Liu Jixiang, Zhong Yulan, Peng Shanshan, Zhou Xiangxiang, Gan Xin
Department of Respiratory Medicine, The First Affiliated Hospital, Nanchang University, Nanchang, China,
Onco Targets Ther. 2018 Dec 3;11:8623-8632. doi: 10.2147/OTT.S181413. eCollection 2018.
PD1/PDL1 blockade is a promising treatment for patients with non-small-cell lung cancer (NSCLC). Here, we employed meta-analysis to evaluate the efficacy and safety of PD1/PDL1 blockades for previously treated NSCLC patients.
Randomized clinical trials were retrieved by searching electronic databases. Data for HRs, 95% CIs for overall survival (OS), progression-free survival (PFS), and adverse events (AEs) were extracted and pooled.
A total of five randomized controlled trials including 2,910 patients were included in this meta-analysis. Pooled HRs (95% CI) were 0.71 (0.63-0.79, <0.0001) for OS and 0.86 (0.73-1.02) for PFS. In the subgroup analysis, the pooled HR (95% CI) for PFS was 0.82 (0.75-0.91, <0.0001) in patients with high PDL1 expression, but no significant difference was seen in patients with low expression (0.97 [0.76-1.24], =0.82). The pooled RR for treatment-related AEs of all grades was 0.32 (0.27-0.38, <0.00001) compared with the docetaxel arm, while that for grade 3-5 treatment-related AEs in the PD1/PDL1-blockade arm was 0.16 (0.10-0.27, <0.00001).
PD1/PDL1 blockades enhanced OS and PFS and led to lower risk of AEs in NSCLC patients. Smoking history and wild-type EGFR were associated with extended OS.
PD1/PDL1阻断疗法是治疗非小细胞肺癌(NSCLC)患者的一种有前景的治疗方法。在此,我们采用荟萃分析来评估PD1/PDL1阻断疗法对既往接受过治疗的NSCLC患者的疗效和安全性。
通过检索电子数据库获取随机临床试验。提取并汇总总生存期(OS)、无进展生存期(PFS)的风险比(HRs)、95%置信区间(CIs)以及不良事件(AEs)的数据。
本荟萃分析共纳入5项随机对照试验,包括2910例患者。OS的汇总HR(95%CI)为0.71(0.63 - 0.79,<0.0001),PFS的汇总HR为0.86(0.73 - 1.02)。在亚组分析中,PDL1高表达患者的PFS汇总HR(95%CI)为0.82(0.75 - 0.91,<0.0001),而低表达患者未见显著差异(0.97 [0.76 - 1.24],=0.82)。与多西他赛组相比,所有级别治疗相关不良事件的汇总相对危险度(RR)为0.32(0.27 - 0.38,<0.00001),而PD1/PDL1阻断治疗组3 - 5级治疗相关不良事件的RR为0.16(0.10 - 0.27,<0.00001)。
PD1/PDL1阻断疗法可提高NSCLC患者的OS和PFS,并降低不良事件风险。吸烟史和野生型表皮生长因子受体(EGFR)与OS延长相关。