Comparison of concurrent chemoradiotherapy followed by immunotherapy and induction chemoimmunotherapy followed by radiotherapy in unresectable stage III NSCLC: a retrospective cohort study.
[BACKGROUND] Concurrent chemoradiotherapy followed by immune consolidation therapy (cCRT+IO, the PACIFIC regimen) is the standard treatment for unresectable stage III non-small cell lung cancer (NSCLC
- p-value p = 0.031
- p-value p = 0.046
- 95% CI 0.45-0.97
APA
Xu Q, Qi Y, et al. (2026). Comparison of concurrent chemoradiotherapy followed by immunotherapy and induction chemoimmunotherapy followed by radiotherapy in unresectable stage III NSCLC: a retrospective cohort study.. Future oncology (London, England), 22(7), 819-829. https://doi.org/10.1080/14796694.2026.2637732
MLA
Xu Q, et al.. "Comparison of concurrent chemoradiotherapy followed by immunotherapy and induction chemoimmunotherapy followed by radiotherapy in unresectable stage III NSCLC: a retrospective cohort study.." Future oncology (London, England), vol. 22, no. 7, 2026, pp. 819-829.
PMID
41760405
Abstract
[BACKGROUND] Concurrent chemoradiotherapy followed by immune consolidation therapy (cCRT+IO, the PACIFIC regimen) is the standard treatment for unresectable stage III non-small cell lung cancer (NSCLC). However, the optimal timing of combining radiotherapy with immunotherapy remains unexplored. This study compared the efficacy and safety of induction chemoimmunotherapy followed by radiotherapy (ICT+RT) with cCRT+IO.
[METHODS] This study included patients with unresectable stage III NSCLC who received cCRT+IO or ICT+RT between January 2021 and August 2023. Efficacy outcomes and safety profiles were assessed.
[RESULTS] A total of 183 eligible patients were enrolled; 108 (59.0%) received cCRT+IO, and 75 (41.0%) received ICT+RT. The median progression-free survival (PFS) was 26.8 months in the cCRT+IO group and 16.4 months in the ICT+RT group (hazard ratio [HR] 0.66; 95%CI 0.45-0.97; p = 0.031). The median overall survival (OS) was 45.4 months in the cCRT+IO group and was not reached in the ICT+RT group (HR 0.57, 95%CI 0.32-0.99; p = 0.046). In the cCRT+IO group, the incidence of grade 3 pneumonitis was 6.48%, whereas it was 13.33% in the ICT+RT group (p = 0.116).
[CONCLUSION] Compared with ICT+RT, cCRT+IO demonstrated superior efficacy with a manageable safety profile in unresectable stage III NSCLC.
[METHODS] This study included patients with unresectable stage III NSCLC who received cCRT+IO or ICT+RT between January 2021 and August 2023. Efficacy outcomes and safety profiles were assessed.
[RESULTS] A total of 183 eligible patients were enrolled; 108 (59.0%) received cCRT+IO, and 75 (41.0%) received ICT+RT. The median progression-free survival (PFS) was 26.8 months in the cCRT+IO group and 16.4 months in the ICT+RT group (hazard ratio [HR] 0.66; 95%CI 0.45-0.97; p = 0.031). The median overall survival (OS) was 45.4 months in the cCRT+IO group and was not reached in the ICT+RT group (HR 0.57, 95%CI 0.32-0.99; p = 0.046). In the cCRT+IO group, the incidence of grade 3 pneumonitis was 6.48%, whereas it was 13.33% in the ICT+RT group (p = 0.116).
[CONCLUSION] Compared with ICT+RT, cCRT+IO demonstrated superior efficacy with a manageable safety profile in unresectable stage III NSCLC.
MeSH Terms
Humans; Carcinoma, Non-Small-Cell Lung; Female; Male; Middle Aged; Chemoradiotherapy; Lung Neoplasms; Retrospective Studies; Aged; Neoplasm Staging; Immunotherapy; Adult; Induction Chemotherapy; Antineoplastic Combined Chemotherapy Protocols; Treatment Outcome
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