Zeng Li, Zhang Yu, Zeng Aiju, Ma Daiyuan
Department of Oncology, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, People's Republic of China.
Cancer Manag Res. 2025 Jul 3;17:1301-1311. doi: 10.2147/CMAR.S517837. eCollection 2025.
The optimal combination of immune checkpoint inhibitors (ICIs), radiotherapy, and chemotherapy for unresectable locally advanced lung squamous cell carcinoma (LA-LUSC) remains undefined. This study evaluated induction chemoimmunotherapy followed by radiotherapy ± consolidation ICI in unresectable LA-LUSC, specifically exploring radiotherapy timing impact.
We retrospectively analyzed 54 unresectable LA-LUSC patients receiving induction chemoimmunotherapy followed by radiotherapy. Patients were grouped by radiotherapy timing: Early (after 2-3 induction cycles, n = 18) and Late (after 4-6 cycles, n = 36). Survival analysis (Kaplan-Meier, Log-rank) compared progression-free survival (PFS), local PFS (LPFS), distant metastasis-free survival (DMFS), overall survival (OS), and safety. Prognostic factors for PFS/OS were explored.
Median follow-up was 30.7 months. Median PFS for all patients was 21.9 months. Early radiotherapy improved PFS (HR = 0.43, p = 0.024) and LPFS (HR = 0.36, p = 0.038). Radiotherapy after 2-3 induction cycles was an independent predictor of improved PFS (p = 0.040). Overall treatment tolerance was good; grade ≥3 pneumonitis incidence was 5.56%. After propensity score matching, OS was significantly longer in patients receiving induction plus consolidation ICI versus induction ICI alone (HR = 0.51, p = 0.038).
Induction chemoimmunotherapy followed by radiotherapy demonstrates promising efficacy and manageable toxicity in unresectable LA-LUSC. Initiating radiotherapy earlier (after 2-3 induction cycles) improves PFS and LPFS and is an independent favorable prognostic factor. Consolidation ICI after combined chemoimmunotherapy and radiotherapy further extends OS compared to induction ICI alone.
免疫检查点抑制剂(ICI)、放疗和化疗对于不可切除的局部晚期肺鳞状细胞癌(LA-LUSC)的最佳联合方案仍未明确。本研究评估了不可切除的LA-LUSC患者接受诱导化疗免疫治疗后序贯放疗±巩固性ICI的疗效,特别探讨了放疗时机的影响。
我们回顾性分析了54例接受诱导化疗免疫治疗后序贯放疗的不可切除LA-LUSC患者。根据放疗时机将患者分组:早期(诱导化疗2 - 3周期后,n = 18)和晚期(诱导化疗4 - 6周期后,n = 36)。采用生存分析(Kaplan-Meier法、Log-rank检验)比较无进展生存期(PFS)、局部无进展生存期(LPFS)、远处转移无进展生存期(DMFS)、总生存期(OS)及安全性。探索PFS/OS的预后因素。
中位随访时间为30.7个月。所有患者的中位PFS为21.9个月。早期放疗改善了PFS(HR = 0.43,p = 0.024)和LPFS(HR = 0.36,p = 0.038)。诱导化疗2 - 3周期后进行放疗是PFS改善的独立预测因素(p = 0.040)。总体治疗耐受性良好;≥3级肺炎发生率为5.56%。倾向评分匹配后,接受诱导化疗加巩固性ICI的患者的OS显著长于单纯接受诱导性ICI的患者(HR = 0.51,p = 0.038)。
诱导化疗免疫治疗后序贯放疗在不可切除的LA-LUSC中显示出有前景的疗效和可管理的毒性。更早开始放疗(诱导化疗2 - 3周期后)可改善PFS和LPFS,且是一个独立的有利预后因素。与单纯诱导性ICI相比,化疗免疫治疗和放疗联合后进行巩固性ICI可进一步延长OS。