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

被引:318
作者
Byrd, JC
Rai, K
Peterson, BL
Appelbaum, FR
Morrison, VA
Kolitz, JE
Shepherd, L
Hines, JD
Schiffer, CA
Larson, RA
机构
[1] Ohio State Univ, Div Hematol Oncol, Dept Med, Columbus, OH 43210 USA
[2] Long Isl Jewish Med Ctr, Div Hematol, New Hyde Pk, NY 11042 USA
[3] Long Isl Jewish Med Ctr, Div Oncol, New Hyde Pk, NY 11042 USA
[4] Ctr Stat, CALGB, Durham, NC USA
[5] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[6] Univ Minnesota, Hematol Oncol Sect, Vet Affairs Med Ctr, Minneapolis, MN USA
[7] Cornell Univ, Coll Med, Dept Med, N Shore Univ Hosp, Manhasset, NY 11030 USA
[8] Kingston Gen Hosp, Dept Pathol, NCI, Canada Clin Trials Grp, Kingston, ON K7L 2V7, Canada
[9] Case Western Reserve Univ, Sch Med, Dept Med, Cleveland, OH 44106 USA
[10] Wayne State Univ, Dept Med, Sch Med, Detroit, MI 48202 USA
[11] Univ Chicago, Dept Med, Chicago, IL 60637 USA
关键词
D O I
10.1182/blood-2004-03-0796
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页码:49 / 53
页数:5
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