Rituximab Plus Fludarabine and Cyclophosphamide Prolongs Progression-Free Survival Compared With Fludarabine and Cyclophosphamide Alone in Previously Treated Chronic Lymphocytic Leukemia

被引:385
作者
Robak, Tadeusz [1 ]
Dmoszynska, Anna
Solal-Celigny, Philippe
Warzocha, Krzysztof
Loscertales, Javier
Catalano, John
Afanasiev, Boris V.
Larratt, Loree
Geisler, Christian H.
Montillo, Marco
Zyuzgin, Ilya
Ganly, Peter S.
Dartigeas, Caroline
Rosta, Andras
Maurer, Joerg
Mendila, Myriam
Saville, M. Wayne
Valente, Nancy
Wenger, Michael K.
Moiseev, Sergey I.
机构
[1] Med Univ Lodz, Dept Hematol, PL-93510 Lodz, Poland
关键词
MONOCLONAL-ANTIBODY THERAPY; MINIMAL RESIDUAL DISEASE; TIME QUANTITATIVE PCR; CLINICAL ACTIVITY; INITIAL THERAPY; TRIAL; CHEMOIMMUNOTHERAPY; LYMPHOMA; GUIDELINES; DIAGNOSIS;
D O I
10.1200/JCO.2009.26.4556
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Rituximab, a monoclonal antibody that targets the CD20 cell surface antigen, has clinical activity in patients with non-Hodgkin's lymphoma and other B-lymphocyte disorders when administered alone or in combination with chemotherapy. Promising results have previously been reported in nonrandomized studies in patients with chronic lymphocytic leukemia (CLL). This trial was designed to compare chemoimmunotherapy with chemotherapy alone in patients with previously treated CLL. Patients and Methods This international, multicenter, randomized trial compared six cycles of rituximab plus fludarabine and cyclophosphamide (R-FC) with six cycles of fludarabine and cyclophosphamide alone (FC) in patients with previously treated CLL. A total of 552 patients with Binet stage A (10%), B (59%), or C (31%) disease entered the study and were randomly assigned to receive R-FC (n = 276) or FC (n = 276). Results After a median follow-up time of 25 months, rituximab significantly improved progression-free survival in patients with previously treated CLL (hazard ratio = 0.65; P < .001; median, 30.6 months for R-FC v 20.6 months for FC). Event-free survival, response rate, complete response rate, duration of response, and time to new CLL treatment or death were also significantly improved. Although the rates of adverse events, grade 3 or 4 events, and serious adverse events were slightly higher in the R-FC arm, R-FC was generally well tolerated, with no new safety findings and no detrimental effect on quality of life. Conclusion R-FC significantly improved the outcome of patients with previously treated CLL. J Clin Oncol 28: 1756-1765. (C) 2010 by American Society of Clinical Oncology
引用
收藏
页码:1756 / 1765
页数:10
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