首页> 美国卫生研究院文献>HemaSphere >Rituximab Maintenance Versus Observation After Immunochemotherapy (R-CHOP R-MCP and R-FCM) in Untreated Follicular Lymphoma Patients: A Randomized Trial of the Ostdeutsche Studiengruppe Hämatologie und Onkologie and the German Low-Grade Lymphoma Study Group
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Rituximab Maintenance Versus Observation After Immunochemotherapy (R-CHOP R-MCP and R-FCM) in Untreated Follicular Lymphoma Patients: A Randomized Trial of the Ostdeutsche Studiengruppe Hämatologie und Onkologie and the German Low-Grade Lymphoma Study Group

机译:在未处理的滤泡淋巴瘤患者中免疫化学疗法(R-ChecR-MCP和R-FCM)后的rituximab维持与观察结果:Ostdeutsche StudiengruppeHämatologieundonkologie和德国低级淋巴瘤研究组的随机试验

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摘要

The German study groups, the German Low-Grade Lymphoma Study Group (GLSG) and Ostdeutsche Studiengruppe Hämatologie und Onkologie (OSHO), initiated in 2007 a double randomized trial to investigate efficacy and safety of rituximab maintenance versus observation in remission after randomly assigned induction treatment in the first-line follicular lymphoma. Previously untreated patients with stage II–IV follicular lymphoma in need of therapy were randomized to receive 6 cycles of R-CHOP, R-MCP, or R-FCM. Responding patients were subsequently randomized to 2 years rituximab maintenance or observation, stratified by type of immunochemotherapy, quality of remission, and Follicular Lymphoma International Prognostic Index (FLIPI). Recruitment was stopped in 2011 after the PRIMA results had been published. Median age of the 206 recruited patients was 66 years (range, 24–86), and (FLIPI) was low in 13%, intermediate in 28%, and high in 60%. High and comparable overall response rates were observed after R-CHOP (88%), R-MCP (89%), and R-FCM (91%). Rituximab maintenance substantially prolonged progression-free survival (PFS) in comparison to observation in remission (hazard ratio 0.39, P = 0.0064). In the rituximab maintenance group, the 3-year PFS was 89% compared with 69% in the observation group. No differences in overall survival were observed for maintenance vs. observation (hazard ratio 1.04, 95% confidence interval 0.32–3.43, P = 0.95). In this randomized trial, 2 years of rituximab maintenance was associated with significantly prolonged PFS in comparison to observation after response to first-line immunochemotherapy in follicular lymphoma. Our data represent an independent confirmation of the PRIMA trial results.
机译:德国学习组,德国低级淋巴瘤研究组(GLSG)和OSTDEUTSCHE StudiengruppeHämatologieundonkologie(OSHO),在2007年开始进行双重随机试验,以研究随机分配的感应治疗后Rituximab维持对缓解的疗效和安全性的疗效和安全性在一线卵泡淋巴瘤中。以前未经治疗的患有治疗的II-IV型卵泡淋巴瘤的患者被随机化以获得6个R-Chec,R-MCP或R-FCM的循环。随后响应患者随后随机〜2年的rituximab维持或观察,通过免疫化学疗法,缓解质量和卵泡淋巴瘤国际预后指数(FLIPI)分层。在发布了Prima结果后,2011年招聘是在2011年停止的。 206名募集患者的中位年龄为66岁(范围,24-86),(FLIPI)低13%,中间体28%,高60%。 R-Chec(88%),R-MCP(89%)和R-FCM(91%)后观察到高且相当的总反应速率。 Rituximab维持基本上延长的无进展存活(PFS)与缓解症(危险比0.39,P = 0.0064)相比,无效的进展存活率(PFS)。在Rituximab维持群中,3年的PFS为89%,而观察组的69%。对于维持和观察(危险比1.04,95%置信区间0.32-3.43,P = 0.95),没有观察到总存活的差异。在该随机试验中,与滤泡淋巴瘤中的一线免疫化学治疗后的观察相比,2年的利妥昔单抗维持与显着延长的PFS相关。我们的数据代表了Prima试验结果的独立确认。

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