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贝伐珠单抗(阿瓦斯汀)对转移性实体瘤生存的影响——一项荟萃分析和系统评价。

The impact of Bevacizumab (Avastin) on survival in metastatic solid tumors--a meta-analysis and systematic review.

机构信息

Institute of Oncology, Rabin Medical Center, Beilinson Campus, Petach Tiqwa, Israel.

出版信息

PLoS One. 2013;8(1):e51780. doi: 10.1371/journal.pone.0051780. Epub 2013 Jan 22.

Abstract

PURPOSE

To evaluate the effect of Bevacizumab in combination with chemotherapy on overall survival of patients with metastatic solid tumors.

DESIGN

A systematic literature search to identify randomized trials comparing chemotherapy with and without Bevacizumab in metastatic cancer. The primary end point was overall survival (OS) and the secondary end points were progression free survival (PFS) and toxicity. A meta-analysis was performed for each tumor type and for the combination of all tumors.

RESULTS

24 randomized trials with 8 different types of malignancies were included in this meta-analysis. Patients treated with Bevacizumab had an OS benefit, hazard ratio (HR) 0.89 (95% CI 0.84-0.93, P<0.00001 I(2)-4%). The combined analysis showed a PFS benefit with a HR 0.71 (95% CI 0.68-0.74, P<0.00001, I(2)-54%). The toxicity analysis showed a statistically significant increase in fatal adverse events (FAEs) in the Bevacizumab treatment arm, risk ratio (RR) 1.47 (95% CI 1.1-1.98). A separate analysis of the lung cancer trials showed an increased risk of fatal pulmonary hemorrhage with a RR of 5.65 (95% CI 1.26-25.26). The risk of G3-4 adverse events was increased: RR 1.2 (95% CI 1.15-1.24).

CONCLUSION

in this combined analysis Bevacizumab improved OS (with little heterogeneity) and PFS. These results should be considered in the light of lack of markers predictive of response and the increased severe and fatal toxicity seen with Bevacizumab treatment.

摘要

目的

评估贝伐珠单抗联合化疗对转移性实体瘤患者总生存期的影响。

设计

系统文献检索,以确定比较转移性癌症中贝伐珠单抗联合化疗与单纯化疗的随机试验。主要终点是总生存期(OS),次要终点是无进展生存期(PFS)和毒性。对每种肿瘤类型和所有肿瘤的联合进行了荟萃分析。

结果

共有 24 项随机试验纳入了 8 种不同类型的恶性肿瘤。接受贝伐珠单抗治疗的患者 OS 获益,风险比(HR)为 0.89(95%可信区间 0.84-0.93,P<0.00001 I(2)-4%)。联合分析显示 PFS 获益,HR 为 0.71(95%可信区间 0.68-0.74,P<0.00001,I(2)-54%)。毒性分析显示贝伐珠单抗治疗组致命不良事件(FAEs)发生率有统计学意义增加,风险比(RR)为 1.47(95%可信区间 1.1-1.98)。对肺癌试验的单独分析显示致命性肺出血的风险增加,RR 为 5.65(95%可信区间 1.26-25.26)。3-4 级不良事件的风险增加:RR 为 1.2(95%可信区间 1.15-1.24)。

结论

在这项联合分析中,贝伐珠单抗改善了 OS(异质性较小)和 PFS。在考虑到缺乏反应预测标志物以及贝伐珠单抗治疗中观察到的严重和致命毒性增加的情况下,应考虑这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d1f/3551962/23848da21b0d/pone.0051780.g001.jpg

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