首页> 美国卫生研究院文献>Neuro-Oncology >AT-55FINAL ANALYSIS OF THE BELOB TRIAL (A RANDOMIZED PHASE II STUDY ON BEVACIZUMAB VERSUS BEVACIZUMAB PLUS LOMUSTINE VERSUS LOMUSTINE SINGLE AGENT IN RECURRENT GLIOBLASTOMA) AND FIRST RADIOLOGY REVIEW RESULTS
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AT-55FINAL ANALYSIS OF THE BELOB TRIAL (A RANDOMIZED PHASE II STUDY ON BEVACIZUMAB VERSUS BEVACIZUMAB PLUS LOMUSTINE VERSUS LOMUSTINE SINGLE AGENT IN RECURRENT GLIOBLASTOMA) AND FIRST RADIOLOGY REVIEW RESULTS

机译:贝特洛尔试验的AT-55最终分析(复发性胶质母细胞中贝伐单抗对贝伐单抗加洛美汀对洛美单药的随机II期研究)和首次放射学检查结果

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摘要

INTRODUCTION: Bevacizumab (BEV) is widely used in recurrent glioblastoma, alone or in combination with other agents. There is however no controlled trial to support this use. MATERIAL AND METHODS: In a Dutch multicenter randomized phase II study patients were assigned to BEV 10 mg/kg day 1, 15 and 29 iv, BEV 10 mg/kg day 1, 15 and 29 iv in combination with 110 mg/m2 lomustine orally on day 1, or lomustine 110 mg/m2 orally on day 1, in a 6- weekly schedule . Eligible were patients with histologically proven glioblastoma, first recurrence after chemo-irradiation with temozolomide, having concluded radiotherapy more than 3 months ago, with adequate bone marrow, renal and hepatic function, and WHO performance status (PS) 0-2. Primary endpoint was 9 months overall survival (OS). RESULTS: Between December 2009 and November 2011, 148 eligible patients were enrolled . Median age was 57 years (range, 24-77) and median WHO PS was 1. After a preplanned safety review after the first 8 patients the lomustine dose in the combination arm was reduced to 90 mg/m2, 44 patients were treated at this dose level. 130 patients were evaluable for response. Nine month OS [95% confidence interval] was 43% [29, 57] in the lomustine arm, 38% [25, 51] in the BEV arm, and 59% [43, 72] in the BEV/lomustine 90 arm. Objective response rate (complete or partial response) by local investigator was 5% in the lomustine arm, 38% in the BEV arm and 34% in the BEV/lomustine 90 arm. CONCLUSION: The combination bevacizumab/lomustine warrants further investigation, and is currently investigated in the randomized controlled phase III EORTC trial 26101. At the meeting the analysis based on IDH and MGMT status and the first results on the radiology review, pattern of progression and clinical impact of isolated T2/FLAIR progression will be presented.
机译:简介:贝伐单抗(BEV)被单独或与其他药物联合广泛用于复发性胶质母细胞瘤。但是,没有对照试验来支持这种用法。材料和方法:在荷兰的一项多中心随机II期研究中,患者分别于第1、15和29天静脉注射BEV 10 mg / kg,第1、15和29天静脉注射BEV 10 mg / kg以及110 mg / m 2 洛莫斯汀,或在第1天口服洛莫斯汀110 mg / m 2 。有组织学证明为胶质母细胞瘤,替莫唑胺化学放疗后首次复发,3个月前结束放疗,骨髓,肾和肝功能良好,WHO表现状态(PS)为0-2的患者是合格的。主要终点为9个月的总生存期(OS)。结果:2009年12月至2011年11月,招募了148例合格患者。中位年龄为57岁(范围24-77),中位WHO PS为1。在对前8例患者进行了预先计划的安全性检查后,联合用药组中的洛莫司汀剂量降低至90 mg / m2,在此情况下治疗了44例患者剂量水平。 130名患者的反应可评估。洛莫司汀组的9个月OS [95%置信区间]为43%[29,57],BEV组为38%[25,51],BEV /洛米汀90组为59%[43,72]。本地研究者的客观缓解率(完全或部分缓解)在洛莫司汀组为5%,BEV组为38%,BEV /洛美他汀90组为34%。结论:贝伐单抗/洛美司汀组合值得进一步研究,目前正在随机对照III期EORTC试验26101中进行研究。在会议上,根据IDH和MGMT的状态以及放射学评价,进展模式和临床的初步结果进行了分析。将介绍孤立的T2 / FLAIR进展的影响。

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