Management varies with type of lymphoma and pt factors (co-morbidities, age, performance status, pt...
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Transcript of Management varies with type of lymphoma and pt factors (co-morbidities, age, performance status, pt...
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
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) Allogeneic haematopoeitic 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 allogeneic
haematopoeitic 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 autologous
haematopoeitic 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 + autologous haematopoeitic 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 autologous haematopoeitic stem cell transplantation 50% long term lymphoma-free survival
Not pie charts
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/ lge mediastinal 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, pulm tox (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 autologous haematopoeitic stem cell transplatation 35-50% cure
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