ArticleQuantitative imaging in medicine and surgery2025
Predicting pathogenic DNA damage repair gene mutations in prostate cancer patients: a multi-center magnetic resonance imaging radiomics study.
Article in Quantitative imaging in medicine and surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Biomarkers for Precision Prognosis in Prostate Cancer: Imaging, Molecular, and Integrated Approaches.Cancers · 2026Review
- Review
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Authors and funding
25 authors.
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Abstract
Background: Genetic testing for pathogenic DNA damage repair gene (pDDRg) mutations has clinical benefits for prostate cancer (PCa) patients, but its real-world application faces challenges due to its high associated costs. We sought to develop a magnetic resonance imaging (MRI)-based radiomics model capable of assessing the likelihood of PCa patients harboring pDDRg mutations. We then rigorously validated its predictive value in two external validation cohorts. Methods: A total of 225 patients with both multiparametric MRI data before prostate biopsy and genetic testing information for pDDRg mutations were included in this study. The radiomics features were extracted from the T2-weighted imaging (T2WI) and apparent diffusion coefficient (ADC) sequences of the MRI images in the training cohort (N=101) using the least absolute shrinkage and selection operator (LASSO) algorithm. The area under the curve (AUC) values of the receiver operating characteristic (ROC) curves and a decision curve analysis (DCA) were used to validate the predictive value of the model in both the internal (N=41) and external (N=83) validation cohorts. Results: In total, 48 of the 225 (21.3%) patients in our cohort were identified by genetic testing as having positive pDDRg mutations, including Conclusions: Our MRI radiomics-based predictive model is a promising pre-testing tool for pDDRg mutation prediction in patients with PCa. Prospective studies need to be conducted to further validate the power of this predictive model before its clinical application.
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