Juemin Yu , Xinchen Shen , Jialiang Wen , Tao Chen, Yunlang She, Deping Zhao, Chang Chen, Jiajun Deng
{"title":"Prognostic impact and characteristics of ROS1 fusion in patients with surgically resected lung adenocarcinoma","authors":"Juemin Yu , Xinchen Shen , Jialiang Wen , Tao Chen, Yunlang She, Deping Zhao, Chang Chen, Jiajun Deng","doi":"10.1016/j.lungcan.2025.108743","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>We aimed to investigate the prognostic significance of <em>ROS1</em> fusion in surgically resected lung adenocarcinoma (LUAD).</div></div><div><h3>Materials and methods</h3><div>Consecutive patients who underwent complete resection and <em>ROS1</em> testing between 2015 and 2020 were included. Propensity score matching (1:2) was applied to balance baseline characteristics. Disease-free survival (DFS), overall survival (OS), and cumulative incidence of recurrence (CIR) were compared overall and by TNM stage. Recurrence patterns and post-recurrence survival (PRS) in <em>ROS1</em> fusion-positive patients were also analyzed.</div></div><div><h3>Results</h3><div>Overall, 16,779 patients met the inclusion criteria (216 <em>ROS1</em> fusion-positive and 16,563 <em>ROS1</em> fusion-negative). After matching, 216 <em>ROS1</em> fusion-positive and 432 <em>ROS1</em> fusion-negative patients were included in survival analysis. In the overall cohort, the <em>ROS1</em> fusion-positive group had similar DFS (5-year: 72.7 % vs. 66.4 %; p = 0.074) and OS (5-year: 87.6 % vs. 80.7 %; p = 0.055) compared with the<!--> <em>ROS1</em> <!-->fusion-negative group. Subgroup analysis showed that <em>ROS1</em> fusion was associated with better DFS (hazard ratio [HR], 0.609; 95 % confidence interval [CI], 0.376–0.986; p = 0.043) and OS (HR, 0.481; 95 % CI, 0.242–0.958; p = 0.037) in stage I, with similar outcomes in stages II–III. In addition, recurrence patterns and CIR analyses were consistent with these findings. Among patients who experienced recurrence, ROS1 tyrosine kinase inhibitors (TKIs) significantly improved PRS (median PRS: 65 vs. 20 months; p < 0.001). In multivariate Cox regression analysis, ROS1-TKI therapy remained an independent protective factor for PRS (HR = 0.259; 95 % CI, 0.103–0.647; p = 0.004).</div></div><div><h3>Conclusion</h3><div><em>ROS1</em> fusion was associated with better prognosis in stage I LUAD, and ROS1-TKI therapy conferred a survival advantage after recurrence.</div></div>","PeriodicalId":18129,"journal":{"name":"Lung Cancer","volume":"208 ","pages":"Article 108743"},"PeriodicalIF":4.4000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lung Cancer","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S016950022500635X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
We aimed to investigate the prognostic significance of ROS1 fusion in surgically resected lung adenocarcinoma (LUAD).
Materials and methods
Consecutive patients who underwent complete resection and ROS1 testing between 2015 and 2020 were included. Propensity score matching (1:2) was applied to balance baseline characteristics. Disease-free survival (DFS), overall survival (OS), and cumulative incidence of recurrence (CIR) were compared overall and by TNM stage. Recurrence patterns and post-recurrence survival (PRS) in ROS1 fusion-positive patients were also analyzed.
Results
Overall, 16,779 patients met the inclusion criteria (216 ROS1 fusion-positive and 16,563 ROS1 fusion-negative). After matching, 216 ROS1 fusion-positive and 432 ROS1 fusion-negative patients were included in survival analysis. In the overall cohort, the ROS1 fusion-positive group had similar DFS (5-year: 72.7 % vs. 66.4 %; p = 0.074) and OS (5-year: 87.6 % vs. 80.7 %; p = 0.055) compared with the ROS1 fusion-negative group. Subgroup analysis showed that ROS1 fusion was associated with better DFS (hazard ratio [HR], 0.609; 95 % confidence interval [CI], 0.376–0.986; p = 0.043) and OS (HR, 0.481; 95 % CI, 0.242–0.958; p = 0.037) in stage I, with similar outcomes in stages II–III. In addition, recurrence patterns and CIR analyses were consistent with these findings. Among patients who experienced recurrence, ROS1 tyrosine kinase inhibitors (TKIs) significantly improved PRS (median PRS: 65 vs. 20 months; p < 0.001). In multivariate Cox regression analysis, ROS1-TKI therapy remained an independent protective factor for PRS (HR = 0.259; 95 % CI, 0.103–0.647; p = 0.004).
Conclusion
ROS1 fusion was associated with better prognosis in stage I LUAD, and ROS1-TKI therapy conferred a survival advantage after recurrence.
期刊介绍:
Lung Cancer is an international publication covering the clinical, translational and basic science of malignancies of the lung and chest region.Original research articles, early reports, review articles, editorials and correspondence covering the prevention, epidemiology and etiology, basic biology, pathology, clinical assessment, surgery, chemotherapy, radiotherapy, combined treatment modalities, other treatment modalities and outcomes of lung cancer are welcome.