首页> 美国卫生研究院文献>Blood >Phase 3 clinical trial of steroids/mycophenolate mofetil vs steroids/placebo as therapy for acute GVHD: BMT CTN 0802
【2h】

Phase 3 clinical trial of steroids/mycophenolate mofetil vs steroids/placebo as therapy for acute GVHD: BMT CTN 0802

机译:类固醇/霉酚酸酯与类固醇/安慰剂治疗急性GVHD的3期临床试验:BMT CTN 0802

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Corticosteroids are the accepted primary therapy for acute graft-versus-host disease (GVHD), but durable responses are seen in only about half of the patients. Blood and Marrow Transplant Clinical Trials Network (BMT CTN) 0802, a phase 3 multicenter randomized double-blinded trial, was designed to test whether mycophenolate mofetil (MMF) plus corticosteroids was superior to corticosteroids alone as initial therapy for acute GVHD. Patients with newly diagnosed acute GVHD were eligible if they required systemic therapy. Patients were randomized to receive prednisone with either MMF or placebo. The primary end point was acute or chronic GVHD-free survival at day 56 after initiation of therapy. A futility rule for GVHD-free survival at day 56 was met at a planned interim analysis after 235 patients (of 372) were enrolled: 116 MMF, 119 placebo. Baseline characteristics were well balanced between treatment groups including grade and organ distribution of GVHD. GVHD-free survival at day 56, cumulative incidence of chronic GVHD at 12 months, overall survival, Epstein-Barr virus reactivation, severe, life-threatening infections, relapse at 12 months, and quality of life were similar. The addition of MMF to corticosteroids as initial therapy for acute GVHD does not improve GVHD-free survival compared with corticosteroids alone. This trial was registered at as #.
机译:皮质类固醇是公认的急性移植物抗宿主病(GVHD)的主要治疗方法,但仅约一半的患者能看到持久的反应。血液和骨髓移植临床试验网络(BMT CTN)0802是一项3期多中心随机双盲试验,旨在测试霉酚酸酯(MMF)加皮质类固醇是否优于单独使用皮质类固醇作为急性GVHD的初始治疗。新诊断为急性GVHD的患者如果需要全身治疗,则符合条件。患者被随机分配接受泼尼松和MMF或安慰剂。主要终点是治疗开始后第56天的急性或慢性无GVHD生存。在计划的中期分析中,纳入235名患者(共372名)后,符合计划中第56天无GVHD生存的无效规则:116例MMF,119例安慰剂。治疗组之间基线特征得到很好的平衡,包括GVHD的等级和器官分布。第56天无GVHD的存活率,12个月时慢性GVHD的累积发生率,总体存活率,爱泼斯坦-巴尔病毒的激活,严重的,威胁生命的感染,12个月的复发以及生活质量相似。与单独使用皮质类固醇相比,在皮质类固醇中添加MMF作为急性GVHD的初始治疗不能改善无GVHD的生存。该试用版注册为#。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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