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RUNNING HEAD: Lung Cancer LUNG CANCER Small-Cell Carcinoma of the Lung SAMANTHA CROWELL GRAND VALLEY STATE UNIVERSITY

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Page 1: LUNG CANCER€¦  · Web view2016. 3. 28. · lung cancer. small-cell carcinoma of the lung. samantha crowell. grand valley state university. samantha crowell. grand valley state

RUNNING HEAD: Lung Cancer

LUNG CANCER

Small-Cell Carcinoma of the Lung

SAMANTHA CROWELL

GRAND VALLEY STATE UNIVERSITY

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Lung Cancer 1

Presenting Signs & Symptoms of Patient

Chief Complaint

This patient is a 72 year old male with the diagnosis of limited stage small-cell lung

carcinoma. He had been doing various chores around the garage such as filling his tires with air

when his wife noticed he was more short of breath than usual. She asked him to get evaluated by

a physician. He underwent a chest x-ray on November 5, 2014 which showed opacity within the

left mid lung.

Medical History

The patient has quite a medical history. He has type 2 diabetes and hypertension. There

has also been a pattern of hyperlipidemia and kidney stones in his past. Both of his knees have

been replaced. He has had a bilateral cataract extraction. Also, he has had hernia repair and

lithotripsy. In late November of 2014, he had a bronchoscopy and mediastinoscopy to look at his

condition.

Family History

There is a significant history for the patient’s father with colon cancer. No other family

history known.

Social History

This patient is a retired engineer. He also used to be a volunteer fire fighter. He has about

a 15-pack-year history of smoking and tends to have about 4 to 5 beers per week.

Epidemiology

Lung cancer as a whole, not including skin cancer, is the second most common cancer

after breast cancer and prostate cancer, in both women and men. The American Cancer Society

estimates that for 2015 in the United States there will be about 221,200 new cases of lung cancer,

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Lung Cancer 2

comprised of 115,610 men and 105,590 women. They also estimate that there will be 158,040

deaths from lung cancer. This number accounts for about 27% of all cancer deaths for 2015.

These estimations include both small cell and non-small cell lung cancers. Accounting for more

than a fourth of all cancer deaths, lung cancer is considerably the most common cause of death

due to cancer for both genders. The older population makes up the majority of lung cancer

patients. Roughly two-thirds of the patients diagnosed with lung cancer are 65 or older. Also,

less than 2% of all lung cancer patients are under the age of 45. This also puts the average age at

time of diagnosis at roughly 70 years of age. The American Cancer Society claims that the

chance of a man developing lung cancer within his life is around 1 in 13. For a woman they

estimate the risk to be near every 1 in 16. However, those statistics take account of both smokers

and non-smokers. The risk for smokers is much higher than that and the risk for non-smokers is

much lower than that. Race can also plays a role in cancer statistics. Black men are nearly 20%

more probable to get lung cancer than white men are. On the other hand, the percentage is about

10% lower in black women than it is in white women. Women in general, regardless of race,

have lower rates of lung cancer than men, but the break between them is tapering. This is

because the rates of lung cancer among men began to drop much sooner than the rates for

women. The majority of lung cancer statistics consist of both small cell and non-small cell lung

cancers. However, only about 10% to 15% of all lung cancers are small cell carcinoma. The

amount of SCLC cases that make up the quantity of all lung cancers has decreased from 17% to

13% in the past 30 years. In 2007, out of the 213,000 cases of lung cancer predicted to occur, an

estimation of about 27,000 of those cases were predicted to be a diagnosis of SCLC. (DeVita, V.,

Lawrence, T., & Rosenberg, S., 2008) Interestingly, black men are roughly 15% less likely to

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Lung Cancer 3

develop small cell lung cancer than white men. The risk is also about 30% lower for black

women than it is for white women. (American Cancer Society)

Etiology

There are many risk factors that increase the chance of developing lung cancer. Some of

these many risk factors include tobacco smoke, radon exposure, asbestos exposure, previous

radiation therapy to the lungs, and having a personal or family history of lung cancer. By far the

biggest risk factor is smoking tobacco. The American Cancer Society estimated that at least 80%

of all lung cancer deaths are due to smoking tobacco. It has also been found that over 95% of

SCLC cases are due to tobacco exposure. The incidence rates of SCLC have been found to

reflect the patterns of smoking rates. (DeVita, V., Lawrence, T., & Rosenberg, S., 2008) Even

just breathing in the secondhand smoke of others can bring the risk of developing lung cancer up

by about 30% and is believed to cause more than 7,000 lung cancer deaths a year. (American

Cancer Society)

Exposure to radon is the second leading cause of lung cancer in the US. Radon is a

radioactive gas that develops organically from the degeneration of uranium soil and rocks. It

does not have a taste or a smell and cannot be seen. In certain geographic areas, there are higher

concentrations of radon in the soil. When people develop a basement or underground living area,

this radioactive gas can build-up and be inhaled. The risk of developing lung cancer from radon

in non-smokers is much lower than the risk of inhaling smoke. Yet, if radon is inhaled by a

smoker, their risk for cancer increases even more. Another risk factor for lung cancer is exposure

to asbestos. Exposure to asbestos is mostly found in people who worked in places where asbestos

can be found like mines, mills, textile plants, and shipyards. These workers have a much higher

risk for dying of lung cancer than people who have not been exposed. Again, if these workers are

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Lung Cancer 4

smokers, than their risk even higher than it would be if you added the risks together separately.

The risk of developing mesothelioma, a type of cancer that starts in the lungs but is not usually

considered a type of lung cancer, is much greater after exposure to asbestos. Although asbestos

has been reduced in common areas, it has not been completely eliminated from working

environments. (American Cancer Society)

Comparison of Patient to the Typical

This patient seems to be very typical as a limited stage small cell lung cancer patient. He

is 72 years of age, which is right around the average age of a patient at time of diagnosis. He also

has a long history with smoking. This is the cause for more than 95% of SCLC cases which

makes him fit perfectly with this statistic. The patient is also a white male which is the most

common race and gender for this malignancy.

Patient Work-Up Information

Date Procedure Results

October – November

2014Chief Complaint Having shortness of breath when doing normal tasks

around the garage

November 5, 2014 Chest X-Ray Opacity found within the left mid lung

November 6, 2014

CT Scan of Abdomen and Pelvis Unremarkable

November 2014 MRI Scan of the Brain No metastatic disease found

November 2014 PET/CT Hilar and mediastinal abnormalities found within

the left upper lobe

November 26, 2014

Bronchoscopy and Mediastinoscopy

No palpable lymphadenopathy, left main and lower lobe appeared normal, left upper lobe bronchial

mucosa was inflamed and friable in apical segment, endoluminal tumor ingrowth biopsied—showed

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Lung Cancer 5

small cell carcinoma

December 8, 2014

Began first cycle of chemotherapy with

cisplatin and etoposide

He had some hemoptysis after the bronchoscopy, however, felt well after chemo thus far

December 11, 2014

Examined by Radiation Oncologist

Decided on standard of care of Chemoradiation therapy, noted to start at the lastest by cycle 2 of his

chemotherapy on December 29, 2014

December 12, 2014

Simulation for Radiation Therapy N/A

Anatomy Discussion

The lungs are two organs which located on either side of the chest that are mainly

responsible for the exchange of oxygen and carbon dioxide of the air outside of the body and the

blood within. Lungs are divided into sponge-like, air-filled lobes. The right lung has three lobes

called the upper, middle, and lower lobe. However, the left lung only has two lobes, upper and

lower, due to the heart taking up more space on the left side. Air is inhaled through either the

nose or the mouth and brought to the trachea. The trachea, also called the windpipe, brings air

down to the chest where it splits off into two other pipes called the left and right primary

bronchi. The section where the bronchi split off of the trachea is called the carina. The primary

bronchi carry the air until they split off into smaller and even smaller branches called

bronchioles. These branches eventually become microscopic. Ultimately, these branches

conclude into clumps of air filled sacs called alveoli. This complex structure of the lungs is

displayed by Figure 1 in the graphics section below. (WebMD)

Another huge portion of the respiratory system is the involvement of blood circulation.

The pulmonary artery carries deoxygenated blood from the heart and brings it toward the lungs.

It then splits into two branches, one for each of the lungs, and then continues to divide into

smaller and smaller subdivisions. This branching is very similar to the branching of the bronchi.

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Lung Cancer 6

The vessels eventually split into a fine web of super tiny tubes called capillaries. The tubes are

positioned as a web around the alveoli. These capillaries are so small that only one blood cell can

pass through at a time. As the blood cells pass through the capillaries, the exchange of gasses

between blood and air occurs with the neighboring alveoli. Alveoli absorb the inhaled oxygen

into the blood, and take the carbon dioxide from the blood into the exhaled air. After sending the

blood cells by the alveoli, the capillaries start to join together again. They branch together,

opposite of before, and eventually come together and form the pulmonary veins which bring the

oxygenated blood back to the heart in order to pump it through the rest of the body. This

branching of the veins, capillaries, and arteries can also be shown in Figure 1. (Lung Anatomy,

2014)

Regional Lymphatic Drainage

The lungs have quite a few paths for lymphatic drainage, all of which are above the

diaphragm. These include the intrathoracic, recurrent laryngeal, cervical, and supraclavicular

nodes. The intrathoracic nodes that are most relevant are broken into two categories the

mediastinal nodes and the intrapulmonary nodes. The mediastinal nodes include the paratracheal

nodes, pretracheal nodes, retrotracheal nodes, aortic nodes, subcarinal nodes, periesophageal

nodes, and inferior pulmonary ligament nodes. The intrapulmonary nodes include the hilar

nodes, peribronchial nodes, and intrapulmonary nodes. (Small Cell Lung Cancer, 2005) The

regional lymph nodes are shown in Figure 1, Figure 2, and Figure 3 in the graphics section

below.

Anatomy & Lymphatic Graphics

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Lung Cancer 7

FIGURE 1.

Non-Small Cell Lung Cancer Treatment (PDQ®). (2014, June 30). Retrieved April 2, 2015, from

http://www.cancer.gov/cancertopics/pdq/treatment/non-small-cell-lung/Patient/page1

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Lung Cancer 8

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Lung Cancer 9

FIGURE 2.

Mediastinal Lymph Node Dissection. (2005). In T. Shields, J. LoCicero, R. Ponn, & V. Rusch

(Eds.), General thoracic surgery (6th ed., Vol. 2). Philadelphia, Pennsylvania: Lippincott

Williams & Wilkins. Retrieved April 9, 2015, from

http://flylib.com/books/en/3.98.1.112/1/

FIGURE 3.

Small Cell Lung Cancer. (2005). In T. Shields, J. LoCicero, R. Ponn, & V. Rusch (Eds.),

General thoracic surgery (6th ed., Vol. 2). Philadelphia, Pennsylvania: Lippincott

Williams & Wilkins. Retrieved April 9, 2015, from

http://flylib.com/books/en/3.98.1.136/1/

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Lung Cancer 10

FIGURE 4.

Small Cell Lung Cancer. (2005). In T. Shields, J. LoCicero, R. Ponn, & V. Rusch (Eds.),

General thoracic surgery (6th ed., Vol. 2). Philadelphia, Pennsylvania: Lippincott

Williams & Wilkins. Retrieved April 9, 2015, from

http://flylib.com/books/en/3.98.1.136/1/

Pathology

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Lung Cancer 11

In order to diagnose small cell lung cancer (SCLC), physicians usually collect small

specimens from either a core biopsy, bronchoscopic biopsy, or a fine needle biopsy. They then

are examine with a light microscopy and characterized by a pathologist. SCLC tumor cells

generally measure to a size less than the diameter of three petite lymphocytes. Their shape can be

round to fusiform and their cytoplasm is meagre. They have a nuclear chromatin that is finely

granular and their nucleoli are discreet or lacking. The typical mitotic rate of SCLC cells is very

high. They also are known for their extensive spreading even at the earliest stages of disease. The

presence of rush artifacts and streaming artifacts are commonly found when looking at SCLC

tumor cells. There are many more pathologies for non-small cell lung cancers (NSCLC). A few

for example are squamous cell carcinoma, adenocarcinoma, large cell carcinoma, and carcinoid

tumors. In general, NSCLC types tend to be much less aggressive than SCLC types. This is one

of the reasons, they are categorized separately. They also look much different under the

microscope than the distinctive structure of a SCLC cell. (DeVita, V., Lawrence, T., &

Rosenberg, S., 2008)

Staging

As a standard way of classifying the degree of a patient’s cancer, the American Joint

Committee on Cancer (AJCC) created the TNM staging system. This staging system can be

applied to staging of small cell, non-small cell, and carcinoid tumors of the lung. Although, it is

used mainly for non-small cell cancers in clinical practice. TNM uses four key concepts which

include the T which refers to the location, size, how far it has spread within the skin and nearby

tissues; the N which describes how much the cancer has spread to nearby lymph nodes; the M

which indicates whether the cancer has metastasized. Each of these three categories have their

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Lung Cancer 12

own staging guide. When all three of them are determined, they are combined in a process called

stage grouping to assign an overall stage for the tumor.

Since small-cell lung cancers are metastatic in about 80% of the cases by the time of

diagnosis, the TMN staging system is not the ideal system for physicians to use. Instead, most

clinical trials and clinical practices use a simpler two-stage system created by the Veterans’

Administration Lung Study Group (VALSG). In the VALSG staging system, a patient is

diagnosed as either having “limited stage” disease or “extensive stage” disease. “Limited stage is

defined as disease confined to one hemithorax that can be “encompassed” in a “tolerable”

radiation field” (DeVita, V., Lawrence, T., & Rosenberg, S., 2008). About one-thirds of SCLC

patients are considered to have limited stage disease. The other two-thirds of the SCLC patients

who do not fall into this category are considered to have extensive stage disease. The VALSG

system does correlate closely to the TNM staging system. The limited stage of SCLC is the same

as stages I through IIIB of the TNM system and the extensive stage is the same as stage IV. For

the use in tumor registries, the TNM system is used for small-cell lung cancers. (Compton, C,

2012)

The following tables were created to show the staging process and all of the different

components involved in it. All of the staging information in the following tables was taken from

the AJCC handbook.

Primary Tumor (T)

TNM Categories Description

TXPrimary tumor cannot be assessed, or tumor proven by the presence of

malignant cells in sputum or bronchial washings but not visualized by imaging or bronchoscopy

T0 No evidence of primary tumor

Tis Carcinoma in situ

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Lung Cancer 13

T1Tumor 3 cm or less in greatest dimension, surrounded by lung or visceral

pleura, without bronchoscopic evidence of invasion more proximal than the lobar bronchus (i.e., not in the main bronchus)

T1a Tumor 2 cm or less in greatest dimension

T1b Tumor more than 2 cm but 3 cm or less in greatest dimension

T2

Tumor more than 3 cm but 7 cm or less or tumor with any of the following features (T2 tumors with these features are classified T2a if 5 cm or less);

Involves main bronchus, 2 cm or more distal to the carina; Invades visceral pleura (PL1 or PL2); Associated with atelectasis or obstructive pneumonitis

that extends to the hilar region but does not involve the entire lung

T2a Tumor more than 3 cm but 5 cm or less in greatest dimension

T2b Tumor more than 5 cm but 7 cm or less in greatest dimension

T3

Tumor more than 7 cm or one that directly invades any of the following: parietal pleural (PL3), chest wall (including superior sulcus tumors),

diaphragm, phrenic nerve, mediastinal pleura, parietal pericardium; or tumor in the main bronchus (less than 2 cm distal to the carina *but without involvement of the carina; or associated atelectasis or obstructive pneumonitis of the entire

lung or separate tumor nodule(s) in the same lobe

T4Tumor of any size that invades any of the following: mediastinum, heart, great vessels, trachea, recurrent laryngeal nerve, esophagus, vertebral body, carina,

separate tumor nodule(s) in a different ipsilateral lobe

Regional Lymph Nodes (N)

TNM Categories Description

NX Regional lymph nodes cannot be assessed

N0 No regional lymph node metastasis

N1 Metastasis in ipsilateral peribronchial and/or ipsilateral hilar lymph nodes and intrapulmonary nodes, including involvement by direct extension

N2 Metastasis in ipsilateral mediastinal and/or subcarinal lymph node(s)

N3 Metastasis in contralateral mediastinal, contralateral hilar, ipsilateral or contralateral scalene, or supraclavicular lymph node(s)

Distant Metastasis (M)

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Lung Cancer 14

TNM Categories Description

M0 No distant metastasisM1 Distant metastasis

M1a Separate tumor nodule(s) in a contralateral lobe tumor with pleural nodules or malignant pleural (or pericardial) effusion

M1b Distant metastasis (in extrathoracic organs)

Anatomic Stage/Prognostic Groups

TNM Stages T N M

Occult carcinoma TX N0 M0

Stage 0 Tis N0 M0

Stage IAT1a N0 M0

T1b N0 M0

Stage IB T2a N0 M0

Stage IIA

T2b N0 M0

T1a N1 M0

T1b N1 M0

T2a N1 M0

Stage IIBT2b N1 M0

T3 N0 M0

Stage IIIA

T1a N2 M0

T1b N2 M0

T2a N2 M0

T2b N2 M0

T3 N1 M0

T3 N2 M0

T4 N0 M0

T4 N1 M0

Stage IIIB T1a N3 M0

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Lung Cancer 15

T1b N3 M0

T2a N3 M0

T2b N3 M0

T3 N3 M0

T4 N2 M0

T4 N3 M0

Stage IVAny T Any N M1a

Any T Any N M1b

Compton, C. (2012). Lung. In AJCC Cancer Staging Atlas: A Companion to the Seventh

Editions of the AJCC Cancer Staging Manual and Handbook (2nd ed., pp. 311-328).

New York, NY: Springer. Retrieved April 2, 2015, from GVSU Online Library.

In addition to these two staging methods, there is another staging scale that is commonly

used to help with treatment planning. This scale is called the Karnofsky Performance Scale

(KPS) and is used to assess the patients’ performance status (PS). It gives the physicians a way to

assess self-described abilities at the time of a patient’s diagnosis. Doctors use this scale to get an

idea of what the quality of life is for their patient. It also helps to develop a plan for treatment

aggressiveness and treatment goals. However, in a study on the use of the Karnofsky

Performance Scale vs. the Physical Performance Test (PPT) to assess the PS of elderly cancer

patients, KPS was not found to be as accurate as the PPT. The KPS is based only on the doctor’s

clinical estimation of the patient and the PPT is based on physical capabilities of the patient

measured through direct observation. So, although KPS is a great representation of overall health

status for predicting mortality of the elderly, it is not the best way to interpret their overall health

status. (Terret, C., Albrand, G., Moncenix, G., & Droz, J., 2011)

Karnofsky Performance Status scale definitions rating (%) criteria

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Lung Cancer 16

Value (%) Level of Functional Capacity

100 Normal, no complaints; no evidence of disease

90 Able to carry on normal activity; minor signs or symptoms of disease

80 Normal activity with effort; some signs or symptoms of disease

70 Cares for self; unable to carry on normal activity or to do active work

60 Requires occasional assistance, but is able to care for most of his personal needs

50 Requires considerable assistance and frequent medical care

40 Disabled; requires special care and assistance

30 Severely disabled; hospital admission is indicated although death not imminent

20 Very sick; hospital admission necessary; active supportive treatment necessary

10 Moribund; fatal processes progressing rapidly

0 Dead

Terret, C., Albrand, G., Moncenix, G., & Droz, J. (2011). Karnofsky Performance Scale (KPS)

or Physical Performance Test (PPT)? That is the question. Critical Reviews in

Oncology/Hematology, 77(2), 142-147. Retrieved April 10, 2015, from ScienceDirect.

Grading

Tumor grades are used to help us assess how abnormal a tumor’s cells and tissue appear

through a microscope compared to the normal. A prediction on how fast a tumor is going to

spread or grow can also be given when using a grading system. When a tumor’s construction of

tissue and cells are comparable to those of ordinary cells and issue, it is categorized as well-

differentiated. If a tumor is well-differentiated, it is believed to be less aggressive and to have a

slower growth rate than those that are categorized as undifferentiated. Tumors that are

considered to be undifferentiated or poorly differentiated have irregular shaped cells and can

have abnormal tissue arrangements. They also tend to mature early and spread quickly, much

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Lung Cancer 17

quicker than well-differentiated tumors. In order to categorize how differentiated the patient’s

cancer is, a histopathological grading system is used. For small cell lung cancer, there isn’t a

specified grading system. The National Cancer Institute stated that when a grading system is not

specified, there is a general grading system to be used. The following table displays the

information given by the National Cancer Institute over the general grading system used.

(National Cancer Institute)

Histological Grade (G) Degree of Differentiation

GX Undetermined grade Grade cannot be assessed

G1 Low grade Well differentiated

G2 Intermediate grade Moderately differentiated

G3 High grade Poorly differentiated

G4 High grade Undifferentiated

Small Cell Lung Cancer Treatment. (n.d.). National Cancer Institute. Retrieved April 7, 2015,

from http://www.cancer.gov/cancertopics/pdq/treatment/small-cell-lung/Patient/page1

Patients Pathology, Stage & Grade

This patient had a bronchoscopy and a mediastinoscopy performed for diagnosis. The

biopsies found the patient to have small cell carcinoma of the lung at a limited stage. There was

no grade stated in the report or in the patient’s charts. In the pathologist report, they stated that

the cells taken from the left upper lobe of his lungs were quite small and had morphologic

features and distinct immunophenotypes. The nodes were found to be negative for metastatic

disease.

Radiation Therapy Treatment Plan & Rx for Patient

The patient was prescribed to a total of 6600 cGy to his Lung/Mediastinum region. This

was to be delivered in 33 fractions of 200 cGy each. His doctor wanted this patient to be treated

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Lung Cancer 18

with a RapidArc technique to target his gross disease and mediastinum. He also wanted to the

patient to be simulated using 4-D equipment to track his breathing patterns.

Radiation Therapy Treatment Information & Patient Set-Up

Simulation for the patient took place on September 8, 2014. He was to lie head first on

the table in a supine position with a wingboard covered with a small vaclok to keep his upper

body in place. Under the vaclok was a size ‘B’ headrest and his hands were to be up on the pegs

to keep his arms out of the field. He also had a large knee sponge under his legs with his feet

banded to keep him still and in place. He used metronome track 1 to keep his breathing even.

There were three tattoos placed. One on his central reference point which is mid-sagittal on his

chest, and one on both of his sides lateral to his central reference point. For treatment he was to

be leveled with his tattoos and then brought right to his central reference point. His SSD needed

to be set to 82.8. This patient was prescribed to 6 different Arcs with image guidance. Images

were to be taken every day to accommodate to the changes in the patients positioning.

Radiation Therapy Treatment Type & Delivery

Field Name

Gantry Angle

Collimator Angle

Couch Angle

Planned SSD

Planned MU Energy Wedge

Factor Bolus

Arc 1 0 to 179 CW 30 0 82.8 cm 177 MU 6 MV 1.0 None

Arc 2 179 to 0 CCW 330 0 83.0 cm 131 MU 6 MV 1.0 None

Arc 1.1

0 to 179 CW 30 0 82.7 cm 180 MU 6 MV 1.0 None

Arc 2.1

179 to 0 CCW 330 0 83.4 cm 124 MU 6 MV 1.0 None

Arc 3 330 to 30 CW 90 270 85.3 cm 56 MU 6 MV 1.0 None

Arc 4 30 to 330

90 270 85.2 cm 32 MU 6 MV 1.0 None

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Lung Cancer 19

CCW

Other Radiation Therapy Treatment Options

Stereotactic body radiotherapy (SBRT) is a treatment option available for patients who

are high risk for surgery or are medically inoperable. If a tumor is small enough and confined

with enough distance from critical structures, the delivery of larger ablative doses, anywhere

from 12-30 Gy per fraction, can be given in a single to a few fractions. SBRT delivers

remarkable primary tumor control along with toxicity being minimal. However, when working

with higher doses per fraction it is even more important to avoid critical structures, especially the

heart, spinal cord, and remaining healthy lung. Tolerance doses for each structure become much

smaller, meaning they cannot take as much radiation before they are at an increased risk of

irreversible late effects. Also, increasing the volume of treatment will decrease the limit of

maximum point dose to a structure, which also increases risks. The total dose given, the amount

of dose per fraction, and the volume of the treated area are all factors that can change the limits

of critical tissue as well as the outcome of treatment. This is the reason only patients with small

tumors in an ideal location can have SBRT as their treatment. It becomes a challenge to create a

plan that will not succeed the max point dose limit of the normal structures. The planning

process grows more complex containing several fields, involving multiple angles, and

calculating several dose points. Although more intricate, this plan is also much more precise.

(Hatton, M., & Martin, J., 2010)

In an article published in the Radiation Oncology Journal, the authors explain that that

are multiple reasons that SBRT is thought to be an ideal alternative to surgery. Due to the fact

the total dose is delivered in only a few treatments, the total treatment will be done within a week

or so. The treatments are outpatient and only last up to a half hour per treatment. This makes it

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Lung Cancer 20

much easier for the patient to maintain a higher quality of life. Also, the use of sedation or

anesthesia is not needed due to it being a painless non-invasive procedure. (Ricardi, U.,

Badellino, S., & Filippi, A., 2015) The practice of SBRT has tightened the gap in survival rates

among operable and inoperable patients with early stage NSCLC. With improved control rates

and lowered toxicity to normal tissues and organs at risk, SBRT is now a standard when caring

for inoperable patients with early stage non-small cell lung cancer. (Kelley, K., et al., 2015)

Radiation Therapy Complications, Side Effects & Treatment

This patient had very few complications from radiation therapy. After 24 Gy in 12

fractions, he mentioned that his breathing had gotten easier and that the rattling in his chest was

gone. Once he reached 54 Gy in 27 fractions the patient began to have a little bit of catching

when he would swallow cold liquids, however, nothing too concerning. The patient had some

mild discomfort when swallowing and a little bit of a cough when he reached 64 Gy in 32

fractions. When the patient was finished with his treatment of 66 Gy in 33 fractions, he did not

have any other complaints or side effects to be noted.

Adjuvant Therapies, Complications, Side Effects & Treatment

For small-cell lung cancer, treatment options vary according to their cancer stage.

Patients with limited-stage SCLC can be treated with a combination of chemotherapy and

radiation therapy, they could have chemotherapy alone, they could have surgery followed by

chemotherapy, they could receive an endoscopic stent, and they could even have a preventative

treatment of radiation to the brain if they have a complete response to primary treatment.

Chemotherapy is used to stop the growth of the cancerous cells. It is a systemic treatment

making it a great option for cancers that have spread or are known to spread throughout the body.

When chemotherapy is used in combination with radiation therapy, the two treatments work

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Lung Cancer 21

together to maximize the outcomes. In a study over tolerance and benefits of treatment in elderly

patients, the survival rate was significantly higher even though the toxicity rate was higher as

well. This is the favorable treatment combination. Surgery can be used for a few limited-stage

patients because their cancer is found in one confined spot. However, this cancer is known to

spread fast. Due to this, surgery is not commonly used. Also, it is dangerous to remove tumors

from this area because it can be in a risky spot. If the doctor has difficulty removing the tumor or

if the tumor has a lot of vascularity, the patient could bleed out. Although it isn’t the best option

for most patients, some SCLC patients might have surgery to remove at risk nodes or to resect

samples of the cancer tissue for pathology. For patients with blocked airways due to their SCLC,

they can have an endoscopic stent placed. This helps the doctors view the tissue directly and also

help them open up blockages. Patients who are diagnosed with extensive-stage SCLC tend to

have less options for treatment. Surgery is not an option because the cancer has already spread

into their system. They often have combination chemotherapy to slow the growth and to relieve

any symptoms they may be having. They can also have radiation to various parts of the body as a

palliative treatment for improving their quality of life. SCLC in its extensive stages usually

recurs. When this happens the treatment options are about the same as they are for the first time

around, chemotherapy to help control the disease and radiation therapy as palliative treatment.

(National Cancer Institute) Since recurrent SCLC can come back with resistance to their chemo

drugs, a new drug might have to be used second time around. There was a study done over target

chemotherapy for hypoxia in small cell cancers. Hypoxia is a micro-environmental pressure that

is present in and important to most solid tumors. It helps the tumor cells adapt to the environment

to survive and reproduce. The study had mixed results with the hypoxia targeted therapy,

however, it could be of use in the near future. (Bryant, J et al., 2014)

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Lung Cancer 22

Other Therapies & Complications the Patient Received

This patient had a bronchoscopy and a mediastinoscopy to help the doctors with

diagnosis. This left the patient with a sore throat and some bleeding, but overall it did not have

many complications. He also had chemotherapy along with his radiation therapy. The doctors

prescribed him to cisplatin and etoposide. He did not have any significant side effects due to his

treatment. He actually had a pretty good reaction to it. The doctor mentioned that he plans on

potentially prescribing this patient with prophylactic cranial irradiation to assure no metastasize

to the brain. Although, he has not met with the patient for his 6 month follow-up yet to discuss it.

Critical Structures & Dose Tolerances

When treating patients with small cell lung cancer, there are three main critical structures

that need to be focused on which are the spinal cord, the heart, and the healthy lung. The reason

these three are primarily focused on is because they are frequently radiated beyond their

tolerance dose when treating SCLC with radiation therapy. Patients with SCLC are usually going

through chemotherapy alongside of radiation giving potential other reaction as well. For these

reasons, radiation to the spinal cord, the heart, and the healthy lung need to be constrained and

the Dosimetrist needs to create a plan that will not exceed their tolerance dose. If the spinal cord

is to exceed its tolerance dose it could result in infarction or necrosis. For the heart and the lung,

after exceeding their tolerance dose they could have pericarditis and pneumonitis. These are to

be avoided at all cost. Although, esophagus, bone marrow, skin, vessels, liver, and bones also

should be paid attention to.

Critical Structure TD 5/5 (cGy)

Spinal cord 5000

Normal lung 2000

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Lung Cancer 23

Heart 4300

Esophagus 5000

Bone marrow 2500

Skin 5500

Liver 3500

Bone 6500

Washington, C., & Leaver, D. (2010). Respiratory System Tumors. In Principles and Practice of

Radiation Therapy (3rd ed., pp. 667-681). St. Louis, Mo.: Mosby Elsevier.

Routes of Spread

Small cell carcinoma of the lung has several different routes of spread. These different

types include through direct extension, through lymphatics, and through the circulatory system.

When the SCLC continues to grow and take over tissue, it can start to take over surrounding

structures as well. This is called direct extension or local extension. The sites that are at risk of

direct extension are the remaining healthy lung, ribs, heart, ribs, vertebral column, and

esophagus. The SCLC cells can break off of the cancerous tumor and travel through the

lymphatic system. If this happens the cells can become stuck within certain nodes until the

lymphatic fluid builds up and pushes the cancerous cells through to other nodes. This can also be

called regional extension. In other cases of lymphatic spread, the cancerous cells can spread

throughout a lymph node and enter the circulatory system supplying the node. If the disease gets

into the circulatory system it can travel all over. Nearly any part of the body can be a metastatic

site for this disease. The most commonly found sites of spread are the brain, liver, kidneys,

bones, pericardium, adrenal glands, subcutaneous tissues, and contralateral lung. (National

Cancer Institute)

Prognosis & Survival

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Lung Cancer 24

The prognosis of patients with small cell carcinoma of the lung in general is not good.

However, it varies by patient. In a study analyzing the University of Toronto database survival

was found to be decent in patients with ‘very limited’ disease. This means that the disease was

confined only to the pulmonary parenchyma. Survival in that group of patients was found to be

50%-60%. They also found that with a combination of chemotherapy and radiation therapy the

‘very limited’ stage patients had a more favorable outcome of survival than the ‘limited’ stage

patients. Also, in this study the median survival was 16 months and the projected 5-year survival

was at about 18%. If the patient’s had mediastinal involvement their 5-year survival went down

to 6% and if they had supraclavicular lymphadenopathy, pleural effusion, pneumonic

consolidation, or atelectasis, their 5-year survival rate went down to 2%. There have been many

other trends found that can help with prognosis of SCLC patients. It has been found that patients

70 years of age and older have responded in the same way to having multiple modalities of

treatment as patients of a younger age and they also have comparable survival rates. Though, the

older patients were found to have a greater toxicity. There is also an association for older patients

with decreased performance status and more comorbid sicknesses. Due to this correlation, there

can be a negotiation of chemotherapy dose intensity. This could be a reason for its prognostic

associations. It is surprising that even though the majority of patients with small cell lung cancer

are over age 65, they comprise only 39% of individuals enrolled on lung cancer clinical trials. It

is very important that physicians are aware of this when attempting to use clinical trial data to

actual care of the growing population. (DeVita, V., Lawrence, T., & Rosenberg, S., 2008) In

another clinical trial, SCLC patient survival rates were found to have improved considerably

between the years of 1986 to 2008. These improvements on survival rate throughout the years

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Lung Cancer 25

are likely due to advancements in technology for treatment and management. (Schabath, M. et

al., 2014).

The numbers below have been taken from the American Cancer Society website. They

are based on patients diagnosed with SCLC between 1988 and 2001. The relative survival rate is

a number representing the comparison of survival rates for people with SCLC to people without

SCLC. The stage of the patient at time of diagnosis is the stage used in these statistics.

(American Cancer Society)

Stage 5-Year Relative Survival Rate

(Limited-stage) I 31%

(Limited-stage) II 19%

(Limited-stage) III 8%

(Extensive-stage) IV 2%

Small cell lung cancer survival rates by stage. (2015, March 9). Retrieved April 8, 2015, from

http://www.cancer.org/cancer/lungcancer-smallcell/detailedguide/small-cell-lung-cancer-

survival-rates

Patient’s Prognosis & Survival

Although this patient’s small cell cancer is limited stage, I do not think that his prognosis

is good. In best case scenario his 5-year relative survival rate is 31%. This is still terrible. SCLC

is known to be aggressive and deadly. After discussing this patient with his radiation oncologist,

I think that the chances of his SCLC recurring are high. Once the cancer recurs, he will not have

very high chances of survival after that. He is a smoker and a white male. He also is old in age.

These are all pointing to recurrence. I believe that his chance of survival are at about 13%. I

think that he will not live longer than a couple years longer.

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Lung Cancer 26

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