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Addition of rituximab to fludarabine may prolong progression-free survival and overall survival in patients with previously untreated chronic lymphocytic leukemia: an updated retrospective comparative analysis of CALGB 9712 and CALGB 9011

Authors :
Frederick R. Appelbaum
Vicki A. Morrison
John D. Hines
Charles A. Schiffer
Jonathan E. Kolitz
Richard A. Larson
Bercedis L. Peterson
John C. Byrd
Kanti R. Rai
Lois E. Shepherd
Source :
Blood. 105:49-53
Publication Year :
2005
Publisher :
American Society of Hematology, 2005.

Abstract

Fludarabine and rituximab combination therapies in chronic lymphocytic leukemia (CLL) have yielded promising early results, but no comparative efficacy data relative to standard fludarabine treatment regimens have been reported. To assess the effect of the addition of rituximab to fludarabine therapy, we retrospectively compared the treatment outcome of patients with similar clinical characteristics enrolled on 2 multicenter clinical trials performed by the Cancer and Leukemia Group B and the US Intergroup that used fludarabine and rituximab (CALGB 9712, n = 104) or fludarabine (CALGB 9011, n = 178). In multivariate analyses controlling for pretreatment characteristics, the patients receiving fludarabine and rituximab had a significantly better progression-free survival (PFS; P < .0001) and overall survival (OS; P = .0006) than patients receiving fludarabine therapy. Two-year PFS probabilities were 0.67 versus 0.45, and 2-year OS probabilities were 0.93 versus 0.81. Infectious toxicity was similar between the 2 treatment approaches. These comparative data are retrospective and could be confounded by differences in supportive care or dissimilar enrollment of genetic subsets on each trial. Confirmation of these findings will require a prospective randomized trial comparing fludarabine and rituximab to fludarabine.

Details

ISSN :
15280020 and 00064971
Volume :
105
Database :
OpenAIRE
Journal :
Blood
Accession number :
edsair.doi.dedup.....272068c6e46480873c8f6895a1e6b933
Full Text :
https://doi.org/10.1182/blood-2004-03-0796