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Machine learning-based differentiation of benign and malignant adrenal lesions using 18F-FDG PET/CT: a two-stage
Yun Wang1, Yuqi Su1,2, Jing Li3
1Department of Nuclear Medicine, Zhejiang Cancer Hospital, Hangzhou, Zhejiang, 310022, China.
Background:
Accurately distinguishing benign from malignant adrenal lesions remains a clinical challenge, especially in oncology patients with indeterminate imaging findings. This study aimed to develop and interpret machine learning (ML) models for classifying adrenal lesions based on 18 F-FDG PET/CT imaging and clinical parameters.
Methods:
A retrospective cohort of 255 patients undergoing 18 F-FDG PET/CT was analyzed. Imaging features-including adrenal SUVmax, SUVpeak, tumor diameter, CT attenuation, and tumor-to-liver SUVmax ratio (T/L SUVmax)-along with clinical variables were extracted. Two classification tasks were constructed: (1) differentiation of benign and malignant adrenal lesions; and (2) subtyping of malignant lesions into lung cancer metastases or lymphoma. Seven ML models were trained and evaluated using 10-fold cross-validation. SHAP (SHapley Additive exPlanations) analysis was applied to elucidate feature contributions.
Results:
For the benign/malignant classification, ensemble models (Random Forest, Bagging, XGBoost) achieved outstanding performance (AUC > 0.99), with Bagging yielding 100% recall. T/L SUVmax, adrenal SUVmax, and CT attenuation emerged as top predictors. In malignancy subtyping, the artificial neural network (ANN) attained the highest AUC (0.887) and F1-score (0.851). SHAP analysis highlighted distinct metabolic patterns, with lymphoma showing higher SUVmax and T/L ratios, and lung metastases associated with higher CT values.
Conclusion:
Machine learning models based on PET/CT-derived features enable highly accurate and interpretable classification of adrenal lesions. Integrating metabolic and anatomical parameters improves diagnostic precision, while SHAP analysis offers clinical transparency, supporting personalized decision-making in adrenal lesion management.
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