Lomustine and Bevacizumab in Progressive Glioblastoma

洛莫司汀 医学 贝伐单抗 危险系数 内科学 临床终点 无进展生存期 置信区间 随机化 外科 联合疗法 肿瘤科 随机对照试验 化疗 长春新碱 环磷酰胺
作者
Wolfgang Wick,Thierry Gorlia,Martin Bendszus,Martin Taphoorn,Felix Sahm,Inga Harting,Alba A. Brandes,Walter Taal,Julien Dômont,Ahmed Idbaïh,Mario Campone,Paul M. Clément,Roger Stupp,Michel Fabbro,Émilie Le Rhun,François Dubois,Michael Weller,Andreas von Deimling,Vassilis Golfinopoulos,Jacoline C. Bromberg
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:377 (20): 1954-1963 被引量:824
标识
DOI:10.1056/nejmoa1707358
摘要

Bevacizumab is approved for the treatment of patients with progressive glioblastoma on the basis of uncontrolled data. Data from a phase 2 trial suggested that the addition of bevacizumab to lomustine might improve overall survival as compared with monotherapies. We sought to determine whether the combination would result in longer overall survival than lomustine alone among patients at first progression of glioblastoma.We randomly assigned patients with progression after chemoradiation in a 2:1 ratio to receive lomustine plus bevacizumab (combination group, 288 patients) or lomustine alone (monotherapy group, 149 patients). The methylation status of the promoter of O6-methylguanine-DNA methyltransferase (MGMT) was assessed. Health-related quality of life and neurocognitive function were evaluated at baseline and every 12 weeks. The primary end point of the trial was overall survival.A total of 437 patients underwent randomization. The median number of 6-week treatment cycles was three in the combination group and one in the monotherapy group. With 329 overall survival events (75.3%), the combination therapy did not provide a survival advantage; the median overall survival was 9.1 months (95% confidence interval [CI], 8.1 to 10.1) in the combination group and 8.6 months (95% CI, 7.6 to 10.4) in the monotherapy group (hazard ratio for death, 0.95; 95% CI, 0.74 to 1.21; P=0.65). Locally assessed progression-free survival was 2.7 months longer in the combination group than in the monotherapy group: 4.2 months versus 1.5 months (hazard ratio for disease progression or death, 0.49; 95% CI, 0.39 to 0.61; P<0.001). Grade 3 to 5 adverse events occurred in 63.6% of the patients in the combination group and 38.1% of the patients in the monotherapy group. The addition of bevacizumab to lomustine affected neither health-related quality of life nor neurocognitive function. The MGMT status was prognostic.Despite somewhat prolonged progression-free survival, treatment with lomustine plus bevacizumab did not confer a survival advantage over treatment with lomustine alone in patients with progressive glioblastoma. (Funded by an unrestricted educational grant from F. Hoffmann-La Roche and by the EORTC Cancer Research Fund; EORTC 26101 ClinicalTrials.gov number, NCT01290939 ; Eudra-CT number, 2010-023218-30 .).
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