Chronic Lymphocytic Leukemia Clinical Trial
Combination Chemotherapy and Rituximab in Treating Patients With Chronic Lymphocytic Leukemia or Lymphocytic Lymphoma
Summary
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 leukemia-cll/" >chronic lymphocytic leukemia or lymphocytic lymphoma.
Full Description
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.
Eligibility Criteria
DISEASE CHARACTERISTICS:
Diagnosis of B-cell chronic lymphocytic leukemia (CLL) or small B-cell lymphocytic lymphoma (SLL) with the following:
Lymph node biopsy interpreted as SLL or consistent with CLL or all of the following:
Peripheral lymphocyte count greater than 5,000/mm^3 with small to moderate peripheral lymphocytes and no more than 55% prolymphocytes
Bone marrow aspirate containing at least 30% lymphoid cells
Immunophenotypic evaluation of peripheral blood lymphocytes demonstrating monoclonality of B lymphocytes with all of the following:
CD19 or CD20 coexpressed with CD5 antigen in the absence of other pan-T- cell markers (e.g., CD2 or CD3)
Expression of CD23 on CLL cells or Dim B-cell expression of kappa or lambda light chains
Measurable disease with any of the following:
1 or more lymph nodes at least 1.5 cm by CT scan
Splenomegaly by CT scan
Peripheral lymphocyte count greater than 5,000/mm3 with coexpression of CD5 and B-cell markers
Bone marrow aspirate with at least 30% lymphoid cells
No mantle cell lymphoma
PATIENT CHARACTERISTICS:
Age
18 and over
Performance status
ECOG 0-2
Life expectancy
At least 2 years
Hematopoietic
See Disease Characteristics
No immune thrombocytopenia
No hemolytic anemia
Hepatic
Bilirubin no greater than 3 times upper limit of normal (ULN)
SGOT no greater than 3 times ULN (unless due to hemolysis or CLL)
No hepatitis
Renal
Creatinine no greater than 1.5 times ULN
Cardiovascular
No cardiac dysfunction
No New York Heart Association class III or IV heart disease
No myocardial infarction within the past month
Other
HIV negative
No active acute or chronic infection
No immunosuppressive diseases
No autoimmune disorder
No secondary malignancy that is projected to limit life expectancy
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception
PRIOR CONCURRENT THERAPY:
Biologic therapy
See Chemotherapy
No prior rituximab
At least 4 weeks since prior biologic therapy
Chemotherapy
At least 4 weeks since prior chemotherapy
No prior combination chemotherapy and rituximab or other antibody therapy
No prior combination chemotherapy comprising an alkylating agent and a purine nucleoside analog (i.e., cyclophosphamide or chlorambucil in combination with fludarabine, cladribine, or pentostatin)
No prior pentostatin
Endocrine therapy
At least 4 weeks since prior corticosteroids
No concurrent supra-physiologic doses of corticosteroids
Radiotherapy
At least 4 weeks since prior radiotherapy
Surgery
At least 4 weeks since prior major surgery
Other
No concurrent immunosuppressive therapy (e.g., cyclosporine)
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There is 1 Location for this study
Newport Beach California, 92658, United States
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