Prediction of EGFR mutation status and mutation sites in lung cancer based on radiomics and deep learning.

Background: Epidermal growth factor receptor (EGFR) mutations are regarded as key predictors for the efficacy of EGFR-tyrosine kinase inhibitors (TKIs), with exon 19 mutations demonstrating a better prognosis compared to exon 21 mutations. Therefore, accurate identification of EGFR mutations and their specific loci (e.g., exon 19 Methods: We retrospectively analyzed clinical and imaging data from 557 NSCLC patients who underwent EGFR genotyping. Radiomics features were extracted from computed tomography (CT) images, and machine learning models, including support vector machine (SVM) and logistic regression (LR), were developed for mutation prediction. Deep learning architectures (ResNet-18 and DenseNet-121) were further employed to extract high-dimensional features from CT images. A combined model integrating radiomics, deep learning, and clinical data was constructed to predict EGFR mutation status and mutation subtypes. Results: The combined model achieved superior performance in predicting EGFR mutation status [area under the curve (AUC): 91.1%, accuracy: 85.6%] and specific mutation sites (AUC: 93.6%, accuracy: 89.9%). Compared to radiomics models, the combined model demonstrated statistically significant improvements (P<0.05). Calibration and decision curve analyses confirmed the clinical applicability of the models in patient stratification and personalized treatment planning. Conclusions: The integration of radiomics and deep learning offers a non-invasive, accurate method for predicting EGFR mutations and subtypes in NSCLC. This integrated approach demonstrates significant potential to optimize clinical decision-making and enable personalized treatment regimens in NSCLC management.