Department of Surgery, Division of Urology, University of Toronto, Toronto, ON, Canada.
Royal College of Surgeons in Ireland School of Medicine, Dublin, Ireland.
Jpn J Clin Oncol. 2020 Jul 9;50(7):800-809. doi: 10.1093/jjco/hyaa021.
Targeting the programmed death ligand 1 (PD-L1) pathway has become standard for many advanced malignancies. Whether PD-L1 expression predicts response is unclear. We assessed the association between PD-L1 expression and immunotherapy response using stratified meta-analysis.
We performed a systematic review of randomized clinical trials published prior to October 2018 comparing overall survival (OS) in patients with advanced solid organ malignancies treated with immunotherapy or standard treatment. Pooled hazard ratios were calculated among patients with high and low PD-L1 levels independently. Differences between the two estimates were assessed using meta-analysis of study-level differences. Our primary analysis assessed a 1% threshold while secondary analyses utilized 5, 10 and 50%.
14 eligible trials reporting on 8887 patients were included. While there was a significant OS benefit for immunotherapy compared with standard treatment for all patients, the magnitude of benefit was significantly larger among those with high PD-L1 expression (P = 0.006). This finding persisted regardless of threshold used and across subgroup analyses according to PD-L1 assay type, tumor histology, line of therapy, type of inhibitor and study methodology.
PD-L1 levels have important predictive value in determining the response to immunotherapy. However, patients with low PD-L1 levels also experience improved survival with immunotherapy compared with standard treatment.
针对程序性死亡配体 1(PD-L1)通路已成为许多晚期恶性肿瘤的标准治疗方法。PD-L1 表达是否能预测治疗反应尚不清楚。我们使用分层荟萃分析评估 PD-L1 表达与免疫治疗反应之间的关联。
我们对截至 2018 年 10 月发表的比较晚期实体器官恶性肿瘤患者接受免疫治疗或标准治疗的总生存期(OS)的随机临床试验进行了系统回顾。分别在 PD-L1 高表达和低表达患者中计算了汇总风险比。使用研究水平差异的荟萃分析评估了两种估计值之间的差异。我们的主要分析评估了 1%的阈值,而次要分析则使用了 5%、10%和 50%的阈值。
纳入了 14 项报告了 8887 例患者的合格试验。虽然与标准治疗相比,免疫治疗对所有患者均有显著的 OS 获益,但在 PD-L1 高表达患者中获益幅度更大(P=0.006)。这一发现无论使用何种阈值以及根据 PD-L1 检测类型、肿瘤组织学、治疗线、抑制剂类型和研究方法进行的亚组分析均持续存在。
PD-L1 水平在确定免疫治疗反应方面具有重要的预测价值。然而,与标准治疗相比,PD-L1 低表达患者接受免疫治疗也能提高生存率。