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PANEL: STUDY METHOD AND RESULTS

机译:面板:研究方法和结果

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摘要

Data from 1966 to 2010 was searched. This threw up 16 trials involving 10,217 patients with a range of advanced solid tumours. A total of 5,589 were available for analysis and 148 patients had fatal adverse events (FAEs).The overall incidence of FAEs with bevacizumab was 2.5 per cent (95 per cent confidence interval 1.7 per cent-3.9 per cent). Compared with chemotherapy alone, the addition of bevacizumab was associated with an increased risk of FAEs, with a relative risk of 1.46 (CI 1.09-1.94; P=0.01; incidence 2.5 per cent versus 1.7 per cent).
机译:检索了1966年至2010年的数据。这项研究进行了16项试验,涉及10,217名患有一系列晚期实体瘤的患者。共有5,589名患者可供分析,其中148名患有致命不良事件(FAE)。贝伐单抗的FAE总体发生率为2.5%(95%的置信区间为1.7%-3.9%)。与单纯化疗相比,添加贝伐单抗与FAE风险增加相关,相对风险为1.46(CI 1.09-1.94; P = 0.01;发生率2.5%vs. 1.7%)。

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