Wang Ziwei, Xu Kunpeng, Sun Han, Liang Jun, Jiang Wei, Wang Luhua
Oncology, Graduate School of Bengbu Medical University, Bengbu, Anhui, China.
Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Front Immunol. 2025 May 9;16:1578057. doi: 10.3389/fimmu.2025.1578057. eCollection 2025.
This study evaluates the impact of thoracic radiotherapy (TRT) combined with immune checkpoint inhibitors (ICIs) treatment-related pneumonitis on tumor progression and prognosis in patients with non-small cell lung cancer (NSCLC).
Data were collected retrospectively from NSCLC patients treated with TRT and ICIs between January 2019 and August 2023. Treatment-related pneumonitis (TRP) was assessed and graded using the Common Terminology Criteria for Adverse Events (CTCAE) and the Chinese Society of Clinical Oncology Guidelines for Managing Immunotherapy-Related Toxicities. Kaplan-Meier curves and log-rank tests examined associations between pneumonitis with local recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), progression-free survival (PFS), and overall survival (OS). COX regression identified prognostic factors in the pneumonitis group.
Among 86 patients, 58 (67.4%) developed TRP, including 37.2% with grade 2 pneumonitis, and no grade ≥3 cases. 12 patients (14.0%) developed mixed radiation and ICIs pneumonitis. The pneumonitis group had significantly shorter DMFS (12.07 vs not reached, p = 0.028) and PFS (9.53 vs 14.27 months, p = 0.040), shorter LRFS compared to the non-pneumonitis group, but similar OS. High-grade pneumonitis correlated with worse outcomes, especially DMFS (p = 0.031), basically no differences among pneumonitis types. Multivariate COX analysis identified solitary pulmonary nodules or masses as independent negative prognostic factors for PFS, while higher MLD (mean lung dose) independently predicted reduced OS.
Pneumonitis resulting from TRT combined with ICIs was associated with shorter PFS but did not affect OS in NSCLC patients. Mixed pneumonitis did not worsen outcomes. Larger prospective studies are needed to validate these findings.
本研究评估胸部放疗(TRT)联合免疫检查点抑制剂(ICIs)治疗相关肺炎对非小细胞肺癌(NSCLC)患者肿瘤进展和预后的影响。
回顾性收集2019年1月至2023年8月接受TRT和ICIs治疗的NSCLC患者的数据。使用不良事件通用术语标准(CTCAE)和中国临床肿瘤学会免疫治疗相关毒性管理指南对治疗相关肺炎(TRP)进行评估和分级。采用Kaplan-Meier曲线和对数秩检验分析肺炎与局部无复发生存期(LRFS)、远处无转移生存期(DMFS)、无进展生存期(PFS)和总生存期(OS)之间的关联。COX回归分析确定肺炎组的预后因素。
86例患者中,58例(67.4%)发生TRP,其中2级肺炎37.2%,无≥3级病例。12例患者(14.0%)发生放疗和ICIs混合性肺炎。肺炎组的DMFS(12.07个月对未达到,p = 0.028)和PFS(9.53个月对14.27个月,p = 0.040)显著缩短,与非肺炎组相比LRFS较短,但OS相似。高级别肺炎与更差的预后相关,尤其是DMFS(p = 0.031),不同类型肺炎之间基本无差异。多因素COX分析确定孤立性肺结节或肿块是PFS的独立阴性预后因素,而较高的平均肺剂量(MLD)独立预测OS降低。
TRT联合ICIs导致的肺炎与NSCLC患者较短的PFS相关,但不影响OS。混合性肺炎并未使预后恶化。需要更大规模的前瞻性研究来验证这些发现。