Chen Haiyan, Xu Yijiao, Liu Jianying, Yang Shuwen, Jiang Hongni, Chen Zhisheng
Zhongshan Hospital (Xiamen), Fudan University, Xiamen, China.
Xiamen Clinical Research Center for Cancer Therapy, Xiamen, China.
Discov Oncol. 2024 Oct 8;15(1):534. doi: 10.1007/s12672-024-01413-2.
Immune checkpoint inhibitors (ICIs) have improved lung cancer treatment but are associated with immune-related adverse events (irAEs). This study analyzes the relationship between irAEs and treatment effectiveness in advanced non-small cell lung cancer (NSCLC) patients.
We conducted a retrospective study of NSCLC patients treated with ICIs from March 2019 to October 2022 at Zhongshan Hospital (Xiamen). Patients were divided into irAE and non-irAE groups, and treatment outcomes were compared.
A total of 154 patients were included, with 36.4% in the irAE group and 63.6% in the non-irAE group. Most irAEs were Grade 1-2 (86.4%), with 13.6% being Grade 3 or higher. The irAE group had higher disease control rates (DCR: 94.6% vs. 76.5%, P = 0.004) and objective response rates (ORR: 42.9% vs. 26.5%, P = 0.037). Median progression-free survival (PFS) was longer in the irAE group (18 vs. 9 months, HR: 0.53, P = 0.001), as was overall survival (OS: 39.5 vs. 16 months, HR: 0.46, P = 0.001). Landmark analysis at 6 and 12 weeks confirmed that irAEs were associated with improved outcomes. Moreover, patients who experienced two or more adverse events during treatment had significantly longer OS compared to those who had only one or no adverse events (41.6 months vs. 34.0 vs. 23.6, P = 0.003).
Patients with irAEs demonstrated better outcomes, including ORR, DCR, PFS, and OS. Further studies on biomarkers and irAE incidence are warranted to improve lung cancer management.
免疫检查点抑制剂(ICI)改善了肺癌治疗,但与免疫相关不良事件(irAE)有关。本研究分析了晚期非小细胞肺癌(NSCLC)患者中irAE与治疗效果之间的关系。
我们对2019年3月至2022年10月在中山医院(厦门)接受ICI治疗的NSCLC患者进行了一项回顾性研究。将患者分为irAE组和非irAE组,并比较治疗结果。
共纳入154例患者,irAE组占36.4%,非irAE组占63.6%。大多数irAE为1-2级(86.4%),13.6%为3级或更高。irAE组的疾病控制率(DCR:94.6%对76.5%,P = 0.004)和客观缓解率(ORR:42.9%对26.5%,P = 0.037)更高。irAE组的中位无进展生存期(PFS)更长(18个月对9个月,HR:0.53,P = 0.001),总生存期(OS:39.5个月对16个月,HR:0.46,P = 0.001)也是如此。6周和12周的标志性分析证实,irAE与更好的预后相关。此外,与仅发生一次或未发生不良事件的患者相比,治疗期间发生两次或更多不良事件的患者的OS明显更长(41.6个月对34.0个月对23.6个月,P = 0.003)。
发生irAE的患者表现出更好的预后,包括ORR、DCR、PFS和OS。有必要对生物标志物和irAE发生率进行进一步研究,以改善肺癌管理。