Rituximab Maintenance Treatment of Relapsed/Resistant Follicular Non-Hodgkin's Lymphoma: Long-Term Outcome of the EORTC 20981 Phase III Randomized Intergroup Study

被引:238
作者
van Oers, Marinus H. J.
Van Glabbeke, Martine
Giurgea, Livia
Klasa, Richard
Marcus, Robert E.
Wolf, Max
Kimby, Eva
van t Veer, Mars
Vranovsky, Andrej
Holte, Harald
Hagenbeek, Anton
机构
[1] EORTC Lymphoma Grp, Hovon, Belgium
[2] Natl Canc Inst Canada, Eortc Data Ctr, Clin Trials Grp, Hematol Grp, Vancouver, BC, Canada
[3] British Natl Lymphoma Invest, London, England
[4] Australasian Leukemia & Lymphoma Grp, Melbourne, Vic, Australia
[5] Nord Lymphoma Grp, Oslo, Norway
关键词
EVENT-FREE SURVIVAL; SIGNIFICANTLY INCREASES; PROLONGS SURVIVAL; CYCLOPHOSPHAMIDE; CHEMOTHERAPY; THERAPY; TRIAL; MITOXANTRONE; VINCRISTINE; COMBINATION;
D O I
10.1200/JCO.2009.26.5827
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose In 2006, we published the results of the European Organisation for Research and Treatment of Cancer phase III trial EORTC 20981 on the role of rituximab in remission induction and maintenance treatment of relapsed/resistant follicular lymphoma (FL). At that time, the median follow-up for the maintenance phase was 33 months. Now, we report the long-term outcome of maintenance treatment, with a median follow-up of 6 years. Patients and Methods Overall, 465 patients were randomly assigned to induction with either six cycles of cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) or rituximab plus CHOP (R-CHOP). Those in complete remission or partial remission after induction (n = 334) were randomly assigned to maintenance treatment with rituximab (375 mg/m(2) intravenously once every 3 months) or observation. Results Rituximab maintenance significantly improved progression-free survival (PFS) compared with observation (median, 3.7 years v 1.3 years; P < .001; hazard ratio [HR], 0.55), both after CHOP induction (P < .001; HR, 0.37) and R-CHOP (P = .003; HR, 0.69). The 5-year overall survival (OS) was 74% in the rituximab maintenance arm, and it was 64% in the observation arm (P = .07). After progression, a rituximab-containing salvage therapy was given to 59% of patients treated with CHOP followed by observation, compared with 26% after R-CHOP followed by rituximab maintenance. Rituximab maintenance was associated with a significant increase in grades 3 to 4 infections: 9.7% v 2.4% (P = .01). Conclusion With long-term follow-up, we confirm the superior PFS with rituximab maintenance in relapsed/resistant FL. The improvement of OS did not reach statistical significance, possibly because of the unbalanced use of rituximab in post-protocol salvage treatment.
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收藏
页码:2853 / 2858
页数:6
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