Comparative outcomes of treatment with versus without definitive thoracic radiotherapy in locally advanced inoperable non-small cell lung cancer during the immunotherapy era: a Chinese real-world study.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
[RESULTS] Among 410 eligible patients, 173 received RT (RT group), while 237 underwent chemoimmunotherapy (CIT) alone (non-RT group).
I · Intervention 중재 / 시술
RT (RT group), while 237 underwent chemoimmunotherapy (CIT) alone (non-RT group)
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
An exploratory analysis suggests that a potential strategy could involve ≤4 cycles of CIT induction followed by concurrent CRT (cCRT) and immune checkpoint inhibitor maintenance. These findings encourage further investigation into RT integration within multimodal treatment, with 50-60 Gy appearing potentially comparable in selected patients.
[BACKGROUND] The heterogeneity of locally advanced non-small cell lung cancer (LA-NSCLC) has led to varied treatment strategies.
- p-value P<0.001
- p-value P=0.04
APA
Zhu X, Liu J, et al. (2025). Comparative outcomes of treatment with versus without definitive thoracic radiotherapy in locally advanced inoperable non-small cell lung cancer during the immunotherapy era: a Chinese real-world study.. Translational lung cancer research, 14(10), 4398-4411. https://doi.org/10.21037/tlcr-2025-701
MLA
Zhu X, et al.. "Comparative outcomes of treatment with versus without definitive thoracic radiotherapy in locally advanced inoperable non-small cell lung cancer during the immunotherapy era: a Chinese real-world study.." Translational lung cancer research, vol. 14, no. 10, 2025, pp. 4398-4411.
PMID
41234562
Abstract
[BACKGROUND] The heterogeneity of locally advanced non-small cell lung cancer (LA-NSCLC) has led to varied treatment strategies. Before the immunotherapy era, definitive chemoradiotherapy (CRT) was the standard for inoperable patients. This real-world study evaluates the role of thoracic radiotherapy (RT) in patients receiving first-line immunotherapy-based treatment.
[METHODS] This retrospective analysis included stage III NSCLC patients from January 2018 to December 2022 who were inoperable or declined surgery and received immunotherapy. Treatment patterns, survival outcomes, and failure modes were assessed. Real-world overall survival (OS), progression-free survival (PFS), and local recurrence-free survival (LRFS) were analyzed using Kaplan-Meier methods.
[RESULTS] Among 410 eligible patients, 173 received RT (RT group), while 237 underwent chemoimmunotherapy (CIT) alone (non-RT group). The RT group demonstrated significantly longer median OS (55.5 26.6 months) and PFS (21.3 14.1 months) compared to the non-RT group (P<0.001). Patients receiving ≤4 CIT induction cycles before RT had improved outcomes versus >4 cycles (P=0.04). No survival difference was observed between RT doses of 50 Gy and 60 Gy.
[CONCLUSIONS] This study confirms that thoracic RT remains essential for inoperable LA-NSCLC in the immunotherapy era. An exploratory analysis suggests that a potential strategy could involve ≤4 cycles of CIT induction followed by concurrent CRT (cCRT) and immune checkpoint inhibitor maintenance. These findings encourage further investigation into RT integration within multimodal treatment, with 50-60 Gy appearing potentially comparable in selected patients.
[METHODS] This retrospective analysis included stage III NSCLC patients from January 2018 to December 2022 who were inoperable or declined surgery and received immunotherapy. Treatment patterns, survival outcomes, and failure modes were assessed. Real-world overall survival (OS), progression-free survival (PFS), and local recurrence-free survival (LRFS) were analyzed using Kaplan-Meier methods.
[RESULTS] Among 410 eligible patients, 173 received RT (RT group), while 237 underwent chemoimmunotherapy (CIT) alone (non-RT group). The RT group demonstrated significantly longer median OS (55.5 26.6 months) and PFS (21.3 14.1 months) compared to the non-RT group (P<0.001). Patients receiving ≤4 CIT induction cycles before RT had improved outcomes versus >4 cycles (P=0.04). No survival difference was observed between RT doses of 50 Gy and 60 Gy.
[CONCLUSIONS] This study confirms that thoracic RT remains essential for inoperable LA-NSCLC in the immunotherapy era. An exploratory analysis suggests that a potential strategy could involve ≤4 cycles of CIT induction followed by concurrent CRT (cCRT) and immune checkpoint inhibitor maintenance. These findings encourage further investigation into RT integration within multimodal treatment, with 50-60 Gy appearing potentially comparable in selected patients.
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