Finding studies
Finding studies
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Lead
Roswell Park Cancer Institute
With
OBJECTIVES: Primary * Determine the safety, including qualitative and quantitative toxic effects and their duration and reversibility, of rituximab and doxorubicin HCl liposome in patients with relapsed or refractory, indolent or aggressive CD20-positive B-cell non-Hodgkin's lymphoma. Secondary * Determine the efficacy, including overall response rate and durability of objective response, of this regimen in these patients. * Correlate pretreatment functional, phenotypic, and genotypic characteristics of host immune effector cells with response in patients treated with this regimen. OUTLINE: This is an open-label, pilot study. Patients receive rituximab IV over 3-8 hours on day 1 and doxorubicin HCl liposome IV over 1-3 hours on day 3. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed periodically for 4 years. PROJECTED ACCRUAL: A total of 42 patients will be accrued for this study.
Age
18–120
Sex
ALL
Healthy volunteers
Not accepted
