Phase III study of R-CVP compared with cyclophosphamide, vincristine, and prednisone alone in patients with previously untreated advanced follicular lymphoma

被引:488
作者
Marcus, Robert
Imrie, Kevin
Solal-Celigny, Philippe
Catalano, John V.
Dmoszynska, Anna
Raposo, Joao C.
Offner, Fritz C.
Gomez-Codina, Jose
Belch, Andrew
Cunningham, David
Wassner-Fritsch, Elisabeth
Stein, George
机构
[1] Royal Marsden Hosp, Dept Med, Sutton, Surrey, England
[2] Sunnybrook Reg Canc Ctr, Dept Med Toronto, Toronto, ON, Canada
[3] Cross Canc Inst, Edmonton, AB, Canada
[4] Clin Victor Hugo, Dept Hematol & Med Oncol, Le Mans, France
[5] Monash Med Ctr, Dept Hematol, Clayton, Vic 3168, Australia
[6] Med Univ Lublin, Dept Hematol, Lublin, Poland
[7] Hosp Santa Maria, Serv Hematol, Lisbon, Portugal
[8] Univ Ziekenhuis St Rafael, Ghent, Belgium
[9] Hosp La Fe, Med Oncol Serv, E-46009 Valencia, Spain
关键词
D O I
10.1200/JCO.2007.13.5376
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To compare the long-term outcome of patients with previously untreated follicular lymphoma (FL) needing therapy, after treatment with cyclophosphamide, vincristine and prednisone (CVP) versus CVP plus rituximab (R-CVP) and to evaluate the predictive value of known prognostic factors after treatment with R-CVP. Patients and Methods Patients with previously untreated CD20-positive stage III/ IV FL were randomly assigned to eight cycles of R-CVP (n = 159) or CVP alone (n = 162). The median follow-up period was 53 months. Results The primary end point-time to treatment failure (TTF), which included patients without a response after four cycles as an event-was significantly prolonged in patients receiving R-CVP versus CVP (P < .0001). Improvements in all other end points, including overall and complete response rates (P < .0001), time to progression (TTP; P < .0001), response duration (P < .0001), time to next antilymphoma treatment (P < .0001), and overall survival (OS; P = .029; 4-year OS: 83% v 77%;) were achieved with R-CVP versus CVP alone. Univariate analyses demonstrated an improvement in TTP with R-CVP versus CVP irrespective of the Follicular Lymphoma International Prognostic Index (FLIPI) subgroup, the International Prognostic Index (IPI) subgroup, baseline histology, and the presence or absence of B symptoms or bulky disease. By multivariate analysis, FLIPI retains a strong predictive power for TTP in the presence of the trial treatment effect. Conclusion Analysis of all outcome measures, including OS, confirm the benefit of adding R to CVP in the front-line treatment of FL.
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页码:4579 / 4586
页数:8
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