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. 2025 Jul:208:110911.
doi: 10.1016/j.radonc.2025.110911. Epub 2025 Apr 27.

Salvage thoracic reirradiation for recurrent non-small cell lung cancer: Clinical efficacy and the impact of consolidative immunotherapy

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Salvage thoracic reirradiation for recurrent non-small cell lung cancer: Clinical efficacy and the impact of consolidative immunotherapy

Jenna Rocchetti et al. Radiother Oncol. 2025 Jul.
Free article

Abstract

Purpose: To describe clinical outcomes in a large patient cohort treated with salvage thoracic reirradiation (reRT) for isolated locoregional recurrence of non-small cell lung cancer (NSCLC).

Methods: Between 2011 and 2021, 1219 patients received thoracic radiotherapy for NSCLC; 130 patients underwent reRT, with doses ranging from 60-72 Gy. Primary outcomes were overall survival (OS), progression-free survival (PFS), and reRT toxicity; secondary outcomes were locoregional failure (LRF) and distant failure (DF). The Kaplan-Meier method and cumulative incidence with death as a competing risk were used for analysis, with multivariable modeling via Cox proportional hazards. Toxicity outcomes included grade 3 + non-hematologic event, hospitalization within 90 days of reRT, and grade 5 toxicity per Common Terminology Criteria for Adverse Events, version 5.0.

Results: Median OS and PFS for the entire cohort were 17.4 months (95 % CI 14.1-22.9) and 8.1 months (95 % CI 6.7-10.8), respectively. 3-year OS was 25.9 % (95 % CI 19.3-34.8 %). The 3-year cumulative incidence of DF and LRF were 44 % and 46 %, respectively. Recipients of consolidative immunotherapy after reRT had improved OS (27.8 months [95 %CI 18.4-not reached] vs 15.8 months [95 %CI 12.1-22.1]; p = 0.035) and locoregional-free survival (22.8 months [95 %CI 9.8-not reached] vs 8.8 months [95 %CI 7.6-12.6]; p = 0.009). Multivariable analysis showed consolidative immunotherapy (HR 0.56, 95 %CI 0.32-1.03, p = 0.065) and hospitalization within 90 days of reRT (HR 2.03, 95 %CI 1.24-3.33, p = 0.005) were associated with OS. Nine patients (6.9 %) experienced grade 5 toxicities.

Conclusion: Thoracic reRT is a safe treatment option associated with long-term cure in select patients. Immunotherapy consolidation was associated with improved clinical outcomes.

Keywords: Chemoimmunotherapy; Intrathoracic recurrence; Locoregional failure; Non-small cell lung cancer; Reirradiation.

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Conflict of interest statement

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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