3.8

CiteScore

2.4

Impact Factor
  • ISSN 1674-8301
  • CN 32-1810/R
Ruozhou Sun, Dan Zong, Xin Chen, Yizhi Ge, Ning Jiang, Lijun Zhao, Xue Song, Xia He, Xiangzhi Zhu. The effect and toxicity profile of consolidative or salvage thoracic radiotherapy following chemoimmunotherapy in patients with extensive-stage small cell lung cancer[J]. The Journal of Biomedical Research. DOI: 10.7555/JBR.39.20250067
Citation: Ruozhou Sun, Dan Zong, Xin Chen, Yizhi Ge, Ning Jiang, Lijun Zhao, Xue Song, Xia He, Xiangzhi Zhu. The effect and toxicity profile of consolidative or salvage thoracic radiotherapy following chemoimmunotherapy in patients with extensive-stage small cell lung cancer[J]. The Journal of Biomedical Research. DOI: 10.7555/JBR.39.20250067

The effect and toxicity profile of consolidative or salvage thoracic radiotherapy following chemoimmunotherapy in patients with extensive-stage small cell lung cancer

  • The present study assessed the efficacy and safety of thoracic radiotherapy (TRT) following first-line chemotherapy or chemoimmunotherapy in patients with extensive-stage small cell lung cancer (ES-SCLC), focusing on the influence of different TRT timing strategies (consolidative vs. salvage) on survival rates. We retrospectively analyzed a total of 54 ES-SCLC patients treated between January 2019 and July 2022. Patients receiving consolidative TRT (cTRT) within three months after first-line treatment completion were compared with those receiving salvage TRT (sTRT) following disease progression. The primary endpoints were overall survival (OS), progression-free survival (PFS), locoregional-free survival (LRFS), and distant metastasis-free survival (DMFS); the secondary endpoint included safety. The cTRT group (n = 41) showed significantly longer median OS (26.6 vs. 14.8 months, P = 0.048), PFS (12.9 vs. 3.5 months, P < 0.0001), and DMFS (10.7 vs. 3.4 months, P = 0.0044) than the sTRT group (n = 13). Multivariate analysis revealed cTRT as an independent favorable prognostic factor. No significant differences in OS or LRFS were observed between high-dose (≥ 50 Gy) and low-dose (< 50 Gy) TRT. Hematologic and respiratory toxicities were the most frequently reported adverse events, with acceptable tolerability. In conclusion, cTRT after chemoimmunotherapy significantly improves survival outcomes for ES-SCLC patients, and low-dose TRT may be a suitable option.
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