Department of Thoracic Oncology, Osaka International Cancer Institute, 3-1-69 Otemachi, Osaka, 541-8567, Japan.
Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Invest New Drugs. 2020 Feb;38(1):211-218. doi: 10.1007/s10637-019-00882-5. Epub 2019 Nov 30.
Associations between treatment outcomes of immune checkpoint inhibitors and metastatic sites in advanced non-small cell lung cancer (NSCLC) are not well known. Therefore, this multicenter retrospective study aimed to investigate the predictive factors of metastatic sites after first-line pembrolizumab treatment for advanced NSCLC with a PD-L1 tumor proportion score (TPS) ≥50%. We retrospectively analyzed advanced NSCLC patients with a PD-L1 TPS ≥50% who underwent first-line pembrolizumab therapy at 11 institutions between February 2017 and April 2018. Clinical data collected from medical records included metastatic sites at the time of pembrolizumab treatment. Treatment outcomes of pembrolizumab were assessed according to the Response Evaluation Criteria in Solid Tumors, version 1.1. In total, 213 patients were included in the study. The median age was 71 years (range 39-91 years). Of the 213 patients, 176 (83%) were men and 172 (81%) had an Eastern Cooperative Oncology Group performance status (ECOG-PS) score of 0-1. The most common metastases were thoracic lymph node metastasis (77%), intrapulmonary metastasis (31%), bone metastasis (28%), and malignant pleural effusion (26%). On multivariate analysis, a poor ECOG-PS score (hazard ratio: 1.95, 95.0% confidence interval: 1.25-3.04; P = 0.003) and malignant pleural effusion (hazard ratio: 1.52, 95.0% confidence interval: 1.01-2.29; P = 0.043) were independent predictors of shorter progression-free survival in patients treated with pembrolizumab. For NSCLC patients with malignant pleural effusion, pembrolizumab monotherapy is not a suitable first-line treatment because of its insufficient effectiveness, even though their PD-L1 TPS was high.
免疫检查点抑制剂治疗晚期非小细胞肺癌(NSCLC)的疗效与转移部位之间的关系尚不清楚。因此,本项多中心回顾性研究旨在探讨 PD-L1 肿瘤比例评分(TPS)≥50%的晚期 NSCLC 患者接受一线帕博利珠单抗治疗后的转移部位的预测因素。我们回顾性分析了 2017 年 2 月至 2018 年 4 月期间在 11 家机构接受一线帕博利珠单抗治疗的 PD-L1 TPS≥50%的晚期 NSCLC 患者。从病历中收集的临床数据包括帕博利珠单抗治疗时的转移部位。根据实体瘤反应评估标准,版本 1.1 评估帕博利珠单抗的治疗效果。共有 213 例患者纳入本研究。中位年龄为 71 岁(范围 39-91 岁)。213 例患者中,176 例(83%)为男性,172 例(81%)ECOG-PS 评分为 0-1。最常见的转移部位是胸内淋巴结转移(77%)、肺内转移(31%)、骨转移(28%)和恶性胸腔积液(26%)。多因素分析显示,较差的 ECOG-PS 评分(风险比:1.95,95.0%置信区间:1.25-3.04;P=0.003)和恶性胸腔积液(风险比:1.52,95.0%置信区间:1.01-2.29;P=0.043)是帕博利珠单抗治疗患者无进展生存期较短的独立预测因素。对于恶性胸腔积液的 NSCLC 患者,即使 PD-L1 TPS 较高,由于其疗效不足,帕博利珠单抗单药治疗也不是一种合适的一线治疗方法。