Department of Oncology, Geneva University Hospital, Geneva, Switzerland.
Santa Maria della Misericordia Hospital, Azienda Ospedaliera di Perugia, Perugia, Italy.
Acta Oncol. 2020 Sep;59(9):1058-1063. doi: 10.1080/0284186X.2020.1781249. Epub 2020 Jun 17.
We retrospectively analysed patients with advanced non-small-cell lung cancer (NSCLC) harbouring high PD-L1 expression (>50%) and treated with front-line pembrolizumab, comparing outcomes of patients with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) 2 to those with PS 0-1. Data were collected by 16 participating centres. All patients with NSCLC and high PD-L1, treated with first-line pembrolizumab were included. We collected medical data from patient files, pathology and laboratory reports. Patient characteristics, comorbidities, PS, and tumour characteristics were reported. Overall survival (OS), progression-free survival (PFS) and response rate (RR) were calculated. 302 patients were included, 246 with PS 0-1, 56 with PS 2. RR was 72% among patients with PS 0-1 compared to 45% with PS2 (odds ratio (OR) 0.31 (95% CI: 0.17-0.57), < .001). Median PFS was 2.6 months (95% CI: 1.9-5.1) among patients with PS2 and 11.3 months (95% CI: 8.5-14.4) among those with PS 0-1. Median OS was 7.8 months (95% CI: 2.5-10.7) in the PS2 group, not reached in the PS 0-1 group. PS 2 remained predictive of poor outcomes in multivariate analysis. PS 2 is a strong independent predictor of poor response and survival in NSCLC patients with high PD-L1, treated with front-line pembrolizumab. Prospective randomised trials comparing immunotherapy to chemotherapy in this population would be welcome.
我们回顾性分析了接受一线帕博利珠单抗治疗的高 PD-L1 表达(>50%)的晚期非小细胞肺癌(NSCLC)患者,比较了东部肿瘤协作组(ECOG)体力状态(PS)2 与 PS 0-1 的患者的结局。数据由 16 个参与中心收集。所有接受一线帕博利珠单抗治疗的 PD-L1 高表达的 NSCLC 患者均纳入本研究。我们从患者病历、病理学和实验室报告中收集了医疗数据。报告了患者特征、合并症、PS 和肿瘤特征。计算了总生存期(OS)、无进展生存期(PFS)和缓解率(RR)。共纳入 302 例患者,其中 PS 0-1 246 例,PS 2 56 例。PS 0-1 患者的 RR 为 72%,而 PS 2 患者的 RR 为 45%(优势比(OR)0.31(95%CI:0.17-0.57),<0.001)。PS 2 组患者的中位 PFS 为 2.6 个月(95%CI:1.9-5.1),PS 0-1 组患者的中位 PFS 为 11.3 个月(95%CI:8.5-14.4)。PS 2 组患者的中位 OS 为 7.8 个月(95%CI:2.5-10.7),PS 0-1 组患者未达到。多变量分析显示 PS 2 仍然是不良结局的预测因素。在 PD-L1 高表达的接受一线帕博利珠单抗治疗的 NSCLC 患者中,PS 2 是不良反应和生存的独立强预测因素。欢迎开展比较该人群免疫治疗与化疗的前瞻性随机试验。