Yoshimura Akihiro, Takeda Takayuki, Kataoka Nobutaka, Tanimura Keiko, Fukui Mototaka, Chihara Yusuke, Takei Shota, Kawachi Hayato, Nakanishi Kentaro, Yamanaka Yuta, Tamiya Nobuyo, Honda Ryoichi, Okura Naoko, Yamada Takahiro, Uryu Kiyoaki, Murai Junji, Shiotsu Shinsuke, Yoshioka Hiroshige, Yamada Tadaaki, Kurata Takayasu, Takayama Koichi
Department of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan.
Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Front Oncol. 2024 Jan 26;14:1303543. doi: 10.3389/fonc.2024.1303543. eCollection 2024.
The efficacy of second-line immune checkpoint inhibitor (ICI) therapy is limited in non-small cell lung cancer (NSCLC) patients with ≤ 49% PD-L1 expression. Although chemoimmunotherapy is a promising strategy, platinum-based chemotherapy followed by ICI monotherapy is often used to avoid synergistic adverse events. However, predictors of the efficacy of ICI monotherapy after platinum-based chemotherapy in NSCLC with ≤ 49% PD-L1 expression remain scarce.
This multicenter retrospective study evaluated 54 advanced or recurrent NSCLC patients with ≤ 49% PD-L1 expression who were treated with second-line ICI monotherapy following disease progression on first-line platinum-based chemotherapy at nine hospitals in Japan. The impact of response to platinum-based chemotherapy on the efficacy of subsequent ICI monotherapy was investigated.
The response to first-line platinum-based chemotherapy was divided into two groups: the non-progressive disease (PD) group, which included patients who did not experience disease progression after four cycles of chemotherapy, and the PD group, which included patients who showed initial PD or could not maintain disease control during the four cycles of chemotherapy and switched to second-line ICI monotherapy. Among the 54 patients, 32 and 22 were classified into the non-PD and PD groups, respectively. The non-PD group showed better response rates (p = 0.038) and longer overall survival (OS) with ICI monotherapy (p = 0.023) than the PD group. Multivariate analysis identified that maintaining a non-PD status after four cycles of chemotherapy was an independent prognostic factor for ICI monotherapy (p = 0.046). Moreover, patients with a modified Glasgow Prognostic Score (mGPS) of 0 showed a tendency for longer OS with ICI monotherapy (p = 0.079), and there was a significant correlation between maintaining non-PD after four cycles of chemotherapy and an mGPS of 0 (p = 0.045).
Maintaining a non-PD status after four cycles of platinum-based chemotherapy was a predictor of OS after second-line ICI monotherapy. These findings will help physicians select the most suitable treatment option for NSCLC patients who were treated with platinum-based chemotherapy and switched to second-line treatment. Those who experienced early PD during platinum-based chemotherapy should not be treated with ICI monotherapy in the second-line setting.
二线免疫检查点抑制剂(ICI)疗法对程序性死亡受体-配体1(PD-L1)表达≤49%的非小细胞肺癌(NSCLC)患者疗效有限。尽管化疗免疫疗法是一种很有前景的策略,但铂类化疗后序贯ICI单药治疗常被采用以避免协同不良事件。然而,对于PD-L1表达≤49%的NSCLC患者,铂类化疗后ICI单药治疗疗效的预测指标仍然匮乏。
这项多中心回顾性研究评估了54例PD-L1表达≤49%的晚期或复发性NSCLC患者,这些患者在日本9家医院接受一线铂类化疗疾病进展后接受二线ICI单药治疗。研究了铂类化疗反应对后续ICI单药治疗疗效的影响。
一线铂类化疗反应分为两组:疾病无进展(PD)组,包括化疗4个周期后未出现疾病进展的患者;以及PD组,包括初始即出现PD或在化疗4个周期内无法维持疾病控制而转为二线ICI单药治疗的患者。54例患者中,分别有32例和22例被归入非PD组和PD组。非PD组ICI单药治疗的缓解率(p = 0.038)和总生存期(OS)更长(p = 0.023)。多因素分析确定化疗4个周期后维持非PD状态是ICI单药治疗的独立预后因素(p = 0.0A6)。此外,改良格拉斯哥预后评分(mGPS)为0的患者ICI单药治疗有OS更长的趋势(p = 0.079),且化疗4个周期后维持非PD状态与mGPS为0之间存在显著相关性(p = 0.045)。
铂类化疗4个周期后维持非PD状态是二线ICI单药治疗后OS的预测指标。这些发现将有助于医生为接受铂类化疗并转为二线治疗的NSCLC患者选择最合适的治疗方案。在铂类化疗期间早期出现PD的患者在二线治疗中不应接受ICI单药治疗。