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Discovery of tumour indicating morphological changes in benign prostate biopsies through AI
Department of Information Technology and SciLifeLab, Uppsala University, Uppsala, Sweden.
Department of Information Technology and SciLifeLab, Uppsala University, Uppsala, Sweden.
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Pathology.ORCID iD: 0009-0002-0666-8952
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Pathology.
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2025 (English)In: Scientific Reports, E-ISSN 2045-2322, Vol. 15, no 1, article id 30770Article in journal (Refereed) Published
Abstract [en]

Diagnostic needle biopsies that miss clinically significant prostate cancer (PCa) often sample benign tissue near hidden cancers. Such benign samples might still display subtle morphological signs of cancer elsewhere in the prostate. This study examined if artificial intelligence (AI) could detect these morphological clues in benign biopsies from men with elevated prostate-specific antigen (PSA) levels to predict subsequent diagnosis of clinically significant PCa within 30 months. We analysed biopsies from 232 men initially diagnosed as benign, matched for age, diagnosis year, and PSA levels-half were later diagnosed with PCa, while the rest remained cancer-free for at least eight years. The AI model accurately predicted future PCa diagnosis from initial benign biopsies (AUC = 0.82), highlighting patterns such as changes in stromal collagen and altered glandular epithelial cells. This demonstrates that AI analysis of routine haematoxylin-eosin biopsy sections can detect subtle signs indicating clinically significant PCa before it becomes histologically apparent. Such morphological patterns shed light on the broader tissue alterations induced by prostate cancer, even in benign tissue, potentially enhancing early detection and clinical decision-making.

Place, publisher, year, edition, pages
Springer Nature, 2025. Vol. 15, no 1, article id 30770
National Category
Cancer and Oncology Urology Nephrology
Identifiers
URN: urn:nbn:se:umu:diva-243736DOI: 10.1038/s41598-025-15105-6PubMedID: 40841408Scopus ID: 2-s2.0-105013890997OAI: oai:DiVA.org:umu-243736DiVA, id: diva2:1995343
Funder
EU, European Research Council, CoG 682810Swedish Cancer Society, 21-1856Science for Life Laboratory, SciLifeLabAvailable from: 2025-09-05 Created: 2025-09-05 Last updated: 2025-09-05Bibliographically approved

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Järemo, HelenaAndersson, PernillaBergh, Anders

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