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纳武利尤单抗联合伊匹木单抗与现有免疫疗法治疗PD-L1阳性晚期非小细胞肺癌患者的系统评价和网状Meta分析

Nivolumab plus Ipilimumab versus Existing Immunotherapies in Patients with PD-L1-Positive Advanced Non-Small Cell Lung Cancer: A Systematic Review and Network Meta-Analysis.

作者信息

Ando Koichi, Kishino Yasunari, Homma Tetsuya, Kusumoto Sojiro, Yamaoka Toshimitsu, Tanaka Akihiko, Ohmori Tohru, Ohnishi Tsukasa, Sagara Hironori

机构信息

Division of Respiratory Medicine and Allergology, Department of Medicine, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8666, Japan.

Advanced Cancer Translational Research Institute (Formerly, Institute of Molecular Oncology), Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.

出版信息

Cancers (Basel). 2020 Jul 15;12(7):1905. doi: 10.3390/cancers12071905.

Abstract

No head-to-head trials have compared the efficacy and safety of nivolumab (Niv) plus ipilimumab (Ipi) combination therapy (Niv+Ipi) and existing regimens with immunotherapies approved as first-line treatment in patients with programmed cell death ligand 1 (PD-L1)-positive previously untreated advanced non-small cell lung cancer (NSCLC). We conducted a network meta-analysis of four relevant Phase Ⅲ trials to compare the efficacy and safety of Niv+Ipi, pembrolizumab (Pem) plus platinum-based chemotherapy (PBC) (Pem+PBC), Pem, Niv, or PBC using Bayesian analysis. The primary efficacy endpoint was progression-free survival (PFS) in patients with advanced NSCLC with PD-L1 expression ≥1%. The primary safety endpoint was the incidence of Grade 3-5 drug-related adverse events (G3-5AEs). Efficacy and safety were ranked using surface under the cumulative ranking curve (SUCRA). With regard to PFS, Niv+Ipi was inferior to Pem+PBC, and superior to Pem, Niv, or PBC alone. SUCRA ranking showed Pem+PBC had the highest efficacy for PFS, followed by Niv+Ipi, Niv, PBC, and Pem. The safety outcome analysis revealed Niv+Ipi was generally well tolerated compared to existing immunotherapy regimens. These results provide clinical information regarding the efficacy and safety of Niv+Ipi and indicate the possibility of the Niv+Ipi combination as a new therapeutic option in PD-L1-positive advanced NSCLC.

摘要

尚无头对头试验比较纳武利尤单抗(Niv)联合伊匹木单抗(Ipi)的联合疗法(Niv+Ipi)与已获批作为一线治疗方案的现有免疫疗法在程序性死亡配体1(PD-L1)阳性、先前未接受治疗的晚期非小细胞肺癌(NSCLC)患者中的疗效和安全性。我们对四项相关的Ⅲ期试验进行了网络荟萃分析,以使用贝叶斯分析比较Niv+Ipi、帕博利珠单抗(Pem)联合铂类化疗(PBC)(Pem+PBC)、Pem、Niv或PBC的疗效和安全性。主要疗效终点是PD-L1表达≥1%的晚期NSCLC患者的无进展生存期(PFS)。主要安全终点是3-5级药物相关不良事件(G3-5AEs)的发生率。使用累积排名曲线下面积(SUCRA)对疗效和安全性进行排名。在PFS方面,Niv+Ipi不如Pem+PBC,且优于单独使用的Pem、Niv或PBC。SUCRA排名显示,Pem+PBC对PFS的疗效最高,其次是Niv+Ipi、Niv、PBC和Pem。安全性结果分析显示,与现有的免疫治疗方案相比,Niv+Ipi总体耐受性良好。这些结果提供了关于Niv+Ipi疗效和安全性的临床信息,并表明Niv+Ipi联合疗法有可能成为PD-L1阳性晚期NSCLC的一种新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4ee/7409193/13264e0341eb/cancers-12-01905-g001.jpg

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