Fan Pengyu, Sheng Zhenxin, Ji Shuyu, Hu Shiqi, Zhang Peng, Wang Haifeng, Shen Ziyun
Department of Thoracic Surgery, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China.
Department of Thoracic Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou Medical University, Wenzhou, China.
J Thorac Dis. 2025 Aug 31;17(8):5893-5903. doi: 10.21037/jtd-2025-576. Epub 2025 Aug 16.
Platinum-based chemotherapy is the most common combination regimen with immune checkpoint inhibitors (ICIs) in neoadjuvant therapy for resectable non-small cell lung cancer (NSCLC), yet the multimodal strategies of neoadjuvant therapy have not been fully explored. Antiangiogenic therapy is known to modify the tumor immune microenvironment, making it a potential candidate. This study aimed to explore the pathological and survival outcomes of neoadjuvant immunotherapy (IO) combined with antiangiogenic therapy and compare the outcomes with neoadjuvant chemoimmunotherapy (IO + CT) in resectable NSCLC.
The clinical and pathological characteristics of NSCLC patients who underwent neoadjuvant immunotherapy plus antiangiogenic therapy (IO + AA) or IO + CT before radical surgery at a high-volume single center between December 2019 and June 2024 were retrospectively collected. The IO + CT group was matched 4:1 with the IO + AA group by propensity score matching (PSM). The surgical and survival outcomes were systematically collected and analyzed.
During a nearly 6-year study period, the majority of patients (411 of 431, 95.4%) underwent neoadjuvant IO + CT, while 20 patients (4.6%) underwent neoadjuvant IO + AA. Following PSM, the major pathological response (MPR) was comparable between the two groups (66.7% 63.3%, P=0.81), whereas the pathological complete response (pCR) had a trend toward reduction (13.3% 38.3%, P=0.07). Meanwhile, the neoadjuvant IO + AA group did not increase the surgical complexity or the overall postoperative complications (20.0% 23.3%, P=0.78). Additionally, no significant difference was observed between the two groups in terms of disease-free survival (DFS) and overall survival (OS) (P=0.16 and P=0.47, respectively).
This finding suggests that neoadjuvant IO + AA demonstrates no superiority over neoadjuvant IO + CT in terms of pathological and survival outcomes. Although it may serve as a chemo-free alternative for selective patients, the current evidence supports IO + CT as the standard neoadjuvant strategy in resectable NSCLC.
在可切除的非小细胞肺癌(NSCLC)新辅助治疗中,铂类化疗是与免疫检查点抑制剂(ICI)联合使用最常见的方案,但新辅助治疗的多模式策略尚未得到充分探索。已知抗血管生成疗法可改变肿瘤免疫微环境,使其成为一个潜在的选择。本研究旨在探讨新辅助免疫治疗(IO)联合抗血管生成疗法的病理及生存结局,并将其与可切除NSCLC的新辅助化疗免疫治疗(IO + CT)的结局进行比较。
回顾性收集2019年12月至2024年6月期间在一家大型单中心接受根治性手术前接受新辅助免疫治疗加抗血管生成疗法(IO + AA)或IO + CT的NSCLC患者的临床和病理特征。IO + CT组与IO + AA组按倾向评分匹配(PSM)以4:1进行匹配。系统收集并分析手术及生存结局。
在近6年的研究期间,大多数患者(431例中的411例,95.4%)接受了新辅助IO + CT,而20例患者(4.6%)接受了新辅助IO + AA。PSM后,两组之间的主要病理反应(MPR)相当(66.7%对63.3%,P = 0.81),而病理完全缓解(pCR)有降低趋势(13.3%对38.3%,P = 0.07)。同时,新辅助IO + AA组并未增加手术复杂性或总体术后并发症(20.0%对23.3%,P = 0.78)。此外,两组在无病生存期(DFS)和总生存期(OS)方面未观察到显著差异(分别为P = 0.16和P = 0.47)。
这一发现表明,新辅助IO + AA在病理及生存结局方面并不优于新辅助IO + CT。尽管它可能作为选择性患者的无化疗替代方案,但目前的证据支持IO + CT作为可切除NSCLC的标准新辅助策略。