A radiomics-based machine learning model for the preoperative differentiation of lung adenocarcinoma subtypes.
Authors
Affiliations (4)
Affiliations (4)
- Department of Radiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
- Department of Radiology, Tongde Hospital of Zhejiang Province Affiliated to Zhejiang Chinese Medical University (Tongde Hospital of Zhejiang Province), Hangzhou, China.
- Department of Radiology, Taizhou Municipal Hospital, Taizhou, China.
- Department of Radiology, Anqing Municipal Hospital, Anqing, China.
Abstract
The preoperative differentiation of lung adenocarcinoma subtypes is critical for implementing personalized treatment but is difficult to accomplish with conventional imaging. This study aimed to develop an interpretable multimodal model integrating clinical, peritumoral, radiomic, and deep learning features to improve diagnostic accuracy. A total of 3,038 patients from four hospitals were divided into training (n=1,822), test (n=608), and validation (n=608) sets. Two radiologists manually segmented two-dimensional tumor regions on computed tomography using ITK-SNAP software. After Pearson correlation analysis and least absolute shrinkage and selection operator regression, the radiomic score and deep learning score were generated. Clinical features were selected via univariate analysis, the Boruta algorithm, and recursive feature elimination (RFE). Individual logistic models were built and fused with the optimal combination selected via support vector machine-synthetic minority oversampling technique and extreme gradient boosting. Performance was evaluated in terms of the Obuchowski index, accuracy, F1-score, calibration, and decision curves, while interpretability was assessed via Shapley additive explanations (SHAP) and individual conditional expectation (ICE). The fused model achieved Obuchowski indices of 0.85 [95% confidence interval (CI): 0.84-0.87], 0.81 (95% CI: 0.78-0.83), and 0.79 (95% CI: 0.76-0.81) in the training, test, and validation sets, respectively outperforming the single-modality models. The F1-scores for the lepidic, acinar/papillary, and solid/micropapillary subtypes, respectively, were 0.77, 0.61, and 0.63 in the training set; 0.72, 0.57, and 0.59 in the test set; and 0.74, 0.54, and 0.52 in the validation set. Calibration and decision curve analysis confirmed the robustness and clinical utility of the model. SHAP analysis identified ResNet-101 feature as the best predictor, followed by peritumoral radiomic score, and lobulation. ICE plots revealed the linear and monotonic relationships between key features and predicted probabilities across subtypes. The radiomics model developed in this study facilitates the accurate and interpretable preoperative classification of lung adenocarcinoma subtypes. Fusion of clinical, peritumoral, and deep learning features enhances diagnostic performance and supports clinical decision-making.