Nokihara Hiroshi, Kijima Takashi, Yokoyama Toshihide, Kagamu Hiroshi, Suzuki Takuji, Mori Masahide, Santorelli Melissa L, Taniguchi Kazuko, Kamitani Tetsu, Irisawa Masato, Kanda Kingo, Abe Machiko, Burke Thomas, Goto Yasushi
Department of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences, Tokushima University, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.
Department of Respiratory Medicine and Hematology, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya 663-8501, Japan.
Cancers (Basel). 2022 Jun 9;14(12):2846. doi: 10.3390/cancers14122846.
The aims of this study were to describe systemic treatment patterns and clinical outcomes for unresectable advanced/metastatic non-small-cell lung cancer (NSCLC) by first-line regimen type in real-world clinical settings in Japan after the introduction of first-line immune checkpoint inhibitor (ICI) monotherapy in 2017. Using retrospective chart review at 23 study sites, we identified patients ≥20 years old initiating first-line systemic therapy from 1 July 2017 to 20 December 2018, for unresectable stage IIIB/C or IV NSCLC; the data cutoff was 30 September 2019. Eligible patients had recorded programmed death-ligand 1 (PD-L1) tumor proportion score (TPS) and no known actionable EGFR/ALK/ROS1/BRAF genomic alteration. Kaplan-Meier method was used to determine time-to-event endpoints. Of 1208 patients, 647 patients (54%) received platinum doublet, 463 (38%) received ICI monotherapy, and 98 (8%) received nonplatinum cytotoxic regimen as first-line therapy. PD-L1 TPS was ≥50%, 1−49% and <1% for 44%, 30%, and 25% of patients, respectively. Most patients with PD-L1 TPS ≥50% received ICI monotherapy (453/529; 86%). Excluding 26 patients with ECOG performance status of 3−4 from outcome analyses, the median patient follow-up was 11.3 months. With first-line platinum doublet, ICI monotherapy, and nonplatinum cytotoxic regimens, median overall survival (OS) was 16.3 months (95% CI, 14.0−20.1 months), not reached, and 14.4 months (95% CI, 10.3−21.2 months), respectively; 24-month OS was 40%, 58%, and 31%, respectively. Differences in OS relative to historical cohort data reported in Japan are consistent with improvement over time in real-world clinical outcomes for advanced NSCLC.
本研究旨在描述2017年一线免疫检查点抑制剂(ICI)单药疗法引入日本后,在真实世界临床环境中,不可切除的晚期/转移性非小细胞肺癌(NSCLC)按一线治疗方案类型划分的系统治疗模式和临床结局。通过对23个研究地点的病历进行回顾性分析,我们确定了2017年7月1日至2018年12月20日期间开始接受一线系统治疗的年龄≥20岁的不可切除的IIIB/C期或IV期NSCLC患者;数据截止日期为2019年9月30日。符合条件的患者记录了程序性死亡配体1(PD-L1)肿瘤比例评分(TPS),且不存在已知的可操作的表皮生长因子受体(EGFR)/间变性淋巴瘤激酶(ALK)/ROS1/ 原癌基因B(BRAF)基因组改变。采用Kaplan-Meier方法确定事件发生时间终点。在1208例患者中,647例患者(54%)接受铂类双联化疗,463例(38%)接受ICI单药治疗,98例(8%)接受非铂类细胞毒性方案作为一线治疗。PD-L1 TPS≥50%、1%-49%和<1%的患者分别占44%、30%和25%。大多数PD-L1 TPS≥50%的患者接受了ICI单药治疗(453/529;86%)。在结局分析中排除26例东部肿瘤协作组(ECOG)体能状态为3-4的患者后,患者的中位随访时间为11.3个月。一线铂类双联化疗、ICI单药治疗和非铂类细胞毒性方案的中位总生存期(OS)分别为16.3个月(95%置信区间[CI],14.0-20.1个月)、未达到以及14.4个月(95%CI,10.3-21.2个月);24个月总生存率分别为40%、58%和31%。与日本报告的历史队列数据相比,总生存期的差异与晚期NSCLC真实世界临床结局随时间的改善一致。