Department of Respiratory Medicine, Hiroshima University Hospital, Hiroshima, Japan.
Department of Respiratory Internal Medicine, JA Onomichi General Hospital, Hiroshima, Japan.
Thorac Cancer. 2022 Jun;13(11):1611-1618. doi: 10.1111/1759-7714.14428. Epub 2022 Apr 30.
Pembrolizumab is the recommended first-line therapy for patients with advanced non-small-cell lung cancer (NSCLC) and a programmed death ligand-1 (PD-L1) tumor proportion score (TPS) of ≥50% without driver mutations. However, its efficacy and safety for patients ≥75 years have not been prospectively investigated; this was the aim of this study.
This multicenter and open-label single-arm phase II study was conducted at 12 institutions. Chemotherapy-naïve patients with advanced NSCLC and a PD-L1 TPS of ≥50% without EGFR mutations or translocation of the ALK received pembrolizumab every 3 weeks. The primary endpoint was progression-free survival (PFS) with a threshold of 4.3 months. The secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR), safety, and quality of life.
Twenty-six patients were enrolled between October 2017 and March 2020. The median PFS was 9.6 (95% confidence interval [CI] 2.1-20.6) months. The lower limit of the 95% CI did not exceed the target. The median OS was 21.6 months. The ORR and DCR were 41.7% and 70.8%, respectively. The proportion of patients with grade ≥3 treatment-related adverse events was 15.4%. The quality of life score did not change significantly during treatment.
While this study showed that pembrolizumab was a tolerable treatment for elderly patients, the safety requires further confirmation in a larger study. Although the primary endpoint, the median PFS (9.6 months), was slightly shorter than that (10.3 months) of the previous phase III study (KEYNOTE-024 study), the median PFS did not achieve the expected value.
对于无驱动基因突变、PD-L1 肿瘤比例评分(TPS)≥50%的晚期非小细胞肺癌(NSCLC)患者,推荐使用派姆单抗作为一线治疗药物。然而,对于年龄≥75 岁的患者,尚未前瞻性地研究其疗效和安全性;这是本研究的目的。
这是一项在 12 家机构进行的多中心、开放标签、单臂 II 期研究。无化疗史、晚期 NSCLC 且 PD-L1 TPS≥50%且无 EGFR 突变或 ALK 易位的患者接受派姆单抗每 3 周一次治疗。主要终点是无进展生存期(PFS),阈值为 4.3 个月。次要终点包括总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)、安全性和生活质量。
2017 年 10 月至 2020 年 3 月期间共纳入 26 例患者。中位 PFS 为 9.6(95%置信区间 [CI]:2.1-20.6)个月。95%CI 的下限未超过目标值。中位 OS 为 21.6 个月。ORR 和 DCR 分别为 41.7%和 70.8%。≥3 级治疗相关不良事件的患者比例为 15.4%。治疗期间生活质量评分无显著变化。
虽然本研究表明派姆单抗对老年患者是一种可耐受的治疗方法,但安全性需要在更大的研究中进一步证实。虽然主要终点中位 PFS(9.6 个月)略短于之前的 III 期研究(KEYNOTE-024 研究)的中位 PFS(10.3 个月),但中位 PFS 未达到预期值。