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Cancer Survivorship Endometrial Cancer Module Part 2 Start Case ©2007. David Geffen School of Medicine, UCLA

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Page 1: Cancer Survivorship Endometrial Cancer Module

Cancer Survivorship

Endometrial Cancer ModulePart 2

StartCase©2007. David Geffen School of Medicine, UCLA

Page 2: Cancer Survivorship Endometrial Cancer Module

Goal of this Module

This is an interactive and self-directed learning module intended to build a foundation of knowledge around the epidemiology and late effects of cancer survival. This is one of several educational modules you will complete during your core clinical clerkships. Themes emphasized in this, and other modules, are:

Epidemiology of survival Late effects Psychosocial concerns Secondary prevention Strategies for behavior change

Next

Page 3: Cancer Survivorship Endometrial Cancer Module

Part 2 Case Summary

Ms. Johnson, an obese (BMI =37), 64 year-old, Caucasian woman, gravida 1, para 1, came to see you because she was having post menopausal bleeding over the past month. She had no other symptoms. She did not receive hormone replacement therapy with estrogen or progesterone. Endometrial biopsy revealed endometrial cancer.

Next

Page 4: Cancer Survivorship Endometrial Cancer Module

Summary Continued

Ms. Johnson was treated with an exploratory laparotomy, total abdominal hysterectomy and bilateral salpingo-oophorectomy (TAH & BSO) pelvic and para-aortic lymphadenectomy and adjuvant chemotherapy (paclitaxel, doxorubicin and cisplatin (CAP) chemotherapy). She was staged as endometrial cancer stage 2A.

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Page 5: Cancer Survivorship Endometrial Cancer Module

Paclitaxel

Licensed to University of California ©2006 UpToDate ® U.S. BRAND NAMES — Abraxane® PHARMACOLOGIC CATEGORY

Antineoplastic Agent, AntimicrotubularAntineoplastic Agent, Natural Source (Plant) Derivative

USE — Treatment of relapsed or refractory breast cancer Adverse reactions

Back to Case

Page 6: Cancer Survivorship Endometrial Cancer Module

Paclitaxel (Adverse Reactions)

>10%:  Cardiovascular: EKG abnormal (60%)  Dermatologic: Alopecia (90%)  Gastrointestinal: Nausea (30%; grades 3/4: 3%), diarrhea (27%; grades 3/4: <1%), vomiting (18%; grades 3/4: 4%)  Hematologic: Neutropenia (80%; grade 4: 9%), anemia (33%; grades 3/4: 1%)  Hepatic: AST increased (39%), alkaline phosphatase increased (36%), GGT increased (grades 3/4: 14%)  Neuromuscular & skeletal: Sensory neuropathy (71%; grades 3/4: 10%; dose dependent; may be cumulative), weakness (47%), myalgia/arthralgia (44%)  Ocular: Vision disturbance (13%; severe [keratitis, blurred vision]: 1%)  Respiratory: Dyspnea (12%)  Miscellaneous: Infection (24%; primarily included oral candidiasis, respiratory tract infection, and pneumonia)

1% to 10%:  Cardiovascular: Edema (10%), hypotension (5%), cardiovascular events (grades 3/4: 3%; included chest pain, cardiac arrest, supraventricular tachycardia, edema, thrombosis, pulmonary thromboembolism, pulmonary emboli, and hypertension)  Gastrointestinal: Mucositis (7%; grades 3/4: <1%)  Hematologic: Bleeding (2%), neutropenic fever (2%), thrombocytopenia (2%; grades 3/4: 1%)  Hepatic: Bilirubin increased (7%)  Neuromuscular and skeletal: Peripheral neuropathy (grade 3: 10%)  Renal: Creatinine increased (11%; severe 1%)  Respiratory: Cough (7%)  Miscellaneous: Hypersensitivity reaction (4%)

<1% (Limited to important or life-threatening): Bradycardia, cardiac ischemia, cerebrovascular attack, cranial nerve palsies, embolism, erythema, hand-foot syndrome (in patients previously exposed to capecitabine), injection site reaction, maculopapular rash, MI, motor neuropathy, nail discoloration, nail pigmentation changes, photosensitivity reaction, pneumothorax, pruritus, radiation recall, stroke, thrombosis, transient ischemic attack

Adverse reactions reported with paclitaxel, which may occur with paclitaxel (protein bound): Autonomic neuropathy, cellulitis, conjunctivitis, extravasation recall, fibrosis, hepatic necrosis, hepatic encephalopathy, induration, intestinal obstruction, intestinal perforation, interstitial pneumonia, ischemic colitis, lacrimation increased, lung fibrosis, necrosis, neutropenic enterocolitis (typhlitis), optic nerve damage (persistent), pancreatitis, paralytic ileus, phlebitis, radiation pneumonitis with concurrent radiation therapy, skin exfoliation, Stevens-Johnson syndrome, toxic epidermal necrolysis

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Page 7: Cancer Survivorship Endometrial Cancer Module

Doxorubicin

Licensed to University of California ©2006 UpToDate ® U.S. BRAND NAMES — Adriamycin PFS®; Adriamycin

RDF®; Rubex® PHARMACOLOGIC CATEGORY

Antineoplastic Agent, Anthracycline USE — Treatment of leukemias, lymphomas, multiple

myeloma, osseous and nonosseous sarcomas, mesotheliomas, germ cell tumors of the ovary or testis, and carcinomas of the head and neck, thyroid, lung, breast, stomach, pancreas, liver, ovary, bladder, prostate, uterus, and neuroblastoma

Adverse reactions

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Page 8: Cancer Survivorship Endometrial Cancer Module

Doxorubicin(Adverse Reactions)

>10%:  Cardiovascular: Transient ECG abnormalities (supraventricular tachycardia, S-T wave changes, atrial or ventricular extrasystoles); generally asymptomatic and self-limiting. CHF, dose related, may be delayed for 7-8 years after treatment. Cumulative dose, mediastinal/pericardial radiation therapy, cardiovascular disease, age, and use of cyclophosphamide (or other cardiotoxic agents) all increase the risk.    Recommended maximum cumulative doses:      No risk factors: 550 mg/m2       Concurrent radiation: 450 mg/m2       Note: Regardless of cumulative dose, if the left ventricular ejection fraction is <30% to 40%, the drug is usually not given.  Dermatologic: Alopecia  Gastrointestinal: Acute nausea and vomiting (21% to 55%), mucositis, ulceration, and necrosis of the colon, anorexia, and diarrhea, stomatitis, esophagitis  Genitourinary: Discoloration of urine (red)  Hematologic: Myelosuppression, leukopenia (75%), dose-limiting toxicity    WBC: Moderate    Platelets: Moderate    Onset (days): 7    Nadir (days): 10-14    Recovery (days): 21-28  Local: Vesicant chemotherapy

1% to 10%:  Cardiovascular: Acute: Arrhythmias, heart block, pericarditis-myocarditis, facial flushing; Delayed: CHF (related to cumulative dose; usually a maximum total lifetime dose of 450-550 mg/m2; possibly higher if given by continuous infusion)  Dermatologic: Hyperpigmentation of nail beds, erythematous streaking along the vein if administered rapidly  Endocrine & metabolic: Hyperuricemia

<1% (Limited to important or life-threatening):  Pediatric patients may be at increased risk of later neoplastic disease, particularly acute myeloid leukemia (pediatric patients). Prepubertal growth failure may result from intensive chemotherapy regimens.  Radiation recall: Noticed in patients who have had prior irradiation; reactions include redness, warmth, erythema, and dermatitis in the radiation port. Can progress to severe desquamation and ulceration. Occurs 5-7 days after doxorubicin administration; local therapy with topical corticosteroids and cooling have given the best relief.

Back tocase

Page 9: Cancer Survivorship Endometrial Cancer Module

Cisplatin

Licensed to University of California ©2006 UpToDate ® U.S. BRAND NAMES — Platinol®-AQ [DSC] PHARMACOLOGIC CATEGORY

Antineoplastic Agent, Alkylating Agent USE — Treatment of bladder, testicular, and ovarian cancer USE - UNLABELED / INVESTIGATIONAL —

Treatment of head and neck, breast, gastric, lung, esophageal, cervical, prostate and small cell lung cancer; Hodgkin's and non-Hodgkin's lymphoma; neuroblastoma; sarcomas, myeloma, melanoma, mesothelioma, and osteosarcoma

Adverse reactions

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Page 10: Cancer Survivorship Endometrial Cancer Module

Cisplatin(Adverse Reactions)

>10%:  Central nervous system: Neurotoxicity: Peripheral neuropathy is dose- and duration-dependent.  Dermatologic: Mild alopecia  Gastrointestinal: Nausea and vomiting (76% to 100%)  Hematologic: Myelosuppression (25% to 30%; mild with moderate doses, mild to moderate with high-dose therapy)    WBC: Mild    Platelets: Mild    Onset: 10 days    Nadir: 14-23 days    Recovery: 21-39 days  Hepatic: Liver enzymes increased  Renal: Nephrotoxicity (acute renal failure and chronic renal insufficiency)  Otic: Ototoxicity (10% to 30%; manifested as high frequency hearing loss; ototoxicity is especially pronounced in children)

1% to 10%:  Gastrointestinal: Diarrhea  Local: Tissue irritation

<1% (Limited to important or life-threatening): Anaphylactic reaction, arrhythmias, blurred vision, bradycardia, cerebral blindness, hemolytic anemia, liver enzymes increased, mild alopecia, mouth sores, optic neuritis, papilledema

Central nervous system: Peripheral and autonomic neuropathy, ototoxicity Endocrine & metabolic: Hypokalemia, hypomagnesemia Gastrointestinal: Highly emetogenic Hematologic: Myelosuppression Renal: Acute renal failure, increased serum creatinine, azotemia Miscellaneous: Transient pain at tumor, transient autoimmune disorders

Back tocase

Page 11: Cancer Survivorship Endometrial Cancer Module

Presenting Complaint

Four weeks into her treatment and 8 weeks after her diagnosis, Ms Johnson notices her bed is full of hair when she wakes up. She also loses a lot of hair when she brushes. She is very agitated because she is very proud of her wavy curly blonde hair.

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Page 12: Cancer Survivorship Endometrial Cancer Module

Question #1

She comes to your office seeking an explanation about her hair loss. What is the most likely diagnosis?

A. Alopecia areata

B. Telogen effluvium

C. Cicatricial alopecia

D. Traumatic alopecia

E. Drug induced alopecia

Page 13: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

B. Alopecia areata Alopecia areata causes one or more patches of scalp hair loss. Tends to affect younger individuals, both male and female. It is an autoimmune disorder, in which the immune system

attacks hair follicles. The condition resolves without treatment within a year, but

hair loss is sometimes permanent. Treatments may be steroid injections and cream (such as

clobetasol or fluocinonide), minoxidil, irritants (anthralin or topical coal tar), and topical immunotherapy (cyclosporine).

Back toQuestion 1

Page 14: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

B. Alopecia areata Alopecia areata causes one or more patches of scalp hair loss. Tends to affect younger individuals, both male and female. It is an autoimmune disorder, in which the immune system

attacks hair follicles. The condition resolves without treatment within a year, but hair

loss is sometimes permanent. Treatments may be steroid injections and cream (such as

clobetasol or fluocinonide), minoxidil, irritants (anthralin or topical coal tar), and topical immunotherapy (cyclosporine).

Continue Case

Teaching Points for Incorrect Answers

Page 15: Cancer Survivorship Endometrial Cancer Module

Minoxidil BRAND NAME: Rogaine DRUG CLASS AND MECHANISM: Oral minoxidil, a medication that originally was used

to treat high blood pressure, has been found to increase hair growth. This lead to the development of topical (solution applied to the skin) minoxidil. Topical minoxidil (Rogaine) has been shown to stimulate hair growth on the bald spot of the back of the head in men. In women, Rogaine can increase hair growth in the forehead areas. Minoxidil is in a class of drugs called hair growth stimulants.

DRUG INTERACTIONS: Oral minoxidil can cause a fall in blood pressure, an increase in the heart rate, and weight gain (fluid retention). An increase in the absorption of minoxidil from the scalp can occur in patients with inflamed or abnormal scalps, leading to side effects mentioned above. Patients with heart failure or significant coronary heart disease should avoid Rogaine because of these side effects. Rogaine's alcohol base can irritate the eyes. Rogaine should not be used with other topical medications because they may increase its absorption and side effects. Rogaine should be used with caution in those with high blood pressure.

PREGNANCY: Rogaine should not be used in pregnancy. NURSING MOTHERS: Rogaine should not be used by nursing women. SIDE EFFECTS: Skin side effects are seen at times with Rogaine, including irritation, itch,

contact dermatitis, hives, swelling, and sensitivity.

Back to Case

Page 16: Cancer Survivorship Endometrial Cancer Module

Minoxidil BRAND NAME: Rogaine DRUG CLASS AND MECHANISM: Oral minoxidil, a medication that originally was used

to treat high blood pressure, has been found to increase hair growth. This lead to the development of topical (solution applied to the skin) minoxidil. Topical minoxidil (Rogaine) has been shown to stimulate hair growth on the bald spot of the back of the head in men. In women, Rogaine can increase hair growth in the forehead areas. Minoxidil is in a class of drugs called hair growth stimulants.

DRUG INTERACTIONS: Oral minoxidil can cause a fall in blood pressure, an increase in the heart rate, and weight gain (fluid retention). An increase in the absorption of minoxidil from the scalp can occur in patients with inflamed or abnormal scalps, leading to side effects mentioned above. Patients with heart failure or significant coronary heart disease should avoid Rogaine because of these side effects. Rogaine's alcohol base can irritate the eyes. Rogaine should not be used with other topical medications because they may increase its absorption and side effects. Rogaine should be used with caution in those with high blood pressure.

PREGNANCY: Rogaine should not be used in pregnancy. NURSING MOTHERS: Rogaine should not be used by nursing women. SIDE EFFECTS: Skin side effects are seen at times with Rogaine, including irritation, itch,

contact dermatitis, hives, swelling, and sensitivity.

Back to Incorrect Answers

Page 17: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

C. Telogen effluvium Telogen effluvium is nonscarring alopecia with diffuse hair

shedding. A reactive process caused by a metabolic, hormonal stress or

medications that shifts follicles in anagen to a telogen-predominant distribution.

Generally, recovery is spontaneous and occurs by 6 months. Acute telogen effluvium is hair shedding lasting < 6 months. Usually initiated by metabolic or physiologic stressors. Papulosquamous diseases of the scalp, such as psoriasis and

seborrheic dermatitis, can produce telogen effluvium. Chronic telogen effluvium is hair shedding lasting > 6 months.

Back toQuestion 1

Page 18: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

C. Telogen effluvium Telogen effluvium is nonscarring alopecia with diffuse hair

shedding. A reactive process caused by a metabolic, hormonal stress or

medications that shifts follicles in anagen to a telogen-predominant distribution.

Generally, recovery is spontaneous and occurs by 6 months. Acute telogen effluvium is hair shedding lasting < 6 months. Usually initiated by metabolic or physiologic stressors. Papulosquamous diseases of the scalp, such as psoriasis and

seborrheic dermatitis, can produce telogen effluvium. Chronic telogen effluvium is hair shedding lasting > 6 months.

Continue Case

Teaching Points for Incorrect Answers

Page 19: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

D. Cicatricial alopecia Cicatricial alopecia is hair loss from scalp and hair

follicle damage. The scalp usually has an abnormal appearance. Plaques of erythema, scaling or pustules occur. Associations include infections (e.g., syphilis,

tuberculosis, acquired immunodeficiency syndrome, herpes zoster), autoimmune disease (discoid lupus erythematosus), sarcoidosis, scalp trauma (e.g., injuries, burns), and radiation therapy.

Back toQuestion 1

Page 20: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

D. Cicatricial alopecia Cicatricial alopecia is hair loss from scalp and hair

follicle damage. The scalp usually has an abnormal appearance. Plaques of erythema, scaling or pustules occur. Associations include infections (e.g., syphilis,

tuberculosis, acquired immunodeficiency syndrome, herpes zoster), autoimmune disease (discoid lupus erythematosus), sarcoidosis, scalp trauma (e.g., injuries, burns), and radiation therapy.

Continue Case

Teaching Points for Incorrect Answers

Page 21: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

E. Traumatic alopecia Traumatic alopecia is caused by cosmetic

practices that damage hair follicles over time. Cosmetic alopecia has been linked to the use of

brush rollers, curling irons, hair brushes with square or angular tips, and tight braiding of the hair.

Back toQuestion 1

Page 22: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #1

E. Traumatic alopecia Traumatic alopecia is caused by cosmetic

practices that damage hair follicles over time. Cosmetic alopecia has been linked to the use of

brush rollers, curling irons, hair brushes with square or angular tips, and tight braiding of the hair.

Continue Case

Teaching Points for Incorrect Answers

Page 23: Cancer Survivorship Endometrial Cancer Module

Correct. Question #1F. Drug induced alopecia Anagen effluvium occurs after insult to hair follicle that impairs mitotic or

metabolic activity. Due to exposure to chemotherapeutic agents Inhibition of cell division in the hair matrix leads to thin, weakened hair

shaft likely to fracture with minimal trauma May cause complete failure of hair formation. Worse with combination chemotherapy and higher doses. Hair loss usually begins 7-14 days after exposure and is clinically most

apparent after 1-2 months. Reversible; hair growth resumes few weeks after treatment cessation;

regrows in 3-5 months; color or texture of new hair may differ from

original hair. Continue

CaseTeaching Points

for Incorrect Answers

Page 24: Cancer Survivorship Endometrial Cancer Module

Question #1 Incorrect Answers

Alopecia areata Telogen effluvium Cicatricial alopecia Traumatic alopecia

ContinueCase

Page 25: Cancer Survivorship Endometrial Cancer Module

Case Continued

After discussing her options Ms Johnson is fitted with a wig.

Four months after her treatment and 5 months after diagnosis. Mrs. Johnson comes to see you and states: “ I have noticed that over the last 2 months my shoes don’t fit and I can only wear bathroom slippers. Both my legs feel tight and appear very swollen but I don’t feel much pain. What is happening to me?”

Next

Page 26: Cancer Survivorship Endometrial Cancer Module

Question #2

What is the most likely diagnosis?

A. Deep venous thrombosis

B. Lymphedema

C. Compartment syndrome

D. Femoral artery ligation

E. Necrotizing fascitis

Page 27: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2A. Deep venous thrombosis Cancer results in a hypercoagulable state. Deep venous thrombosis occurs in up to 11% of

cancer patients and is an important cause of death Usually unilateral and about half are asymptomatic. Symptoms of include swelling, pain, and

discoloration. Physical examination may reveal a palpable cord

(reflecting a thrombosed vein), ipsilateral edema, warmth, and/or superficial venous dilation.

Diagnosed by: venography of the legs, Doppler ultrasound, plethysmography, D-dimer blood test

Back toQuestion 2

Page 28: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2A. Deep venous thrombosis Cancer results in a hypercoagulable state. Deep venous thrombosis occurs in up to 11% of cancer

patients and is an important cause of death Usually unilateral and about half are asymptomatic. Symptoms of include swelling, pain, and discoloration. Physical examination may reveal a palpable cord

(reflecting a thrombosed vein), ipsilateral edema, warmth, and/or superficial venous dilation.

Diagnosed by: venography of the legs, Doppler ultrasound, plethysmography, D-dimer blood test

Continue Case

Teaching Points for Incorrect Answers

Page 29: Cancer Survivorship Endometrial Cancer Module

Correct. Question #2

B. Lymphedema Lymphedema is nonpitting swelling of an extremity,

usually bilateral. In cancer is due to lymphatic obstruction from node

dissection, radiation or malignant obstruction. Treated by exercise, gradient pressure garments,

massage or external pneumatic compression. Patients undergoing dissection or radiation of lymph

nodes should be counseled on preventing lymphedema; which are: elevating limb, avoiding constricting garments that cause a tourniquet effect, meticulous skin hygiene and nail care.

Continue Module

Stage 3

Teaching Points for Incorrect Answers

Page 30: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2

C. Compartment syndrome Compartment syndrome is increased tissue

pressure in a closed muscle compartment compromising local circulation and neuromuscular function.

Requires 1:constricting envelope (fascia or cast) 2: increase in volume (blood, edema).

Fascia of leg muscles do not allow muscle expansion when significant edema occurs.

Due to a direct blow, usually to an unpadded soft-tissue area. Causes pain that is more severe than physical findings.

Treatment is fasciotomy: longitudinal incisions in affected compartments.

Back toQuestion 2

Page 31: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2

C. Compartment syndrome Compartment syndrome is increased tissue

pressure in a closed muscle compartment compromising local circulation and neuromuscular function.

Requires 1:constricting envelope (fascia or cast) 2: increase in volume (blood, edema).

Fascia of leg muscles do not allow muscle expansion when significant edema occurs.

Due to a direct blow, usually to an unpadded soft-tissue area. Causes pain that is more severe than physical findings.

Treatment is fasciotomy: longitudinal incisions in affected compartments.

Continue Case

Teaching Points for Incorrect Answers

Page 32: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2

D. Femoral artery ligation Femoral artery ligation will result in

pulselessness and lower extremity ischemia. If not corrected, will result in lower limb

ischemia and necrosis necessitating amputation.

It may occurs as an inadvertent injury following extensive and difficult surgery for extensive cancer.

Back toQuestion 2

Page 33: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2

D. Femoral artery ligation Femoral artery ligation will result in

pulselessness and lower extremity ischemia. If not corrected, will result in lower limb

ischemia and necrosis necessitating amputation.

It may occurs as an inadvertent injury following extensive and difficult surgery for extensive cancer.

Continue Case

Teaching Points for Incorrect Answers

Page 34: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2E. Necrotizing fascitis Necrotizing fasciitis is an insidiously advancing soft

tissue infection with widespread fascial necrosis. Mixed infection after surgery with diabetes or

peripheral vascular disease. Systemic toxicity and high mortality. Extensive tissue destruction, thrombosis of blood

vessels, bacteria spread along fascial planes. Unexplained pain. Erythema darken to a reddish-

purple color, with blisters and bullae. Treatment is early and aggressive surgical

exploration and debridement of necrotic tissue, antibiotics, and hemodynamic support.

Back toQuestion 2

Page 35: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #2E. Necrotizing fascitis Necrotizing fasciitis is an insidiously advancing soft

tissue infection with widespread fascial necrosis. Mixed infection after surgery with diabetes or

peripheral vascular disease. Systemic toxicity and high mortality. Extensive tissue destruction, thrombosis of blood

vessels, bacteria spread along fascial planes. Unexplained pain. Erythema darken to a reddish-

purple color, with blisters and bullae. Treatment is early and aggressive surgical

exploration and debridement of necrotic tissue, antibiotics, and hemodynamic support.

Continue Case

Teaching Points for Incorrect Answers

Page 36: Cancer Survivorship Endometrial Cancer Module

Question #2 Incorrect Answers

A. Deep venous thrombosis

C. Compartment syndrome

D. Femoral artery ligation

E. Necrotizing fascitis

Continue Case

Page 37: Cancer Survivorship Endometrial Cancer Module

Case Continued

She is started on an exercise program, fitted with gradient pressure garments and diuretics were prescribed.

Three months later and seven months after diagnosis she comes to see you. She is very distraught and agitated. She tells you “I cry a lot and have lost interest in almost everything. I don’t sleep well and I don’t want to eat. I’ve lost weight. I think the cancer has come back.”

Next

Page 38: Cancer Survivorship Endometrial Cancer Module

Question #3

Of the following, what is the most likely explanation?

A. Insomnia

B. Nutritional imbalance

C. Depression

D. Recurrence of the cancer

Page 39: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #3A. Work-up for insomnia is helpful but does not explain all the other

symptoms that she has.

Sedatives should be used with caution since tolerance or dependence can develop. Time and effort should be spent in finding the cause of insomnia.

Causes of insomnia include:

Back toQuestion 3

Psychiatric disease: SchizophreniaAnxietyDepression

Medical disease:Alcoholism Degenerative Neurological Disorders Alzheimer’s diseaseParkinson’s disease Fatal Familial Insomnia (FFI)Headaches

Medical disease cont.Chronic Obstructive Pulmonary Disease (COPD) Sleep apneaAsthma Gastroesophageal Reflux Fibromyalgia HypothyriodismMedications

Page 40: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #3A. Work-up for insomnia is helpful but does not explain all the other

symptoms that she has.

Sedatives should be used with caution since tolerance or dependence can develop. Time and effort should be spent in finding the cause of insomnia.

Causes of insomnia include:

Continue Case

Psychiatric disease: Schizophrenia AnxietyDepression

Medical disease:Alcoholism Degenerative Neurological Disorders Alzheimer’s diseaseParkinson’s Disease Fatal Familial Insomnia (FFI)Headaches

Medical disease cont.Chronic Obstructive Pulmonary Disease (COPD) Sleep apneaAsthma Gastroesophageal Reflux Fibromyalgia HypothyriodismMedications

Teaching Points for Incorrect Answers

Page 41: Cancer Survivorship Endometrial Cancer Module

Alcoholism

Alcoholism Alcohol may induce sleep for up to four hours, but after that it can lead to frequent awakenings and sleep fragmentation. Insomnia is a common symptom of alcoholism.

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Page 42: Cancer Survivorship Endometrial Cancer Module

Alcoholism

Alcoholism Alcohol may induce sleep for up to four hours, but after that it can lead to frequent awakenings and sleep fragmentation. Insomnia is a common symptom of alcoholism.

Back to Incorrect Answers

Back to Insomnia

Page 43: Cancer Survivorship Endometrial Cancer Module

Degenerative Neurological Disorders

Insomnia is often associated with degenerative neurological disorders, such as Alzheimer's disease, Pick's disease, and hydrocephalus. People with dementia who require institutionalization typically have insomnia.

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Page 44: Cancer Survivorship Endometrial Cancer Module

Degenerative Neurological Disorders

Insomnia is often associated with degenerative neurological disorders, such as Alzheimer's disease, Pick's disease, and hydrocephalus. People with dementia who require institutionalization typically have insomnia.

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Back to Insomnia

Page 45: Cancer Survivorship Endometrial Cancer Module

Alzheimer’s disease

Alzheimer's disease (AD) is an irreversible, progressive disorder in which brain cells (neurons) deteriorate, resulting in the loss of cognitive functions, primarily memory, judgment and reasoning, movement coordination, and pattern recognition. In advanced stages of the disease, all memory and mental functioning may be lost.

The condition predominantly affects the cerebral cortex and hippocampus, which lose mass and shrink (atrophy) as the disease advances.

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Page 46: Cancer Survivorship Endometrial Cancer Module

Alzheimer’s disease

Alzheimer's disease (AD) is an irreversible, progressive disorder in which brain cells (neurons) deteriorate, resulting in the loss of cognitive functions, primarily memory, judgment and reasoning, movement coordination, and pattern recognition. In advanced stages of the disease, all memory and mental functioning may be lost.

The condition predominantly affects the cerebral cortex and hippocampus, which lose mass and shrink (atrophy) as the disease advances.

Back to Incorrect Answers

Back to Insomnia

Page 47: Cancer Survivorship Endometrial Cancer Module

Parkinson's Disease

Insomnia is a common complication of Parkinson's disease and of the medications used to treat it. Other causes of insomnia in people with Parkinson's disease include periodic limb movements and sleep-related breathing disorders. Parkinson's patients also don't move much in bed and experience pain from agitated pressure-point arousal. Rapid eye movement disorder is thought to precede Parkinson's disease.

Back to Case

Page 48: Cancer Survivorship Endometrial Cancer Module

Parkinson's Disease

Insomnia is a common complication of Parkinson's disease and of the medications used to treat it. Other causes of insomnia in people with Parkinson's disease include periodic limb movements and sleep-related breathing disorders. Parkinson's patients also don't move much in bed and experience pain from agitated pressure-point arousal. Rapid eye movement disorder is thought to precede Parkinson's disease.

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Back to Insomnia

Page 49: Cancer Survivorship Endometrial Cancer Module

Fatal Familial Insomnia

Fatal familial insomnia is an extremely rare, infectious prion disease. It involves proteinaceous cells, probably of the thalamus, that lack the ability to produce nucleic acid. It is a progressive disorder that begins with difficulty initiating sleep and leads to total lack of sleep within a few months. It can be fatal within 7 to 13 months after symptoms begin but may last longer.

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Page 50: Cancer Survivorship Endometrial Cancer Module

Prion

A microscopic protein particle similar to a virus but lacking nucleic acid, responsible for certain degenerative diseases of the nervous system.

Back to FFI

Page 51: Cancer Survivorship Endometrial Cancer Module

Fatal Familial Insomnia

Fatal familial insomnia is an extremely rare, infectious prion disease. It involves proteinaceous cells, probably of the thalamus, that lack the ability to produce nucleic acid. It is a progressive disorder that begins with difficulty initiating sleep and leads to total lack of sleep within a few months. It can be fatal within 7 to 13 months after symptoms begin but may last longer.

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Back to Insomnia

Page 52: Cancer Survivorship Endometrial Cancer Module

Prion

A microscopic protein particle similar to a virus but lacking nucleic acid, responsible for certain degenerative diseases of the nervous system.

Back to FFI

Page 53: Cancer Survivorship Endometrial Cancer Module

Headaches

Any type of headache that occurs during sleep may wake a person up. For example, hypnic (sleep-inducing) headaches are characterized by generalized pulsating pain and may occur three times a night for 30 minutes for several consecutive nights. They are benign and usually affect people over the age of 60. They sometimes respond to lithium treatment

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Page 54: Cancer Survivorship Endometrial Cancer Module

Headaches

Any type of headache that occurs during sleep may wake a person up. For example, hypnic (sleep-inducing) headaches are characterized by generalized pulsating pain and may occur three times a night for 30 minutes for several consecutive nights. They are benign and usually affect people over the age of 60. They sometimes respond to lithium treatment

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Back to Insomnia

Page 55: Cancer Survivorship Endometrial Cancer Module

Chronic Obstructive Pulmonary Disease (COPD)

Many aspects of COPD can disturb one's sleep. Low blood oxygen levels, coughing to clear secretions from the lungs, bronchospasm (narrowing and obstruction of airways), and the side effects of the medications used to treat the condition can create a night of broken sleep.

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Page 56: Cancer Survivorship Endometrial Cancer Module

Chronic Obstructive Pulmonary Disease (COPD)

Many aspects of COPD can disturb one's sleep. Low blood oxygen levels, coughing to clear secretions from the lungs, bronchospasm (narrowing and obstruction of airways), and the side effects of the medications used to treat the condition can create a night of broken sleep.

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Page 57: Cancer Survivorship Endometrial Cancer Module

Asthma

Asthma-related bronchospasm and subsequent airway obstruction is often worse during the night. This may lead to shortness of breath that causes a person to wake up. As with COPD, many asthma medications can cause insomnia, including theophylline, beta agonists (used as inhalants), and corticosteroids.

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Page 58: Cancer Survivorship Endometrial Cancer Module

Asthma

Asthma-related bronchospasm and subsequent airway obstruction is often worse during the night. This may lead to shortness of breath that causes a person to wake up. As with COPD, many asthma medications can cause insomnia, including theophylline, beta agonists (used as inhalants), and corticosteroids.

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Page 59: Cancer Survivorship Endometrial Cancer Module

Gastroesophageal Reflux and Heartburn

Nocturnal acid reflux and its characteristic chronic burning sensation in the lower esophagus can arouse one from sleep. If the symptoms are pronounced before going to sleep, they may cause sleep-onset difficulties. Heartburn often wakes people up and makes it difficult to go back to sleep. Avoiding fatty foods before sleep may help reduce heartburn and sleep disturbance.

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Page 60: Cancer Survivorship Endometrial Cancer Module

Gastroesophageal Reflux and Heartburn

Nocturnal acid reflux and its characteristic chronic burning sensation in the lower esophagus can arouse one from sleep. If the symptoms are pronounced before going to sleep, they may cause sleep-onset difficulties. Heartburn often wakes people up and makes it difficult to go back to sleep. Avoiding fatty foods before sleep may help reduce heartburn and sleep disturbance.

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Page 61: Cancer Survivorship Endometrial Cancer Module

Fibromyalgia

People with fibromyalgia often complain of light sleep and nonrestorative sleep. Fibromyalgia causes chronic pain in muscles and joint tissue, which can significantly disrupt or prevent sleep.

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Page 62: Cancer Survivorship Endometrial Cancer Module

Fibromyalgia

People with fibromyalgia often complain of light sleep and nonrestorative sleep. Fibromyalgia causes chronic pain in muscles and joint tissue, which can significantly disrupt or prevent sleep.

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Back to Insomnia

Page 63: Cancer Survivorship Endometrial Cancer Module

Medications There are numerous medications for which insomnia is a predictable

side effect. The most common ones are listed below:

Decongestants (pseudoephedrine) Bronchodilators (beta-2 agonists, theophylline) Antihypertensives (hydrochlorothiazide, nifedipine, methyldopa, propranolol) Antidepressants (fluoxetine, bupropion, sertraline) Antidepressants that may cause daytime drowsiness (desipramine, imipramine,

nortriptyline) Diuretics (furosemide) Antiepileptics (phenytoin) Antiarrhythmic agents (quinidine, propranolol, verapamil) Histamine H2 inhibitors (cimetidine -for gastrointestinal conditions) Thyroid medications Alcohol, caffeine, nicotine

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Page 64: Cancer Survivorship Endometrial Cancer Module

Medications There are numerous medications for which insomnia is a predictable

side effect. The most common ones are listed below:

Decongestants (pseudoephedrine) Bronchodilators (beta-2 agonists, theophylline) Antihypertensives (hydrochlorothiazide, nifedipine, methyldopa, propranolol) Antidepressants (fluoxetine, bupropion, sertraline) Antidepressants that may cause daytime drowsiness (desipramine, imipramine,

nortriptyline) Diuretics (furosemide) Antiepileptics (phenytoin) Antiarrhythmic agents (quinidine, propranolol, verapamil) Histamine H2 inhibitors (cimetidine -for gastrointestinal conditions) Thyroid medications Alcohol, caffeine, nicotine

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Back to Insomnia

Page 65: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #3

B. Nutritional Imbalance

Nutrition evaluation is always important but must not prevent physicians from making a diagnosis that maybe potentially life-threatening and treatable.

Back to Question 3

Page 66: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #3

B. Nutritional Imbalance

Nutrition evaluation is always important but must not prevent physicians from making a diagnosis that maybe potentially life-threatening and treatable.

Continue Case

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Page 67: Cancer Survivorship Endometrial Cancer Module

Correct. Question #3

C. Depression Clinical depression occurs in about 25% with

cancer, causing distress, impaired functioning, and less ability to follow treatment and is treatable. Symptoms of clinical depression that our patient has are:

Sad or "empty" mood Loss of interest or pleasure Significant weight changes “Slowed down" or restless and agitated Sleeping disorders Continue

CaseTeaching Points

for Incorrect Answers

Page 68: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #3

D. Recurrence of the cancerCancer recurrence is always a concern. A thorough physical examination would be the first step, including an MRI. However the patient has other symptoms that need to be evaluated.

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Page 69: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #3

D. Recurrence of the cancerCancer recurrence is always a concern. A thorough physical examination would be the first step, including an MRI. However the patient has other symptoms that need to be evaluated.

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Page 70: Cancer Survivorship Endometrial Cancer Module

Question #3 Incorrect Answers

A. Insomnia

B. Nutritional imbalance

D. Recurrence of the cancer

Continue Case

Page 71: Cancer Survivorship Endometrial Cancer Module

Case Continued

She is started on an SSRI, psychotherapy sessions are initiated and she joins a cancer support group.

A year after her diagnosis, Ms. Johnson, comes for her check-up with her oncologist. Clinical evaluation and follow-up MRI shows that she has a suspicious enlarged para-aortic lymph node. Further therapy is suggested.

Next

Page 72: Cancer Survivorship Endometrial Cancer Module

Question #4

Of the following, which is the best management?

A. Surgical removal of lymph node

B. Combined chemotherapy

C. Brachytherapy

D. External pelvic and abdominal radiation

E. Tamoxifen

Page 73: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4

A. Surgical removal of lymph nodeSurgical removal of the lymph node will increase the risk of disseminating cancerous tissue. It is not curative since the exact extent of local spread cannot be determined.

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Page 74: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4

A. Surgical removal of lymph nodeSurgical removal of the lymph node will increase the risk of disseminating cancerous tissue. It is not curative since the exact extent of local spread cannot be determined.

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Page 75: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4

B. Combined chemotherapyPatient has previously been treated with chemotherapy. Repeat chemotherapy is not felt to be effective and will increase morbidity with little or no benefit.

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Page 76: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4

B. Combined chemotherapyPatient has previously been treated with chemotherapy. Repeat chemotherapy is not felt to be effective and will increase morbidity with little or no benefit.

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Page 77: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4C. Brachytherapy

Brachyterapy is, giving a high radiation dose to the tumor while reducing the radiation exposure in the surrounding healthy tissues by using radioactive seeds or applicators placed in or near the tumor itself. It allows use of a higher total dose of radiation to treat a smaller area and in a shorter time than is possible with external radiation treatment. It is given at a short distance: internally, localized, precise, and high-tech. This is not possible with lymph nodes. Some of the tumors treated with: Breast , Lung, Esophageal, cervical, Anal/Rectal, head and neck cancers and Sarcomas

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Page 78: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4C. Brachytherapy

Brachyterapy is, giving a high radiation dose to the tumor while reducing the radiation exposure in the surrounding healthy tissues by using radioactive seeds or applicators placed in or near the tumor itself. It allows use of a higher total dose of radiation to treat a smaller area and in a shorter time than is possible with external radiation treatment. It is given at a short distance: internally, localized, precise, and high-tech. This is not possible with lymph nodes. Some of the tumors treated with: Breast , Lung, Esophageal, Cervical, Anal/Rectal, head and neck cancers and Sarcomas

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Page 79: Cancer Survivorship Endometrial Cancer Module

Correct. Question #4

D. External pelvic and abdominal radiation

Radiation therapy may be used in combination with other forms of cancer treatment, or when surgery is not an option.

Radiotherapy uses high-energy rays to destroy or impede tumor growth. External Beam Radiation Therapy, or EBRT involves focusing a “beam” of radiation from an external source on the cancerous internal organ and/or tissue.

Radiotherapy should be considered for women with endometrial cancer who suffer a localized relapse following surgery. It can be curative in a select group of previously non-irradiated women.

In the literature, long-term survival rates in women who undergo irradiation after relapse range from 25 to 71 percent, with most reporting five-year survival rates between 40 and 55 percent.

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Page 80: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4

E. Tamoxifen Tamoxifen, a selective estrogen receptor modulator

(SERM), appears to have some efficacy in women with advanced endometrial cancer as a single agent, with response rates of 10 to 22 percent .

It is inactive in women who are resistant to progestins or chemotherapy.

Low-grade endometrial cancers are far more likely to respond to tamoxifen than are high-grade tumors. There is a more effective therapy for this patient

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Page 81: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #4

E. Tamoxifen Tamoxifen, a selective estrogen receptor modulator

(SERM), appears to have some efficacy in women with advanced endometrial cancer as a single agent, with response rates of 10 to 22 percent .

It is inactive in women who are resistant to progestins or chemotherapy.

Low-grade endometrial cancers are far more likely to respond to tamoxifen than are high-grade tumors. There is a more effective therapy for this patient

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Page 82: Cancer Survivorship Endometrial Cancer Module

Tamoxifen

Licensed to University of California ©2006 UpToDate ® U.S. BRAND NAMES — Nolvadex®; Soltamox™ PHARMACOLOGIC CATEGORY

Antineoplastic Agent, Estrogen Receptor Antagonist USE — Palliative or adjunctive treatment of advanced

breast cancer; reduce the incidence of breast cancer in women at high risk; reduce risk of invasive breast cancer in women with ductal carcinoma in situ (DCIS); metastatic female and male breast cancer

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Page 83: Cancer Survivorship Endometrial Cancer Module

Tamoxifen

Licensed to University of California ©2006 UpToDate ® U.S. BRAND NAMES — Nolvadex®; Soltamox™ PHARMACOLOGIC CATEGORY

Antineoplastic Agent, Estrogen Receptor Antagonist USE — Palliative or adjunctive treatment of advanced

breast cancer; reduce the incidence of breast cancer in women at high risk; reduce risk of invasive breast cancer in women with ductal carcinoma in situ (DCIS); metastatic female and male breast cancer

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Page 84: Cancer Survivorship Endometrial Cancer Module

Question #4 Incorrect Answers

A. Surgical removal of lymph node

B. Combined chemotherapy

C. Brachytherapy

E. Tamoxifen

Continue Case

Page 85: Cancer Survivorship Endometrial Cancer Module

Case Continued

Six months later and 18 months after her diagnosis, Ms Johnson receives external pelvic and abdominal radiation.

A repeat MRI shows resolution of the enlarged lymph node.

Mrs Johnson returns to your office and states; “ My bladder is very painful, I have strong urgency with frequent urination and sometimes lose my urine before I get to the bathroom. Also my urine is very bloody. Is it happening again?

Next

Page 86: Cancer Survivorship Endometrial Cancer Module

Question #5

What is the most likely diagnosis?

A. Urinary tract infectionB. Estrogen loss cystitisC. Irradiation cystitis D. Recurrence of endometrial cancerE. Detrusor instability

Page 87: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #5

A. Urinary tract infectionBecause of a short urethra, urinary tract infection is common in women but is usually not associated with hematuria.

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Page 88: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #5

A. Urinary tract infectionBecause of a short urethra, urinary tract infection is common in women but is usually not associated with hematuria

Continue Case

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Page 89: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #5

B. Estrogen loss cystitis Estrogen deficiency may lead to vaginal atrophy

resulting in vaginal dryness and dyspareunia. The mucosal lining of the vagina and urethra are

very sensitive to estrogen, and thinning of the vaginal epithelium occurs after the menopause. Estrogen deprivation is unlikely to cause bladder inflammation.

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Page 90: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #5

B. Estrogen loss cystitis Estrogen deficiency may lead to vaginal atrophy

resulting in vaginal dryness and dyspareunia. The mucosal lining of the vagina and urethra are

very sensitive to estrogen, and thinning of the vaginal epithelium occurs after the menopause. Estrogen deprivation is unlikely to cause bladder inflammation.

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Page 91: Cancer Survivorship Endometrial Cancer Module

Correct. Question #5

C. Irradiation cystitis

Continue Case

Radiation results in cell death, vasculitis, fibrosis and neuritis. Early findings (<12 mo) are submucosal inflammation and fibrosis, perineural inflammation, surface ulceration, and epithelial atypiaLate findings (>12 mo) include luminal occlusion, vascular ectasia, and necrosis of vessel walls. Acute symptoms consist of urgency, frequency, dysuria, and hematuria. Chronic symptoms are due to ischemia and fibrosis resulting in contracted bladders, ulcer formation, fistulas, and bladder dysfunction; therefore, clinical presentation can include frequency, urgency, dysuria, hematuria, incontinence, hydronephrosis,

pneumaturia, and fecaluria. Teaching Points for Incorrect Answers

Page 92: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #5

D. Recurrence of endometrial cancerSince the lymph node has resolved, recurrence of the endometrial cancer is less likely. Also endometrial cancer does not commonly present as heamturia.

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Page 93: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #5

D. Recurrence of endometrial cancerSince the lymph node has resolved, recurrence of the endometrial cancer is less likely. Also endometrial cancer does not commonly present as heamturia.

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Page 94: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question # 5

E. Detrusor instability

Detrusor instability is due to uninhibited bladder contractions of detrusor overactivity resulting in urgency, frequency, and nocturia, and urge incontinence but does not cause heamturia.

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Page 95: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question # 5

E. Detrusor instability

Detrusor instability is due to uninhibited bladder contractions of detrusor overactivity resulting in urgency, frequency, and nocturia, and urge incontinence but does not cause heamturia.

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Teaching Points for Incorrect Answers

Page 96: Cancer Survivorship Endometrial Cancer Module

Question #5 Incorrect Answers

A. Urinary tract infection

B. Estrogen loss cystitis

D. Recurrence of endometrial cancer

E. Detrusor instability

Continue Case

Page 97: Cancer Survivorship Endometrial Cancer Module

Case Continued

She is treated with hyperbaric oxygen and alum irrigation with good results.

Six months, later and 20 months after her diagnosis, Ms Johnson calls your office. “I am really mad. My daughter, who takes care of me, is being threatened with termination from her job because of all the time she has taken off work to help me during my treatment.”

Next

Page 98: Cancer Survivorship Endometrial Cancer Module

Question #6

Which federal law best protects her caregiver?

A. American with disabilities act of 1990(ADA), P.L. 101-336B. Family medical Leave Act of 1993 (FMLA), P.L. 103-3C. Federal Rehabilitation Act of 1973, P.L. 93-112(amended 19

98)D. Employee Retirement Income Security Act of 1974E. Consolidated Omnibus Budget Reconciliation Act of 1985 (C

OBRA), P.L. 99-272F. Health Insurance Portability and Accountability Act of 1996

Page 99: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

A. American with disabilities act of 1990(ADA), P.L. 101-336The ADA prohibits employers with 15 or more employees from treating a cancer survivor or the family of a cancer survivor differently from other employees. The ADA requires employees to make reasonable accommodations to the survivor’s work schedule, work environment or duties if needed.

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Page 100: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

A. American with disabilities act of 1990(ADA), P.L. 101-336The ADA prohibits employers with 15 or more employees from treating a cancer survivor or the family of a cancer survivor differently from other employees. The ADA requires employees to make reasonable accommodations to the survivor’s work schedule, work environment or duties if needed.

Continue Case

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Page 101: Cancer Survivorship Endometrial Cancer Module

Correct. Question #6

B. Family medical Leave Act of 1993 (FMLA), P.L. 103-3 FMLA states: Subject to section 103, an eligible employee shall be entitled

to a total of 12 work weeks of leave during any 12-month period for any of the following:

A) Birth of a son or daughter of the employee and in order to care for such son or daughter.

(B) Placement of a son or daughter with the employee for adoption or foster care.

(C) In order to care for the spouse, or a son, daughter, or parent, of the employee, if such spouse, son, daughter, or parent has a serious health condition.

(D) Serious health condition that makes the employee unable to perform the functions of the position of such employee.

Employers with at least 50 employees are required to provide up to 12 weeks of unpaid leave to care for a spouse, child or oneself with a serious medical condition. The leave need not be taken at once. The person is entitled to health benefits and must be allowed to return to his or her job or an equivalent position. Continue

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Page 102: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

C. Federal Rehabilitation Act of 1973, P.L. 93-112(amended 1998)

This legislation bans discrimination of employees that are not covered under the ADA. These include the Federal Government, Federal contract receivers who have less than 15 employees and Federal assistance receivers who have less than 15 employees.

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Page 103: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

C. Federal Rehabilitation Act of 1973, P.L. 93-112(amended 1998)

This legislation bans discrimination of employees that are not covered under the ADA. These include the Federal Government, Federal contract receivers who have less than 15 employees and Federal assistance receivers who have less than 15 employees.

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Page 104: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

D. Employee Retirement Income Security Act of 1974

ERISA sets minimum standards for established pensions and health plans in private industry and protects the individuals in these plans. It stipulates that a person cannot be fired because the employer thinks the individual’s health care will cost too much.

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Page 105: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

D. Employee Retirement Income Security Act of 1974

ERISA sets minimum standards for established pensions and health plans in private industry and protects the individuals in these plans. It stipulates that a person cannot be fired because the employer thinks the individual’s health care will cost too much.

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Page 106: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

E. Consolidated Omnibus Budget Reconciliation Act of 1985 (COBRA), P.L. 99-272Consolidated Omnibus Budget Reconciliation Act of 1985 (COBRA), P.L. 99-272 is the legislation that enables a worker at a company of more than 20 employees who must leave his/her job for health reasons to continue to participate in the employer’s group health plan. The employee must pay the full monthly premium plus an administrative fee.

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Page 107: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #6

E. Consolidated Omnibus Budget Reconciliation Act of 1985 (COBRA), P.L. 99-272Consolidated Omnibus Budget Reconciliation Act of 1985 (COBRA), P.L. 99-272 is the legislation that enables a worker at a company of more than 20 employees who must leave his/her job for health reasons to continue to participate in the employer’s group health plan. The employee must pay the full monthly premium plus an administrative fee.

Continue Case

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Page 108: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question # 6

F. Health Insurance Portability and Accountability Act of 1996

Employees must be allowed to join a group health plan without an exclusion or waiting period for coverage of pre-existing conditions as long as they have had continuous “credible” coverage without a break for 63 days.

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Page 109: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question # 6

F. Health Insurance Portability and Accountability Act of 1996

Employees must be allowed to join a group health plan without an exclusion or waiting period for coverage of pre-existing conditions as long as they have had continuous “credible” coverage without a break for 63 days.

Continue Case

Teaching Points for Incorrect Answers

Page 110: Cancer Survivorship Endometrial Cancer Module

Question #6 Incorrect Answers

A. American with disabilities act of 1990(ADA), P.L. 101-336

C. Federal Rehabilitation Act of 1973, P.L. 93-112(amended 1998)

D. Employee Retirement Income Security Act of 1974E.

Consolidated Omnibus Budget Reconciliation Act of 1985 (COBRA), P.L. 99-272

F. Health Insurance Portability and Accountability Act of 1996

Continue Case

Page 111: Cancer Survivorship Endometrial Cancer Module

Case Continued

With the assistance of an employment attorney, her daughter is able to retain her job.You have a counseling session with Mrs. Johnson. At the end of the visit she responds; “I was concerned about the status of my cancer. My diagnosis of cancer was made about 3 years ago. I am relieved that you state that I am in remission. I am now ready to face the fact that I am a cancer survivor.”

Next

Page 112: Cancer Survivorship Endometrial Cancer Module

Question #7

How can her current status be best categorized?

A. Acute survivor

B. Extended survivor

C. Permanent survivor

D. End of life survivor

Page 113: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #7

A. Acute survivorBegins at diagnosis and continues till end of treatment. This “season of life” is dominated by cancer treatment including medical, surgical and radiological. Fear and anxiety are important elements of this phase. Pain is common and the person for the first time may have to deal with the fact that they may die.

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Page 114: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #7

A. Acute survivorBegins at diagnosis and continues till end of treatment. This “season of life” is dominated by cancer treatment including medical, surgical and radiological. Fear and anxiety are important elements of this phase. Pain is common and the person for the first time may have to deal with the fact that they may die.

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Page 115: Cancer Survivorship Endometrial Cancer Module

Correct. Question #7

B. Extended Survivor Begins at the conclusion of treatment and lasts until

the risk of recurrence has decreased. This is the period of watchful waiting, periodic examinations and intermittent therapy. This phase is dominated by the fear of recurrence.

The 5 year survival for endometrial cancer stage 2A is about 78%. There is probably an increased of risk till 5 years after diagnosis, thus this patient is most likely an extended survivor.

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Page 116: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #7

C. Permanent Survivor The period when the activity of the disease or the

likelihood of its recurrence is sufficiently small that the cancer can now be considered permanently arrested.

This encompasses the duration of survivor’s life. This is the period that the individual deals with employment; insurance and discrimination issues. Secondary effects such as sterility, secondary tumors, and radiation effects are a concern.

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Page 117: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #7

C. Permanent Survivor The period when the activity of the disease or the

likelihood of its recurrence is sufficiently small that the cancer can now be considered permanently arrested.

This encompasses the duration of survivor’s life. This is the period that the individual deals with employment; insurance and discrimination issues. Secondary effects such as sterility, secondary tumors, and radiation effects are a concern.

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Page 118: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #7

D. End of Life Survivor

Weeks or months at the end of life associated with palliative care.

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Page 119: Cancer Survivorship Endometrial Cancer Module

Incorrect. Question #7

D. End of Life Survivor

Weeks or months at the end of life associated with palliative care.

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Page 120: Cancer Survivorship Endometrial Cancer Module

Question #7 Incorrect Answers

A. Acute Survivor

C. Permanent Survivor

D. End of Life Survivor

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Page 121: Cancer Survivorship Endometrial Cancer Module

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For More Information: Visit the National Cancer Institute (NCI)

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