AUTHOR=You Shuailin , Fan Ying , Yang Zhiguang , Yang Chunna , Sun Yiyao , Luo Yahong , Wang Zekun , Sun Bo , Jiang Wenyan 

TITLE=Deep learning on brain metastasis for predicting EGFR genotype and EGFR-TKI therapy response in metastatic NSCLC: a multicenter study

JOURNAL=Frontiers in Bioengineering and Biotechnology

VOLUME=Volume 13 - 2025

YEAR=2025

URL=https://www.frontiersin.org/journals/bioengineering-and-biotechnology/articles/10.3389/fbioe.2025.1637095

DOI=10.3389/fbioe.2025.1637095

ISSN=2296-4185

ABSTRACT=BackgroundBrain metastases are common in patients with advanced non-small cell lung cancer (NSCLC), particularly those harboring EGFR mutations, and accurate prediction of EGFR mutation status and therapeutic response is crucial for guiding targeted therapy. This study aims to conduct a deep learning (DL) approach to automatically predict epidermal growth factor receptor (EGFR) genotype and response to EGFR-tyrosine kinase inhibitor (TKI) therapy in NSCLC patients with brain metastatic tumor (BM).MethodsFor training and validating the DL models, 388 patients were enrolled from three centers between Jul. 2014 and Dec.2022 (230 from center 1, 80 from center 2 and 78 from center 3). Contrast-enhanced T1-weighted (T1CE) and T2-weighted (T2W) brain MRI images before treatment for each patient were obtained for analyses. We developed an EGFR-TKI system (ETS) for automated detection of brain metastatic (BM) lesions and to differentiate EGFR mutation status and predict response to EGFR-TKI therapy. The models underwent rigorous evaluation through receiver operating characteristic (ROC) curve analyses, where metrics such as area under the curve (AUC), sensitivity, and specificity were examined.ResultsFor prediction of EGFR mutation status, the ETS integrating radiological-based features and clinical factors achieved AUCs of 0.842, 0.833 and 0.832 on the internal validation, external validation 1 and external validation 2 cohort, respectively. For forecasting response to EGFR-TKI therapy, the fusion model created by amalgamating MRI with clinical factors generated AUCs of 0.747, 0.726 and 0.728 on the internal validation, external validation 1, and external validation 2 cohort, respectively.ConclusionThe ETS may have the potential to work as a non-invasive tool for predicting EGFR mutation status and response to EGFR-TKI therapy, which holds promise as a non-invasive tool to assist clinicians in making decisions about personalized treatment strategies.