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首页> 外文期刊>The Lancet >Ramucirumab monotherapy for previously treated advanced gastric or gastro-oesophageal junction adenocarcinoma (REGARD): an international, randomised, multicentre, placebo-controlled, phase 3 trial
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Ramucirumab monotherapy for previously treated advanced gastric or gastro-oesophageal junction adenocarcinoma (REGARD): an international, randomised, multicentre, placebo-controlled, phase 3 trial

机译:雷米库单抗单药治疗先前治疗的晚期胃或胃食管交界性腺癌(REGARD):一项国际,多中心,安慰剂对照的3期临床试验

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Background Vascular endothelial growth factor (VEGF) and VEGF receptor-2 (VEGFR-2)-mediated signalling and angiogenesis can contribute to the pathogenesis and progression of gastric cancer. We aimed to assess whether ramucirumab, a monoclonal antibody VEGFR-2 antagonist, prolonged survival in patients with advanced gastric cancer.Methods We did an international, randomised, double-blind, placebo-controlled, phase 3 trial between Oct 6, 2009, and Jan 26, 2012, at 119 centres in 29 countries in North America, Central and South America, Europe, Asia, Australia, and Africa. Patients aged 24-87 years with advanced gastric or gastro-oesophageal junction adenocarcinoma and disease progression after first-line platinum-containing or fluoropyrimidine-containing chemotherapy were randomly assigned (2:1), via a central interactive voice-response system, to receive best supportive care plus either ramucirumab 8 mg/kg or placebo, intravenously once every 2 weeks. The study sponsor, participants, and investigators were masked to treatment assignment. The primary endpoint was overall survival. Analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00917384.
机译:背景技术血管内皮生长因子(VEGF)和VEGF受体2(VEGFR-2)介导的信号传导和血管生成可以促进胃癌的发病和发展。我们旨在评估单克隆抗体VEGFR-2拮抗剂雷莫昔单抗是否能延长晚期胃癌患者的生存期。方法我们在2009年10月6日至2009年10月之间进行了一项国际,随机,双盲,安慰剂对照的3期临床试验2012年1月26日,在北美,中南美洲,欧洲,亚洲,澳大利亚和非洲的29个国家/地区的119个中心举行。通过中央交互语音应答系统将一线含铂或含氟嘧啶的一线化疗后年龄为24-87岁,患有晚期胃或胃食管连接腺癌且疾病进展的患者通过中央交互式语音应答系统随机分配(2:1)最好的支持治疗,加用拉莫昔单抗8 mg / kg或安慰剂,每2周静脉注射一次。研究赞助商,参与者和研究者都被掩盖了治疗任务。主要终点是总体生存率。分析是按意向进行的。该试验已在ClinicalTrials.gov上注册,编号为NCT00917384。

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