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首页> 外文期刊>BMC Cancer >Effects of bevacizumab plus irinotecan on response and survival in patients with recurrent malignant glioma: a systematic review and survival-gain analysis
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Effects of bevacizumab plus irinotecan on response and survival in patients with recurrent malignant glioma: a systematic review and survival-gain analysis

机译:贝伐单抗联合伊立替康对复发性恶性神经胶质瘤患者反应和生存的影响:系统评价和生存获益分析

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Background The combination of bevacizumab and irinotecan is a new chemotherapy protocol increasingly used for recurrent malignant glioma. Results from phase II trials suggest this drug combination is beneficial to patients, but no conclusive comparisons between this and other treatment protocols have been published. Methods We performed a systematic review and survival gain analysis of phase II studies to evaluate the efficacy and safety of bevacizumab plus irinotecan treatment. To do this, we utilized a preexisting database from which the mean overall survival and response rate of patients could be predicted. Survival gain, which characterized the influence of treatment, was defined as the difference between observed and predicted mean overall survival. Response gain was calculated similarly. Results 741 cohorts were enrolled in the database. Among them, 282 cohorts were based on recurrent adult HGG, mean reported median overall survival was 10.96 ± 8.4 months, and mean response rate was 18.9% ± 20.5. We found that compared with other treatment protocols, bevacizumab plus irinotecan largely improved response rates ( P = 0.00002) and had a possible moderate effect on overall survival time ( P = 0.024). Hemorrhage, thromboembolic complications, and gastrointestinal toxicities were the most frequently reported side effects. Conclusion The combination of bevacizumab and irinotecan might improve outcome in patients with recurrent malignant glioma. Randomized controlled trials are recommended to evaluate this treatment protocol and the additional value of irinotecan.
机译:背景:贝伐单抗和伊立替康的组合是一种新的化疗方案,越来越多地用于复发性恶性神经胶质瘤。 II期试验的结果表明,这种药物组合对患者有益,但尚未发表此治疗方案与其他治疗方案之间的确切比较。方法我们对II期研究进行了系统的回顾和生存获益分析,以评估贝伐单抗联合伊立替康治疗的疗效和安全性。为此,我们利用了一个现有数据库,可以从中预测患者的平均总生存率和反应率。表征治疗效果的生存增益定义为观察到的平均预期生存与预期平均生存之间的差异。响应增益的计算方法类似。结果741个队列被纳入数据库。其中,282例基于成人复发性HGG,平均报告中位总生存期为10.96±8.4个月,平均缓解率为18.9%±20.5。我们发现,与其他治疗方案相比,贝伐单抗加伊立替康可显着提高缓解率(P = 0.00002),并且可能对总体生存时间有中等影响(P = 0.024)。出血,血栓栓塞并发症和胃肠道毒性是最常报告的副作用。结论贝伐单抗联合伊立替康可改善复发性恶性神经胶质瘤患者的预后。建议进行随机对照试验以评估该治疗方案和伊立替康的附加价值。

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