Treatment Plan for Lymphoma
For CD20-positive diffuse large B-cell lymphoma (the most common type), the standard curative treatment is R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) given every 21 days for 6-8 cycles. 1, 2
Initial Diagnostic Requirements
Before initiating treatment, confirm the diagnosis and complete staging:
- Obtain excisional lymph node biopsy (not fine needle aspiration) with WHO classification and CD20 immunohistochemistry to determine B-cell versus T-cell lineage 1, 2, 3
- Complete staging workup including CT chest/abdomen/pelvis, bone marrow aspirate and biopsy, complete blood count, LDH, uric acid, and screening for HIV, hepatitis B and C 1, 2, 4
- Calculate International Prognostic Index (IPI) using age, stage, LDH, performance status, and number of extranodal sites for prognostic stratification 1, 2
- Stage according to Ann Arbor system with notation of bulky disease (>10 cm) 1, 3
Treatment Algorithm by Lymphoma Subtype
CD20-Positive Large B-Cell Lymphoma (Most Common)
Standard curative regimen: R-CHOP every 21 days for 8 cycles 1, 2
- Rituximab 375 mg/m² IV
- Cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP chemotherapy)
- Consider shortening interval to 14 days with growth factor support in select cases 1
Critical management points:
- Avoid dose reductions for hematological toxicity; instead use prophylactic growth factors (G-CSF) if febrile neutropenia develops 1
- Document cumulative anthracycline dose due to cardiotoxicity risk 1
T-Cell Lymphoma
Standard regimen: CHOP chemotherapy alone (rituximab not indicated as T-cells lack CD20) every 21 days for 8 cycles 1
High-Risk Patients (IPI ≥2)
- Consider prophylactic CNS treatment with intrathecal cytarabine or methotrexate at time of diagnostic lumbar puncture, particularly if bone marrow, testis, spine, or skull base involvement 1, 4
- High-dose chemotherapy with stem cell transplantation remains investigational in first-line setting 1
Response Monitoring
Perform radiological assessment:
- After 2-4 cycles of therapy 1, 3
- After completion of all treatment 1
- Whenever response is questioned 1
If bone marrow or CSF initially involved: Repeat bone marrow biopsy/lumbar puncture at end of treatment 1, 4
For inadequate response: Immediately evaluate for salvage chemotherapy regimens 2, 3
Radiotherapy Considerations
Consolidation radiotherapy to bulky disease sites has NOT proven benefit and is not routinely recommended 1
Exception: May consider involved-field radiation in select cases with residual masses after chemotherapy 1
Relapsed/Refractory Disease
For chemosensitive relapsed disease in transplant-eligible patients:
- Salvage chemotherapy (R-DHAP, R-ESHAP, R-ICE, or R-EPOCH) followed by high-dose chemotherapy with autologous stem cell transplantation is standard 1, 2
- Rituximab shows considerable single-agent activity even after failed transplantation in CD20-positive disease 1
Surveillance After Treatment Completion
Clinical monitoring:
- History and physical examination every 3 months for 2 years, then every 6 months for 3 additional years, then annually 1, 2
- Monitor specifically for secondary malignancies including transformation 1, 3
Laboratory monitoring:
- Complete blood count and LDH at 3,6,12, and 24 months, then only as clinically indicated 1, 2
- TSH monitoring at 1,2, and 5 years if neck irradiation received 1, 3
Imaging surveillance:
Special considerations:
- Women receiving chest radiation before age 25 require clinical breast cancer screening and mammography starting at age 40-50 1
Critical Pitfalls to Avoid
- Do not use fine needle aspiration alone for initial diagnosis—inadequate tissue for proper classification 2, 3
- Do not reduce chemotherapy doses for cytopenias—use growth factor support instead to maintain dose intensity 1
- Do not delay salvage therapy in patients with inadequate response—early intervention improves transplant outcomes 2, 3
- Do not omit hepatitis B screening—reactivation with rituximab can be fatal 4