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抗血管生成药物联合厄洛替尼治疗晚期非小细胞肺癌的疗效与安全性:一项随机临床试验的荟萃分析

Efficacy and safety of anti-angiogenic drugs combined with erlotinib in the treatment of advanced non-small cell lung cancer: a meta-analysis of randomized clinical trials.

作者信息

Chen Zheng, Jiang Shu, Li Xuechun, Zhang Jingyao, Liu Liu, Li Juan, Cao Peiyu, Xin Yong, Zhang Longzhen

机构信息

Department of Radiotherapy, Xuzhou Medical College Affiliated Hospital, Xuzhou, China.

Cancer Institute, Xuzhou Medical University, Xuzhou, China.

出版信息

Ann Palliat Med. 2021 Mar;10(3):2687-2698. doi: 10.21037/apm-20-1621. Epub 2021 Feb 2.

Abstract

BACKGROUND

To determine the efficacy and safety of anti-angiogenic drugs combined with erlotinib in the treatment of advanced non-small cell lung cancer (NSCLC), we performed a meta-analysis of 10 randomized controlled trials (RCTs).

METHODS

An electronic literature search of PubMed, Cochrane Library, Embase, and other databases was performed. Literature was retrieved on December 2, 2019. We collected and compared RCTs on antiangiogenic drugs combined with erlotinib (A + E) for NSCLC, and analyzed outcomes including overall survival (OS), objective response rate (ORR), progression-free survival (PFS), and incidence of severe adverse events (grade ≥3 AEs).

RESULTS

Compared with the control group, combined treatment did not increase the ORR (RR 1.03, 95% CI: 0.95-1.11, P=0.52) or prolong OS (HR 1.03, 95% CI: 0.91-1.17, P=0.24); however, a significant improvement was seen in PFS (HR 0.63, 95% CI: 0.57-0.70, P<0.001). The subgroup analysis showed that patients with epidermal growth factor receptor (EGFR) mutations and patients with adenocarcinoma could benefit from combination therapy, as could those from Asian populations. Although combination therapy was found to carry an increased incidence of grade 3 or higher adverse events including diarrhea and proteinuria, these remained within controllable levels.

CONCLUSIONS

Anti-angiogenic drugs used in combination with erlotinib can significantly prolong PFS in patients with advanced NSCLC.

摘要

背景

为了确定抗血管生成药物联合厄洛替尼治疗晚期非小细胞肺癌(NSCLC)的疗效和安全性,我们对10项随机对照试验(RCT)进行了荟萃分析。

方法

对PubMed、Cochrane图书馆、Embase和其他数据库进行电子文献检索。文献检索于2019年12月2日进行。我们收集并比较了抗血管生成药物联合厄洛替尼(A+E)治疗NSCLC的RCT,并分析了总生存期(OS)、客观缓解率(ORR)、无进展生存期(PFS)和严重不良事件(≥3级AE)发生率等结局指标。

结果

与对照组相比,联合治疗并未提高ORR(RR 1.03,95%CI:0.95-1.11,P=0.52)或延长OS(HR 1.03,95%CI:0.91-1.17,P=0.24);然而,PFS有显著改善(HR 0.63,95%CI:0.57-0.70,P<0.001)。亚组分析表明,表皮生长因子受体(EGFR)突变患者、腺癌患者以及亚洲人群患者可从联合治疗中获益。虽然联合治疗发现3级或更高不良事件(包括腹泻和蛋白尿)的发生率增加,但这些仍在可控范围内。

结论

抗血管生成药物与厄洛替尼联合使用可显著延长晚期NSCLC患者的PFS。

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