首页> 外文期刊>The Lancet >Rituximab maintenance for 2 years in patients with high tumour burden follicular lymphoma responding to rituximab plus chemotherapy (PRIMA): a phase 3, randomised controlled trial.
【24h】

Rituximab maintenance for 2 years in patients with high tumour burden follicular lymphoma responding to rituximab plus chemotherapy (PRIMA): a phase 3, randomised controlled trial.

机译:高肿瘤负荷滤泡性淋巴瘤患者对利妥昔单抗联合化疗(PRIMA)有反应时,利妥昔单抗维持2年:3期随机对照试验。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Patients with follicular lymphoma can have long survival times, but disease progression typically occurs 3-5 years after initial treatment. We assessed the potential benefit of 2 years of rituximab maintenance after first-line treatment in patients with follicular lymphoma receiving a rituximab plus chemotherapy regimen. METHODS: The randomised, open-label PRIMA study was undertaken in 223 centres in 25 countries. 1217 patients with previously untreated follicular lymphoma needing systemic therapy received one of three non-randomised immunochemotherapy induction regimens used in routine practice. 1019 patients achieving a complete or partial response were then randomly assigned to receive 2 years of rituximab maintenance therapy (375 mg/m(2) every 8 weeks) or observation. Treatment was assigned equally by centralised block randomisation, stratified by induction regimen, response, region, and centre. Neither the participants nor those giving the interventions, assessing outcomes, and analysing data were masked to group assignments. The primary endpoint was progression-free survival (PFS). Analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00140582. FINDINGS: 505 patients were assigned to rituximab maintenance and 513 to observation (one patient died during randomisation). With a median follow-up of 36 months (IQR 30-42), PFS was 74.9% (95% CI 70.9-78.9) in the rituximab maintenance group (130 patients progressed) and 57.6% (53.2-62.0) in the observation group (218 progressed; hazard ratio [HR] 0.55, 95% CI 0.44-0.68, p<0.0001). 2 years after randomisation, 361 patients (71.5%) in the rituximab maintenance group were in complete or unconfirmed complete response versus 268 (52.2%) in the observation group (p=0.0001). Overall survival did not differ significantly between groups (HR 0.87, 95% CI 0.51-1.47). Grade 3 and 4 adverse events were recorded in 121 patients (24%) in the rituximab maintenance group and 84 (17%) in the observation group (risk ratio 1.46, 95% CI 1.14-1.87; p=0.0026). Infections (grades 2-4) were the most common adverse event, occurring in 197 (39%) and 123 (24%) patients, respectively (risk ratio 1.62, 95% CI 1.35-1.96; p<0.0001). INTERPRETATION: 2 years of rituximab maintenance therapy after immunochemotherapy as first-line treatment for follicular lymphoma significantly improves PFS. FUNDING: Groupe d'Etude des Lymphomes de l'Adulte (GELA) and F Hoffmann-La Roche.
机译:背景:滤泡性淋巴瘤患者的生存时间可能较长,但疾病进展通常在初始治疗后3-5年发生。我们评估了接受利妥昔单抗联合化疗方案的滤泡性淋巴瘤患者在一线治疗后维持利妥昔单抗2年的潜在益处。方法:在25个国家/地区的223个中心进行了随机,开放标签的PRIMA研究。 1217例先前未接受治疗的滤泡性淋巴瘤患者需要系统治疗,接受了常规实践中使用的三种非随机免疫化学诱导方案之一。然后将1019名完全或部分缓解的患者随机分配接受2年的利妥昔单抗维持治疗(每8周375 mg / m(2))或观察。通过集中式区组随机分配治疗方案,并按诱导方案,反应,区域和中心分层。参与者和进行干预,评估结果以及分析数据的参与者都没有被掩盖到小组任务中。主要终点是无进展生存期(PFS)。分析是按意向进行的。该试验已在ClinicalTrials.gov上注册,编号为NCT00140582。结果:505例患者接受了利妥昔单抗维持治疗,513例进行了观察(一名患者在随机分组期间死亡)。中位随访36个月(IQR 30-42),利妥昔单抗维持组(进展为130例患者)的PFS为74.9%(95%CI 70.9-78.9),观察组为PFS为57.6%(53.2-62.0) (进展为218;危险比[HR] 0.55,95%CI 0.44-0.68,p <0.0001)。随机分组后2年,利妥昔单抗维持组的361例患者(71.5%)完全或未确认完全缓解,而观察组为268例(52.2%)(p = 0.0001)。两组之间的总生存期无显着差异(HR 0.87,95%CI 0.51-1.47)。利妥昔单抗维持组的121例患者(24%)和观察组的84例(17%)记录了3级和4级不良事件(风险比1.46,95%CI 1.14-1.87; p = 0.0026)。感染(2-4级)是最常见的不良事件,分别发生在197(39%)和123(24%)患者中(风险比1.62,95%CI 1.35-1.96; p <0.0001)。解释:免疫化学治疗后2年的利妥昔单抗维持治疗是滤泡性淋巴瘤的一线治疗,可显着改善PFS。资金:爱德华·德·林普之家集团(GELA)和霍夫曼·拉罗什(F Hoffmann-La Roche)。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号