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

Author:

Robak Tadeusz1,Dmoszynska Anna1,Solal-Céligny Philippe1,Warzocha Krzysztof1,Loscertales Javier1,Catalano John1,Afanasiev Boris V.1,Larratt Loree1,Geisler Christian H.1,Montillo Marco1,Zyuzgin Ilya1,Ganly Peter S.1,Dartigeas Caroline1,Rosta András1,Maurer Jörg1,Mendila Myriam1,Saville M. Wayne1,Valente Nancy1,Wenger Michael K.1,Moiseev Sergey I.1

Affiliation:

1. From the Department of Hematology, Medical University, Lodz; Department of Hemato-Oncology and Bone Marrow Transplantation, Medical University, Lublin; Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland; Department of Hematology, Clinique Victor Hugo, Le Mans; Department of Hematology, Centre Hospitalier Universitaire Bretonneau, Tours, France; Department of Hematology, Hospital Universitario de la Princesa, Madrid, Spain; Haematology Department and Dorevitch...

Abstract

PurposeRituximab, 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 MethodsThis 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 (1%), B (59%), or C (31%) disease entered the study and were randomly assigned to receive R-FC (n = 276) or FC (n = 276).ResultsAfter 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.ConclusionR-FC significantly improved the outcome of patients with previously treated CLL.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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