Tao Ye, Li Xiang, Cui Xinrun, Zhao Dachuan, Liu Bing, Wang Yaqi, Du Haoxuan, Wen Zengjin, Yan Shi, Wu Nan
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Thoracic Surgery II, Peking University Cancer Hospital & Institute, Beijing, China.
State Key Laboratory of Molecular Oncology, Beijing Key Laboratory of Carcinogenesis and Translational Research, Department of Thoracic Surgery II, Peking University Cancer Hospital & Institute, Beijing, China.
Eur J Surg Oncol. 2025 May 13;51(9):110148. doi: 10.1016/j.ejso.2025.110148.
This study aims to compare the survival benefits of perioperative versus neoadjuvant immune checkpoint inhibitors (ICI)-based therapy in patients with resectable non-small cell lung cancer (NSCLC), focusing specifically on those who achieve major pathological response (MPR) or pathological complete response (pCR) following neoadjuvant ICI-based treatment.
s: A systematic literature review was performed using PubMed, Embase, Cochrane Library, and ClinicalTrials.gov databases. A trial-level proportional meta-analysis was conducted to compare the two treatment modalities. A patient-level-based analysis was also conducted to obtain more evidence of different perioperative treatment regimens. Cox regression and accelerated failure time models were used to analyze the survival benefits in patients who achieved MPR or pCR for the proper treatment modality.
Twenty-three studies were included in the trial-level proportional meta-analysis, wherein no statistical significance was observed in the 1-, 2-, and 3-year event-free survival (EFS) rates between patients with MPR and pCR receiving perioperative or neoadjuvant ICI-based therapy. The pooled median EFS (mEFS) was 40.1 and 32.1 months in patients with MPR receiving perioperative and neoadjuvant ICI-based therapies, respectively. Meanwhile, the pooled mEFS was 35.4 and 34.2 months in patients with pCR receiving perioperative and neoadjuvant ICI-based therapies, respectively. Multivariable Cox analysis showed that perioperative chemoimmunotherapy was a favorable prognostic factor compared with neoadjuvant chemoimmunotherapy in MPR patients (P = 0.038), but not in those with pCR (P = 0.408).
The EFS were similar among patients with NSCLC who received neoadjuvant and perioperative ICI-based treatment and achieved MPR or pCR. Multivariable Cox analysis indicated that perioperative chemoimmunotherapy was a favorable prognostic factor in patients who achieved MPR after neoadjuvant chemoimmunotherapy, but not in those who reached pCR.
本研究旨在比较围手术期与新辅助免疫检查点抑制剂(ICI)为基础的治疗对可切除非小细胞肺癌(NSCLC)患者的生存获益,特别关注新辅助ICI为基础治疗后达到主要病理缓解(MPR)或病理完全缓解(pCR)的患者。
使用PubMed、Embase、Cochrane图书馆和ClinicalTrials.gov数据库进行系统文献综述。进行试验水平的比例荟萃分析以比较两种治疗方式。还进行了基于患者水平的分析以获得不同围手术期治疗方案的更多证据。使用Cox回归和加速失效时间模型分析达到MPR或pCR的患者采用适当治疗方式后的生存获益。
试验水平的比例荟萃分析纳入了23项研究,其中接受围手术期或新辅助ICI为基础治疗的MPR和pCR患者在1年、2年和3年无事件生存(EFS)率方面未观察到统计学显著性差异。接受围手术期和新辅助ICI为基础治疗的MPR患者的汇总中位EFS(mEFS)分别为40.1个月和32.1个月。同时,接受围手术期和新辅助ICI为基础治疗的pCR患者的汇总mEFS分别为35.4个月和34.2个月。多变量Cox分析显示,与新辅助化疗免疫治疗相比,围手术期化疗免疫治疗是MPR患者的有利预后因素(P = 0.038),但在pCR患者中并非如此(P = 0.408)。
接受新辅助和围手术期ICI为基础治疗并达到MPR或pCR的NSCLC患者的EFS相似。多变量Cox分析表明,围手术期化疗免疫治疗是新辅助化疗免疫治疗后达到MPR患者的有利预后因素,但在达到pCR的患者中并非如此。