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A phase III study of gemcitabine ± docetaxel
for metastatic soft tissue sarcoma
Maki RG, Wathen JK, Patel SR, Priebat DA, Okuno S, Samuels B, Harmon DC, Fanucchi M,
Hensley ML, Reinke D, Thall PF, Benjamin RS, Baker LH
CTOS 2005, Boca Raton, FL
Rationale for phase III study
• Gemcitabine alone has at least activity in some sarcomas (LMS, osteosarcoma, angiosarcoma)
• Two phase II studies show activity of gemcitabine + docetaxel in soft tissue sarcoma (STS)– There appears to be synergy in sarcoma cell lines
between the two drugs when given in the sequence gem→doc
Merimsky O et al. Cancer Chemother Pharmacol 2000; 45:177Patel SR et al. J Clin Oncol 2001;19:3483. Svankarova L et al. Eur J Cancer 2002; 38:556 Okuno S et al. Cancer 2003; 97:1969 Hensley ME et al. JCO 2002; 20:2824Leu KM et al. JCO 2004; 22: 1706
Purpose
• Execute a phase III study of gemcitabine +/- docetaxel in patients with up to 3 prior lines of therapy for metastatic disease– Is it the controlled rate infusion of gemcitabine that
yields the activity in this combination?– In which subtypes is combination active? Is the
combination better, or more toxic, or both?
• Utilize a novel Bayesian design, dynamic randomization, to minimize the number of patients necessary to determine a statistically significant difference between arms
Entry Criteria
• Soft tissue sarcoma, no GIST, KS, meso• Age ≥ 10• Measurable disease• No more than 3 prior regimens for metastatic
disease• Good organ function; T Bili ≤ ULN, Cr ≤ 2• Not pregnant• No neuropathy > G1• No uncontrolled CNS metastases
Phase III regimens
No prior pelvic XRT Prior Pelvic XRT
Arm A
G 1200 mg/m2 over 120 min, d 1, d8,
q21d + GCSF
G 900 mg/m2 over 90 min, d 1, d8, q21d + GCSF
Arm B
G 900 mg/m2 over 90 min, d1, d8, Doc 100
mg/m2 d8, q21d + GCSF
G 675 mg/m2 over 60-75 min, d1, d8, Doc 75 mg/m2 d8,
q21d + GCSF
● Dynamic randomization: Bayesian model● 120 patient enrollment target● Restage after cycles 2, 4, 6, 8, then ~Q 3 months
Definition of response
• RECIST used for classic response criteria• For purposes of the dynamic randomization model,
a different definition of success was defined:– Any PR or better after 2, 4, 6, 8 cycles = success– Any RECIST progression = failure– Stability recorded as SD for any of the 1st four time points– We arbitrarily decided that lowering the failure rate is 1.3
times as important as increasing the response rate– This weighs stable disease as more important in the
model than frank response
Dose adjustments
• Recover to ANC > 1K, PLT > 100K each cycle• Sliding scale dose on d8
– ANC > 1000: full dose day 8– ANC 500-999 or PLT 50-99: 75% dose G, (Doc)– ANC < 500 or PLT < 50: Hold Rx
• Febrile neutropenia, G 3-4 non heme toxicity → 25% dose reduction
• May reduce dose up to twice before stopping
Status as of 3 October 2005
120 patients are enrolled; 118 are assessable for use in the dynamic randomization model
U Michigan 30MDACC 27Washington Hosp Center 17MSKCC 16Mayo 14Lutheran General, Chicago 10Emory 5MGH/Partners 2
Tumor histologyLeiomyosarcoma 36
Liposarcoma 19
WD/DD 12
Myxoid / RC 4
Pleomorphic 3
MFH (includes 1 myxofibro) 19
Unclassified 9
Synovial 8
MPNST 7
Angiosarcoma 3
Fibrosarcoma (2 SEF) 3
HPC/SFT 3
Rhabdomyosarcoma 2
Epithelioid 2
Others 9
TOTAL 120
All events: toxicity data for 120 patients
As of 02 Nov 2005, NCI-CTC 2.0. G2 allergic reaction = Rash, Urticaria, Drug Fever
Type of toxicity TotalGEM
(n= 46)GEM+DOC
(n=74)
ANC G3 19 14 5
ANC G4 13 5 8
Hemoglobin G3 19 12 7
Platelets G3 83 26 57
Platelets G4 13 3 10
Blood transfusions 36 15 21
Platelet txfusion (some require > 1) 32 8 24
Febrile neutropenia 7 3 4
Allergic reaction G2 3 2 1
Pulmonary G3 9 2 7
Pulmonary G4 2 2 0
Edema G3 3 0 3
Neuropathy G2 3 0 3
Cumulative toxicity by patient, n=120
Type of toxicity TotalGEM
(n=46)GEM+DOC
(n=74)
ANC G3 12 8 4
ANC G4 13 5 8
Hemoglobin G3 11 6 5
Platelets G3 36 13 23
Platelets G4 10 3 7
Blood transfusions 21 9 12
Platelet transfusion 16 5 11
Febrile neutropenia 7 3 4
Allergic reaction G2 (no G3, G4) 2 1 1
Pulmonary G3 6 1 5
Pulmonary G4 2 2 0
Edema G3 3 0 3
Neuropathy G2 (no G3, G4) 3 0 3
Other toxicity (all events)
*Other G3 includes: lymphopenia (4), GI bleed (2), abdominal pain, diarrhea,mucositis, cough, pleural effusion, hiccups, bone pain, back spasm/pain, rash, nail changes, hypokalemia; data as of 02 Nov 2005
Event Gem (n=46) Gem/Doc (n=74)Fatigue G3-4 7 17
Myalgia / Muscle weakness G3
1 9
DVT / PE G3 2 3
Nausea / Vomiting / anorexia G3
0 5
All other G3 1 (glucose G3) 17*
Totals 11 51
Interim statistical model results
• Dynamic randomization model includes 100 of 110 patients accrued as of June, 2005
• p < 0.01 boundary stopping rule was not crossed for either leiomyosarcoma nor non-leiomyosarcoma groups
Randomization probability
(after n=100 patients)
NO YES
LMS
Gem/Doc 0.87 0.76
Gem 0.13 0.24
NON-LMS
Gem/Doc 0.66 0.60
Gem 0.34 0.40
Prior Irradiation
Conclusions
• In analysis of the randomization of patients, gemcitabine + docetaxel appears superior to higher dose single agent gemcitabine for patients with leiomyosarcoma.
• There is a trend toward improved response rate with the combination of therapy for patients with other types of soft tissue sarcomas
• Low platelet count most common toxicity– Nearly no febrile neutropenia using (peg)-filgrastim– Fatigue, edema, myalgias occasionally dose limiting
• Dynamic randomization is an effective study design to minimize the number of patients receiving the less active therapy
• More data will be presented tomorrow!