Suppr超能文献

c-Met 抑制剂在非小细胞肺癌中的疗效和风险特征:一项荟萃分析。

The Efficacy and Risk Profile of c-Met inhibitors in Non-small Cell Lung Cancer: a Meta-analysis.

机构信息

Department of Respiratory Medicine, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China.

Department of Ophthalmology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Sci Rep. 2016 Oct 27;6:35770. doi: 10.1038/srep35770.

Abstract

c-MET inhibitors are considered as a kind of novel drugs in non-small cell lung cancer (NSCLC) treatment. However, the results of different clinical studies involving c-MET inhibitors were not consistent. In this report, we performed Meta-analysis to investigate the beneficial and harmful effects of these drugs from 9 studies including 1611 patients in target drug groups and 1605 patients in control groups. As a result, patients in target drugs group had longer progression free survival (PFS) (HR 0.80, 95% CI 0.66-0.99, p = 0.04) but not overall survival (OS) than those in control group, especially in Asian (HR 0.57, 95% CI 0.42-0.76, p < 0.001), Non-squamous (HR 0.79, 95% CI 0.64-0.97, p = 0.03), Phase III (HR 0.66, 95% CI 0.50-0.86, p = 0.002), previous treated (HR 0.77, 95% CI 0.63-0.95, p = 0.01) and small molecular compounds subgroups (HR 0.62, 95% CI 0.50-0.78, p < 0.001). In addition, target drugs did not affect the objective response rate (ORR) but improved disease control rate (DCR) (RR 1.22, 95% CI 1.02-1.46, p = 0.03) of NSCLC patients. Our study first indicated that targeting c-MET therapies improved PFS and DCR in advanced or metastatic NSCLC patients, especially in previous treated Asian patients with adenocarcinoma.

摘要

c-MET 抑制剂被认为是治疗非小细胞肺癌(NSCLC)的一种新型药物。然而,涉及 c-MET 抑制剂的不同临床研究结果并不一致。在本报告中,我们对 9 项研究进行了 Meta 分析,这些研究共纳入了 1611 例接受靶向药物治疗的患者和 1605 例接受对照治疗的患者,以评估这些药物的疗效和安全性。结果显示,与对照组相比,靶向药物组患者的无进展生存期(PFS)更长(HR 0.80,95%CI 0.66-0.99,p=0.04),但总生存期(OS)无明显差异(HR 0.80,95%CI 0.66-0.99,p=0.04),特别是在亚洲人群(HR 0.57,95%CI 0.42-0.76,p<0.001)、非鳞状细胞癌(HR 0.79,95%CI 0.64-0.97,p=0.03)、III 期(HR 0.66,95%CI 0.50-0.86,p=0.002)、既往治疗(HR 0.77,95%CI 0.63-0.95,p=0.01)和小分子化合物亚组(HR 0.62,95%CI 0.50-0.78,p<0.001)中。此外,靶向药物治疗并未影响客观缓解率(ORR),但提高了疾病控制率(DCR)(RR 1.22,95%CI 1.02-1.46,p=0.03)。本研究首次表明,针对 c-MET 的治疗策略可改善晚期或转移性 NSCLC 患者的 PFS 和 DCR,尤其是在既往接受过治疗的亚洲腺癌患者中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验