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A Novel Model for Predicting Microsatellite Instability in Endometrial Cancer: Integrating Deep Learning-Pathomics and MRI-Based Radiomics. | LitMetric

A Novel Model for Predicting Microsatellite Instability in Endometrial Cancer: Integrating Deep Learning-Pathomics and MRI-Based Radiomics.

Acad Radiol

Zhejiang Key Laboratory of Imaging and Interventional Medicine, Lishui Hospital, School of Medicine, Zhejiang University, No 289, Kuocang Road, Lishui 323000, China (L.Z., L.Z., Y.H., Z.W., X.G., Z.Z., M.X., C.L., M.C., J.J.); Department of Radiology, Lishui Central Hospital, the Fifth Affiliated Ho

Published: August 2025


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Article Abstract

Rationale And Objectives: To develop and validate a novel model based on multiparametric MRI (mpMRI) and whole slide images (WSIs) for predicting microsatellite instability (MSI) status in endometrial cancer (EC) patients.

Materials And Methods: A total of 136 surgically confirmed EC patients were included in this retrospective study. Patients were randomly divided into a training set (96 patients) and a validation set (40 patients) in a 7:3 ratio. Deep learning with ResNet50 was used to extract deep-learning pathomics features, while Pyradiomics was applied to extract radiomics features specifically from sequences including T2-weighted imaging (T2WI), diffusion-weighted imaging (DWI), and late arterial phase (AP). we developed a deep learning pathoradiomics model (DLPRM) by multilayer perceptron (MLP) based on radiomics features and pathomics features. Furthermore, we validated the DLPRM comprehensively, and compared it with two single-scale signatures-including the area under the receiver operating characteristic (ROC) curve, accuracy, sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and F1-score. Finally, we employed shapley additive explanations (SHAP) to elucidate the mechanism of prediction model.

Results: After undergoing feature selection, a final set of nine radiomics features and 27 pathomics features were selected to construct the radiomics signature (RS) and the deep learning pathomics signature (DLPS). The DLPRM combining the RS and DLPS had favorable performance for the prediction of MSI status in the training set (AUC 0.960 [95% CI 0.936-0.984]), and in the validation set (AUC 0.917 [95% CI 0.824-1.000]). The AUCs of DLPS and RS ranged from 0.817 to 0.943 across the training and validation sets. The decision curve analysis indicated the DLPRM had relatively higher clinical net benefits.

Conclusion: DLPRM can effectively predict MSI status in EC patients based on pretreatment pathoradiomics images with high accuracy and robustness, could provide a novel tool to assist clinicians in individualized management of EC.

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Source
http://dx.doi.org/10.1016/j.acra.2025.07.050DOI Listing

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