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贝伐珠单抗联合伊立替康治疗复发性恶性脑胶质瘤患者的疗效和生存影响:系统评价和生存获益分析。

Effects of bevacizumab plus irinotecan on response and survival in patients with recurrent malignant glioma: a systematic review and survival-gain analysis.

机构信息

Department of Neurosurgery, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China.

出版信息

BMC Cancer. 2010 Jun 2;10:252. doi: 10.1186/1471-2407-10-252.

Abstract

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.

摘要

背景

贝伐珠单抗联合伊立替康是一种新的化疗方案,越来越多地用于治疗复发性恶性脑胶质瘤。Ⅱ期临床试验结果表明,该药物联合方案对患者有益,但尚未发表关于该方案与其他治疗方案的明确比较。

方法

我们对Ⅱ期研究进行了系统评价和生存获益分析,以评估贝伐珠单抗联合伊立替康治疗的疗效和安全性。为此,我们利用了一个预先存在的数据库,从中可以预测患者的总生存期和应答率的平均值。生存获益用于描述治疗的影响,定义为观察到的和预测的平均总生存期之间的差异。应答获益的计算方法类似。

结果

该数据库共纳入了 741 个队列。其中,282 个队列基于复发性成人高级别脑胶质瘤,报告的中位总生存期为 10.96±8.4 个月,总应答率为 18.9%±20.5%。我们发现,与其他治疗方案相比,贝伐珠单抗联合伊立替康可显著提高应答率(P=0.00002),并可能对总生存时间有中度影响(P=0.024)。出血、血栓栓塞并发症和胃肠道毒性是最常报告的不良反应。

结论

贝伐珠单抗联合伊立替康可能改善复发性恶性脑胶质瘤患者的预后。建议开展随机对照试验,以评估该治疗方案和伊立替康的附加价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823b/2891637/a9d2a692be9f/1471-2407-10-252-1.jpg

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