Impact of radiation dose to immune cells on survival in patients with extensive-stage small cell lung cancer receiving consolidative thoracic radiotherapy after chemoimmunotherapy.
1/5 보강
[BACKGROUND] Consolidative thoracic radiotherapy (RT) following chemo-immunotherapy is increasingly used in extensive-stage small cell lung cancer (ES-SCLC).
- HR 0.56
APA
Feng C, Wang K, et al. (2026). Impact of radiation dose to immune cells on survival in patients with extensive-stage small cell lung cancer receiving consolidative thoracic radiotherapy after chemoimmunotherapy.. Future oncology (London, England), 22(2), 217-227. https://doi.org/10.1080/14796694.2025.2609972
MLA
Feng C, et al.. "Impact of radiation dose to immune cells on survival in patients with extensive-stage small cell lung cancer receiving consolidative thoracic radiotherapy after chemoimmunotherapy.." Future oncology (London, England), vol. 22, no. 2, 2026, pp. 217-227.
PMID
41466536 ↗
Abstract 한글 요약
[BACKGROUND] Consolidative thoracic radiotherapy (RT) following chemo-immunotherapy is increasingly used in extensive-stage small cell lung cancer (ES-SCLC). This study investigates the prognostic value of the estimated radiation dose to immune cells (EDRIC) and its determinants in these patients.
[METHODS] This retrospective study included 173 ES-SCLC patients between 2020 and 2023. EDRIC was calculated as a function of the number of fractions and the average doses to the lungs, heart, and remaining body. Kaplan-Meier and Cox regression analyses were performed to evaluate overall survival (OS) and progression-free survival (PFS).
[RESULTS] GTV, PTV, and N stage were positively correlated with EDRIC (r = 0.2577, = 0.0006; r = 0.3541, < 0.01; r = 0.2259, = 0.0028), while lymphocyte nadir was negatively correlated (r = -0.2190, = 0.0038). Median OS and PFS were longer in the EDRIC ≤4.68 Gy group (OS: 24.9 vs. 17.4 months, = 0.003; PFS: 12.4 vs. 10.1 months, = 0.038). Patients in the EDRIC ≤4.68 Gy group had significantly better OS (HR = 0.56, = 0.003) and PFS (HR = 0.68, = 0.039). Bone metastasis was associated with worse OS (HR = 1.88, = 0.002), and liver metastasis with shorter PFS (HR = 2.05, = 0.001).
[CONCLUSIONS] EDRIC is an independent predictor of OS and PFS in ES-SCLC. These findings highlight the need to optimize radiation exposure to the immune system in cancer treatment.
[METHODS] This retrospective study included 173 ES-SCLC patients between 2020 and 2023. EDRIC was calculated as a function of the number of fractions and the average doses to the lungs, heart, and remaining body. Kaplan-Meier and Cox regression analyses were performed to evaluate overall survival (OS) and progression-free survival (PFS).
[RESULTS] GTV, PTV, and N stage were positively correlated with EDRIC (r = 0.2577, = 0.0006; r = 0.3541, < 0.01; r = 0.2259, = 0.0028), while lymphocyte nadir was negatively correlated (r = -0.2190, = 0.0038). Median OS and PFS were longer in the EDRIC ≤4.68 Gy group (OS: 24.9 vs. 17.4 months, = 0.003; PFS: 12.4 vs. 10.1 months, = 0.038). Patients in the EDRIC ≤4.68 Gy group had significantly better OS (HR = 0.56, = 0.003) and PFS (HR = 0.68, = 0.039). Bone metastasis was associated with worse OS (HR = 1.88, = 0.002), and liver metastasis with shorter PFS (HR = 2.05, = 0.001).
[CONCLUSIONS] EDRIC is an independent predictor of OS and PFS in ES-SCLC. These findings highlight the need to optimize radiation exposure to the immune system in cancer treatment.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Small Cell Lung Carcinoma
- Male
- Female
- Lung Neoplasms
- Middle Aged
- Aged
- Retrospective Studies
- Neoplasm Staging
- Prognosis
- Radiotherapy Dosage
- 80 and over
- Adult
- Chemoradiotherapy
- Immunotherapy
- Kaplan-Meier Estimate
- Extensive-stage small cell lung cancer
- estimated dose of radiation to immune cells
- immunology
- lymphocyte nadir
- survival
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