Hematologic Malignancies Flashcards
Lymphomas
2 major types
Hodgkins lymphoma which is characterized by reed-sternberg cells
AND
Non-Hodgkins lymphoma which has 30+ unigue histopathologic diseases
90% are B cells
Chemotherapy is backbone of treatment
Hodgkins lymphoma
Reed-sternberg cells that originated from B-lymphocytes
B cells lose ability to do apoptosis, and cause proliferation of the cells
Hodgkins lymphoma Risk factors
Viral exposure
- EBV infection
patient older than 50
impaired immune function
- congenital immunodeficiencies
- solid organ transplant
- HIV infection
genetic factors
- ataxia telangiectasia
Hodgkins lymphoma symptoms
tends to be painless rubbery enlarged lymph nodes
Patients may present with B symptoms: fever over 100.4, drenched night sweats, unintentional weight loss of greater than 10% in less than or equal to 6 months
also can present with itching but does not have any rash visible on skin
Hodgkins lymphoma - diagnosis
Excisional biopsy should be preformed which is removal of the entire lymph node
in advanced stages you can do a bone marrow biopsy to see if disease is stage 4
Staging HL
Early-stage favorable (stage I-II without unfavorable factors)
Early stage unfavorable (Stage I-II with unfavorable factors)
Advanced stage (Stage III-IV)
Unfavorable factors include:
B symptoms, Elevated ESR, large mediastinal adenopathy, multiple invovled nodal regions
Early stage disease treatment HL
ABVD chemotherapy regimen for 2-4 cycles
Advanced stage treatment HL
6 cycles of ABVD or AAVD chemotherapy
Relapsed disease treatment HL
Autologous stem cell rescue
- high dose of chemo followed by patients own stem cells as a rescue dose
Maintenance therapy treatment HL
Brentuximab Vedotin
ABVD chemo regimen HL
Doxorubicin
Bleomycin
Vinblastine
Dacarbazine
- can cause cardiotoxicity, pulmonary toxicity, myelosupression, peripheral neuropathy, nausea and vomiting
AAVD chemo regimen HL
Doxorubicin
Brentuximab vendotin
Vinblastine
Dacarbazine
can cause cardiotoxicity, myelosupression, peripheral neuropathy, nausea and vomiting
Non-hodgkins lymphoma
malignant B or T lymphocytes
Non-hodgkins lymphoma Presentation
depends on tumor location
B symptoms are present in 40% of patients
primary CNS lymphoma
Extranodal involvement in 10-35% of patients with GI, skin, testes, and bone
NHL - diagnosis
Excisional biopsy is best
bone marrow biopsy
lumbar puncture in patients at high risk or who have testicular involvement because the testes have similar barrier to the brain so if they lymphocytes are able to get into the testes theres a high probability they are in the brain as well
Follicular Lymphoma - NHL
2nd most common NHL
indolent grade 1-2
median age 60
median survival: 8-10 years
treated if symptomatic or patient preference becuase studies have shown patients who get chemo with follicular lymphoma has the same survival rate as those who go untreated so no point unless symptoms or patient got that money money
Richters transformation - NHL
follicular lymphoma that can transofrm into a more agressive NHL known as DLBCL
DLBCL treatment - NHL
and relapse DLBCL
median age is 70
30-40% present with extranodal disease
6 cycles of R-Chop
Curative - CART therapy
Palliative - Brentuximab + Rituximab + Polatuzumab regimen
BITE - Epcoritamab
Glofitamab
R-CHOP
for treatment of DLBCL
rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone
thrombocytopenia, infection, anemia, peripheral neuropathies
NHL - rituximab and Hepatitis B
Hepatitis B surface ANTIGEN and Hepatitis B CORE ANTIBODY must be tested prior to anti-CD20 directed therapy
CAR-T cell process
- Take the patients cells through leukapheresis
- activate the patients T cells outside of the body
- allow T cells to grow and multiple outside the patient
- chemotherapy to get rid of the patients T cells that are not activated in the body
- T-cell infusion - add the active cells back into the patient so they will attack the cancer
What to Car-T therapy target
CD19 on B cells
Cytokine release syndrome (CRS) and Immune effector Cell associated neurotoxicity syndrome (ICANS)
cytokine release in the body and patients have fever, tachycardia, and hypotension
Treat CRS with Tocilizumab (does not affect the activation and action of the Car-Tcell or BiTe drugs)
ICANS - symptoms include tremor, confusion, altered mental status, seizures - patient should be asked to write and if handwritting is altered usually a sign
treat ICANS with corticosteroids (downside that this will effect the T cell treatment that patient just spend their damn life saving on but cannot use tocilizumab because it doesnt cross BBB)
If patient is presenting with both of these they must be treated with corticosteroids
Multiple Myeloma Presentation (CRAB)
hyperCalcemia - calcium greater than 11.5
Renal dysfunction SCr greater than 2 or CrCl less than 40
Anemia Hgb less than 10 or 2 below normal level
Bone: one or more osteolytic lesions or pathologic fractures