医学
美罗华
内科学
危险系数
长春新碱
切碎
国际预后指标
强的松
人口
弥漫性大B细胞淋巴瘤
外科
胃肠病学
养生
临床终点
无进展生存期
化疗方案
环磷酰胺
淋巴瘤
化疗
随机对照试验
置信区间
环境卫生
作者
Christian Récher,Bertrand Coiffier,Corinne Haïoun,Thierry Jo Molina,Christophe Fermé,Olivier Casasnovas,Catherine Thiéblemont,André Bosly,Guy Laurent,Franck Morschhauser,Hervé Ghesquières,Fabrice Jardin,Serge Bologna,Christophe Fruchart,Bernadette Corront,Jean Gabarre,Christophe Bonnet,Maud Janvier,Danielle Canioni,Jean‐Philippe Jaïs
出处
期刊:The Lancet
[Elsevier]
日期:2011-11-01
卷期号:378 (9806): 1858-1867
被引量:353
标识
DOI:10.1016/s0140-6736(11)61040-4
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.
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