Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, 465, Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.
Department of Respiratory Medicine, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
J Cancer Res Clin Oncol. 2022 Nov;148(11):2985-2994. doi: 10.1007/s00432-021-03866-2. Epub 2021 Nov 26.
The primary objective of this study was to identify the potential predictors to assess the impact of maintenance therapy after induction immunochemotherapy in the real-world setting of patients with advanced non-small cell lung cancer (NSCLC).
We retrospectively identified 152 patients with advanced NSCLC who received immunochemotherapy at 8 hospitals in Japan between January 2019 and December 2019. Patients who received at least four cycles of induction immunochemotherapy and one cycle of maintenance therapy with immune checkpoint inhibitors were included. We investigated the biomarkers for progression-free survival (PFS) for maintenance therapy after induction immunochemotherapy.
Out of the 92 patients with advanced NSCLC included in the study, 42 received maintenance therapy with cytotoxic agents, whereas 50 received maintenance therapy without cytotoxic agents. Among those who received maintenance therapy without cytotoxic agents, responders to prior immunochemotherapy had significantly longer PFS than non-responders (p = 0.004), except those with maintenance therapy with cytotoxic agents. In non-responders to prior immunochemotherapy, patients with maintenance therapy with cytotoxic agents had significantly longer PFS than those with maintenance therapy without cytotoxic agents (log-rank p = 0.007), whereas, among responders to prior immunochemotherapy, there was no significant difference in PFS for different maintenance regimens (log-rank p = 0.31).
This retrospective study showed that response to prior immunochemotherapy was associated with clinical outcomes among patients with advanced NSCLC who received maintenance therapy.
本研究的主要目的是确定潜在的预测因素,以评估在晚期非小细胞肺癌(NSCLC)的真实世界环境中,诱导免疫化疗后维持治疗的影响。
我们回顾性地确定了 2019 年 1 月至 2019 年 12 月期间在日本 8 家医院接受免疫化疗的 152 名晚期 NSCLC 患者。纳入至少接受了四个周期的诱导免疫化疗和一个周期的免疫检查点抑制剂维持治疗的患者。我们研究了诱导免疫化疗后维持治疗的无进展生存期(PFS)的生物标志物。
在研究的 92 名晚期 NSCLC 患者中,42 名患者接受了细胞毒性药物维持治疗,而 50 名患者接受了无细胞毒性药物维持治疗。在未接受细胞毒性药物维持治疗的患者中,先前免疫化疗的应答者比无应答者的 PFS 显著延长(p=0.004),但不包括接受细胞毒性药物维持治疗的患者。在先前免疫化疗无应答者中,接受细胞毒性药物维持治疗的患者 PFS 明显长于接受无细胞毒性药物维持治疗的患者(对数秩 p=0.007),而在先前免疫化疗的应答者中,不同的维持方案对 PFS 无显著差异(对数秩 p=0.31)。
这项回顾性研究表明,对先前免疫化疗的反应与接受维持治疗的晚期 NSCLC 患者的临床结果相关。