Department of Oncology, National Taiwan University Hospital Yunlin Branch, Yunlin, Taiwan.
Department of Medical Oncology, National Taiwan University Cancer Center, Taipei, Taiwan.
Cancer Med. 2023 Oct;12(19):20035-20051. doi: 10.1002/cam4.6563. Epub 2023 Sep 22.
Immune checkpoint inhibitors have revolutionized the treatment of malignancies. However, disproportionate enrollment among races and ethnicities places the generalizability of global trial results in doubt.
In this systematic review, phase 3 randomized controlled trials investigating pembrolizumab in advanced cancers and providing subgroup analyses of Asian and non-Asian participants were included. The primary and secondary effect measures were the mean differences (MDs) in the natural logarithms of the hazard ratios (HRs) for overall survival (OS) and progression-free survival (PFS) between these two subgroups, respectively. We used random-effects meta-analysis to calculate the pooled ratios of HRs (i.e., exp(MD)) and implemented a meta-regression analysis to identify significant covariates.
A total of 17 and 11 trials were included in the meta-analyses of OS and PFS, respectively. These trials included 2732 (25.49%) Asian and 7000 (65.32%) non-Asian participants in the OS analysis and 1438 (22.5%) Asian and 4129 (64.61%) non-Asian participants in the PFS analysis. The pooled ratio of HRs for OS was 0.87 (95% CI: 0.76-0.99; p = 0.0391), favoring Asian participants, but no significant difference was found in PFS (pooled ratio of HRs: 0.93; 95% CI: 0.82-1.07; p = 0.2391). Both linear meta-regression analyses revealed an open-label design as a crucial covariate, which indicated more benefits for non-Asian participants.
Compared with non-Asian patients, Asian patients with advanced cancers may derive superior OS benefits from pembrolizumab. Although the results warrant further exploration, this meta-analysis provides insight into clinical research design.
免疫检查点抑制剂彻底改变了恶性肿瘤的治疗方法。然而,不同种族和族裔人群之间的不成比例入组使得全球试验结果的普遍性受到质疑。
在这项系统评价中,纳入了评估派姆单抗治疗晚期癌症并提供亚洲和非亚洲参与者亚组分析的 III 期随机对照试验。主要和次要疗效指标分别为这两个亚组之间总生存期(OS)和无进展生存期(PFS)的风险比(HR)自然对数的平均值差异(MD)。我们使用随机效应荟萃分析计算 HR 的合并比值(即 exp(MD)),并进行了荟萃回归分析以确定显著的协变量。
共纳入了 17 项和 11 项 OS 和 PFS 的荟萃分析研究,这些试验中,OS 分析分别纳入了 2732 例(25.49%)亚洲人和 7000 例(65.32%)非亚洲人,PFS 分析分别纳入了 1438 例(22.5%)亚洲人和 4129 例(64.61%)非亚洲人。OS 的合并 HR 比值为 0.87(95%CI:0.76-0.99;p=0.0391),有利于亚洲参与者,但在 PFS 中未发现显著差异(合并 HR 比值:0.93;95%CI:0.82-1.07;p=0.2391)。线性荟萃回归分析均表明开放标签设计是一个关键的协变量,这表明非亚洲参与者获益更多。
与非亚洲患者相比,晚期癌症的亚洲患者可能从派姆单抗治疗中获得更好的 OS 获益。尽管这些结果需要进一步探索,但本荟萃分析为临床研究设计提供了新的视角。