El Helali Aya, Tao Jun, Wong Charlene H L, Chan Wendy Wing-Lok, Mok Ka-Chun, Wu Wing Fong, Shitara Kohei, Mohler Markus, Boku Narikazu, Pang Herbert, Lam Ka On
Department of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong SAR, China.
School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
Front Oncol. 2022 Oct 31;12:908026. doi: 10.3389/fonc.2022.908026. eCollection 2022.
While the efficacy of immune checkpoint inhibitors (ICIs) is increasingly recognized in advanced gastric cancer (aGC), overall survival (OS) has not been consistently improved across the different randomized controlled trials (RCTs). This meta-analysis aimed to quantify the efficacy and safety of ICI and explore potential predictive tumor tissue biomarkers in aGC.
A random-effect pairwise meta-analysis was used to evaluate the primary outcome of OS. Sensitivity analysis was performed to investigate the effects of ICIs on PD-L1 status, TMB, MSI-H, and the Asian patient population. We extracted the OS Kaplan-Meier curves from the included trials to compare the effect of PD-L1 status on response to ICIs using DigitizeIt 2.5 and Guyot's algorithm.
A pairwise meta-analysis of seven RCTs included in this study showed that ICIs were more effective than the comparator in improving OS (pooled HR: 0.84). We demonstrated that PD-1 ICIs were additive when combined with the comparator arm (pooled HR: 0.79). A sensitivity analysis showed that PD-1 ICIs were associated with better OS outcomes in the Asian patient population as monotherapy (pooled HR: 0.66) or in combination with chemotherapy (pooled HR: 0.83). We demonstrated that tumors with PD-L1 ≥1 ( = 0.02) and PD-L1 ≥10 ( = 0.006) derived OS benefit from ICI monotherapy. Equally, MSI-H (0.00001) and TMB-high (0.0001) tumors derived favorable survival benefits from ICIs.
The results of this meta-analysis suggest that ICIs result in improved OS outcomes in aGC. The benefits varied with different ethnicities, class of ICI, PD-L1 expression, MSI status, and TMB.
https://www.crd.york.ac.uk/prospero, identifier (CRD42019137829).
尽管免疫检查点抑制剂(ICI)在晚期胃癌(aGC)中的疗效日益得到认可,但在不同的随机对照试验(RCT)中,总生存期(OS)并未持续改善。本荟萃分析旨在量化ICI在aGC中的疗效和安全性,并探索潜在的预测性肿瘤组织生物标志物。
采用随机效应成对荟萃分析来评估OS这一主要结局。进行敏感性分析以研究ICI对PD-L1状态、肿瘤突变负荷(TMB)、微卫星高度不稳定(MSI-H)以及亚洲患者群体的影响。我们从纳入的试验中提取OS的Kaplan-Meier曲线,使用DigitizeIt 2.5和Guyot算法比较PD-L1状态对ICI反应的影响。
本研究纳入的7项RCT的成对荟萃分析表明,ICI在改善OS方面比对照更有效(合并风险比:0.84)。我们证明,PD-1 ICI与对照臂联合使用时具有累加效应(合并风险比:0.79)。敏感性分析表明,PD-1 ICI作为单药治疗(合并风险比:0.66)或与化疗联合使用(合并风险比:0.83)时,在亚洲患者群体中与更好的OS结局相关。我们证明,PD-L1≥1(P = 0.02)和PD-L1≥10(P = 0.006)的肿瘤从ICI单药治疗中获得OS获益。同样,MSI-H(P = 0.00001)和TMB高(P = 0.0001)的肿瘤从ICI中获得良好的生存获益。
本荟萃分析结果表明,ICI可改善aGC的OS结局。获益因不同种族、ICI类别、PD-L1表达、MSI状态和TMB而异。