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MRI-based patient selection for active surveillance in prostate cancer using U-Found: a generalized deep learning model.

Cancer imaging : the official publication of the International Cancer Imaging Society 2026 Vol.26(1) p. 26

Lowry NC, Breto AL, Wallaengen V, Algohary A, Tapia-Stoll N, Gaston SM, Prakash NS, Freitas PFS, Kryvenko ON, Castillo P, Saltz J, Kurc T, Ritch CR, Nahar B, Gonzalgo ML, Parekh DJ, Mahal B, Spieler BO, Pra AD, Abramowitz MC, Pollack A, Punnen S, Stoyanova R

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[BACKGROUND] Current MRI prostate cancer risk assessment methods focus mainly on detecting tumor lesions, ignoring the prostate gland macro-environment which may also impact disease progression.

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BibTeX ↓ RIS ↓
APA Lowry NC, Breto AL, et al. (2026). MRI-based patient selection for active surveillance in prostate cancer using U-Found: a generalized deep learning model.. Cancer imaging : the official publication of the International Cancer Imaging Society, 26(1), 26. https://doi.org/10.1186/s40644-026-00988-z
MLA Lowry NC, et al.. "MRI-based patient selection for active surveillance in prostate cancer using U-Found: a generalized deep learning model.." Cancer imaging : the official publication of the International Cancer Imaging Society, vol. 26, no. 1, 2026, pp. 26.
PMID 41555464

Abstract

[BACKGROUND] Current MRI prostate cancer risk assessment methods focus mainly on detecting tumor lesions, ignoring the prostate gland macro-environment which may also impact disease progression. A generalized deep-learning model for prostate may help capture these gland-level characteristics through deep embeddings which can be used for a variety of downstream tasks. This study aims to assess whether U-Found, a generalized multiparametric (mp)MRI-based model, offers added value in predicting histopathological progression in active surveillance (AS) patients. The prostate macro-environment, captured in U-Found embeddings, is hypnotized to play a significant role in differentiating patients who progress to definitive treatment from those whose tumor is kept at bay.

[METHODS] U-Found was trained on a dataset comprising over 3000 mpMRIs from in-house and public sources using self-supervised learning. Axial slices were represented in a 128-dimentional space. The physical interpretation of the embeddings was explored by investigating images that are closest to the centroid of embeddings clusters. U-Found was tested on a downstream task: identifying cancer in an independent dataset (publicly available UCLA dataset,  = 1,151). To determine the added value of U-Found embeddings to clinical and intratumoral radiomics features, we compared models for predicting histopathological progression in 144 participants of a prospective AS trial. In addition, associations between U-Found embeddings and lesion- and prostate radiomics were investigated.

[RESULTS] Our findings suggest that U-Found captures key characteristics of the prostate gland’s macro-environment. U-Found successfully detected cancer in an independent UCLA dataset without being explicitly trained for lesion detection (AUC = 0.79). The prediction model incorporating a combination of clinical variables, mpMRI-derived intratumoral radiomics features and deep embeddings generated by U-Found achieved AUC = 0.86, outperforming models solely based on clinical and/or radiomics features. There were clear associations between U-Found embeddings and radiomics features.

[CONCLUSIONS] U-Found was designed as a generalized self-supervised foundation model for prostate imaging, enabling the model to learn intrinsic imaging structures. We demonstrate that U-Found embeddings capture key features of the prostate macro-environment, which appear to contribute to disease progression, albeit to a lesser extent than tumor-specific imaging features.