<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Morgan TM</submitter><funding>NCI NIH HHS</funding><pubmed_abstract>&lt;h4>Background and objective&lt;/h4>Biochemical recurrence (BCR) after radical prostatectomy (RP) is a heterogeneous disease state in prostate cancer with multiple treatment options. Improved risk stratification could enable more personalized decision-making. We developed and validated a digital pathology-based multimodal artificial intelligence (MMAI) model to predict outcomes in post-RP BCR patients undergoing salvage therapy.&lt;h4>Methods&lt;/h4>An MMAI model was trained to predict distant metastasis (DM) using prostate histopathology image features and clinical variables (pathologic grade group, pathologic T stage, prostate-specific antigen level before salvage radiotherapy [SRT], age, and surgical margin). The locked model was validated in 533 patients from NRG/RTOG 9601 and 0534 treated with</pubmed_abstract><journal>European urology</journal><pagination>S0302-2838(25)04859-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12774449</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development and Validation of a Multimodal Artificial Intelligence-derived Digital Pathology-based Biomarker Predicting Metastasis Among Patients with Biochemical Recurrence After Radical Prostatectomy in NRG/RTOG Trials.</pubmed_title><pmcid>PMC12774449</pmcid><funding_grant_id>UG1 CA189867</funding_grant_id><funding_grant_id>U24 CA196067</funding_grant_id><funding_grant_id>U10 CA180868</funding_grant_id><funding_grant_id>U10 CA180822</funding_grant_id><pubmed_authors>Zwerink W</pubmed_authors><pubmed_authors>Efstathiou JA</pubmed_authors><pubmed_authors>Ren Y</pubmed_authors><pubmed_authors>Pugh SL</pubmed_authors><pubmed_authors>Michalski JM</pubmed_authors><pubmed_authors>Greenberg MJ</pubmed_authors><pubmed_authors>Feng FY</pubmed_authors><pubmed_authors>Martin AG</pubmed_authors><pubmed_authors>Ross AE</pubmed_authors><pubmed_authors>Hoffman KE</pubmed_authors><pubmed_authors>Tang S</pubmed_authors><pubmed_authors>Pollack A</pubmed_authors><pubmed_authors>Esteva A</pubmed_authors><pubmed_authors>Nguyen PL</pubmed_authors><pubmed_authors>Mitani A</pubmed_authors><pubmed_authors>Spratt DE</pubmed_authors><pubmed_authors>Tran PT</pubmed_authors><pubmed_authors>Bahary JP</pubmed_authors><pubmed_authors>Simko JP</pubmed_authors><pubmed_authors>Sandler HM</pubmed_authors><pubmed_authors>Chen E</pubmed_authors><pubmed_authors>DeVries S</pubmed_authors><pubmed_authors>Wilke D</pubmed_authors><pubmed_authors>Royce TJ</pubmed_authors><pubmed_authors>Morgan TM</pubmed_authors><pubmed_authors>Huang HC</pubmed_authors><pubmed_authors>Balogh AG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and Validation of a Multimodal Artificial Intelligence-derived Digital Pathology-based Biomarker Predicting Metastasis Among Patients with Biochemical Recurrence After Radical Prostatectomy in NRG/RTOG Trials.</name><description>&lt;h4>Background and objective&lt;/h4>Biochemical recurrence (BCR) after radical prostatectomy (RP) is a heterogeneous disease state in prostate cancer with multiple treatment options. Improved risk stratification could enable more personalized decision-making. We developed and validated a digital pathology-based multimodal artificial intelligence (MMAI) model to predict outcomes in post-RP BCR patients undergoing salvage therapy.&lt;h4>Methods&lt;/h4>An MMAI model was trained to predict distant metastasis (DM) using prostate histopathology image features and clinical variables (pathologic grade group, pathologic T stage, prostate-specific antigen level before salvage radiotherapy [SRT], age, and surgical margin). The locked model was validated in 533 patients from NRG/RTOG 9601 and 0534 treated with</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T10:52:52.817Z</modification><creation>2026-05-29T03:12:38.999Z</creation></dates><accession>S-EPMC12774449</accession><cross_references><pubmed>41436315</pubmed><doi>10.1016/j.eururo.2025.12.007</doi></cross_references></HashMap>