-months follow-

s between groupsgroup differences,oup differences)

atigue over time

treatment for adult

Measure poin

s ,

Baseline (withiprior to startingdarbepoetin alpost-interventioweeks after theexercise progrFACT-AN scal

t cancer patients

nt Int

in 10days g fa) and at on (1-2 e 12-week ram) le

Coproae3 tca

tervention chara

ontrol group: askeogram during inte

erobic exercise tratimes per week atpacity, for 12 wee

cteristics

ed not to initiate a rvention periodInt

aining ( cycle ergot 60-100% of baseeks

KCE Report

structured exercistervention group: metry sessions)

eline exercise

t 185

se

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KCE Report 185

4.6.4 SafetyNo adverse eve

Conclusions • No eviden

5

y ents related to the

ce is available.

e exercise interven

Exercise t

ntion were reporte

treatment for adult

ed. 5TptridofubtrlyinwepOqFaeincliInothredHacainbcin

t cancer patients

5 DISCUSThis report providphysical exercise reatment with chdentified, with stuoutcomes of effeunction and fatigbenefits of exercisrue for most cancymphoma patienncluded outcomeswhy the exercise ieffect, since the populations in termOn the contrary, wquality of life or caFurthermore, theradjuvant therapy exercise-related anterpreted with cacancer types, hmitations. n systematic revieon the quality of this report, only veemaining had an

decision was madHowever, an adeqa very limited numconcealing allocaassociated with ovnterventions, inclblinding. The optiocommonly lackingncreased risk of b

SSION des an overview

interventions inemotherapy and/

udies on breast caectiveness, inclu

gue, there was nse, with trials oftecer types with th

nts that reporteds without the repintervention in thipatients in the

ms of age or treatmwe found no consardiopulmonary fure was some efor cancer patien

adverse events. Imaution due to the heterogeneity be

ews and guidelinethe supporting every few trials had either moderate

de from the startquate method of amber of the trials. ation sequencesverestimations of luding exercise, on of blinding the g in the study

biased assessmen

of studies that nvolving cancer p/or radiation. A toancer patients beiding quality of o clear or consis

en reporting conflie exception of th

d significantly poorting of adverses cancer type prostudy did not diment type. istent evidence th

unction, or increasvidence that exents, although notmportantly, our colow number of R

etween studies

es, evidence-basevidence. Of the 33

a low risk of bias(11 studies) or hit of the project t

allocation concealInadequate meth are prone to the intervention eit is not possiblassessment of odesigns. Conse

nt and inflated trea

evaluated a rangpatients during aotal of 33 RCTs ing most commonlife, cardiopulmo

stent evidence octing results. This

he study performeositive results o

e events. It is not oduced such a poiffer from other

hat exercise hampsed fatigue sympercise is safe dt all trials reporteonclusions need

RCTs included for and methodolo

ed conclusions de3 studies assesses (4 studies), whiligh risk (18 studieto include RCTs ment was describ

hods of generatingselection bias

effect54. In behave to perform doutcome measures

equently, there iatment effect.

55

ge of active were

n. For onary n the s was ed on on all

clear ositive study

pered toms.

during ed on to be most

ogical

epend ed for le the es). A

only. bed in g and

and ioural

ouble-s was s an

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56

A number of stuthus failed to tathat efficacy esvalidity of the snot based on poDue to major patient demogrreceiving activetype. A generaadherence) anpopulation diffpopulations seland/or carefullyonly include Rexercise treatmFor other cancavailable, but tconclusions. The large variefrequency andsomewhat elusbased intervenonly possible fTherefore, it iintervention. Trecommendatiothat take canceExercise studiewith Belgian exwas defined focardiopulmonarpatients undergtypes of exercoutcomes it waof exercise, i.etypes on all rem

udies failed to anaake advantage of

stimates become tstudies are the relower calculationsdifferences in disraphics it was de cancer treatme

alization of the rend conclusions ferences in cancected for the trialsy screened befor

RCTs has led toment for those cacer types, evidenthis type of evid

ety of exercise inted duration madesive. An attempt ntions and aerobifor breast canceris impossible to

To allow for theons new studies ser type, stage and es often assess mxercise and cancor cancer patientry function, fatigugoing adjuvant tr

cise without the s not possible to

e. studies had comaining outcomes

alyze data on an f randomization atoo high. Additionlatively small sam. sease- and treat

decided to only tent and to synthesults (including thmight still not cer stage and s were often recrure participation. A a selective repncer types for wnce from observaence was not ta

erventions with ree a comparisonto compare inst

ic exercise with r and did not pro

o recommend ine development ohould focus on optreatment side-ef

multiple outcome mcer specialists a ls in the acute pe and safety. Thereatment for canrisk of major adelucidate consiste

onflicting results w.

Exercise t

intention-to treat and risking the ponally, a large threample sizes that we

ment-related facttreat studies onesize studies perhe reporting of ube appropriate treatment regimeuited on a voluntaAbove this, the cporting on the efhich RCTs are aational studies maken into accoun

espect to intensityof study interv

itution-based withresistance exerc

oduce consistent favour of a pof more cancerptimal exercise mffects into account

measures. In collalist of four key ouphase, i.e. qualityere is some evidecer can perform

dverse events. Foent results on the within the various

treatment for adult

principle ossibility at to the ere often

tors and patients

r cancer ptake or due to

es. The ary basis hoice to ffects of vailable.

might be nt in our

y, mode, ventions h home-cise was

results. particular r-specific odalities t.

aboration utcomes y of life, ence that

several or other benefits

s cancer

ThTsodosthdaadodmthradTtrsSimepvfo(reafoAesrec

t cancer patients

The large varietyhampered our abilThere were a brosame outcome. Woutcome conflictindifficult to assess or a result of diffescales. Within thehere seem to be adisease-specific inand patients first aare affected by a disease-specific ioverlooked. Prefedisease-specific ameasure, cardiopuhe included studiate, timed walking

direct comparison The literature sereatment for cansystematic reviewSports Medicine amportant bias anexpert panel, whicpresent report, focvery positive concor cancer patientIKNL) recently ehabilitation64. Pa

and was identifiedound as for the pA potential explaexclusively are bastudy, enabling a mefers to systema

cancer patients bo

y in outcome mlity to compare treoad selection of

When studies deplong results were whether the effec

erence in sensitive subjective outcoa lack of agreemenstrument. It can and foremost are disease. Howevenstrument there rably, studies sh

and a generic instulmonary functionies. A decision wg tests and VO2mof these measure

earch did not idcer patients in th

w. A consensus appears to be wind therefore not ch involved manycused on RCTs wclusions and recos. The Comprehepublished eviden

art of this guidelin through our searresent report, but

anation is that thased on a criticamore in-depth anatic reviews and m

oth in the acute an

measure points aeatment effects. outcome scales oyed more than ooften reported.

ct measure was dity among the larome measures, inent on whether to

be assumed thainterested in the

er, by only assessis a risk that imould measure qu

trument. Our primn, was measured was made to inclu

ax measures, withes might not be apdentify many guhe acute phase tguideline of the idely accepted63, included in our y authors of the with positive resu

ommendations aboensive Cancer Cence-based guidee was published arch1. In general, tht more positive cohe conclusions o

al appraisal at thealysis and criticismmeta-analyses thand post-acute trea

KCE Report

across studies fu

used to measurone scale for the

It was consequdue to the interverge variety of meancluding quality ouse a generic and

at health professidimensions of life

sing quality of lifemportant domainsuality of life by b

mary objective outin a variety of wa

ude measures of h the awareness tppropriate. uidelines on exethat were based American Collegbut was subjectevidence review.RCTs included i

ults and ended upout exercise treatentre The Netherelines on oncoloas a systematic rehe same evidence

onclusions were dof the present re level of the prm. The Dutch guidat included studie

atment phase9,25.

t 185

urther

re the same uently ntion, asure

of life, d/or a onals e that

e by a s are oth a come ays in heart that a

ercise on a

ge of ted to . The n the

p with tment rlands ogical eview e was rawn. report imary deline es on

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KCE Report 185

Combination oheterogeneity ofor these guidein line with oursAccording to thprograms focusscope of the document for tcollaboration wthe acute phaspecific cancerrehabilitation pfact, a controlleevaluate the eftreatment and pFinally, it shoulhealth in genertrials and metamortality and th

5

of these trials in of the used outcoelines. Nevertheles (see Chapter 6).e consulted expes on the (post-acupresent report, the cancer guideith the College of

ase encompassinr types. Nevertheeriod after cance

ed trial is being seffectiveness of mpsychological supd be stressed tharal, regardless of a-analysis showedhe risk of cardiova

a meta-analysisome scales, was ss, the Dutch rec

erts, most Belgian ute) rehabilitation as it was intend

elines that are def Oncology, guideng diagnosis, steless, a separateer treatment contet up by Belgian remultimodality treat

port) after the treaat physical activity

the health statusd a positive effe

ascular disease65, 6

Exercise t

s, partly becauseconsidered inapp

commendations a

oncological rehaperiod. This was

ded to be a sueveloped by the lines that mainly faging and treatme report focusingtinues to be releehabilitation spectment (including atment for breast y has beneficial efs of a person. Nuct of physical ac66.

treatment for adult

e of the propriate re much

bilitation s not the upportive

KCE in focus on ment of

g on the evant. In cialists to exercise cancer. ffects on umerous ctivity on

66

6

t cancer patients

6 RECOM6.1 Clinical re

• In the abseffects of function treatment,favour of agenerally for healthHence, it iof the pati

• As there iwould be not be recommen

6.2 Research

• Since thereffectiveneand fatigupatients uneeded.

• For outcoshould uscommunityinstrumen

• For future magnitudesignificanc

MMENDATIOecommendatio

sence of consistenexercise treatme

and fatigue for , we cannot forma specific type of accepted counse (weak recommeis advisable to takent into account.is no consistent eharmful for cance

discouraged tndation; very low

h agenda

re is a lack of coness (in terms of que) and on safendergoing active

omes such as qse standardized,y should agree ot to render the resstudies it is cruci

e of effect for oce.

ONS ns

nt evidence on thent on quality ofr cancer patientulate more precisexercise treatme

elling that physicaendation; very loke the local conte

evidence either ther patients under to do physicalevel of evidence)

sistent and high-qquality of life, carety of exercise treatment, large

uality of life and validated scale

on a generic and sults comparable.ial to pre-define moutcome measur

e short-term benef life, cardiopulmots undergoing ase recommendatint, over and aboval activity is bene

ow level of evidext and the prefere

hat exercise treattreatment, they sal activities. ().

quality evidence ordiopulmonary funtreatment for cahigh-quality RCT

d fatigue, researes and the rese

on a disease-sp

main outcomes anres based on cl

57

eficial onary active ion in ve the eficial ence). ences

tment hould (weak

on the nction ancer

Ts are

chers earch

pecific

nd the linical

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58

7 APPEN7.1 Append7.1.1 AMST

Question

1. Was an ‘a prThe research q

2. Was there dThere should be

3. Was a compAt least two eleMEDLINE). Keyshould be suppstudy, and by re

4. Was the statThe authors shexcluded any re

NDICES dix 1: Quality aTAR

riori’ design provuestion and inclus

uplicate study se at least two inde

prehensive literatectronic sources y words and/or Mplemented by coneviewing the refer

tus of publicatioould state that theeports (from the sy

appraisal instru

vided? sion criteria shoul

election and datependent data ext

ture search perfoshould be search

MESH terms musnsulting current crences in the stud

on (i.e. grey literaey searched for reystematic review)

Exercise t

ments

d be established

a extraction? tractors and a con

ormed? hed. The report mst be stated and contents, reviewsies found.

ature) used as aneports regardless), based on their p

treatment for adult

before the conduc

nsensus procedur

must include yeawhere feasible th, textbooks, spec

n inclusion criters of their publicatiopublication status,

t cancer patients

ct of the review.

re for disagreeme

rs and databaseshe search strategcialized registers,

rion? on type. The auth language etc.

nts should be in p

s used (e.g. Cengy should be prov or experts in th

hors should state w

place.

tral, EMBASE, anvided. All searche particular field

whether or not th

KCE Report

Answer

� Yes � No � Can’t answ� Not applic

� Yes � No � Can’t answ� Not applic

nd es of

� Yes � No � Can’t answ� Not applic

ey � Yes � No � Can’t answ� Not applic

t 185

wer able

wer able

wer able

wer able

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KCE Report 185

Question

5. Was a list ofA list of include

6. Were the chIn an aggregateThe ranges of severity, or othe

7. Was the scie‘A priori’ methodouble-blind, plrelevant.

8. Was the scieThe results of texplicitly stated

9. Were the meFor the pooled for homogeneitshould be taken

5

f studies (included and excluded st

aracteristics of ted form such as acharacteristics in

er diseases shoul

entific quality of ods of assessmenacebo controlled

entific quality of the methodologica in formulating rec

ethods used to cresults, a test sh

ty, I²). If heterogen into consideratio

ed and excludedtudies should be p

the included studa table, data from n all the studies d be reported.

the included stunt should be provstudies, or alloca

the included stual rigor and scientcommendations.

combine the findiould be done to e

eneity exists a raon (i.e. is it sensib

Exercise t

d) provided? provided.

dies provided? the original studieanalyzed e.g. ag

udies assessed avided (e.g., for efftion concealment

udies used approtific quality should

ings of studies aensure the studie

andom effects moble to combine?).

treatment for adult

es should be provge, race, sex, rel

and documentedfectiveness studiet as inclusion crite

opriately in formud be considered i

appropriate? s were combinab

odel should be us

t cancer patients

vided on the particevant socioecono

d? es if the author(seria); for other type

ulating conclusion the analysis an

ble, to assess theised and/or the cl

cipants, interventiomic data, diseas

) chose to includees of studies alter

ons? d the conclusions

ir homogeneity (i.linical appropriate

ions and outcomese status, duratio

e only randomizernative items will b

s of the review, an

e. Chi-squared teeness of combinin

Answer

� Yes � No � Can’t answ� Not applic

es. on,

� Yes � No � Can’t answ� Not applic

ed, be

� Yes � No � Can’t answ� Not applic

nd � Yes � No � Can’t answ� Not applic

est ng

� Yes � No � Can’t answ� Not applic

59

wer able

wer able

wer able

wer able

wer able

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60

Question

10. Was the likAn assessmenttests (e.g., Egg

11. Was the coPotential source

7.1.2 Cochr

Domain

Selection bias

Random seque

Allocation con

Performance b

Blinding of papersonnel Assessments each main outoutcomes)

kelihood of publit of publication biaer regression test

onflict of interestes of support shou

rane Collaborati

ence generation

ncealment

bias

rticipants and

should be madecome (or class o

cation bias asseas should include t).

t stated? uld be clearly ack

ion’s tool for ass

Suppo

Describsequenwhethe

Describsequeninterveadvanc

for of

Describparticipinterverelating

Exercise t

essed? a combination of

knowledged in bot

sessing risk of bi

ort for judgement

be the method usnce in sufficient deer it should produc

be the method usnce in sufficient dention allocations c

ce of, or during, en

be all measures upants and personnntion a participang to whether the in

treatment for adult

f graphical aids (e

th the systematic r

ias

t

ed to generate theetail to allow an ace comparable gro

ed to conceal the etail to determine could have been fnrolment

used, if any, to blinnel from knowledgt received. Providntended blinding w

t cancer patients

e.g., funnel plot, ot

review and the inc

e allocation ssessment of oups

allocation whether

foreseen in

nd study ge of which de any informationwas effective

ther available test

cluded studies.

Review auth

Selection biasdue to inadeqsequence

Selection biasdue to inadeqto assignmen

n

Performance interventions the study

ts) and/or statistic

hors’ judgement

s (biased allocatioquate generation o

s (biased allocatioquate concealmennt

bias due to knowby participants an

KCE Report

Answer

cal � Yes � No � Can’t answ� Not applic

� Yes � No � Can’t answ� Not applic

on to interventionsof a randomised

on to interventionsnt of allocations pr

wledge of the allocnd personnel duri

t 185

wer able

wer able

s)

s) rior

cated ng

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KCE Report 185

Domain

Detection bias

Blinding of ouAssessments each main outoutcomes)

Attrition bias

Incomplete ouAssessments each main outoutcomes)

Reporting bias

Selective repo

Other bias

Other sources

5

s

tcome assessmeshould be madecome (or class o

tcome data should be madecome (or class o

s

orting

s of bias

Suppo

ent for

of

Describassessparticipwhethe

for of

Describoutcomanalysireporte(compaattritionanalyse

State hexamin

State athe othIf particreview’questio

Exercise t

ort for judgement

be all measures usors from knowledpant received. Proer the intended bli

be the completeneme, including attritis. State whether

ed, the numbers inared with total rann/exclusions wheres performed by t

how the possibilityned by the review

any important conher domains in thecular questions/en’s protocol, responon/entry

treatment for adult

t

used, if any, to blindge of which intervovide any informatnding was effectiv

ess of outcome daion and exclusionattrition and exclu

n each interventiondomized participare reported, and athe review authors

y of selective outcauthors, and wha

cerns about bias e tool ntries were prespenses should be pr

t cancer patients

nd outcome vention a tion relating to ve

ata for each mainns from the usions were n group ants), reasons for any reinclusions ins

ome reporting waat was found

not addressed in

ecified in the rovided for each

Review auth

Detection biainterventions

rn

Attrition bias incomplete ou

as Reporting bia

Bias due to ptable

hors’ judgement

as due to knowledby outcome asse

due to amount, nautcome data

as due to selective

problems not cove

ge of the allocateessors

ature or handling

e outcome reporti

ered elsewhere in

61

d

of

ng

the

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62

7.2 Append7.2.1 Syste

7.2.1.1 OV1 exp Ne2 Neopla3 cancer$4 tumor$5 tumour6 carcino7 neoplas8 lympho9 melano10 staging11 metasta12 metasta13 exp Ne14 exp neo15 neoplas16 non sm17 adenoc18 squamo19 nsclc.ti20 osteosa21 phyllod22 cystosa23 fibroade24 (non ad25 (non ad26 (nonsm27 plasma28 myelom29 multiple30 lympho31 lympho32 lympho

dix 2: Search smatic reviews

VID Medline eoplasms/ (232736asm Staging/ (103$.ti,ab. (863951) .ti,ab. (820330)

r$.ti,ab. (175521) oma$.ti,ab. (40779sm$.ti,ab. (85745

oma.ti,ab. (97206)oma.ti,ab. (64929)g.ti,ab. (41905) as$.ti,ab. (183033atic.ti,ab. (117234

eoplasm Metastasoplastic processestic process$.ti,ab

mall cell.ti,ab. (235carcinoma$.ti,ab. ous cell.ti,ab. (554,ab. (12889) arcoma$.ti,ab. (13es.ti,ab. (1142)

arcoma$.ti,ab. (54enoma$.ti,ab. (27dj small adj cell).tidj2 small adj2 cell

mall adj2 cell).ti,abacytoma$.ti,ab. (49ma.ti,ab. (31766) e myeloma.ti,ab. (oblastoma$.ti,ab. (ocytoma$.ti,ab. (25osarcoma$.ti,ab. (3

syntax by datab

65) 545)

98) ) ) )

3) 4) is/ (141345) s/ (298816) b. (2088) 591) (81736) 422)

3022)

44) 715) ,ab. (23591) ).ti,ab. (23800)

b. (1482) 946)

(19914) (259) 52) 3572)

Exercise t

base

treatment for adultt cancer patients

33 immunocy34 sarcoma$35 hodgkin$.t36 (nonhodgk37 or/1-36 (2638 exp Exerc39 exp Exerc40 exp Exerc41 exp Muscu42 Rehabilita43 "Physical T44 Exercise M45 "physical t46 "physical f47 motor acti48 (treatment49 (treatment50 (therapy a51 (training a52 (fitness ad53 (activity ad54 (movemen55 (treatment56 (therapy a57 (training a58 (fitness ad59 (activity ad60 (movemen61 (physical a62 rehabilitat63 or/38-62 (364 37 and 6365 meta-anal66 review.pt. 67 search:.tw68 or/65-67 (69 64 and 68

ytoma.ti,ab. (400).ti,ab. (65098) ti,ab. (47627) kin$ or non hodgk667070)

cise/ (58830) cise Therapy/ (246cise Therapy/ (246uloskeletal Manip

ation/ (16315) Therapy (SpecialtMovement Technitraining".mp. (395fitness".mp. (2094vity.mp. or Motor t adj3 exercise) {It adj3 exercise).m

adj3 exercise).mp.adj3 exercise).mp.dj3 exercise).mp. dj3 exercise).mp. nt adj3 exercise).mt adj3 physical).m

adj3 physical).mp.adj3 physical).mp. dj3 physical).mp. (dj3 physical).mp. nt adj3 physical).mand exercise).mp.ion.mp. (98440) 351321)

3 (13676) ysis.mp,pt. (5035(1707163)

w. (174318) 1843870)

8 (2608)

kin$).ti,ab. (27245

668) 668) ulations/ (10808)

ty)"/ (1843) iques/ (271)

57) 47) Activity/ (73372)ncluding Related

mp. (1965) . (23618) (9686) (671) (2519)

mp. (421) mp. (2736)

(31743) (14740)

(21202) (40715)

mp. (300) . (80606)

55)

KCE Report

5)

Terms} (8200)

t 185

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KCE Report 185

70 limit 69

7.2.1.2 OV1 tumor$2 tumour3 carcino4 neoplas5 lympho6 melano7 Staging8 metasta9 metasta10 neoplas11 non sm12 adenoc13 squamo14 nsclc.a15 osteosa16 phyllod17 cystosa18 fibroade19 (non ad20 (non ad21 (nonsm22 plasma23 myelom24 multiple25 lympho26 lympho27 lympho28 immono29 sarcom30 hodgkin31 (nonho32 cancer$33 or/1-3234 "physic

5

9 to yr="2002 - 201

VID PreMedline .ab,ti. (31351)

r$.ab,ti. (7527) oma$.ab,ti. (15670sm$.ab,ti. (2990)

oma.ab,ti. (3167) oma$.ab,ti. (2194)g.ab,ti. (1846) as$.ab,ti. (7988) atic.ab,ti. (5370) stic process$.ab,t

mall cell.ab,ti. (170carcinoma$.ab,ti. ous cell.ab,ti. (237b,ti. (1139) arcoma$.ab,ti. (46es.ab,ti. (40)

arcoma$.ab,ti. (10enoma$.ab,ti. (98dj small adj cell).adj2 small adj2 cell

mall adj2 cell).ab,tiacytoma$.ab,ti. (88ma.ab,ti. (967) e myeloma.ab,ti. (oblastoma$.ab,ti. (ocytoma$.ab,ti. (5)osarcoma$.ab,ti. (7ocytoma.ab,ti. (0)

ma$.ab,ti. (2641) n$.ab,ti. (1246) dgkin$ or non hod$.ab,ti. (43124)

2 (79297) cal training".mp. (1

11" (1685)

0)

)

ti. (59) 07) (3200) 77)

69)

0) 8) ab,ti. (1707) ).ab,ti. (1712) . (92) 8)

(742) (11) ) 78)

dgkin$).ab,ti. (772

112)

Exercise t

2)

treatment for adultt cancer patients

35 "physical f36 motor acti37 (treatment38 (treatment39 (therapy a40 (training a41 (fitness ad42 (activity ad43 (movemen44 (treatment45 (therapy a46 (training a47 (fitness ad48 (activity ad49 (movemen50 (physical a51 rehabilitat52 or/34-51 (953 33 and 5254 meta-anal55 review.pt. 56 search:.tw57 or/54-56 (58 53 and 5759 limit 58 to

fitness".mp. (244)vity.mp. (259) t adj3 exercise) (2t adj3 exercise).m

adj3 exercise).mp.adj3 exercise).mp.dj3 exercise).mp. dj3 exercise).mp. nt adj3 exercise).mt adj3 physical).m

adj3 physical).mp.adj3 physical).mp. dj3 physical).mp. (dj3 physical).mp. nt adj3 physical).mand exercise).mp.ion.mp. (4218) 9491)

2 (465) ysis.mp,pt. (2791(463)

w. (14775) 16781)

7 (25) yr="2002 - 2011"

)

2720) mp. (118) . (191) (473) (46) (158)

mp. (15) mp. (191)

(763) (181)

(299) (2993)

mp. (24) . (1536)

)

(23)

63

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64

7.2.1.3 EM'neoplasm'/exp 'oncogenesis aexercise OR 'mmovement ORtherapy)) ORtherapy'/exp O'locomotion'/expnear AND ('thernear AND ('th('exercise'/exp ('exercise'/exp movement)) O('rehabilitation'/e('rehabilitation'/e'physical trainin(2002:py OR 2OR 2008:py O([cochrane revie

7.2.1.4 Coc#1 MeSH d#2 MeSH d#3 cancer*#4 tumor*:#5 tumour*#6 carcino#7 neoplas#8 lympho#9 melano#10 staging#11 metasta#12 MeSH d#13 MeSH d

MBASE OR 'cancer

and malignant tramotor activity'/exp R ('exercise'/exp 'rehabilitation'/eOR 'physical thp OR locomotion rapy'/exp OR ther

herapy'/exp OR tOR exercise)) OOR exercise

OR ('exercise'/eexp OR rehabilexp OR rehabilng' OR 'physical003:py OR 2004

OR 2009:py OR ew]/lim OR [meta

chrane Library descriptor Neopladescriptor Neopla*:ti,ab ti,ab *:ti,ab

oma*:ti,ab sm*:ti,ab

oma:ti,ab oma:ti,ab :ti,ab a*:ti,ab descriptor Neopladescriptor Neopla

staging'/exp ORansformation'/exp OR 'motor activity

OR exercise exp OR rehabherapy' OR ('gOR motor AND a

rapy)) OR ('exercitherapy)) OR (p

OR (physical ANDAND near AND

exp OR exercitation)) OR (phlitation)) OR 'phl fitness'/exp OR:py OR 2005:py 2010:py OR 201analysis]/lim OR

asms explode all tasm Staging, this t

asm Metastasis exastic Processes ex

Exercise t

R 'metastasis'/eAND ('exercise'/

y' OR 'movement'AND ('therapy'/ebilitation OR 'gait'/exp OR gctivity) OR (physise'/exp OR exerchysical AND ne

D near AND activD ('movement'/e

cise AND neahysical AND neahysical training'/e

R 'physical fitnessOR 2006:py OR 11:py OR 2012:p[systematic review

rees term only

xplode tree 1 xplode tree 1

treatment for adult

xp OR /exp OR /exp OR exp OR 'physical ait OR cal AND

cise AND ar AND vity) OR exp OR r AND ar AND exp OR s') AND 2007:py

py) AND w]/lim)

######################

####

t cancer patients

#14 neoplastic#15 non small #16 adenocarc#17 squamous#18 nsclc:ti,ab#19 osteosarco#20 phyllodes:#21 cystosarco#22 fibroadeno#23 (non NEXT#24 (nonsmall #25 plasmacyt#26 myeloma:t#27 lymphobla#28 lymphocyt#29 lymphosar#30 immunocy#31 sarcoma*:#32 hodgkin*:t#33 nonhodgk#34 non hodgk#35 (#1 OR #2

#10 OR #1#18 OR #1#26 OR #2#34)

#36 MeSH des#37 MeSH des#38 MeSH des#39 MeSH des

c process*:ti,ab cell:ti,ab

cinoma*:ti,ab s cell:ti,ab oma*:ti,ab ti,ab oma*:ti,ab oma*:ti,ab T small NEXT celNEAR/2 cell):ti,ab

toma*:ti,ab ti,ab

astoma*:ti,ab toma*:ti,ab rcoma*:ti,ab ytoma:ti,ab ti,ab

ti,ab in*:ti,ab kin*:ti,ab 2 OR #3 OR #4 O11 OR #12 OR #119 OR #20 OR #227 OR #28 OR #2

scriptor Exercise escriptor Exercise Tscriptor Musculoskscriptor Rehabilita

l):ti,ab b

OR #5 OR #6 OR13 OR #14 OR #121 OR #22 OR #229 OR #30 OR #3

explode tree 1 Therapy explode tkeletal Manipulati

ation, this term onl

KCE Report

R #7 OR #8 OR #15 OR #16 OR #123 OR #24 OR #231 OR #32 OR #3

tree 1 ons explode tree ly

t 185

#9 OR 7 OR

25 OR 33 OR

1

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#40 MeSH d#41 MeSH d#42 physica#43 physica#44 motor a#45 MeSH d#46 (treatm#47 (therap#48 (training#49 (fitness#50 (activity#51 (movem#52 (treatm#53 (therap#54 (training#55 (fitness#56 (activity#57 (movem#58 (physic#59 rehabili#60 (#36 O

OR #44OR #52#59)

#61 (#35 AN#62 (#61), f

5

descriptor Physicadescriptor Exercisal training:ti,ab al fitness:ti,ab activity:ti,ab descriptor Motor Aent NEAR/3 exercy NEAR/3 exercisg NEAR/3 exercis

s NEAR/3 exercisey NEAR/3 exercisement NEAR/3 exeent NEAR/3 physy NEAR/3 physicag NEAR/3 physica

s NEAR/3 physicay NEAR/3 physicament NEAR/3 phyal NEXT exercisetation:ti,ab R #37 OR #38 O4 OR #45 OR #462 OR #53 OR #5

ND #60) from 2001 to 2012

al Therapy Speciase Movement Tec

Activity, this term cise):ti,ab se):ti,ab se):ti,ab e):ti,ab e):ti,ab rcise):ti,ab

sical):ti,ab al):ti,ab al):ti,ab l):ti,ab

al):ti,ab ysical):ti,ab e):ti,ab

OR #39 OR #40 O6 OR #47 OR #4854 OR #55 OR #

2

Exercise t

alty, this term onlychniques, this term

only

OR #41 OR #42 8 OR #49 OR #50 #56 OR #57 OR

treatment for adult

y m only

OR #43 OR #51 #58 OR

7

7123456789111111111122222222

t cancer patients

7.2.2 Random

7.2.2.1 OVID exp Neoplasms

2 Neoplasm Stag3 cancer$.ab,ti. (84 tumor$.ab,ti. (795 tumour$.ab,ti. (16 carcinoma$.ab,t7 neoplasm$.ab,t8 lymphoma.ab,ti.9 melanoma.ab,ti

0 staging.ab,ti. (41 metastas$.ab,t2 metastatic.ab,t3 exp Neoplasm4 exp Neoplastic5 neoplastic proc6 non small cell.7 adenocarcinom8 squamous cell9 nsclc.ab,ti. (12

20 osteosarcoma21 phyllodes.ab,ti22 cystosarcoma$23 fibroadenoma$24 (non adj small 25 (non adj2 sma26 (nonsmall adj227 plasmacytoma

mized controlled t

Medline / (2100323) ing/ (101800) 837076) 96216) 174567) ti. (398903) i. (84170) . (94917) . (63512) 41340) ti. (178868) ti. (114774)

m Metastasis/ (138c Processes/ (292cess$.ab,ti. (2068ab,ti. (23260)

ma$.ab,ti. (79787)l.ab,ti. (54228)

2735) $.ab,ti. (12755) i. (1125) $.ab,ti. (538) $.ab,ti. (2675) adj cell).ab,ti. (23ll adj2 cell).ab,ti. (

2 cell).ab,ti. (1462a$.ab,ti. (4865)

trials

8329) 2261) 8)

)

3260) (23454) )

65

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28 myeloma.ab29 multiple my30 lymphoblas31 lymphocyto32 lymphosarc33 immunocyto34 sarcoma$.a35 hodgkin$.ab36 (nonhodgkin37 1 or 2 or 3

15 or 16 or 27 or 2

38 exp Exercis39 exp Exercis40 exp Muscul41 Rehabilitatio42 Physical Th43 Exercise Mo44 physical tra45 physical fitn46 motor activi47 (treatment a48 (therapy adj49 (training adj50 (fitness adj351 (activity adj352 (movement 53 (treatment a54 (therapy adj55 (training adj

b,ti. (31190) yeloma.ab,ti. (1947toma$.ab,ti. (249)ma$.ab,ti. (252)

coma$.ab,ti. (3533oma.ab,ti. (397) ab,ti. (63959) b,ti. (46774) n$ or non hodgkinor 4 or 5 or 6 or 7or 17 or 18 or 19

28 or 29 or 30 or 3se/ (90515) se Therapy/ (2405oskeletal Manipulon/ (15723)

herapy Specialty/ (ovement Techniqining.mp. (3895)

ness.mp. (20540) ty.mp. or Motor A

adj3 exercise).mpj3 exercise).mp. (j3 exercise).mp. (3 exercise).mp. (63 exercise).mp. (2adj3 exercise).m

adj3 physical).mpj3 physical).mp. (j3 physical).mp. (

70) )

3)

n$).ab,ti. (26683)7 or 8 or 9 or 10 o9 or 20 or 21 or 231 or 32 or 33 or

53) lations/ (10765)

(1834) ues/ (254)

Activity/ (70785) p. (1913) (22952) 9422)

654) 2445) p. (402) . (2672) 31510) 14583)

Exercise t

or 11 or 12 or 13 22 or 23 or 24 or 234 or 35 or 36 (25

treatment for adult

or 14 or 25 or 26 556911)

555566

6666

734567891111111122

t cancer patients

56 (fitness adj3 ph57 (activity adj3 p58 (movement ad59 (physical and e60 rehabilitation.m61 38 or 39 or 40

50 or 51 or(365943)

62 37 and 61 (13263 62 (13200) 64 limit 63 to yr="65 limit 64 to rand

7.2.2.2 OVID 3 cancer$.ab,ti. (44 tumor$.ab,ti. (305 tumour$.ab,ti. (76 carcinoma$.ab,t7 neoplasm$.ab,t8 lymphoma.ab,ti.9 melanoma.ab,ti

0 staging.ab,ti. (1 metastas$.ab,t2 metastatic.ab,t5 neoplastic proc6 non small cell.7 adenocarcinom8 squamous cell9 nsclc.ab,ti. (10

20 osteosarcoma21 phyllodes.ab,ti

hysical).mp. (2078physical).mp. (394dj3 physical).mp. (exercise).mp. (79mp. (96515) 0 or 41 or 42 or 4r 52 or 53 or 54

200)

2010 -Current" (1domized controlled

PreMedline 41236) 0141) 7065) ti. (15000) i. (2928) . (2987) . (2043) 1772) ti. (7702) ti. (5133) cess$.ab,ti. (55) ab,ti. (1557)

ma$.ab,ti. (3047)l.ab,ti. (2231)

020) $.ab,ti. (460) i. (43)

88) 437) 290) 111)

3 or 44 or 45 or 44 or 55 or 56 or

823) d trial (191)

KCE Report

46 or 47 or 48 or 57 or 58 or 59 o

t 185

49 or or 60

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22 cystosarcom23 fibroadenom24 (non adj sm25 (non adj2 sm26 (nonsmall a27 plasmacyto28 myeloma.ab29 multiple my30 lymphoblas31 lymphocyto32 lymphosarc33 immunocyto34 sarcoma$.a35 hodgkin$.ab36 (nonhodgkin37 3 or 4 or 5

or 19 or 30 or 31

44 physical tra45 physical fitn46 motor activi47 (treatment a48 (therapy adj49 (training adj50 (fitness adj351 (activity adj352 (movement 53 (treatment a54 (therapy adj55 (training adj

5

ma$.ab,ti. (9) ma$.ab,ti. (95)

mall adj cell).ab,ti. mall adj2 cell).ab,

adj2 cell).ab,ti. (87ma$.ab,ti. (93) b,ti. (932)

yeloma.ab,ti. (711)toma$.ab,ti. (11) ma$.ab,ti. (5)

coma$.ab,ti. (79) oma.ab,ti. (1) ab,ti. (2568) b,ti. (1179) n$ or non hodgkinor 6 or 7 or 8 or 920 or 21 or 22 oror 32 or 33 or 34 ining.mp. (118)

ness.mp. (239) ty.mp. (264)

adj3 exercise).mpj3 exercise).mp. (j3 exercise).mp. (3 exercise).mp. (43 exercise).mp. (1adj3 exercise).m

adj3 physical).mpj3 physical).mp. (j3 physical).mp. (

(1557) ti. (1562)

7)

)

n$).ab,ti. (735) 9 or 10 or 11 or 1r 23 or 24 or 25 oor 35 or 36 (7598

p. (116) (191) 459)

46) 153) p. (16) . (178) 745) 185)

Exercise t

12 or 15 or 16 or or 26 or 27 or 28 88)

treatment for adult

17 or 18 or 29 or

555566

6666

7'n'otulyOA(sp(cmlyOnOOthOlo((O

t cancer patients

56 (fitness adj3 ph57 (activity adj3 p58 (movement ad59 (physical and e60 rehabilitation.m61 44 or 45 or 46

56 or 57 or 62 37 and 61 (44563 62 (445) 64 limit 63 to yr="65 limit 64 to rand

7.2.2.3 EMBAneoplasm'/exp Ooncogenesis andumor*:ab,ti OR tuymphoma:ab,ti OOR metastatic:ab,AND small:ab,ti squamous:ab,ti A

phyllodes:ab,ti Onon:ab,ti AND sm

cell):ab,ti OR (nomyeloma:ab,ti ymphoblastoma*:OR immunocytomnonhodgkin*:ab,ti OR exercise OR 'mOR movement Oherapy)) OR 'rehaOR 'physical theocomotion OR 'therapy'/exp OR 'therapy'/exp OR

OR exercise)) OR

hysical).mp. (288)physical).mp. (277dj3 physical).mp. (exercise).mp. (14mp. (3986) 6 or 47 or 48 or 458 or 59 or 60 (905)

2010 -Current" (3domized controlled

ASE OR 'cancer stad malignant tranumour*:ab,ti OR c

OR melanoma:ab,,ti OR (neoplastic

AND cell:ab,AND cell:ab,ti) OROR cystosarcomamall:ab,ti AND nexonsmall NEAR/2

OR (multiple:ab,ti OR lymphocma:ab,ti OR saOR (non:ab,ti A

motor activity'/expOR ('exercise'/expabilitation'/exp ORrapy' OR ('gait'/emotor AND acttherapy)) OR ('extherapy)) OR (p

R (physical AND n

) 72) 23) 98)

9 or 50 or 51 or 5005)

313) d trial (2)

aging'/exp OR nsformation'/exp carcinoma*:ab,ti O,ti OR staging:ab

c:ab,ti AND proces,ti) OR adeno

R nsclc:ab,ti OR oa*:ab,ti OR fib

xt:ab,ti AND cell:abcell):ab,ti OR plaab,ti AND cytoma*:ab,ti ORarcoma*:ab,ti ORND hodgkin*:ab,t

p OR 'motor activip OR exercise AR rehabilitation ORexp OR gait ORtivity) OR (physxercise'/exp OR exphysical AND neaear AND activity)

52 or 53 or 54 or

'metastasis'/exp OR cancer*:ab,t

OR neoplasm*:abb,ti OR metastasss*:ab,ti) OR (nonocarcinoma*:ab,ti osteosarcoma*:abbroadenoma*:ab,tib,ti) OR (small NEasmacytoma*:ab,myeloma:ab,ti)

R lymphosarcomaR hodgkin*:ab,titi) AND ('exerciseity' OR 'movemen

AND ('therapy'/exR 'physical therapR 'locomotion'/expical AND near xercise AND nearar AND ('exerciseOR ('exercise'/ex

67

55 or

OR ti OR ,ti OR *:ab,ti n:ab,ti

OR ,ti OR OR

EAR/2 ti OR

OR *:ab,ti i OR e'/exp nt'/exp p OR y'/exp p OR

AND r AND e'/exp xp OR

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68

exercise AND('exercise'/exp rehabilitation)) rehabilitation)) Ofitness'/exp ORAND [embase]/

7.2.2.4 CEN#1 MeSH d#2 MeSH d#3 cancer*#4 tumor*:#5 tumour*#6 carcino#7 neoplas#8 lympho#9 melano#10 staging#11 metasta#12 MeSH d#13 MeSH d#14 neoplas#15 non sm#16 adenoc#17 squamo#18 nsclc:ti,#19 osteosa#20 phyllod#21 cystosa#22 fibroade#23 (non NE

D near AND OR exercise AOR (physical A

OR 'physical trainR 'physical fitnes/lim AND [2001-20

NTRAL descriptor Neopladescriptor Neopla*:ti,ab ti,ab *:ti,ab

oma*:ti,ab sm*:ti,ab

oma:ti,ab oma:ti,ab :ti,ab a*:ti,ab descriptor Neopladescriptor Neoplastic process*:ti,ab

mall cell:ti,ab carcinoma*:ti,ab ous cell:ti,ab ,ab arcoma*:ti,ab es:ti,ab

arcoma*:ti,ab enoma*:ti,ab EXT small NEXT

('movement'/exp AND near ANDAND near AND

ning'/exp OR 'physss') AND [random012]/py

asms explode all tasm Staging, this t

asm Metastasis exastic Processes exb

cell):ti,ab

Exercise t

OR movemen ('rehabilitation'/e

D ('rehabilitation'/esical training' OR mized controlled

rees term only

xplode tree 1 xplode tree 1

treatment for adult

nt)) OR exp OR exp OR 'physical trial]/lim

############

##############

t cancer patients

#24 (nonsmall #25 plasmacyt#26 myeloma:t#27 lymphobla#28 lymphocyt#29 lymphosar#30 immunocy#31 sarcoma*:#32 hodgkin*:t#33 nonhodgk#34 non hodgk#35 (#1 OR #2

#10 OR #1#18 OR #1#26 OR #2#34)

#36 MeSH des#37 MeSH des#38 MeSH des#39 MeSH des#40 MeSH des#41 MeSH des#42 physical tr#43 physical fit#44 motor activ#45 MeSH des#46 (treatment#47 (therapy N#48 (training N#49 (fitness NE

NEAR/2 cell):ti,abtoma*:ti,ab ti,ab

astoma*:ti,ab toma*:ti,ab rcoma*:ti,ab ytoma:ti,ab ti,ab

ti,ab in*:ti,ab kin*:ti,ab 2 OR #3 OR #4 O11 OR #12 OR #119 OR #20 OR #227 OR #28 OR #2

scriptor Exercise escriptor Exercise Tscriptor Musculoskscriptor Rehabilitascriptor Physical Tscriptor Exercise Mraining:ti,ab tness:ti,ab vity:ti,ab scriptor Motor Actt NEAR/3 exercise

NEAR/3 exercise):NEAR/3 exercise):EAR/3 exercise):t

b

OR #5 OR #6 OR13 OR #14 OR #121 OR #22 OR #229 OR #30 OR #3

explode tree 1 Therapy explode tkeletal Manipulati

ation, this term onlTherapy SpecialtyMovement Techni

ivity, this term onle):ti,ab :ti,ab ti,ab i,ab

KCE Report

R #7 OR #8 OR #15 OR #16 OR #123 OR #24 OR #231 OR #32 OR #3

tree 1 ons explode tree ly

y, this term only iques, this term on

ly

t 185

#9 OR 7 OR

25 OR 33 OR

1

nly

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KCE Report 185

#50 (activity#51 (movem#52 (treatm#53 (therap#54 (training#55 (fitness#56 (activity#57 (movem#58 (physic#59 rehabili#60 (#36 O

OR #44OR #52#59)

#61 (#35 AN#62 (#61), f

5

y NEAR/3 exercisement NEAR/3 exeent NEAR/3 physy NEAR/3 physicag NEAR/3 physica

s NEAR/3 physicay NEAR/3 physicament NEAR/3 phyal NEXT exercisetation:ti,ab R #37 OR #38 O4 OR #45 OR #462 OR #53 OR #5

ND #60) from 2001 to 2012

e):ti,ab rcise):ti,ab

sical):ti,ab al):ti,ab al):ti,ab l):ti,ab

al):ti,ab ysical):ti,ab e):ti,ab

OR #39 OR #40 O6 OR #47 OR #4854 OR #55 OR #

2

Exercise t

OR #41 OR #42 8 OR #49 OR #50 #56 OR #57 OR

treatment for adult

OR #43 OR #51 #58 OR

t cancer patients 69

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70

7.3 AppendInstitution-bas

Outcome N st

QOL 5

QOL, physical subscale

4

Home-based e

Outcome N st

QOL 5

QOL, physical subscale

5

Aerobic exerci

Outcome N st

QOL 8

QOL, physical subscale

7

Resistance exe

Outcome N st

QOL 1

dix 3: GRADE sed exercise trea

tudies Risk of

-1

-1

exercise treatmen

tudies Risk of

-2

-2

ise treatment for

tudies Risk of

-1

-1

ercise treatment

tudies Risk of

-1

profiles by inteatment for breast

bias Inconsis

-2

-1

nt for breast can

bias Inconsis

-2

-2

r breast cancer p

bias Inconsis

-2

-2

t for breast cance

bias Inconsis

0

Exercise t

ervention and ot cancer patients

stency Imprec

0

-1

ncer patients.

stency Imprec

0

-1

patients.

stency Imprec

0

0

er patients.

stency Imprec

-2

treatment for adult

outcome s.

cision Indirect

0

0

cision Indirect

0

0

cision Indirect

0

0

cision Indirect

0

t cancer patients

tness Publica

0

0

tness Publica

0

0

tness Publica

0

0

tness Publica

0

ation bias Leve

Very

Very

ation bias Leve

Very

Very

ation bias Leve

Very

Very

ation bias Leve

Very

el of evidence

y low

y low

el of evidence

y low

y low

el of evidence

y low

y low

el of evidence

y Low

KCE Reportt 185

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KCE Report 185

Combined res

Outcome N st

QOL 1

QOL, physical subscale

1

Exercise treatm

Outcome

VO2 peak, absolute

VO2 peak, relative

Other cardiopulmonafunction measures

Fatigue Safety

5

istance and aero

tudies Risk of

-1

-1

ment for breast c

N studies

2 -

2 -

ary 2 -

8 -

5 -

obic exercise trea

bias Inconsis

0

0

cancer patients

Risk of bias

In

-1 -2

-1 -2

-2 -1

-1 -2

-2 0

Exercise t

atment for breas

stency Imprec

-2

-2

nconsistency

2

2

1

2

treatment for adult

st cancer patients

cision Indirect

0

0

Imprecision I

-1 0

-1 0

-2 0

0 0

0 0

t cancer patients

s

tness Publica

0

0

ndirectness P

0 0

0 0

0 0

0 0

0 0

ation bias Leve

Very

Very

Publication bias

0

0

0

0

0

el of evidence

y low

y low

Level of evidence

Very low

Very low

Very low

Very low

Low

71

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72

Exercise treatm

Outcome

QOL

QOL, physicalsubscale

Cardiopulmonfunction

Fatigue

Safety

Exercise treatm

Outcome

QOL

Exercise tolerance

Exercise treatm

Outcome

QOL

Heart rate

Fatigue

ment for prostate

N studies

3 -

2 -

ary 3 -

4 -

2 -

ment for lung ca

N studies

Ris

1 -1

1 -1

ment for colorec

N studies

Ris

1 -2

1 -2

2 -1

e cancer patients

Risk of bias In

-1 -

-2 -

-2 -

-2 -

-1 -2

ncer patients.

sk of bias Inco

0

0

ctal cancer patien

k of bias Inco

0

0

0

Exercise t

s

nconsistency

1

1

1

1

2

onsistency Im

-2

-1

nts.

onsistency Im

-1

-1

-1

treatment for adult

Imprecision

-1 0

-1 0

-1 0

-1 0

-1 0

mprecision Ind

2 0

1 -1

precision Ind

0

0

0

t cancer patients

Indirectness P

0 0

0 0

0 0

0 0

0 0

directness Pu

0

0

irectness Pub

0

0

0

Publication bias

0

0

0

0

0

ublication bias

blication bias

Level of evidence

Very low

Very low

Very low

Very low

Very low

Level of evidence

Very low

Very low

Level of evidence

Very low

Very low

Low

KCE Reportt 185

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KCE Report 185

Exercise treatm

Outcome

QOL

VO2max

Heart rate

Fatigue

Exercise treatm

Outcome

QOL

VO2peak

Fatigue

Exercise treatm

Outcome

Fatigue

Exercise treatm

Outcome

QOL VO2peak

fatigue

5

ment for patients

N studies

Risk

2 -2

1 -2

1 -2

2 -2

ment for lympho

N studies

Risk

1 0

1 0

1 0

ment for leukem

N studies

Risk

1 -2

ment for mixed c

N studies

Risk

4 -2

3 -2

5 -2

s undergoing allo

k of bias Incon

0

0

0

-1

oma patients

k of bias Incon

0

0

0

ia patients

k of bias Incon

0

cancer patients

k of bias Incon

-1

-1

-2

Exercise t

ogeneic hematop

nsistency Imp

-1

-1

-1

-1

nsistency Imp

-1

-1

-1

nsistency Imp

-1

nsistency Imp

0

-1

-2

treatment for adult

poietic stem cell

precision Indir

0

0

0

0

precision Indir

0

0

0

precision Indir

0

precision Indir

0

0

0

t cancer patients

l transplantation

rectness Pub

0

0

0

0

rectness Pub

0

0

0

rectness Pub

0

rectness Pub

0

0

0

.

blication bias Le

V

V

V

V

blication bias Le

M

M

M

blication bias Le

V

blication bias Le

V

V

V

Level of evidence

Very low

Very low

Very low

Very low

Level of evidence

Moderate

Moderate

Moderate

Level of evidence

Very low

Level of evidence

Very low

Very low

Very low

73

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74

7.4 Append7.4.1 Breas

Study ID

Cadmus 200943

dix 4: Evidencest cancer

Method

• Design: Doub2 arms per tridata from IMPstudy is retrie

• Sources of fuLance ArmstrFoundation, American CaSociety, SusaKomen Foundand supportepart by a GenClinical ReseCenter grant home-based intervention oConnecticut widentified throYale-New HaHospital TumRegistry

• Sample size: • Duration: 6 m

e tables

Patien

ble trial, al. Only

PACT eved. nding: rong

ncer an G. dation d in

neral arch Setting:

of women ough aven or

50 months

• Incl• Pre

womAJCcannot beg(≤2 cycphyandbegany

• ExcDiagor pcurr

• Pat• Mea

(8.2• Tre• Rad

CG• Che

CG• Rad

CheCG

Exercise t

t characteristics

usion criteria: - or post-menopamen, ages 35-75 yCC Stages 0-IIIa bncer, recently diag

yet begun or recegun adjuvant treat

weeks radiation oles chemotherapy

ysically able to exed physician consengin an exercise proy activity level clusion criteria: gnosis of other re

primary cancer everent smoker ients characteristian age (+-SD): IG2), CG=54.0 (10.9atment: diation: IG=32%, =32% emotherapy: IG=8=20% diation and emotherapy: IG=5=44%

treatment for adult

s Interve

usal years, breast gnosed, ently ment or ≤ 2 y), ercise nt to ogram,

ecurrent ent,

ics: G=54.5 9)

8%,

56%,

• Interhomintermin daystrial receeduca bincontspecinforPolamonmainat 60predHR).partirecephon

• Comwerecouldtheirchosstudactivwouavai

t cancer patients

ntion(s) Ro

rvention: me-based rvention, 30 activity 5 s/week. At start pt

eived an cational book, nder taining cialized rmation and a ar heart rate nitor (to ntain activity 0-80 % of dicted max . Each icipants

eived weekly ne calls

mparator: CG e told they d exercise on r own if they se but that the y physical

vity program ld not be lable to them

UoagcmAn

Uocm3“pAs(pfac

Results primary outcomes

Unclear reporting of QOL (FACT-B and FACT-G) group comparison measures Authors suggest no significance

Unclear reporting of group comparison measures on SF-36 subscale physical”

Authors suggest significance p<0.05) avouring usual care group

Results secondary andother outcome

• No adverse events relateto the intervention was observe

KCE Report

d es

Critical appraisal ofquality

ed

ed

• Moderateof bias

• 64% of pmeet theof exercis150 min week

• Small sasize

• Difficult toassess thstatistics provided

t 185

f

e risk

pt goal sing per

mple

o he

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KCE Report 185

Study ID

Campbell 200544

Courneya 200745

5

Method

• Design: RCT,arms, pilot stu

• Sources of FuGreater GlasgNHS trust

• Setting: Largeof Scotland CCentre

• Sample size: women with bcancer

• Duration: 12 w

• Design: RCT,• Sources of Fu

Supported byfrom the CanaBreast CanceResearch Allithe CanadianResearch ChProgram, a gfrom NCIC wifunds from thCanadian Ca

Patien

, 2 udy unding: gow

e West Cancer

22 breast

weeks

• Elig• Pat

breaweradjuradi

• Pat• IG ;

(SD• CG

age• Che• Rad• Com

, 3 arms unding: y a grant adian er ance;

n airs rant ith e ncer

• Elig• Eng

spewomstagbegther

• Pat• Mea

78)

Exercise t

t characteristics

gibility criteria: ients who had recast cancer surgerre currently receivuvant iotherapy/chemotients characteristi (n=12) mean age

D+-)=48 (+/- 10) ; (n=10) mean

e=47(+/- 5) emotherapy (n=6)diotherapy (n=6) mbination (n=10)

gibility criteria: glish – or French eaking non-pregnamen ≥18 years oldge I-IIIA breast caginning first line adrapy. ients characteristian age 49.2 (rang

treatment for adult

s Interve

ceived ry and ving

herapy ics: e yrs

)

• IG: sexerweeage hearmaxweeconswarmmin and and perio

• CG: At thstudrececonspersexer

ant d with ancer djuvant

ics: ge 25-

• UC: and initiaexerdurin

• RET3 x wof 8-diff e60-7estimrep mResi

t cancer patients

ntion(s) Ro

supervised rcise 2 x kly at 60-75% adjusted rt rate

ximum for 12 ks. Classes sisted of m-up, 10-20 of exercise a cool down relaxation od. usual care.

he end of y period they

eived help in structing a sonalized rcise plan.

QSvcfagQNcv

usual care asked not to

ate an rcise program ng trial.

T(resistance): weekly 2 sets -12 rep of 9 exercises at 70% of their mated one max. istance

N(Uv(CpU3pA(CA

Results primary outcomes

QOL (FACT-G) Significant p-value group comparison avoring exercise group ( p=0.046) QOL (FACT-B): NS group comparison p-value (p=0.094)

NS for QOL FACT-An)

Unadjusted: RET vs. UC: MD 4.7 CI=-2.7-12.1),

p=0.216 AET vs. UC: MD 3.7(CI=-3.8-11.1), p=0.338, RET vs. AET: MD 1.0 CI=-6.4-8.5)

At 6 month

Results secondary andother outcome

• No effect forfatigue measured byPiper FatiguScale

• No effect forfatigue (measured bFACT-AN subscale “Fatigue”) foany of the twintervention arms at posttest (median17 weeks) aat 6-months

d es

Critical appraisal ofquality

r

y ue

• High riskbias

• Analysis some variablesappropriapoweredsmall samsize a tot19 womefinalized trial IG=1CG=9)

• No ITT analysis

r

by

or wo

t-n and

• Moderateof bias

• Allocationconceale

• No blindioutcome assessm

75

f

of

of

s not ately , mple tal of en the

10,

e risk

n ed ng of

ment

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76

Study ID

Haines

Method

society. • Setting: The C

Cancer Institu(Edmonton, Athe Ottawa HIntegrated CaProgram (OttaOntario) and British ColumCancer Agen(Vancouver, BColumbia)

• Sample size: breast cancerpatients, 201 6months follo

• Duration: durapt chemother(median duraweeks, CI=9-week)

• Design: 2-gro

Patien

Cross ute Alberta), ospital

ancer awa, The

mbia cy British

242 r at

ow-up ation of rapy ation 17 24

oup • Elig

Exercise t

t characteristics

gibility criteria: wom

treatment for adult

s Interve

increwhecomthan

• AETweeergotreadelliptbegiof VOweeprog70%beyo

men • Exer

t cancer patients

ntion(s) Ro

eased by 10% n participants pleted more

n 12 rep. T(aerobic): 3 x kly on cycle

ometer, dmill or tical nning at 60% O2 max for k 1-6,

gressing to % and 80% ond week 12.

foUv(CpU7pA(C

rcise group: 3

Results primary outcomes

ollow-up: Unadjusted: RET vs. UC: MD+2.3 CI=-6.9-11.5),

p=0.620 AET vs. UC: MD 1.9(CI=-7.4-11.3), p=0.686, RET vs. AET: MD 0.4 CI=-8.6-9.4)

3-month:

Results secondary andother outcome

follow-up • Objectively

measured outcomes

• VO2 peak AEgroup supercompared wUC and RET

• Unadjusted:AET vs. UC;MD1.8, (CI=0.5-3.2)p=0.006

• Adjusted: AEvs. UC; MD 2.0, CI=0.6-3.3, P=0.004

• Unadjusted:AET vs. RETMD 1.6, CI=(0.3-2.9),p=0.014

• Adjusted: AEvs. RET; MD1.4, (CI=0.1-2.7 ), p=0.03

• Adverse events: No adverse events reported

• Participant

KCE Report

d es

Critical appraisal ofquality

ET rior with T: ;

),

ET

4 T;

4 ET D -31

• Moderate

t 185

f

e risk

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KCE Report 185

Study ID

201047

5

Method

randomized controlled triablinded outcoassessment aactive (sham intervention) cgroup

• Funding: projgrant from thePrincess AlexHospital CancCollaborative

• Setting: PrincAlexandra Ho(Australia)

• Sample size: baseline, 73 amonth follow-

• Duration: 3, 612months foll

Patien

al with ome and

control

ect e xandra cer Group

cess ospital

89 at at 12--up 6 and low-up

withbreaadjuchefollocritedisehypinjuexe

• Patage55.954.2

Exercise t

t characteristics

h newly diagnosedast cancer underguvant therapy (rademo and hormonaowing surgery; exceria were severe cease, uncontrolledpertension, orthopry, participation in

ercise program ient characteristic

e intervention grou9y (SD 10.5), con2y (SD 11.5) (p=0

treatment for adult

s Interve

d going diation, l) clusion cardiac d edic

n

c: mean up trol

0.47)

homstrenshoucardenduprogmultinstrpackequi

• Contactivinter(flexrelaxactivmateprogactiv

t cancer patients

ntion(s) Ro

me-based ngth, balance, ulder mobility, iovascular urance gram; timedia ructional kage; pment. trol group:

ve sham rvention xibility and xation vities); video erial; no gression of vities

Gre(ines(7(pe0c(0Epfues(8(pe3c(2Mfage1c(pp

Results primary outcomes

Generic health-elated QOL EQ-5D nstrument): VAS exercise group superior 80.6 11.6) vs. control

74.1 (20.6), p=0.006). Utility

exercise group 0.78 (0.19) vs. control 0.84 0.17) (p=0.54)

EORTC C30: physical unctioning exercise group superior; 86.9 10.7) vs. control

86.7 (14.9) p=0.02); fatigue

exercise group 31.8 (20.1) vs. control 34.5 27.9) (p=0.12)

Multidimensional atigue inventory: general fatigue exercise group

1.9 (3.7) vs. control 12.6 (4.3) p=0.52);

physical fatigue

Results secondary andother outcome

adherence higher in firs3 months thain second 3 months

• Adverse events: musculoskeal pain 9 patients, oddratio 2.39 (95%CI 0.5889.92) (p=0.23); fal8patients, odds ratio 0.58 (95%C0.14-2.42) (p=0.48)

d es

Critical appraisal ofquality

st an

let

ds

8-

l

I

of bias • Large

number obetween-group comparis(increasechance otype I statisticaerror

• Considernumber opatients tup form oexercise during tri

• Possible beneficiaeffect of SHAM intervent

77

f

of -

sons e in of

l

rable of took of

al

al

ion

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78

Study ID Method Patien

Exercise t

t characteristics

treatment for adult

s Interve

t cancer patients

ntion(s) Ro

e1c(pree9c(p6NG(ine8c(Ugv(0Epfue8c(fagv

Results primary outcomes

exercise group 0.7 (4.6) vs.

control 10.9 (4.6) p=0.51); educed activity

exercise group 9.8 (4.6) vs. control 10.4 (5.3) p=0.07)

6 months No effect on Generic QOL EQ-5D nstrument): VAS exercise group 80.4 (12.7) vs. control 79.3 14.1) (p=0.09);

Utility exercise group 0.80 (0.21) vs. control 0.83 0.18) (p=0.87)

EORTC C30: physical unctioning exercise group 83.6 (15.8) vs. control 87.5 10.8) (p=0.64); atigue exercise group 27.3 (26.4) vs. control 28.1

Results secondary andother outcome

KCE Report

d es

Critical appraisal ofquality

t 185

f

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KCE Report 185

Study ID

Headley 200448

5

Method

• Design: RCT • Sources of fu

study funded 1999 HoechsMarion RoussInc. Researchfrom the ONSFoundation aUniversity of THealth SciencCenter in the Houston SchoNursing.

• Setting: Outpclinic of comprehensivcancer centersouthwesternStates

Patien

2 arms nding: by the

st sels, h Grant S nd the Texas ce

ool of

atient

ve r,

n United

• EligspestagschoutphavstatZubsit ifor 3accvide

• PatMea(7.1(11(SDCG

Exercise t

t characteristics

gibility criteria: Engeaking, at least 18ge IV breast canceduled to initiate patient chemotherving a performanctus of 2 or less onbrod scale, being an a straight back 30 min and havingess to a television

eo cassette playerients characteristian age (SD): IG=50) CG=52.25 .43)Mean educati

D): IG=14.4 (3.12) =12.6 (2.5)

treatment for adult

s Interve

glish years, er,

rapy, e

n able to chair g n and a r; ics: 50.0

on

• Intermin exerweecomavai(ArmFitneExerProgconsmin min intenrepeexermin Comseatprog

t cancer patients

ntion(s) Ro

(2Mfage1c(ppe1c(p

rvention: 30 seated rcise 3 x kly using a mercially lable video

mchair ess: Gentle rcise). gram sisted of 5 warm-up, 20 moderate-nsity etitive motion rcise and 5 cool down.

mparator: No ted exercise gram,

InreSbepO(dgEdsc(pgpre

Results primary outcomes

20.5) (p=0.29) Multidimensional atigue inventory: general fatigue exercise group

1.1 (4.2) vs. control 11.9 (4.5) p=0.40);

physical fatigue exercise group

0.1 (4.5) vs. control 10.0 (4.1) p=0.95).

nsufficient data eporting

Statistics between endpoints not provided Overall QOL FACIT-F)

declined for both groups Exercise group declining at slower rate than control group p=0.0254, only

graphical presentation of esults)

Results secondary andother outcome

• No adverse events reported

d es

Critical appraisal ofquality

• High riskbias

• Small sa

size • No ITT

analysis • Overall

adherenc75%

79

f

of

mple

ce

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80

Study ID

Hwang 200849

Method

• Sample size: women

• Duration: exeintervention dcycles of chemotherap

• Design: RCT • Sources of fu

none stated • Setting: clinic

setting, Seou• Sample size:

women • Duration: 5 w

Patien

32

ercise during 4

y

2 arms nding:

cal l, Korea 40

weeks

• Eligposwaitwithheaaffeexeunccard

Exercise t

t characteristics

gibility criteria: womst-surgery on outpting list for radioth

h no concurrent malth problems that ect participation inercise program, inccontrolled hypertendiovascular diseas

treatment for adult

s Interve

permcontusuaactiv

men atients

herapy major

could cluding nsion, se,

• Intersupeexerwee(10 m30 mand exercool

t cancer patients

ntion(s) Ro

mitted to tinue any al physical vity

Pbsedsc(pgpreGthgdocc(pmFs“

rvention: ervised rcise 3 x kly for 50 min min warm up,

min stretching aerobic

rcise, 10 min down) Heart

Results primary outcomes

Physical well-being (FACIT-F subscale): exercise group declining at a slower rate than control, p=0.0252, only

graphical presentation of esults)

Graph suggests hat intervention group had less decline in fatigue over time compared with control group p=0.0078),

measured by FACIT-F subscale Fatigue” Positive effect

for WHOQOL-BREF (p<0.001)

Positive effect, p<0.001 (WHOQOL-BREF subscale

Results secondary andother outcome

• No significaexercise-related adverse events werereported

KCE Report

d es

Critical appraisal ofquality

ant

e

• High risk bias

• No allocaconcealm

• No ITT analysis

• Small samsize

• QOL Sca

t 185

f

of

ation ment

mple

ale not

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KCE Report 185

Study ID

Kim 200650

5

Method

• Design: RCT • Sources of fu

supported by from the NatioInstitute of NuResearch andpostdoctoral fellowship awfrom the Korescience and Engineering

Patien

acudisedys

• Pat• Mea

grou• Mea

grou• No

outcbas

2 arms nding: grant

onal ursing d a

ward ea

• Elignewbreaprevall sagerece

• Pat• Mea

(SD• Mea

Exercise t

t characteristics

te or chronic respease, and cognitivfunction. ients characteristian age control up=46.3 (+-9.5) an age exercise up=46.3 (+-7.5) significant differencome measures aseline

gibility criteria: womwly diagnosed withast cancer and novious history of castages of breast ces ≥40 years and eiving cancer treaients characteristian age IG=51.3

D=6.7) an age CG=48.3

treatment for adult

s Interve

piratory ve

ics:

nce on at

rate throuwith encoto wo70%adju

• Com• Patie

wereto peshouexerwereto conorm

men h o ancer, cancer,

atment ics:

• InterAero3 x wmin warmmin 60-7resepeakWeeasse

t cancer patients

ntion(s) Ro

monitored ugh exercise

ouragement ork at 50-

% of age sted max.

mparator: ents in control e shown how erform ulder ROM rcise and e encouraged ontinue with mal activities

rvention: obic exercise, weekly for 30 (+ 5 min m up and 5 cool down) at

70% of HR erve or VO2 k at baseline. ekly essment for

Results primary outcomes

“physical”) Figure

suggests that the control group had a increase in fatigue, that the exercise group had a decrease in fatigue and that there was a significance in difference in the mean fatigue level (measured by Brief Fatigue Inventory) between groups (p<0.05)

No significant group difference in VO2 peak (ml/min)

No significant group difference in resting or maximum heart rate

Results secondary andother outcome

• Secondary outcomes npart of project outcomes

d es

Critical appraisal ofquality

cancer specific

not • High risk

bias • Allocation

concealmnot descr

• High numof drop-o(33 of 74)

• no ITT analysis

81

f

of

n ment ribed

mber uts )

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82

Study ID

Mock 200551

Method

Foundation • Setting: Exerc

facility within School of NurMaryland, Ba

• Sample size: women newlydiagnosed wibreast cancer

• Duration: 8 w

• Design: RCT • Sources of fu

study funded competitive F(Fatigue InitiaResearch andEducation) minstitutional awfrom the OncoNursing SocieFoundation toMock.

• Setting: 4 Unteaching hospNational CancInstitute desigCancer Cente4 community

Patien

cise the rsing,

altimore 41

y th r

weeks

(SD• 40.9

che• 31.8

radi• 27.3

comcheradi

2 arms nding: by a

FIRE ative in d ulti-ward ology ety o Dr.

iversity pitals of cer gnated ers and cancer

• EligageIII bsurgrecethercheconprobpartalrepr w

• Pat• Mea

(8.9• Mea

(9.7• The

Che

Exercise t

t characteristics

D=8.8) 9% receiving

emotherapy 8% receiving iotherapy 3% receiving a

mbination of emotherapy and iotherapy

gibility criteria: Woed 18-70 years, Stbreast cancer by dgery, scheduled toeive outpatient radrapy or adjuvant

emotherapy. Excluncurrent major heablems that could aticipation. Patients

eady exercising >4week were excludients characteristian age IG (SD)=59) an age CG (SD)=7) erapy type IG: emotherapy 41.7%

treatment for adult

s Interve

the fto adpartiresp

• Comusuaincluinforbeneexerspecinstrfurthfor e

omen tage 0-definite o diation

uded if alth affect s 45 min ed ics:

51.3

51.6

%,

• Interhomwrittepreswalkat a pace70%rate.keptand coorweewas coorbiwe

• Comusuaenco

t cancer patients

ntion(s) Ro

first 3 weeks djust for icipants HR

ponses mparator: al care uding general rmation of efits of rcise but no cific ructions or her guidance exercise rvention:

me-based with en

scription to k 5-6 x weekly moderate

e at app. 50-% of max heart

. Patients t daily diaries sent these to

rdinators 1 x kly. Patient contacted by

rdinators eekly mparator: al care, ouraged to

Results primary outcomes

(beats/min)

No effect for fatigue (measured by Piper Fatigue Scale) at post-intervention

Results secondary andother outcome

• No reportingof overall quality of lifmeasure

• Unclear reporting ofgroup comparisonmeasures (SF-36 “Physical Functioningsubscale)

KCE Report

d es

Critical appraisal ofquality

g

fe

f

n

g”

• Moderateof bias

• possible dilution oftreatmenteffect; 39CG exerc28% of IGnot exerc

• unclear reporting

t 185

f

e risk

f t

9% of cised, G did cise

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KCE Report 185

Study ID

Mutrie 200753

5

Method

centers in theEastern US

• Sample size: • Duration: pati

stratified for atherapy form Radiation the(RT) or Chemotherap

• RT pt duratiointervention=6weeks

• CT pt duratiointervention=3months

• Design: RCT • Sources of fu

Cancer ReseUK. CE fundethe UK MedicResearch CoFunders independent fconduct and outcome of thstudy.

• Setting: ThreeNational HeaService Oncoclinics in Scotand communexercise facil

Patien

e

119 ients adjuvant either

erapy

py (CT). n of 6

n of 3-6

Rad• The

CheRad

2 arms nding: arch ed by cal uncil.

from

he

e lth

ology tland ity ities

• EligduristagI-III)

• PatMeaChe

• 15:2RadChe201

Exercise t

t characteristics

diation 58.3% erapy type CG: emotherapy 42.4%diation 57.6%

gibility criteria: woming treatment for ege breast cancer () ients characteristian age=51.6 yearemotherapy= 201, diotherapy=57:201emo+Radiotherap

treatment for adult

s Interve

%,

mainleve

men early (stage

ics: rs.

1, py=129:

• InterEncoattenof mexerweeaddiexerat howeemonensuage maxrate)

• Comusua

t cancer patients

ntion(s) Ro

ntain current l of activity

rvention: ouraged to nd 45 minutes

moderate level rcise 2 x kly and do an tional

rcise session ome each k (women

nitored to ure 50-75% adjusted

ximum heart )

mparator: al care

Results primary outcomes

Significant effect for FACT-B:

12 weeks effect estimate: 2.5 (CI=1.0-3.9), p=0.0007

6 months effect estimate 1.5 (CI=0.1-2.9), p=0.039

No effect for FAGT-G at any measure point

Non-Significant

Results secondary andother outcome

• No adverseevents reported

• Other secondary outcomes npart of project outcomes

d es

Critical appraisal ofquality

e

not

• Low risk obias

• Allocationconcealmblinding ooutcome assessmeITT-analy

• Number oclasses attended the participannot report

83

f

of

n ment, of

ent, ysis of

by

nts ted

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84

Study ID Method

• Sample size: women

• Duration: 12 w

Patien

203

weeks

Exercise t

t characteristics

treatment for adult

s Interve

t cancer patients

ntion(s) RoResults primary outcomes

effect for FACT-F subscale (fatigue) at 12 weeks and 6 months

Results secondary andother outcome

KCE Report

d es

Critical appraisal ofquality

t 185

f

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KCE Report 185

Study ID

Schwartz 200755

5

Method

• Design: RCT (aerobic, resisor usual care

• Sources of fuNot stated

• Setting: Two National CancInstitute-desigcancer centermetropolitan a(US)

• Sample Size:women

• Duration:6 mo

Patien

3 arms stance ) nding:

cer gnated rs in area

66

onths

• Pat• Bre

stagche

• Meagrou

• Meaexe

• Meagrou

Exercise t

t characteristics

ient characteristicast cancer patienge I-III beginning emotherapy an age aerobic exup=48 years an age resistance

ercise group=50 yean age usual careup=46 years

treatment for adult

s Interve

cs ts,

xercise

e ears e

• Usuainstrconttheiractiv

• Aerobaseto chaerotheywalkjoggexer30 mdaysdurindura

• Resiinstrexerfour weeTherresisand Partgivediffeexerwerecomsets repe

t cancer patients

ntion(s) Ro

al care: ructed to tinue with r usual vities obic: home-ed, instructed hoose an obic activity y enjoyed (e.g. king or ing) and

rcise for 15-minutes four s pr. Week ng study ation istance: ructed to rcise at home days per k using ra-Band stance band tubing. icipants were n two rent sets of rcises and e asked to plete two of 8-10

etitions and

Results primary outcomes

Primary outcomes were not part of project defined outcomes

Results secondary andother outcome

• Aerobic capacity at months : Effect on 12minute walktest for aerobic exercise, mean change all groups=94.(95%CI=812-104.6), p=0.02. Resistance exercise group had slight increase in aerobic capacity. Usual Caregroup had decline in aerobic capacity.

d es

Critical appraisal ofquality

6

2 k-

5 -

• High risk bias

• No descr

of allocatconcealmor blindinoutcome assessme

• Small sam

size • Authors u

ITT princi

85

f

of

iption ion

ment g of

ent

mple

used iples

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86

Study ID

Segal 200156

Method

• Design: RCT (self-directedsupervised orcare)

• Sources of fuSupported byNational CancInstitute of Cawith funds froCanadian CaSociety

• Setting: OttawRegional CanCenter, Cana

• Sample size: women

• Duration:26 w

Patien

3 arms , r usual

nding: y the cer anada om the ncer

wa ncer ada

123

weeks

• Elig • Wo

breawithof pther

• Pat• Mea

8.7)• SD

8.7)• Sup

G=5

Exercise t

t characteristics

gibility criteria:

men with stages Iast cancer recruithin 2 weeks of initprescribed adjuvanrapy ient characteristican age ; CG=50.3) exercise G=51.0 ) pervised exercise 51.4 (SD 8.7)

treatment for adult

s Interve

alterexerwithi

I and II ed tiation nt

cs: 3 (SD

(SD

• Intero arm:

exerexerwee

o arm:exerweewalkat prpaceto exhomwee

• Contusua(gen

t cancer patients

ntion(s) Ro

rnate the rcise sets in each week. rvention: : self-directed rcise at home rcising 5 x kly : supervised rcise 3 x pr k (mainly

king exercise rescribed e) + expected xercise at

me 2 other kdays trol arm: al care neral advice)

Results primary outcomes

No effect for FACT-G and FACT-B in patients receiving chemotherapy

No effect for “physical functioning” (SF-36) in institution-based study arm for patients receiving chemotherapy

Positive effect on SF-36 “Physical functioning” (p=0.03) for patient in self-directed arm receiving chemotherapy

Results secondary andother outcome

• Relative VOpeak(ml/kg/in):

• No effect foself-directedinterventionarm compared with control(based datafrom patienreceiving adjuvant therapy)

• No effect fo

supervised interventionarm compared with control(based on data from patients receiving adjuvant therapy)

KCE Report

d es

Critical appraisal ofquality

O2 /m

or d n

l a ts

or

n

l

• Moderateof bias

• Allocationconcealed

• Analysescarried ouan ITT ba

• No blindinoutcome assessme

t 185

f

e risk

n d ut on asis ng of

ent

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KCE Report 185

Study ID

Wang 201158

5

Method

• Design: RCT-• Sources of fu

Mark DiamonResearch FunGraduate StuAssociate, Unat Buffalo, theUniversity of York

• Setting: Homeintervention wpatients from Gung MemorHospital and National TaiwUniversity Ho

• Sample size: • Duration: 6 w

Patien

-2 arms nding:

nd nd,

udent niversity e State New

e-based with

Chang-rial

wan ospital

72 weeks

• Elig18 tdiagstagexp

• follosurgwritcritemasexcjoin

• degadvto e

• recophywomaneand(4) exedysbonnauprobconexebrearepotype

• Aveyea

Exercise t

t characteristics

gibility Criteria: woto 72 years, newlygnosed with stagege II breast cance

pecting chemotherowing recovery frogery, and able to te Chinese. Excluseria: (1) obesity (bss index Q30 kg/mluded to avoid bot problems); (2)

generative arthritisverse effects or inaexercise as ommended by theysicians for exampmen with leukopenemia, thrombocytod high fever up to unsafe conditions

ercise; (5) limiting pnea with exertio

ne pain; (7) severeusea; (8) psychiatrblems; (9)

ntraindications to ercise; (10) recurreast cancer; and (1orted history of otes of cancer. erage age; all=50.ars, exercise=48.4

treatment for adult

s Interve

omen y e I or er, rapy om read or sion body m2; ne and

s; (3) ability

eir ple, nia, openia, 102-F;

s to

n; (6) e ric

ent 11) a ther

42 40

• Exerinterweebaseprogmodintenmeahearmaxmax60%modScal0.5 a

• 3 to per wleastper saccu10-msess30 m

t cancer patients

ntion(s) Ro

rcise rvention; 6-ks, home-ed walking gram, low to erate

nsity asured by a rt rate

ximum (HR x) from 40% to % or the

ified Borg le between and 2, 5 sessions week, and at t 30 minutes session or the umulation of minute sions to reach minutes

Results primary outcomes

QOL (FACT-G, Chinese version):

Hierarchical linear model analysis: pattern

of change between the 2 groups was significantly different

at linear growth rate (t70=3.76, p<.001) and quadratic growth rate (t70=2.64, p=.011). (results provided in text and graphs only)

Fatigue (FACIT-F):

Significant differences between the 2 groups were detected only

Results secondary andother outcome

• Not reportewhether there were any adverseevents

d es

Critical appraisal ofquality

d

e

• High risk bias

• High

contaminrate in uscare grou(30.4%),

• Missing lo

from 17.7usual cargroup

• No descr

of randomizprocess oallocationconcealm

87

f

of

ation sual up

ogs 7% in re

iption

zation or n ment

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88

Study ID

7.4.2 Prosta

Study ID

Galvao 201046

Method

ate cancer

Method

• Design: RCT-2• Sources of fun

the Cancer Cof Western Au

• Setting: Sir ChGairdner Hos(Perth, WesteAustralia)

• Sample size: 5• Duration: 12 w

Patien

yeayea

Patien

2 arms ding:

Council ustralia arles

spital ern

57 weeks

• IncludoccanexpthanevidactiremsubMedphy

• PatieMea7.3)

• Prev

Exercise t

t characteristics

ars, usual care=52ars

t characteristics

sion criteria: histocumented prostatencer, minimum prioposure to AST no n 2 months, withodence of disease vity, and anticipat

main hypogonadal bsequent 6 monthsdical clearance froysician. ents characteristican age; IG=69.5(S), CG=70.1 (SD 7ious radiation;

treatment for adult

s Interve

2.3

s Interve

orically e or longer

out PSA

ted to for the s. om

cs: SD .3)

• IntervComprogresisaero2 x wweeResiexerchesseatshoutriceleg pexte

t cancer patients

ntion(s) Ro

ntion(s) Ro

vention: mbined gressive stance and obic exercise weekly for 12 ks. istance rcise included st press, ted row, ulder press, ps extension,

press, leg nsion and leg

QSGAdmoM2PcAdm

Results primary outcomes

at the nadir (time 3=8.52, P<.001) and at the end of the

program (time 4=5.78, P<.001).

(results provided in text and graphs only)

Results primary outcomes

QOL (general): SF-36; General health: Adjusted group difference in mean changes over 12 weeks: MD=12.9 (CI; 1.9-23.9), p=0.022 Physical health composite: Adjusted group difference in mean changes

Results secondary andother outcome

Results secondary another outcom

QOL (cancer specific): QLQ-C30; fatigue subsca(p=0.021) No adverse events during testing or exerc

KCE Report

d es

Critical appraisal ofquality

d es

Critical appraisal quality

ale:

cise

• Moderateof bias

• • Low pow• • Cardiopu

ary measnot alignwith projedefined

t 185

f

of

e risk

wer

ulmonsures ed ect

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KCE Report 185

Study ID

Windsor 200459

5

Method

• Design: RCT 2• Sources of fun

none stated • Setting: home

intervention, Dundee, Sco

• Sample size: • Duration: 4 we

Patien

IG=• Curre

CG

2 arms nding:

e-based

otland 66 eeks

• EligiboutpradiradiprosExcfrailcomor s

Exercise t

t characteristics

=37.9%, CG=39.3%ent radiation; IG=2=21.4%

bility criteria: men patient waiting listical conformal iotherapy for locastate carcinoma.

clusion criteria: phty due to age and

morbidities e.g. unsevere angina, rec

treatment for adult

s Interve

% 27.6%,

curl,abdocrunResiexerdesigprogto-6-maxto foexeraerocomincluminucardexerwalkat 65maxrate.

• Comp• Usual

on t for

lized

hysical d nstable cent

• Intervhommodintencontwalkmin daysdurin

t cancer patients

ntion(s) Ro

with ominal

nches. istance rcise was gned to

gress from 12--repitition

ximum for two our sets per rcise. The obic ponent

uded 15-20 utes of iovascular

rcise (cycling, king, jogging) 5% to 85% ximum heart . parator: l care

oM9QsQNdd

vention: me-based,

erate-nsity, tinuous king for 30 at least 3 s per week ng

FNdmbra(w

Results primary outcomes

over 12 weeks: MD=5.0(CI; 0.81-9.2), p=0.02 QOL (cancer specific): QLQ-C30; No significant difference for domain “physical”

Fatigue: No significant difference for mean BFI score btwn groups after adiotherapy p=0.18) or at

week 8 follow-up

Results secondary another outcom

Cardio-pulmonfunctioning: No significant group differencin pre-post testresting HR or pto-posttest exercise HR.

d es

Critical appraisal quality

nary

ce t pre-

• High riskbias

• No allocaconcealm

• Low pow

89

of

k of

ation ment wer

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90

Study ID

Monga 200752

Method

(duration of radiotherapy

• Design: RCT • Sources of fu

not reported• Setting: Acad

Medical CenUS

• Sample size: with prostatecancer

• Duration: 8 w

Patien

y) myodem

• Patie• Mean• CG=• IG=6

2 arms nding: emic

nter ,

21 men e

eeks

• Eligibwithdiagambcommea

• Patie• Exerc

68 (• Cont

70.6

Exercise t

t characteristics

ocardial infarctionmentia. ents characteristicn age (+- standard69.3 (+-1.3)

68.3 (+-0.9)

bility criteria: patieh first time cancer gnosis, had to be bulatory and able

mplete self-report asures ents characteristiccise group, mean(+-4.2) rol group, mean a6 (+-5.3)

treatment for adult

s Interve

, or

cs: d error)

radioHR 6calcuHR.

• Comppatiediscoperfonormbut arest thingbeca

ents

to

cs: age:

age:

• IntervSupeaeroprogweeweeaeroat tarate HR –rest

• Compstaninclueducradio

t cancer patients

ntion(s) Ro

otherapy at 60-70% of ulated max

parator: ents not ouraged from orming mal activities advised to and take

gs easy if they ame fatigue.

(InsgfaCndfaIG

vention: ervised

obic exercise gram 3 x kly for 8 ks 30 min

obic exercise arget heart

(.65) x (max – rest HR) + HR

parator: dard care

uding cation and otherapy

CbcMmOsde+FgPmfa-4pQ

Results primary outcomes

p=0.197) n time a significant within group increase foratigue scores in CG (p=0.013) but not a significant difference in atigue scores for G (p=0.203)

Cardiac fitness btwn group omparison

METS:(MET=3.5 ml O2·kg−1·min−1) ignificant mean ifference favoring

exercise=2.8 (SD +- 1.8), p=0.006 Fatique btwn

roup comparison PFS significant mean difference avoring exercise=4.3(SD +-2.1),

p<0.001 QOL (FACT-P)

Results secondary another outcom

r

g

Significant withgroup improvement fexercise grouppre-post intervention Cardiac fitness(METS): p<0.0Fatique: p=0.0FACT-P: p=0.0Physical well-being: p=0.002Significant withgroup decline fcontrol groupIncrease in fatique score,

KCE Report

d es

Critical appraisal quality

hin

for p

s 001 02 04

2 hin for

• High riskbias

• Low pow• Possibly

biased towards healthierprostate cancer patients

• no descriptioof allocatconcealm

t 185

of

k of

wer

r

on tion

ment

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KCE Report 185

Study ID

Segal 200957

5

Method

• Design: RCT Resistance e(RET), Aerobexercise (AEusual care (U

• Sources of funSupported bfrom the CanProstate CanResearch Fu

• Setting: OttawHospital RegCancer CentOttawa, Can

• Sample size: men

• Duration: 24 w

Patien

3 arms, exercise bic

ET) or UC) nding: y Grant nadian ncer und wa gional tre,

nada 121

weeks

• Eligibdoccanrecewithby t

• Patie• Mean

(SD• Marr• Com

Col• Emp• Canc

Exercise t

t characteristics

bility criteria: histocumented prostatencer, scheduled toeive radiotherapy hout ADT and apptreating oncologisent characteristicsn age; 66.3 years

D=7.0) ied=82.6% pleted University lege=51.2% loyed full-time=23cer stage II=78.5%

treatment for adult

s Interve

orically e o

with or proved t

s:

or

3.9% %

• Interv• 1. arm

exergrouexerweerep oexer70%

• 2. armtrain(AET3 x pbegi60%predVO2weeprog75%24

• 3.arm

t cancer patients

ntion(s) Ro

bcSde+sw(p

vention; m: Resistance rcise training up (RET) rcising 3x pr k (2 x 8-12 of 10 diff rcises at 60-

% of 1RM) m: Aerobic ning group T) exercising pr week nning at 50-

% of determined

peak for k 1-4,

gressing to 70-% for week 5-

m: Usual care

F(dSf1(M7Sf1(M7Sf2t(PN

Results primary outcomes

btwn group omparison

Significant mean ifference favoring

exercise=13.8 (SD+-10.1), p=0.006, ubscale “physical

well-being” p<0.001)

FACT-Fatique unadjusted group

differences): Significant effect for RET vs. UC at 12 weeks midpoint);

M=4.11 (CI=0.87-7.35), p=0 .010 Significant effect for AET vs. UC at 12 weeks midpoint);

M=4.64 (CI=1.47-7.80) P=0.004 Significant effect for RET vs. UC at 24 weeks (post-est ); M=4.78 CI=1.77-7.78)

P=0.002 Not significant for

Results secondary another outcom

g D

l

p=0.004, decliin social well-being; p<0.05

p Objectively measured outcomes Group differen(baseline to potest) Unadjusted VOpeak RET vs. MD=1.5 (CI=03.0) P=0.041 AET vs. UC; MD=1.4 (CI=-02.8) P=0.52 (NAdjusted VO2 peak RET vs. UC ; MD=1.6 (CI=13.1) P=0.037 AET vs. UC ; MD=1.4 (CI=02.8) P=0 .063

d es

Critical appraisal quality

ne

nce ost-

O2 UC; .06-

0.1-NS)

.0-

.08-

• Moderaterisk of bia

• Centralizwith allocationconcealmbefore assignme

91

of

e as zed

n ment

ent.

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92

Study ID

Results retrieved

Method

d from a systematic

Patien

review by M.J. Velth

Exercise t

t characteristics

huis, 2010 2

treatment for adult

s Interve

grouwas initiadurin

t cancer patients

ntion(s) Ro

up (UC). UC asked not to

ate exercise ng trial

AwM0FsRw(24FfNFin

Results primary outcomes

AET vs. UC at 24 wks MD=2.65(CI=-0.29-5.58),P=0.08FACT-G significant for RET vs. UC at 12 weeks ; MD 4.76 p=0;017) and at

24 weeks; MD 4.43 (p=0;015) FACT-G no effect for aerobic vs. UCNo effect for FACT-P in any ntervention arm

Results secondary another outcom

8

C

(NS) Adverse event3 adverse eveof these one serious adversevent occurrinthe group performing aerobic exercison day 3 of training protoc(acute myocarinfarction, patierecovered but not complete intervention)

KCE Report

d es

Critical appraisal quality

ts : nts

se g in

se

col rdial ents did

t 185

of

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KCE Report 185

7.4.3 Lung

Study ID

Arbane 201127

5

cancer

Method

• Design: RCT, 2• Sources of Fun

St Georges HoTherapies ChaFunding and thFaculty of HeaSocial Care Sc

• Setting: St GeoHealthcare, LoUK

• Sample size: 5patients attendthoractomy for cancer

• Duration: 1-5 dpost-operative further 12 weeoperative with supervised homexercises

Patien

2 arms nding: ospital aritable he lth and

ciences orge

ondon,

53 ding

lung

days and a ks post-

me

• Eligibwith lung thoraassis

• PatieMean47), Imale

Exercise t

t characteristics

bility criteria: PatieNSCLC referred fresection via ope

actomy or visual sted thoractomy ent characteristicsn age CG=62.6y (IG=65.4y (47-82),

es, 25 females

treatment for adult

s Interventio

ents for n

s: (32-, 28

• Intervent(n=22): uplus 2x/dand mob(walking,the spot, bike exerbedside aleg raisesankle weday 1 to dpostoper80% of m+ a 12-wof home

• Compara(n=21): uincludingphysiothetreatmenclearancemobilizatand uppeactivitiesmonthly tcalls proveducation

t cancer patients

on(s) Ro

tion group usual care day strength ility training marching on recumbent

rcises at and seated s with 2-4lb

eights) from day 5 rative, at 60-max heart rate eek program support

ator group usual care, g routine erapy

nts, airway e techniques, tions as able er limb , (1x/day), telephone viding n

QCsdwbE(fIGmd(CCod4

Results primary outcomes

QOL (EORTC-C30): non-significant difference both within groups and between groups EORTC-C30 functional): G: pre to post-op mean difference=2.0 CI=-5.5-9.3)

CG: pre to post-op mean difference=2.7 (-4.7-10.0)

Results secondary another outcomes

Secondary outcomes not part of project outcomes

d Critical appraisal ofquality

(+)moderateof bias randomizatiocodes kept bindependentteam membe

93

f

risk

on by t er

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94

7.4.4 Colore

Study ID

Courneya, 200332

ectal cancer

Method

• Design: RCT, 2assigned in a 2

• Sources of fungrant from the National Canceinstitute of Can

• Setting: Cross Institute, EdmoCanada

• Sample size: 1colorectal cancsurvivors

• Duration: 16 w

Patien

2 arms 2:1 ratio ding:

er nada Cancer

onton,

02 cer

weeks

• Eligibcolor3 mosurgeattenundewritteEngliPhysQuescontras demaxifitnes

• Patie• Age

IG=5• CG=• Patie

chemCG=

• PatieIG=2

Exercise t

t characteristics

bility criteria: Surgrectal cancer withionths, recovery froery as indicated b

nding physician, aerstand and providen informed conseish, passed the re

sical Activity Readstionnaire and no raindications to exetermined by a sumal cardio respirass test. ents characteristic(mean, SD);

59.92(10.73) 61.13(9.93)

ents % on motherapy: IG=6367.7%

ents % on radiothe23.0%, CG=16.1%

treatment for adult

s Interve

gery for in past om by bility to de ent in evised diness

xercise ub atory

cs:

.9%,

erapy: %

• Interv(n=62preschomepersoexerc(cardiand flexerctimes 20-3065-75predicmax.)phoneprojecreportlevel oand aquest

• Comp(n=31askeda struexercand wan expresc

t cancer patients

ntion(s) Ro

vention group 2): ription of a

e-based, onalized ise program ovascular exibility ises, 3-5 per week, for

0 minutes at 5% of cted HR ) + weekly e calls from ct director to t participants of exercise

answer any ions.

parator group ): were

d not to begin ctured ise program

were not given ercise ription.

Qbmb15(aoincfiwdcfisfop

DbinbinF(pF(p

Results primary outcomes

QOL (measured by FACT-C): mean change between groups=-

.3(95%CI -7.8-5.1), p=0.679 Exploratory

ancillary analysis of patients with ncreased cardiorespiratory itness compared with patients with decreased cardiorespiratory itness showed a significant effect or FACT-C, p=0.038)

Difference between groups n change from baseline to post-ntervention: FACT-C Scale p=0.679)

FACT-G scale p=0.652)

Results secondary another outcomes

Cardiopulmonay function Mean change iresting HR=-2.(95%CI 3.2 to 8.6) (p=0.361) Remaining outcomes not part of guidelinoutcomes

KCE Report

d Critical appraisal ofquality

ar

in 7 -

ne

moderate risbias ITT analysis Blinding of assessors No allocationconcealmentExercise grodid not perfoappreciably mmoderate/strus exercise tcontrol group

t 185

f

sk of

n t

oup orm more renuothan p

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KCE Report 185

Study ID

Houborg 200638

5

Method

• Design: RCT, • Sources of fun

Danish ReseaAgency, DanisCancer SocietDanish HealthInsurance Foundation, DCancer SocietClinical ReseaUnit

• Setting: AarhuUniversity HosDenmark

• Sample size: • Duration: until

Patien

2 arms nding: arch sh ty, h

Danish ty’s arch

us spital,

n=119 l

• Eligib>60yelectcolor

• Excluinflamdissesignifdiseamedi

• • Patie

30 wage 7wom72y (

Exercise t

t characteristics

bility criteria: patiey old when admitteive, abdominal

rectal surgery usion: patients witmmatory bowel diseminated cancer, ficant psychiatric ase or dementia ocal reason

ent characteristicsomen, 30 men, m72y (SD 7) CG: 29en, 30 men, mean(SD 7)

treatment for adult

s Interve

ents ed for

th sease,

or other

s: IG: mean

9 n age

• Interv(n=37mobilstrengupperextremaerobmin/semobilaerob1/3 sttraininextremlower load oone remaxim

t cancer patients

ntion(s) Ro

Tinpbfubebsbcs(p

vention group 7): izations, gth training of r and lower mities and bic training, 45 ession (1/3 ization or

bic training, rength ng upper mity, 1/3 extremity),

of 50-80% of epetition mum.

FP7in1(P3sdbinfapm

Results primary outcomes

Trial outcome ndex (p=0.903) physical well-being (p=0.898) unctional well-being (p=0.987) emotional well-being (p=0.082), social/family well-being (p=0.933), colorectal cancer subscale p=0.839)

Fatigue (VAS): Postoperative day7: more increase n CG 2.3 (95%CI.8-2.9) p=0.0007)

Postoperative day30 and 90: no significant differences between groups n change in atigue score (no p-value mentioned)

Results secondary another outcomes

y

y

d Critical appraisal ofquality

Low risk of b High numberdrop-outs, nodirect measuremenone repetitiomaximum, nmonitoring oactivities besintervention

95

f

bias

r of o

nt of on o

of side

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96

Study ID

7.4.5 Haem

Study ID

Baumann 201128

Method

discharge

matological cance

Method

• Design: RCT 2• Sources of fun

the German JoCarreras LeukeFoundation, thStefan MorschFoundation, Förderverein Transplantationum

• Setting: centertransplantation

Patien

ers

Patien

2-arm ding:

osé emia e

nszentr

r for n ,

• Eligibwith schegood

• Excludiseathe lethrombleedsoma

• Patie

Exercise t

t characteristics

t characteristics

bility criteria: patiemalignant diseaseduled for HSCT, >

d German skills usion: severe cardase, orthopedic illnegs, bone metastambopenia, acute dings, acute healtatic complaints ent characteristics

treatment for adult

s Interve

• Comp(n=48positiostretcneck ashouldtighterelaxaexercwrappmassa(45mi

s Interve

ents e, >18y,

diac ness of ases,

th or

s:

• Interv(n=17endur(cycletraininachiev-20%,withouinterruADL-t(durinchem

t cancer patients

ntion(s) Ro

parator group 8): turning and oning in bed, hing, relaxing and ders, ning and ation ises, hot

pings, age n/session)

ntion(s) Ro

vention group 7): aerobic rance training e ergometer, ng intensity ved watt load , 10-20min ut uption) and training

ng otherapy and

Q(COdtiIG6+C5(n

Results primary outcomes

Results primary outcomes

Quality of life EORTC-QLQ-

C30): Overall QOL difference over ime G: 63.7±19.7 vs. 68.6±11.2, +7.7%) CG: 62.5±23.9 vs.56.3±17.6, -9.9%) no p-values

Results secondary another outcomes

Results secondary another outcomes

Fatigue (EORTC-QLQ-C30) Difference ovetime IG: 41.8±25.3 vs. 43.8±22.7, +4.8%, no p-value mentioneCG: 36.1±24.5vs. 52.8±27.1, +46.3%,

KCE Report

d Critical appraisal ofquality

d Critical appraisal ofquality

-

er

ed 5

High risk of b Contaminatiocontrol groupITT analysisreporting of allocation concealment

t 185

f

f

bias

on in p, no , no

t

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KCE Report 185

Study ID

5

Method

Germany • Sample size: n• Duration: until

discharge

Patien

n=47 • IG: n

mean• CG:

wom(SD

Exercise t

t characteristics

=17, 11 men, 6 wn age 41.41y (SDn=16, 5 men, 11 en, mean age 42.14.04)

treatment for adult

s Interve

women, 11.75)

.81y

after ediffereon strcoordstretcand s20-30twice conduprofestherapdays transpuntil d

• Comp(n=16standphysioprograconsisindividmobiltreatmand pmethointens20mindays/wconduphysiostart otransp

t cancer patients

ntion(s) Ro

engraftment, ent exercises rength, ination, hing, walking tair climbing,

0min/day), a day,

ucted by ssional pist, start 6 prior to plantation discharge parator group 6): clinic’s ard otherapy am, sting of dualized ization

ment (active passive ods with low sities), n/session, 5 week, ucted by otherapist, one day after plantation

m

PfudtiIG62C52

Results primary outcomes

mentioned)

Physical unctioning difference over ime G: 83.1±16.9 vs. 65.9±16.5, -20.7%, p=0.005 CG: 79.6±19.2 vs.59.6±22.9, -25.1%, p=0.002

Results secondary another outcomes

p=0.046

d Critical appraisal ofquality

97

f

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98

Study ID

Coleman 200331

Jarden 200939

Method

• Design: RCT 2• Sources of fun

University of Arkansas for MSciences MedEndowment Research FunOncology NurFoundation, thKnudsen ChaFoundation

• Setting: ArkanSample size:

• Duration: durachemotherapy6 months)

• Design: RCT, armed

• Sources of funthe Lundbeck Foundation, thNordic Foundthe Danish CaSociety, the Copenhagen Hospital Corpand the Danis

Patien

2-arm nding:

Medical dical

nd, the rsing he Earl ritable

nsas n=24 ation of y (+/-

• Eligibpatiechemperiptranstreatmmyelrisk f

• Patieage 574 yemen,

two-

nding:

he Novo ation, ancer

poration sh

• Eligibsche

• Exclurecenpulmabnopsycmotoneurobonyanem

Exercise t

t characteristics

bility characteristicents receiving highmotherapy and ranpheral blood stem splantation for the ment of multiple oma, >40y, not atfor pathologic fracent characteristics55 years, age ranears, 10 women, 1, all white

bility criteria: 18-6duled for HDSCTusion: prior HSCTnt cardiovascular onary disease,

ormal electrocardiohiatric disorder an

or, musculoskeletaological dysfunctio

y metastasis, infecmia, neutropenia,

treatment for adult

s Interve

until ddischa

cs: h-dose ndem cell

t high cture s: mean ge 42-14

• Interv(n=14basedprogracombresistaaerob3x weminut

• Comp(n=10and encouremai

5y,

T, or

ogram, nd al or on, ction,

• Interv(n=21plus mintervconsiswarm(statio15-30max hdays/wdynam

t cancer patients

ntion(s) Ro

day before arge

vention group 4): Home-d exercise am, ination of ance and

bic exercise, eekly for 20 es

parator group 0): usual care

uragement to n active

Fntiam

vention group ): usual care

multimodal ention, sting of 4min -up onary cycling, 0min,<75% of heart rate, 5 week), mic and

Qfu(CDpgIG7C

Results primary outcomes

Fatigue (POMS): no reduction over ime (no changes and p-values mentioned)

QOL-Physical unctioning EORTC-QLQ-

C30): Difference pre-post between groups G:82.9±16.3 vs 75.3±17.4 CG: 83.8±13.4 vs

Results secondary another outcomes

Adverse eventa broken centrvenous cathetestick

Fatigue (EORTC-QLQ-C30): Difference pre-post between groups IG:33.9±28.2 v50.3±24.6 CG: 34.9±28.4vs 58.8±26.0

KCE Report

d Critical appraisal ofquality

ts: ral er

Low sample size, study underpowereUnclear reporting (stusplit results opatients on othalidomide therapy thusonly 10 patieare reported exercise versnot exercise)No reportingcompletion ror adherenceexercise

-

-

vs

4

High risk of bControl grouwas free to increase physical activSmall samplsize

t 185

f

ed

udy of or off

s ents

on sus ) of ate e to

bias p

vity e

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KCE Report 185

Study ID

5

Method

Nursing Socie• Setting: Unive

Hospital of Copenhagen, Denmark

• Sample size: • Duration: 4-6

Patien

ety ersity

n=42 week

throm• Patie• IG: n

(SD • CG:

(SD

Exercise t

t characteristics

mbocytopenia ents characteristic=21, mean age 413.3) n=21, mean age 311.1)

treatment for adult

s Interve

cs: 0.9y

37.4y

stretcexerc20mindays/wresista(15-203daysprogrerelaxa2dayspsych

• Comp(n=21(rangeresistamassa

t cancer patients

ntion(s) Ro

hing ises (15-

n, 5 week), ance training 0min, s/week), essive ation (20min, s/week) and ho-education parator group ): usual care e of motion, ance and age)

6(D3gIG7C6(D6gIG8C7(

QDpgIG8C6(

Results primary outcomes

63.5±22.6 p=0.089)

Difference pre-3months between groups G: 82.9±16.3 vs 77.1±18.1 CG: 83.8±13.4 vs 67.7±23.1 p=0.325)

Difference pre-6months between groups G: 82.9±16.3 vs 87.1±13.2 CG: 83.8±13.4 vs 74.4±23.1 p=0.131)

QOL-FACT-g: Difference pre-post between groups G:87.0±10.9 vs 81.6±14.5 CG: 77.8±14.7 vs 69.0±11.5 p=0.298)

Results secondary another outcomes

(p=0.405) Difference pre-3months between groupIG:33.9±28.2 v44.4±25.0 CG: 34.9±28.4vs 57.3±26.0 (p=0.302) Difference pre-6months between groupIG:33.9±28.2 v29.6±21.3 CG: 34.9±28.4vs 49.6±34.1 (p=0.097) Fatigue (FACTAn) Difference pre-post between groups IG:39.6±6.7 vs33.9±9.7 CG: 37.5±8.9 v27.8±9.0 (p=0.218)

d Critical appraisal ofquality

-

ps vs

4

-

ps vs

4

T-

-

s

vs

99

f

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100

Study ID Method Patien

Exercise t

t characteristics

treatment for adult

s Interve

t cancer patients

ntion(s) Ro

D3gIG8C7(6(D6gIG9C7(

QDpgIG1Cv(

Results primary outcomes

Difference pre-3months between groups G:87.0±10.9 vs 85.6±9.9 CG: 77.8±14.7 vs 71.3±13.0 p=0.241)

67.7±23.1 p=0.241)

Difference pre-6months between groups G:87.0±10.9 vs 90.1±11.9 CG: 77.8±14.7 vs 78.1±18.0 p=0.620)

QOL-FACT-An: Difference pre-post between groups G:149.2±18.0 vs 36.5±26.1

CG: 136.4±24.6 vs 115.8±21.6 p=0.225)

Results secondary another outcomes

Difference pre-3months between groupIG:39.6±6.7 vs37.1±8.9 CG: 37.5±8.9 v31.2±11.9 (p=0.312) Difference pre-6months between groupIG:39.6±6.7 vs40.1±10.6 CG: 37.5±8.9 v33.2±13.0 (p=0.325) Cardiopulmonay function (VO2peak) Difference pre-post IG: 1.97±0.53 v2.03±0.59 (mean % change 0.01) CG: 2.03±0.58vs 1.45±0.46 (mean %

KCE Report

d Critical appraisal ofquality

-

ps s

vs

-

ps s

vs

ar

-

vs

8

t 185

f

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KCE Report 185

Study ID

Courneya 200934

5

Method

• Design: RCT, • Sources of Fu

Lance ArmstroFoundation, thCanada ReseChair programHealth Studenships, Senior Scholar AwardClinical InvestAward from thAlberta HeritaFoundation fo

Patien

2 arms unding: ong he earch m, nt –Health d, and tigator he age or

• EligibspeahistoNHL,chemtreatm

• Patieage: Canc(42%(39.3lympstatu

Exercise t

t characteristics

bility criteria: Englaking, ≥18 years, rically confirmed H, receiving

motherapy or no ment

ent characteristics53.2 (range 18-80

cer type: NHL indo%), NHL aggressiv3%), Hodgkins homa (18%) Treas: Chemotherapy

treatment for adult

s Interve

ish

HL or

s: Mean 0) olent ve

atment y

• Interv(n=60exercfor 12intenspeak first wincreaeach (week15-204, incmin p45min

t cancer patients

ntion(s) Ro

D3gIG1Cv(D6gIG1Cv(

vention group 0): aerobic ise 3xweekly

2 weeks, sity at 60% of power output

week, ased by 5% week to 75% k 4), duration 0 min week 1-reased by 5 r week to 40-n (week 9).

Cfu(DpIG+0C-00Ud

Results primary outcomes

Difference pre-3months between groups G:149.2±18.0 vs 45.6±19.9

CG: 136.4±24.6 vs 121.7±25.2 p=0.167)

Difference pre-6months between groups G:149.2±18.0 vs 53.8±25.1

CG: 136.4±24.6 vs 131.7±34.6 p=0.395)

Cardiopulmonary unction (VO2peakl/min))

Difference pre-post G: mean change +0.40 (95%CI 0.34-0.47) CG: mean change0.03 (95%CI -

0.09-0.03) Unadjusted group difference in

Results secondary another outcomes

change -27.68p<0.0001

k

e

Fatigue (FACTAn) Difference pre-post IG: mean change +4.5 (95%CI 1.9-7.1CG: mean change -0.1 (95%CI -2.7-2.Unadjusted group differencin mean chang

d Critical appraisal ofquality

)

T-

-

1)

.4)

ce ge

moderate risbias allocation sequence generated independentand concealein opaque envelopes frthe study coordinator wassigned participants t

101

f

sk of

tly ed

om

who

to

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102

Study ID Method

Medical Resegrant from NaCancer instituCanada, by Canadian CanSociety and thNCIC/CCS SociobehavioCancer ReseaNetwork

• Setting: CrossCancer instituEdmonton, AlCanada

• Sample size: lymphoma pat

• Duration: 12 w

Patien

arch, ational ute of

ncer he

ural arch

s ute, berta,

122 tients weeks

(44.3treatmtreatm

Exercise t

t characteristics

3%) but stratified fment status Off ment (55.7%)

treatment for adult

s Interve

for Additisessiotraininventila(weeksessiopeak trainin

• Comp(n=62and aincreaaboveduring

t cancer patients

ntion(s) Ro

onally one on of interval ng above ator threshold k 7) and one on of VO2 interval ng (week9) parator group 2): usual care asked not to ase exercise e baseline g trial

m+0(Adm+0(

QDpIG+4C+6Udm+1Adm+1

Results primary outcomes

mean change +0.43 (95%CI 0.34-0.52) p<.001)

Adjusted group difference in mean change +0.43 (95%CI 0.34-0.52) p<.001)

QOL (FACT-An) Difference pre-post G: mean change +10.6 (95%CI 4.9-16.3) CG: mean change+1.1 (95%CI -4.5-6.7) Unadjusted group difference in mean change +9.5 (95%CI 1.5-

7.5) (p=0.021) Adjusted group difference in mean change +7.2 (95%CI 0.4-

4.1)(p=0.039)

Results secondary another outcomes

e

+4.6 (95%CI 1.0-8.3) (p=0.013) Adjusted groupdifference in mean change +4.0 (95%CI 0.9-7.0)(p=0.012)Treatment status (on or ochemo) did notmoderate effecfor any objectively measured outcomes: Adverse evenNo serious adverse event but 3 adverse event (back, hiand knee pain)related to exercise. Patients with knee pain withdrew. The two other patients continued with

KCE Report

d Critical appraisal ofquality

p

ff t ct

ts

ip )

groups

t 185

f

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KCE Report 185

Study ID

Dimeo 199735

5

Method

• Design: RCT, • Sources of fun

the Nenad KeFoundation Preventive MeFreisburg in Breisgau, Ger

• Setting: FreibuUniversity MeCentre

• Sample size: • Duration: indiv

duration depeon hospitaliza(11-18 days)

Patien

2arms nding:

eul

edicine,

rmany urg dical

70 vidual

ending ation

• Eligibconfiperfo60y, impapulmfunctmetaextretransperip

• Patiemean10), m(+-11

Exercise t

t characteristics

bility criteria: maligrmed by biopsy, E

ormance score 0-2no evidence of

airment of cardiac,onary, renal and tion; absence of bastases in the loweemities; and splantation of CD 3pheral blood stem ents characteristicn age IG 39 yearsmean age CG 40 1)

treatment for adult

s Interve

gnancy ECOG 2, 18-

, hepatic

bony er

34+ cells.

cs: s (+-years

• Interv(n=33exercergominterv15 daat mincardia

• Comp(n=37

t cancer patients

ntion(s) Ro

vention group 3): aerobic ises on bed

meter, als of 1 min x

aily, intensity n 50% of ac reserve parator group 7): no exercise

CfuraMraIGCpMraIGCp

%mraIGCp%mraIG

Results primary outcomes

Cardiopulmonary unction (heart ate)

Maximal heart ate at admissionG: 170±18 CG: 168±16 p=0.58 Maximal heart ate at dischargeG: 166±21 CG: 168±19 p=0.84

% of estimated maximal heart ate at admissionG: 94±7 CG: 94±8 p=0.89 % of estimated maximal heart ate at admissionG: 92±10

Results secondary another outcomes

modified exercise program

Adverse eventless severity ofcomplications IG: Diarrhea: p=0.04 Pain: p=0.01 One severe adverse event exercise groupdeemed to be highly unlikely related to exercise (patiedied of hepatichemorrhage)

d Critical appraisal ofquality

ts f in

in p

ent c

high risk of b multiple comparisonsincreased risspurious find randomizationot well described no descriptioallocation concealment

103

f

bias

s, sk of dings

on

on of

t

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104

Study ID

Chang 200830

Method

• Design: RCT, • Sources of fun

none stated • Setting: medic

centre in centTaiwan

• Sample size: 2patients with A

• Duration: 3 we

Patien

2 arms nding:

cal ral

22 AML eeks

• Eligibof agand aprescsatisfcondECOwillin

• Patiemean(SD=(SD=

Exercise t

t characteristics

bility criteria: > 18 ge diagnosed withaware of their diagcribed chemotherafactory functional ition as determine

OG-PS (rating of 0-g to sign consent

ents characteristicn age IG=49.4 yea=15.3), CG=53.3 y=13.6)

treatment for adult

s Interve

years AML gnosis, apy, in

ed by -3.), t form cs: ars years

• Interv(n=11walkinhallwaper wweeks

• Comp(n=11invasicare

t cancer patients

ntion(s) Ro

Cp

vention group ): 12 min

ng in hospital ay, five days eek for 3 s parator group ): non-ive routine

FAindbA(90A(90A(90

WindbA(90A(91A(9

Results primary outcomes

CG: 93±9 p=0.69

Fatigue Average fatigue ntensity: difference between groups At day 7: -3.64 95%CI -6.65 to -

0.62) p=0.02 At day 14: -3.73 95%CI -6.65 to -

0.81) p=0.010 At day 21: -2.55 95%CI -5.62 to -

0.53) p=0.100

Worst fatigue ntensity: difference between groups At day 7: -4.73 95%CI -8.73 to -

0.72) p=0.02 At day 14: -4.27 95%CI -7.53 to -.01) p=0.01

At day 21: -3.36 95%CI -6.74 to

Results secondary another outcomes

Secondary outcomes not part of project outcomes No adverse events

KCE Report

d Critical appraisal ofquality

high risk of ballocation concealmentdescribed small samplesize lacks patientsimilarity at baseline

t 185

f

bias

t not

e

t

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KCE Report 185

Study ID

5

Method Patien

Exercise t

t characteristics

treatment for adult

s Interve

t cancer patients

ntion(s) Ro

0FindbA(90A(90A(90

Results primary outcomes

0.01) p=0.05 Fatigue nterference difference between groups At day 7: -2.58 95%CI -5.06 to -

0.09) p=0.04 At day 14: -2.83 95%CI -5.56 to -

0.11) p=0.04 At day 21: -3.32 95%CI -6.18 to -

0.46) p=0.02

Results secondary another outcomes

d Critical appraisal ofquality

105

f

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106

7.4.6 Mixed

Study ID

Rummans 200641

d cancers

Method

• Design: RCT, tarms

• Sources of funthe Linse BockFoundation, SaMarys HospitaSponsorship B

• Setting: Mayo Cancer Center

• Sample size: n• Duration: 4 we

Patien

two-

ding: k aint l

Board Clinic r n=103 eks

• EligibdiagncancsurviplannweekExcluon FostatumoreCoopGroudisorongosubsradiaof dis

• Patien=4911.4959.4y

Exercise t

t characteristics

bility criteria: newlnosed with advancer, estimated 5-yeval rate of 0-50% ned to receive at lks of radiation theusion: scored 20 oolstein mini mentas examination, 3

e on the Eastern perative Oncologyup, active thought rder or suicidality, oing alcohol or tance abuse, prev

ation therapy, recusease ent characteristics9, mean age 59.7y9), CG n=54, meay (SD 10.62)

treatment for adult

s Interve

y ced ear who east 2 rapy. or less al or

y

vious urrence

s: IG: y (SD an age

• Interv(n=49sessiocompweeksenrollpsychpsychfacilitanursetherapor soc20minexerceducainstru20minexerc

• Comp(n=54

t cancer patients

ntion(s) Ro

vention group 9): 8x90min-ons, leted within 4 s after ment, led by

hiatrist or hologist co ated by

e, physical pist, chaplain cial worker, n conditioning ises,

ational ction and n relaxation ises.

parator group 4): usual care

QUAAoObIGCpOwIGCpOwIGCpOwIGCpNd

Results primary outcomes

QOL (Spitzer QOLUniscale + Linear Analogue Scales oAssessment (LASAof QOL) Overall QOL at baseline G: 70.0±21.89 CG: 73.0±20.80 p=0.4829 Overall QOL at week 4 G: 72.8±20.62 CG: 64.1±22.53 p=0.0469 Overall QOL at week 8 G: 71.9±19.41 CG: 68.4±23.48 p=0.4229 Overall QOL at week 27 G: 72.1±19.49 CG: 72.1±18.97 p=0.9922 No significant difference in overa

Results secondary aother outcom

L

of A)

all

Secondary outcomes noof project outcomes

KCE Report

and mes

Critical appraisaquality

ot part High risk bias Small samsize Heterogeof study populatio

t 185

al of

of

mple

eneity

on

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KCE Report 185

Study ID

Adamsen 200926

5

Method

• Design: RCT 2• Sources of fun

The LundbeckFoundation, TNovo NordiskEgmont FounThe Danish CSociety, The SAndersen Foundation, TAase and EjnaDanielsen Foundation, TBeckett FoundThe Wedell-Wedellsborg Foundation, THede Nielsen Foundation, TGangsted Foundation, Copenhagen University Hos

• Setting: Two University Hosin CopenhageDenmark

Patien

2 arms nding: k The , The dation,

Cancer Svend

The ar

The dation,

The Family

The

spital

spitals en,

• Eligibof caleastchemdiseatreatmperfoand 1

• Patiemen,47 ye21dif59 diregim

Exercise t

t characteristics

bility criteria: diagnancer, having rece

one cycle of motherapy for advaase or as adjuvanment, having a Wormance status of 18-65 years ents characteristic, 196 women, meaears (range 20-65fferent cancer diagfferent chemothe

mes

treatment for adult

s Interve

nosis eived at

anced t

WHO 0 or 1,

cs: 73 an age

5), gnosis, rapy

• Interv(n=11basedhigh aintensintervsupertrainespeciaphysiohigh itraininminutfor 6 wactivitequivatotal ohours

• Comp(n=11convemedicalloweincreaactivitprograsix we

t cancer patients

ntion(s) Ro

Qgd(nm

vention group 8): Group

d multimodal and low sity exercise ention rvised by ed nurse alist and otherapist, ntensity ng for 90 es 3 x weekly weeks, ties alent to a of 43 MET s per week parator group 7):

entional cal care + ed freely to ase physical ty + exercise am after the eek

QQGsd6IG6C6M27

Pfud6IG8C8M25

Results primary outcomes

QOL in interventiogroup, a significandecrease in QOL no p-value

mentioned)

QOL (EORTC QLQ-C30) Global health status/QOL: difference baseline6weeks G: 63.8±21.1 vs 67.2±20.3 CG: 60.2±22.4 vs 63.3±22.4 Mean difference: 2.2 (95%CI -2.7-7.1), p=0.4

Physical unctioning: difference baseline6weeks G: 84.7±14.5 vs 89.0±12.4 CG: 84.0±15.7 vs 86.4±14.5 Mean difference: 2.4 (95%CI -0.4-5.1), p=0.09

Results secondary aother outcom

on nt

e-

e-

Fatigue (EORQLQ-C30) Difference baseline-6weIG: 39.7±25.834.6±24.3 CG: 43.0±2341.0±22.7 Mean differe6.6 (95%CI -to -0.9), p=0. Adverse eveOne patient wbrain tumor experienced grade 3 seizupost cardiovascultraining (recovered bsubsequentlyexcluded fromtrial)

and mes

Critical appraisaquality

RTC-

eeks 8 vs

3.9 vs

nce: --12.3 .02

nts with

ure

ar

but y m

Low risk bias Randomion using CITMAS AllocationconcealeOutcomemeasureskeyed ananalyzedindependresearch assistant Analysescarried ouon an ITTbasis

107

al of

of

zati

n ed e s

nd by

dent

s ut T

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108

Study ID

Mustian 200940

Method

• Sample size: 2patients with c(mixed)

• Duration: 6 we

• Design: RCT 2• Sources of fun

the National CInstitute

• Setting: UniveRochester JamWilmot CanceCenter

• Sample size: (breast and prcancer patient

• Duration: 4 we

Patien

269 cancer

eeks

2-arms nding: Cancer

ersity of mes P. er

n=38 rostate ts) eeks

• Eligibwith with begintherametadiseacontrschetreatmlifesty

• Patien=19CG:

Exercise t

t characteristics

bility criteria: wombreast cancer andprostate cancer nning standard radapy, no distant astases, no recurrease, no raindications, at leduled radiation ments, sedentary yle

ent characteristics9, 6 men, 13 women=19, 5 men, 14 w

treatment for adult

s Interve

asses

men d men

diation

ent

east 30

s: IG: en, women

• Interv(n=19therapindividhomeprogrewalkinheart a weeweekstherapresistaprogra(modeintensprogreresistaexercweek

t cancer patients

ntion(s) Ro

ssment CfuinD6IG1C1M00

vention group 9): radiation py+ dually tailored

e-based, essive ng (60-70% of rate, 7 days

ek for 4 s) and peutic ance band am erately se essive ance ise, 7 days a for 4 weeks,

FDpIG10(C20(

Din3IG10

Results primary outcomes

Cardiopulmonary unction (VO2peakn l/min) Difference baselin6weeks G: 1.82±0.4 vs .96±0.5

CG: 1.90±0.5 vs .88±0.5

Mean difference: 0.16 (95%CI 0.1-0.2), p<0.0001

Fatigue (BFI) Difference baselinpost-intervention G:1.85±1.87 vs .60±1.36 (-

0.25±1.24) Cohen’s d=-0.15)

CG: 2.62±2.14 vs 2.44±2.08 (-0.18±1.16) Cohen’s d=-0.08)

Difference post-ntervention-3months G:1.60±1.36 vs .16±0.98 (-

0.66±1.52)

Results secondary aother outcom

k

e-

e-

)

)

Secondary outcomes noof project outcomes

KCE Report

and mes

Critical appraisaquality

ot part Low risk bias Patients blinded, rof experimebias, participanexpectaneffect or nonspecitreatmeneffects

t 185

al of

of

not risk

enter

nt ncy

fic t

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KCE Report 185

Study ID

5

Method Patien

Exercise t

t characteristics

treatment for adult

s Interve

focusebody)

• Compconvemedic(radia

t cancer patients

ntion(s) Ro

ed on upper ) parator group: entional cal care ation therapy)

(C2(0(

FDpIG4((C31(

Din3IG4((C4((

Results primary outcomes

Cohen’s d=-0.58)CG: 2.44±2.08 vs 2.73± 2.60 0.12±1.95) Cohen’s d=0.04)

Fatigue (FACIT-F)Difference baselinpost-intervention G:38.68±11.66 vs41.79±8.99 3.11±8.69) Cohen’s d=0.29)

CG: 36.89±11.73 v35.84±12.08 (-

.05±4.84) Cohen’s d=-0.09)

Difference post-ntervention-3months G:41.79±8.99 vs 43.17±7.74 3.89±7.77) Cohen’s d=0.45)

CG: 35.84±12.08 v40.35±12.24 3.88±6.97) Cohen’s d=0.29)

Results secondary aother outcom

)

) e-

s

vs

)

vs

and mes

Critical appraisaquality

109

al of

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110

Study ID Method Patien

Exercise t

t characteristics

treatment for adult

s Interve

t cancer patients

ntion(s) Ro

CfuDpIGv(4(C112(

Din3IGv((C11((

QDp

Results primary outcomes

Cardiopulmonary unction (6MWT) Difference baselinpost-intervention G:1894.37±296.7vs 1937.95±261.943.58±227.84) Cohen’s d=0.16)

CG: 478.21±401.02 v425.28±438.27 (-

28.44±303.75) Cohen’s d=-0.13)

Difference post-ntervention-3months G:1937.95±261.9vs 2020.59± 386.3133.53±396.79) Cohen’s d=0.37)

CG: 425.28±438.27 v600.33±468.86 78.73±484.12) Cohen’s d=0.28)

QOL (FACIT-F) Difference baselinpost-intervention

Results secondary aother outcom

e-

8 9

vs -

)

9 36

vs

e-

KCE Report

and mes

Critical appraisaquality

t 185

al of

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KCE Report 185

Study ID

Griffith 200937

5

Method

• Design: RCT 2• Sources of fun

The National Institutes of HNational CentResearch resoNIH RoadmapMedical Rese

• Setting: univeteaching hospcommunity cacenter in Balti

Patien

2-arms nding:

Health, ter for ources, p for arch rsity

pital and ancer more

• Eligibdiagncancto recradiaexcluindivthan

• Patien=6810.8)60.6y

Exercise t

t characteristics

bility criteria: >21ynosis of stage I to er who were scheceive chemothera

ation therapy or bousion: comorbiditieiduals exercising 120min per week

ent characteristics8, mean age 59.8y), CG: n=58, meany (SD 10.8)

treatment for adult

s Interve

y, II

eduled apy, oth, es, more

k s: IG: y (SD n age

• Interv(n=68interv70% oheart 20-30followslowe(cool times biweecall by

t cancer patients

ntion(s) Ro

IG1(6(Cv0(Din3IG11CCv(8(

vention group 8): walking ention, 50-of maximum rate, brisk

0 min walk wed by 5 min er walking down), 5 per week +

ekly telephone y study nurse

CfuDIGCp

Results primary outcomes

G:124.19±25.12 v30.19±20.13 6.00±18.31) Cohen’s d=0.26)

CG: 117.59±29.65vs 116.92±30.58 (0.67±11.51) Cohen’s d=-0.02)

Difference post-ntervention-3months G:130.19±20.13 v32.96± 6.41(8.76±16.51)

Cohen’s d=0.41) CG: 116.92±30.58vs 126.13±31.81 8.55±11.28) Cohen’s d=0.28)

Cardiopulmonary unction (VO2peakDifference pre-posG: -2.9% CG: +5.6% p=0.26

Results secondary aother outcom

vs

5 -

)

vs

)(

8

k) st

Cardiopulmofunction (VO2peak) Difference prpost (dose-response analysis) Prostate grou+8% Nonprostate group:->9%

and mes

Critical appraisaquality

onary

re-

up:

High risk bias Adherencproblemssmall samsize, limitpower forsubset analysis, of 2 methodos for

111

al of

of

ce s, mple ted r

use

logie

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112

Study ID

Brown 200629

Method

• Sample size: • Duration: ?

• Design: RCT 2• Sources of fun

the Linse BocFoundation anSaint Mary’s HSponsorship B

• Setting: DivisiRadiation OncMayo Clinic, Rochester

• Sample size: • Duration: 4we

Patien

n=126

2-arms nding:

ck nd the Hospital Board on of cology

n=115 eeks

• Eligibdiagnmontat leasurvimorerecom2 weless tor mosubsthougplans

• Patien=49

Exercise t

t characteristics

bility criteria: cancnosis within the paths, expected survast 6 months, 5-yeval probability of n

e than 50%, treatmmmendation for aeks, exclusion: Mthan 20, ECOG score, active alcohotance abuse, activght disorder, suicis ent characteristics9, CG: n=54

treatment for adult

s Interve

• Comp(n=58phonestudy patienencoumaintcurrenactivit

cer ast 12 vival of ear no ment t least MSE core 3

ol or ve dal

s: IG:

• Interv(n=49sessioweeksrangeexercand loextremresistwith estretcexercfunctioextremto incendurrelaxaexercindividhome

• Comp(n=54medic

t cancer patients

ntion(s) Ro

parator group 8): biweekly e calls by nurse +

nts were uraged to ain their nt level of ty vention group 9): 8x90-min ons over 4 s, seated

e of motion ises of upper

ower mities, ive exercises

elastic band, hing ises, onal lower mity exercises rease rance, ation ises and a dualized

e program parator group 4): standard cal care (not

FDgPinPaSpLS

Dgofa(

Dg

Results primary outcomes

Fatigue Difference betweegroups at baselinePOMS fatigue-nertia: p=0.3934POMS vigor-activity: p=0.2495SDS Fatigue: p=0.9887 LASA: p=0.7950 STAI: p=0.9302

Difference betweegroups at week 4:overall higher atigue QOL-scorep=0.047) in IG

Difference betweegroups at week 8

Results secondary aother outcom

p=0.008

en e:

en

es

en

Secondary outcomes noof project outcomes

KCE Report

and mes

Critical appraisaquality

cardiorestory fitnesassessm

ot part High risk bias Complianto exercisinstructiounknownamount oexercisesknown in control gr

t 185

al of

spirass ent

of

nce se

ons ,

of s not

roup

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KCE Report 185

Study ID

Dodd 201036

5

Method

• Design: RCT • Sources of fun

the National CInstitute, the Cand TranslatioScience InstituClinical ReseaCenter

• Setting: 6 outpsettings in SaFrancisco Bay

• Sample size: • Duration: 1y

Patien

3-arms nding: Cancer Clinical onal ute, arch

patient n y Area n=119

• Eligib>18ybreascancchemPerfo60 orconcboneuncodiabeinten3, lytorthoof madisorwithinAIDSleuke

• Patien=448.2); 52.0yn=36

Exercise t

t characteristics

bility criteria: womy, confirmed diagnst, colorectal or over, beginning first

motherapy, Karnoformance Status scr greater, exclusiourrent radiation th

e marrow transplaontrolled hypertensetes mellitus, painsity score greateric bone lesion,

opedic limitations, ajor depression, srders, chemotheran past year, diagn

S-related malignanemia ent characteristics4, mean age 49.4y

CG: n=39, mean y (SD 10.8); Post-6, mean age 50.4y

treatment for adult

s Interve

furthe

men, nosis of varian t fsky core of on: herapy, ntation, sion, n r than

history sleep apy nosis of ncy,

s: IG: y (SD age

-IG: y (SD

• Interv(n=37prescweeklfrom etraineof indcardioobic etimes heart 80% V30mincontinexerc

• Later-groupsimilaintervcompcance

• Comp(n=37(no ex

t cancer patients

ntion(s) Ro

er described) ndtrfa(inSp

vention group 7): exercise ription with ly phone calls exercise

ers, consisting ividualized ovascular/aerexercises, 3-5 per week, rate at 60-

VO2peak, 20-n of nuous ises -intervention p (n=32): ar exercise ention after letion of

er treatment parator group 7): usual care xercise

FCp

CpNm

Results primary outcomes

no significant differences, but rend towards bettatigue-score in CGPOMS Fatigue-nertia p=0.065 anSDS Fatigue p=0.098)

Fatigue (PFS) Change over timep=0.084

Change over time per group No p-value mentioned

Results secondary aother outcom

ter G

d

Adverse eveHip pain, scia(n=16), arm discomfort (nknee discom(n=10), anklediscomfort (nfoot discomfo(n=8), asymptomatiischemic chaelectrocardio(n=10), asymptomatibigeminy (n=premature ventricular complexes (n

and mes

Critical appraisaquality

nts atica

n=4), fort

e n=3), ort

ic anges ogram

ic =6),

n=9)

Moderaterisk of biaOnly 3 assessmin 1 year period to capture effect

113

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ents

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114

Study ID

Courneya 200833

Method

• Design: RCT, • Funding: fund

drug supply pby Amgen, CaInc.

• Setting: CrossCancer InstituEdmonton, Ca

• Sample size: to-moderatelyanemic cancepatients

• Duration: 12 w

Patien

9.0)

2 arms ding and rovided anada,

s ute, anada 55 mild-

y er

weeks

• EligibconficancleverEasteOncostatudefinsurvispeaage, thera

• Patieage=(81.8chemnot snon-c

Exercise t

t characteristics

bility criteria: histormed nonmyoloider diagnosis, an H

r of 80-110 g/l, an ern Cooperative ology group perfors of 0-2, completeitive surgery, expval ≥3 months, En

aking and ≥18 yeadarbepoetin alfa

apy ent characteristics=56 (25-77), Fema8%), Current motherapy=51 (92stratified for chemochemo

treatment for adult

s Interve

prescweeklby res

orically

Hb

rmance ed ected nglish

ars of

s: mean ale 45

.7%), o vs.

• Interv(n=26ergomsessiofor 12100%peak

• Comp(n=29askedinitiateexercduringperiod

t cancer patients

ntion(s) Ro

ription) + ly phone calls search nurse vention group 6):3 x cycle metry ons pr week 2 weeks at 60-

% of baseline power output

parator group 9):usual care, d not to e a structured ise program g intervention d

QMbp+2C9Ud(9pAd(9p

FMbp+1C4Ud

Results primary outcomes

QOL ( FACT-An)Mean change baseline-postintervention IG+13.4 (95%CI 2.5-24.2) CG: +20.3 (95%C9.2-31.4) Unadjusted group difference: -6.9 95%CI -22.1-8.3)

p=0.363 Adjusted group difference: -3.2 95%CI -16.7-10.4

p=0.637

Fatigue (FACT-AnMean change baseline-postintervention IG+7.8 (95%CI 2.8-

2.8) CG: +9.1 (95%CI 4.4-13.8) Unadjusted group difference: -1.3

Results secondary aother outcom

G: -

I

,

4),

n)

G:

Cardiopulmofunction (VO2peak) VO2peak (ml/kg/min) Unadjusted gdifference: +(95%CI -1.2-p=0.001 Adjusted grodifference: +(95%CI 1.1-5p=0.003 VO2peak (l/mUnadjusted gdifference: +(95%CI 0.080.34), p=0.00Adjusted grodifference: +(95%CI 0.080.37), p=0.00

KCE Report

and mes

Critical appraisaquality

onary

group 3.0 -4.7),

oup 3.0 5.0),

min) group 0.21 -01

oup 0.22 -04

moderaterisk of biaITT analyAppropriaallocationconcealm

t 185

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KCE Report 185

Study ID

Schwartz 200942

5

Method

• Design: RCT • Funding: Natio

Institutes of Hgrant

• Setting: 3 majcancer centrecommunity meoncology prac

• Sample size: women

• Duration: 12m

Patien

3 arms onal

Health

jor s and edical ctices 101

months

• Eligibwith neopspeaambuexercchemradiobeginwith aantiepsyccardimovepulm6 mostudyhyperheumankymeta

• Patien=34n=34n=33

Exercise t

t characteristics

bility criteria: womhistologically conf

plasia, >18y, able ak and read Englisulatory, cised<120min per

motherapy and otherapy naïve, nning chemotheraa steroid or as an

emetic, exclusion: hiatric illness, ovascular disease

ement-limiting arthonary diseases, s

onths prior to starty, Paget’s disease

erparathyroidism, matoid arthritis, losing spondylitis

abolic bone diseasent characteristics4, mean age 48y; 4, mean age 47y; 3, mean age 48y

treatment for adult

s Interve

men firmed to

sh,

r week,

apy

e, hritis, steroids t of e,

, other ses s: AG: RG: CG:

• Intervaerobgroup4days30minintensbearinactivittelephup

• Intervresistagroupspecifwith thon weequip3 setsrepetisets orepetion surepetimaximtelephup

t cancer patients

ntion(s) Ro

(9pAd(9p

vention bic exercise p (AG)(n=34): s/week, 20-n, low sities, weight ng aerobic ties + hone follow-

vention ance exercise

p (RG)(n=34): fic exercises heraband or eight ment, at least

s of 12 tions or 2

of 18-20 tions (based bjects 1-tion

mum)+ hone follow-

CfuCA16(m1R16(m1C1619DgA6

Results primary outcomes

95%CI -8.0-5.4), p=0.694 Adjusted group difference: +2.1 95%CI -2.8-7.1),

p=0.388

Cardiopulmonary unction (12MWT) Change over timeAG: baseline

017.3 (SD 210), a6 months 1219.2 SD 178), at 12

months 1201 (SD 83)

RG: baseline 021.7 (SD 186), a

6 months 1174.7 SD 191), at 12

months 1144 (SD 85)

CG: baseline 035.4 (SD 200), a

6 months 911.1 (S94), at 12 months

983 (SD 193) Difference betweegroups AG:+16%, mean 661±9ft at 6 and

Results secondary aother outcom

at

at

at SD s

en

Adherence rain AG 94% (7at 12months)RG 74% andat 12 months

and mes

Critical appraisaquality

ate: 79% ), in

d 65% s

High risk bias Problemswith adherencrate in RG

115

al of

of

s

ce G

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116

Study ID

Method Patien

Exercise t

t characteristics

treatment for adult

s Interve

• Comp(n=33teleph

t cancer patients

ntion(s) Ro

parator group 3): only hone call

1R41Cain1dto

Results primary outcomes

2months RG:+11%, mean 401±28ft at 6 and

2months (p<0.05CG: 12% decreaseat 6 months, ncrease at 2months but 5%

decline compared o baseline

Results secondary aother outcom

5) e

KCE Report

and mes

Critical appraisaquality

t 185

al of

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KCE Report 185

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