Interpretable LightGBM model with SHAP analysis predicts non‐excellent response to initial radioiodine therapy in differentiated thyroid carcinoma
Year: 2026
Type: article
Study design: Observational Study
Abstract: PURPOSE: I) therapy in differentiated thyroid carcinoma (DTC) and establish an interpretable predictive framework for clinical decision-making. MATERIALS AND METHODS: I therapy was randomly allocated into training (n = 664) and testing (n = 286) cohorts. Multivariable logistic regression (LR) analysis identified response-associated variables, followed by the development of seven machine learning (ML) architectures including decision trees (DT), LR, random forests (RF), support vector machines (SVM), adaptive boosting (AdaBoost), eXtreme gradient boosting (XGBoost), and light gradient boosting machine (LightGBM). Model performance was systematically evaluated through ROC curves (AUC), calibration plots, and decision curve analysis (DCA), complemented by SHapley Additive exPlanationgs (SHAP) interpretability framework for optimal model explanation. RESULTS: I therapeutic interval (TI), tumor multiplicity, maximum tumor diameter (MTD), lymph node metastasis (LNM) topography, stimulated thyroglobulin (sTg), thyroglobulin antibody (TgAb) levels, administered activity (AA), and post-therapy whole-body scan (Rx-WBS) findings as independent predictors of non-excellent response (N-ER).The LightGBM architecture achieved superior predictive accuracy (AUC = 0.896) in the testing cohort, outperforming conventional LR (AUC = 0.842).SHAP interpretation identified sTg (mean absolute SHAP value = 1.285), TgAb (mean absolute SHAP value = 0.642), and LNM topography (mean absolute SHAP value = 0.308) as principal predictive determinants. DCA confirmed that the model had a net benefit higher than the "full treatment" and "no treatment" strategies at multiple threshold probabilities, indicating its certain application value in clinical decision-making. CONCLUSION: I therapeutic efficacy in DTC patients, with SHAP-driven elucidation of clinical risk factor contributions enabling personalized therapeutic paradigms.Future integration of multicenter prospective data and molecular biomarkers is required to enhance model generalizability.
DOI: 10.1002/acm2.70555
Authors: Zhaoxia Luo, Yangyang Lei, Qing Zhang
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $900
Awards: G3523411110, G7598083677
OpenAlex ID: W7141263984
