Lymphoma Clinical Trial
Official title:
Pentostatin, Cyclophosphamide And Rituximab (PCR) For B-Cell Chronic Lymphocytic Leukemia (CLL) And Small B-Cell Lymphocytic Lymphoma (SLL): Four Phase II Trials With Patient Stratification Based On Prior Therapy
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing
so they stop growing or die. Monoclonal antibodies can locate cancer cells and either kill
them or deliver cancer-killing substances to them without harming normal cells. Combining
chemotherapy with monoclonal antibody therapy may kill more cancer cells.
PURPOSE: Phase II trial to study the effectiveness of combining pentostatin and
cyclophosphamide with rituximab in treating patients who have chronic lymphocytic leukemia
or lymphocytic lymphoma.
OBJECTIVES:
- Determine the efficacy of pentostatin, cyclophosphamide, and rituximab, in terms of
response rate, time to treatment failure, time to disease progression, durability of
response, and overall survival, in patients with B-cell chronic lymphocytic leukemia or
small B-cell lymphocytic lymphoma.
- Determine the safety of this regimen, in terms of acute, subacute, and chronic
toxicity, in patients treated with this regimen.
OUTLINE: This is a multicenter study. Patients are stratified according to prior
chemotherapy (no prior chemotherapy for chronic lymphocytic leukemia vs prior purine
analog-based therapy [fludarabine or cladribine] but no alkylator therapy vs prior
alkylator-based therapy [chlorambucil or cyclophosphamide] but no prior purine analog
therapy vs prior therapy with alkylators and purine analogs, but not as combination
therapy).
- First course: Patients receive rituximab IV over 1-4 hours on days 1-3 and pentostatin
IV over 10-30 minutes and cyclophosphamide IV over 30-60 minutes on day 1.
- All subsequent courses: Patients receive rituximab IV over 60 minutes, pentostatin IV
over 10-30 minutes, and cyclophosphamide IV over 30-60 minutes on day 1. Treatment
repeats every 3 weeks for up to 6 courses in the absence of disease progression or
unacceptable toxicity.
Patients are followed every 3 months for 5 years.
PROJECTED ACCRUAL: A total of 160-240 patients (40-60 per stratum) will be accrued for this
study.
;
Masking: Open Label, Primary Purpose: Treatment
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