Gu Xiaodong, Si Jinfei, Guan Yelan, Xu Yibing, Shao Lan, Zhang Yiping, Xu Chunwei, Pan Weiwei, Lu Yuanzhi, Song Zhengbo, Wang Wenxian
The Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310053, China.
Department of Thoracic Medical Oncology, Chinese Academy of Sciences University Cancer Hospital (Zhejiang Cancer Hospital), Hangzhou, Zhejiang 310022, China.
Open Med (Wars). 2023 Mar 10;18(1):20230653. doi: 10.1515/med-2023-0653. eCollection 2023.
The efficacy of immune checkpoint inhibitors (ICIs) on KRAS-mutant advanced non-small cell lung cancer (NSCLC) remains controversial. This retrospective study compared the effects of ICIs treatment and chemotherapy on the prognosis of patients with KRAS-mutant advanced NSCLC and different mutant subtypes in the real world. The study included 95 patients with KRAS-mutant advanced NSCLC. Patients treated with first-line ICIs plus platinum-containing chemotherapy had better progression-free survival (PFS) (7.4 vs 4.5 months, = 0.035) and overall survival (OS) (24.1 vs 13.2 months, = 0.007) than those receiving platinum-containing chemotherapy alone, and second-line ICI monotherapy was associated with better PFS (4.8 vs 3.0 months, = 0.043) and OS (18.0 vs 13.8 months, = 0.013) than chemotherapy monotherapy. There was no significant difference in PFS (5.267 vs 6.734 months, = 0.969) and OS (19.933 vs 20.933 months, = 0.808) between patients with KRAS-mutant and KRAS-wild-type NSCLC treated with ICIs or between KRAS G12C and KRAS non-G12C patients (PFS: 8.1 vs 4.8 months, = 0.307; OS: 21.3 vs 21.8 months, = 0.434). In summary, patients with advanced NSCLC with KRAS mutations can benefit from ICIs, but no difference between KRAS mutant subtypes was observed.
免疫检查点抑制剂(ICI)对KRAS突变的晚期非小细胞肺癌(NSCLC)的疗效仍存在争议。这项回顾性研究比较了在现实世界中ICI治疗和化疗对KRAS突变的晚期NSCLC患者及不同突变亚型患者预后的影响。该研究纳入了95例KRAS突变的晚期NSCLC患者。一线ICI联合含铂化疗的患者的无进展生存期(PFS)(7.4个月对4.5个月,P = 0.035)和总生存期(OS)(24.1个月对13.2个月,P = 0.007)均优于单纯接受含铂化疗的患者,二线ICI单药治疗的PFS(4.8个月对3.0个月,P = 0.043)和OS(18.0个月对13.8个月,P = 0.013)也优于化疗单药治疗。接受ICI治疗的KRAS突变型和KRAS野生型NSCLC患者之间,以及KRAS G12C和KRAS非G12C患者之间,PFS(5.267个月对6.734个月,P = 0.969)和OS(19.933个月对20.933个月,P = 0.808)均无显著差异(PFS:8.1个月对4.8个月,P = 0.307;OS:21.3个月对21.8个月,P = 0.434)。总之,KRAS突变的晚期NSCLC患者可从ICI中获益,但未观察到KRAS突变亚型之间存在差异。