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不可切除的局部晚期肺鳞状细胞癌诱导化疗免疫治疗后放疗干预时机的回顾性分析

Retrospective Analysis of the Timing of Radiotherapy Intervention After Induction Chemoimmunotherapy in Unresectable Locally Advanced Lung Squamous Cell Carcinoma.

作者信息

Zeng Li, Zhang Yu, Zeng Aiju, Ma Daiyuan

机构信息

Department of Oncology, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, People's Republic of China.

出版信息

Cancer Manag Res. 2025 Jul 3;17:1301-1311. doi: 10.2147/CMAR.S517837. eCollection 2025.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

背景

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。

方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/492c/12235018/eb366e5522bb/CMAR-17-1301-g0001.jpg

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