Tanimura Keiko, Takeda Takayuki, Kataoka Nobutaka, Yoshimura Akihiro, Nakanishi Kentaro, Yamanaka Yuta, Yoshioka Hiroshige, Honda Ryoichi, Uryu Kiyoaki, Fukui Mototaka, Chihara Yusuke, Takei Shota, Kawachi Hayato, Yamada Tadaaki, Tamiya Nobuyo, Okura Naoko, Yamada Takahiro, Murai Junji, Shiotsu Shinsuke, Kurata Takayasu, Takayama Koichi
Department of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto 602-8026, Japan.
Department of Thoracic Oncology, Kansai Medical University Hospital, Hirakata 573-1191, Japan.
Cancers (Basel). 2023 Oct 14;15(20):4988. doi: 10.3390/cancers15204988.
The long overall survival (OS) observed among patients with non-small cell lung cancer (NSCLC) with high programmed death-ligand 1 (PD-L1) expression in chemoimmunotherapy (CIT) groups in previous phase III trials suggests the limited efficacy of CIT among the subgroup with ≤49% PD-L1 expression on tumor cells. Hence, sequential treatment with first-line platinum-based chemotherapy followed by second-line immune checkpoint inhibitor treatment (SEQ) is an option. This study examined whether first-line CIT would provide better outcomes than SEQ in patients with advanced NSCLC with ≤49% PD-L1 expression.
This retrospective study evaluated patients with untreated NSCLC who received first-line CIT or SEQ at nine hospitals in Japan. OS, progression-free survival (PFS), PFS-2 (the time from first-line treatment to progression to second-line treatment or death), and other related outcomes were evaluated between the CIT and SEQ groups.
Among the 305 enrolled patients, 234 eligible patients were analyzed: 165 in the CIT group and 69 in the SEQ group. The COX proportional hazards model suggested a significant interaction between PD-L1 expression and OS ( = 0.006). OS in the CIT group was significantly longer than that in the SEQ group in the 1-49% PD-L1 expression subgroup but not in the <1% PD-L1 expression subgroup. Among the subgroup with 1-49% PD-L1 expression, the CIT group exhibited longer median PFS than the SEQ group (CIT: 9.3 months (95% CI: 6.7-14.8) vs. SEQ:5.5 months (95% CI: 4.5-6.1); < 0.001), while the median PFS in the CIT group was not statistically longer than the median PFS-2 in the SEQ group ( = 0.586). There was no significant difference between the median PFS in the CIT and SEQ groups among the <1% PD-L1 expression subgroup ( = 0.883); the median PFS-2 in the SEQ group was significantly longer than the median PFS in the CIT group (10.5 months (95% CI: 5.9-15.3) vs. 6.4 months (95% CI: 4.9-7.5); = 0.024).
CIT is recommended for patients with NSCLC with 1-49% PD-L1 expression because it significantly improved OS and PFS compared to SEQ. CIT had limited benefits in patients with <1% PD-L1 expression, and the median PFS-2 in the SEQ group was significantly longer than the median PFS in the CIT group. These findings will help physicians select the most suitable treatment option for patients with NSCLC, considering PD-L1 expressions.
在既往III期试验的化疗免疫治疗(CIT)组中,程序性死亡配体1(PD-L1)高表达的非小细胞肺癌(NSCLC)患者观察到较长的总生存期(OS),这表明CIT在肿瘤细胞上PD-L1表达≤49%的亚组中疗效有限。因此,一线铂类化疗序贯二线免疫检查点抑制剂治疗(SEQ)是一种选择。本研究探讨一线CIT在PD-L1表达≤49%的晚期NSCLC患者中是否比SEQ能带来更好的疗效。
这项回顾性研究评估了在日本9家医院接受一线CIT或SEQ治疗的未经治疗的NSCLC患者。在CIT组和SEQ组之间评估OS、无进展生存期(PFS)、PFS-2(从一线治疗到进展至二线治疗或死亡的时间)及其他相关疗效指标。
在305例入组患者中,分析了234例符合条件的患者:CIT组165例,SEQ组69例。COX比例风险模型显示PD-L1表达与OS之间存在显著交互作用(P = 0.006)。在PD-L1表达为1%-49%的亚组中,CIT组的OS显著长于SEQ组,但在PD-L1表达<1%的亚组中并非如此。在PD-L1表达为1%-49%的亚组中,CIT组的中位PFS长于SEQ组(CIT组:9.3个月(95%CI:6.7-14.8) vs. SEQ组:5.5个月(95%CI:4.5-6.1);P<0.001),而CIT组的中位PFS在统计学上并不长于SEQ组的中位PFS-2(P = 0.586)。在PD-L1表达<1%的亚组中,CIT组和SEQ组的中位PFS无显著差异(P = 0.883);SEQ组的中位PFS-2显著长于CIT组的中位PFS(10.5个月(95%CI:5.9-15.3) vs. 6.4个月(95%CI:4.9-7.5);P = 0.024)。
对于PD-L1表达为1%-49%的NSCLC患者,推荐使用CIT,因为与SEQ相比,它能显著改善OS和PFS。CIT在PD-L1表达<1%的患者中获益有限,且SEQ组的中位PFS-2显著长于CIT组的中位PFS。这些研究结果将有助于医生根据PD-L1表达为NSCLC患者选择最合适的治疗方案。