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Epidemiology factors
Represents 4.1% of all new cancers in the US
Higher incidence in Non-Hispanic white males
Higher male predominance than HL
More common in the United States, Canada, and Europe and less likely in Asian countries
Most common age range
65-74
Median = 68
Etiology
Cause unknown
Not caused by inheritance but rather by DNA that has mutated during one's lifetime
Immune system abnormalities
Overexposure to certain chemicals
Radiation exposure: nuclear reactor accidents, radiation therapy, and EBRT with adjuvant chemo
Changes in the structure and function of B or T cells are the source of the progression of cancer
Which autoimmune disorders are associated with increased risk?
Sjögren syndrome, systemic lupus, and rheumatoid arthritis
Which viruses are associated with increased risk?
Epstein–Barr, AIDS, HIV, hepatitis C, or human T-lymphotropic virus type 1 (HTLV-1), or with certain bacteria, such as Helicobacter pylori
Prognostic indicators
More dependent on histology than Hodgkin lymphoma
Two groups: indolent and aggressive
Indolent: slow-growing and causes little problems at the time of diagnosis; median survival time can be as long as 20 years
Aggressive: faster growing
The risk of relapse for both groups is the highest after the first 2 years of treatment
Clinical presentation
Symptoms of NHL mimic those of HL, enlarged lymph nodes, night sweats, weight loss, fever, and itching are all common with diagnosis
Found in lymph nodes but is also in a wide variety of locations in the body
Symptoms manifest according to the location of the disease, the surrounding organs, and the extent of the disease
Most common site of extranodal involvement
GI system, specifically the stomach
Other common sites are Waldeyer's ring, skin, bone marrow, sinuses, thyroid, CNS, and GU system
Detection and Diagnosis
Thorough H&P (knowledge of occupational risks and patient’s medical history can give a suggestion of NHL)
Imaging Studies: chest radiograph, CT, PET, MRI, US helpful in determining extent and initial staging
Lab Studies: CBC (anemia, thrombocytopenia, leukopenia, lymphocytosis, and thrombocytosis could all be signs of disease)
Serum chemistry studies: liver function tests, lactic acid dehydrogenase, and calcium levels may be abnormal
Serum beta-2 microglobulin level may be elevated
HIV serology
Human T- cell lymphotropic virus-1 serology
The relapse of aggressive NHL in the CNS has a good prognosis
False
Why is a prophylactic treatment approach incorporated into the treatment protocols for the aggressive subtypes of lymphoblastic and Burkitt lymphomas?
Recurrence tends to happen early after diagnosis and its incidence is around 30%
Staging
Ann Arbor Staging System
(does not always encompass the variety that may come from the many different types of
NHLs and fails to classify extranodal sites)
Grading of the malignant cells is important in the determination of a treatment plan
True
Primary treatments
chemotherapy, radiation therapy, immunotherapy, and stem cell transplants
What treatment has been proven effective and is almost always given?
Chemotherapy
Most common chemo regimen
CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone)
NHL is radiosensitive, however, radiation therapy is almost always used ________
Adjuvantly or in combination with chemotherapy or another technique
(Indolent NHL in early stages I and II can be treated with radiation alone)
When radiation is given, the involved site is included along with the related drainage clusters nearby. These fields are treated to a dose of _____
35-45 Gy
Patients with ________ can be treated with aggressive chemotherapy and radiation, followed by bone marrow transplant
Advanced or recurrent disease
________ is used to boost the immune system into fighting off cancer cells
Immunotherapy
Prognostic indicators
Varies among the different types. Generally, survival is dependent on age, stage, location, and histology at the time of diagnosis
Overall 5-yr survival
74%
Pattern of spread is …
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