...
首页> 外文期刊>The Lancet >Intensified chemotherapy with ACVBP plus rituximab versus standard CHOP plus rituximab for the treatment of diffuse large B-cell lymphoma (LNH03-2B): an open-label randomised phase 3 trial.
【24h】

Intensified chemotherapy with ACVBP plus rituximab versus standard CHOP plus rituximab for the treatment of diffuse large B-cell lymphoma (LNH03-2B): an open-label randomised phase 3 trial.

机译:含有ACVBP Plus rituximab的增强化疗与标准CheCh Plus Rituximab用于治疗弥漫性大B细胞淋巴瘤(LNH03-2B):开放标签随机相3试验。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

BACKGROUND: The outcome of diffuse large B-cell lymphoma has been substantially improved by the addition of the anti-CD20 monoclonal antibody rituximab to chemotherapy regimens. We aimed to assess, in patients aged 18-59 years, the potential survival benefit provided by a dose-intensive immunochemotherapy regimen plus rituximab compared with standard treatment plus rituximab. METHODS: We did an open-label randomised trial comparing dose-intensive rituximab, doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone (R-ACVBP) with subsequent consolidation versus standard rituximab, doxorubicin, cyclophosphamide, vincristine, and prednisone (R-CHOP). Random assignment was done with a computer-assisted randomisation-allocation sequence with a block size of four. Patients were aged 18-59 years with untreated diffuse large B-cell lymphoma and an age-adjusted international prognostic index equal to 1. Our primary endpoint was event-free survival. Our analyses of efficacy and safety were of the intention-to-treat population. This study is registered with ClinicalTrials.gov, number NCT00140595. FINDINGS: One patient withdrew consent before treatment and 54 did not complete treatment. After a median follow-up of 44 months, our 3-year estimate of event-free survival was 81% (95% CI 75-86) in the R-ACVBP group and 67% (59-73) in the R-CHOP group (hazard ratio [HR] 0.56, 95% CI 0.38-0.83; p=0.0035). 3-year estimates of progression-free survival (87% [95% CI, 81-91] vs 73% [66-79]; HR 0.48 [0.30-0.76]; p=0.0015) and overall survival (92% [87-95] vs 84% [77-89]; HR 0.44 [0.28-0.81]; p=0.0071) were also increased in the R-ACVBP group. 82 (42%) of 196 patients in the R-ACVBP group experienced a serious adverse event compared with 28 (15%) of 183 in the R-CHOP group. Grade 3-4 haematological toxic effects were more common in the R-ACVBP group, with a higher proportion of patients experiencing a febrile neutropenic episode (38% [75 of 196] vs 9% [16 of 183]). INTERPRETATION: Compared with standard R-CHOP, intensified immunochemotherapy with R-ACVBP significantly improves survival of patients aged 18-59 years with diffuse large B-cell lymphoma with low-intermediate risk according to the International Prognostic Index. Haematological toxic effects of the intensive regimen were raised but manageable. FUNDING: Groupe d'Etudes des Lymphomes de l'Adulte and Amgen.
机译:背景:通过加入抗CD20单克隆抗体利妥昔单抗至化疗方案,弥漫性大B细胞淋巴瘤的结果基本上得到了改善。我们的目标是在18-59岁的患者中评估,剂量 - 密集免疫化治疗方案和Rituximab的潜在存活效果与标准治疗加里妥昔单抗相比。方法:采用随后的合并与标准Rituximab,多柔比蛋白,环磷酰胺,长春碱和泼尼松(R-Chec,用后续固结,进行了一种开放标签随机试验比较剂量密集的Rituximab,多柔枯蛋白,环磷酰胺,Vindesine,Bleomycin和Prednisone(R-ACVBP),对二柔枯蛋白,环磷酰胺,血管内(R-Chec )。随机分配用计算机辅助的随机分配序列完成,具有四个块大小。患者年龄18-59岁,未经处理的弥漫性大B细胞淋巴瘤和年龄调整的国际预后指数等于1.我们的主要终点是无事的存活。我们对疗效和安全的分析是有意治疗人口。本研究以ClinicalTrials.gov注册,NCT00140595号码。调查结果:治疗前的一名患者同意,54人没有完全治疗。在44个月的中位随访后,我们在R-ACVBP组和67%(59-73)中,我们的3年的无事项存活率估计为81%(95%CI 75-86),在R-Chec中组(危害比[HR] 0.56,95%CI 0.38-0.83; p = 0.0035)。无进展生存率的3年估计(87%[95%CI,81-91] Vs 73%[66-79]; HR 0.48 [0.30-0.76]; P = 0.0015)和总体存活(92%[87] -95] Vs 84%[77-89]; HR 0.44 [0.28-0.81]; P = 0.0071)在R-ACVBP组中也增加。 R-ACVBP组的196名患者的82名(42%)在R-Chec组中的183名(15%)的183名中经历了严重的不良事件。在R-ACVBP组中,3-4级血液神学毒性效应更常见,具有较高比例的,患者出现发热中性级集(38%[196的75条] Vs 9%[183/16])。解释:与标准R-Chec相比,R-ACVBP的加强免疫化治疗显着改善了18-59岁的患者的存活,弥漫性大B细胞淋巴瘤根据国际预后指数低中间风险。提高了密集方案的血液学毒性效应,但可易于管理。资金:Groupe d'Etudes des Lymphomes de L'Adultee和Amgen。

著录项

相似文献

  • 外文文献
  • 中文文献
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