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Lymphoma tx. Lymphoma tx. Management varies with type of lymphoma and pt factors (co-morbidities, age, performance status, pt preferences) Goal of tx can be curative, to prolong life, or palliative
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Lymphoma tx • Management varies with type of lymphoma and pt factors (co-morbidities, age, performance status, pt preferences) • Goal of tx can be curative, to prolong life, or palliative • Multidisciplinary team (haematologists, medical oncologists, radiation oncologists, anatomical pathologists, surgeons, allied health profs, plus ongoing GP care)
Therapeutic Modalities • Chemotherapy – systemic control • Radiation therapy – local control • Immunotherapy - targeted monoclonals (like that CD20 guy) • Allogeneichaematopoeitic stem cell transplantation • Autologous haematopoietic stem cell transplantation
Non-Hodgkin’s Tx • Tx depends on stage (Ann Arbor) • Indolent • low-grade, aggressive • Intermediate-grade, aggressive • High-grade • Special forms
Indolent • Usually disseminated by time of diagnosis and therefore not curable • Not bulky, not symptomatic no initial tx necessary • Some tx options available, no consensus • Rituximab (the anti-CD20 guy) can be used (low toxicity, avoid chemotherapy) • Or, common chemotherapy regimens (R-CHOP, R-CVP) • Low grade – aggressive allogeneichaematopoeitic stem cell transplantation
Intermediate grade, aggressive (diffuse large B-cell lymphoma) • Tx with curative intent • Short course chemo (x3) R-CHOP + localised radiation • or, 6-8 cycles R-CHOP w/o radiation (especially more advanced) • Very high risk lymphoma autologoushaematopoeitic stem cell transplantation • High grade (Burkitt’s, lymphoblastic) • Intense, cyclic chemo + intrathecal chemo as CNS prophylaxis
Special cases • MALT lymphoma of stomach – kill pylori with combo antibiotics; or, whole stomach radiation • Mantle cell – doesn’t respond to standard chemo; intensive chemo + autologoushaematopoeitic stem cell transplantation • Primary CNS lymphoma – repeated cycles of high-dose methotrexate w/ rituximab
R-CHOP • R – Rituximab (Mabthera) • that monoclonal that binds to CD20 • C - Cyclophosphamide • Nitrogen mustard alkylating agent – adds alkyl group to DNA causing irreversible cross-links • H - Hydroxydaunorubicin (Doxorubicin, Adriamycin) • intercalating agent - damages DNA by inserting itself between DNA bases • O - Oncovin (Vincristine) • prevents cell proliferation by binding to tubulin • P - Prednisone (or prednisolone) • corticosteroid
Side effects of R-CHOP • Nausea/vomiting (antiemetics), • Allopecia • Neutropenia • Tumour-lysis syndrome • caused by the break-down products of dying cancer cells and include hyperkalaemia, hyperphosphataemia, hyperuricaemia and hyperuricosuria, hypocalcaemia, and consequent acute uric acid nephropathy and acute renal failure • Allopurinol - prophylactic to prevent hyperuricaemia
Prognosis – Non-Hodgkin’s • Indolent - med surv 10-15yrs • Intermediate • uses IPI (International Prognostic Index) • Factors – age >60, high serum LDH, stage III/IV dis, poor performance status, more than 1 extranodal site • 0-1 factor 5y surv 73% • 2 factors 5y surv 51% • 3 factors 5y surv 43% • 4-5 factors 5y surv 26% • Relapse after initial chemo autologoushaematopoeitic stem cell transplantation 50% long term lymphoma-free survival
Hodgkin’s Tx • All should be treated with curative intent • Stage IA w/ high cervical lymph node and low ESR – radiation • Stage I/II – short course chemo ABVD + involved-field radiation • Stage III/IV – full course ABVD • Stage II w/ lgemediastinal mass – full course ABVD + mediastinal radiotherapy
ABVD • A - Adriamycin (the H in R-CHOP) • B - Bleomycin • antibiotic that also induces DNA strands to break • V - Vincristine (the O in R-CHOP) • D - Dacarbazine • Alkylating agent – adds alkyl groups to DNA
ABVD side effects • Acute • Alopecia, nausea/vomiting (antiemetics can be given), myelosuppression, allergic reactions to bleomycin (test dose often given first), neuropathy (temp or perm) • Delayed • Infertility, pulmtox (again bleomycin), cardiac tox (adriamycin), secondary malignancies
Prognosis - Hodgkin’s • Influenced by 7 features – stage, age, gender, haemoglobin, albumin, WBC, lymphocyte count • 0-2 features 75% cure • 3+ features 55% • Stage IA/IIA 10y surv >90% • Stage III/IV 10y surv 50-60% • Poor outcomes – older folk, bulky disease, lymphocyte depletion, mixed-cellularity on histo • Relapse after intial chemo autologoushaematopoeitic stem cell transplatation 35-50% cure
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