<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>487(1)</volume><submitter>Hommerding O</submitter><funding>Universitätsklinikum Bonn</funding><pubmed_abstract>The prognostication of individual disease trajectory and selection of optimal therapy in patients with localized, low-grade prostate cancer often presents significant difficulty. The phosphatase and tensin homolog on chromosome 10 (PTEN) has emerged as a potential novel biomarker in this clinical context, based on its demonstrated prognostic significance in multiple retrospective studies. Incorporation into standard clinical practice necessitates exceptional diagnostic accuracy, and PTEN's binary readout-retention or loss-suggests its suitability as a biomarker. This multi-institutional ring trial aimed to validate the diagnostic precision of PTEN immunohistochemistry in localized, low- to intermediate-risk prostate cancer, across ten university pathology institutes in Germany. The trial i</pubmed_abstract><journal>Virchows Archiv : an international journal of pathology</journal><pagination>87-96</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12289804</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High interobserver variability of PTEN immunohistochemistry defining PTEN status in low- to intermediate-risk prostate cancer: results of the first German ring trial.</pubmed_title><pmcid>PMC12289804</pmcid><pubmed_authors>Semjonow A</pubmed_authors><pubmed_authors>Reis H</pubmed_authors><pubmed_authors>Kristiansen G</pubmed_authors><pubmed_authors>Schmid M</pubmed_authors><pubmed_authors>Linxweiler J</pubmed_authors><pubmed_authors>Schildhaus HU</pubmed_authors><pubmed_authors>Brasen JH</pubmed_authors><pubmed_authors>Darr C</pubmed_authors><pubmed_authors>Wulf AL</pubmed_authors><pubmed_authors>Baretton G</pubmed_authors><pubmed_authors>Seidl M</pubmed_authors><pubmed_authors>Esposito I</pubmed_authors><pubmed_authors>Stahl PR</pubmed_authors><pubmed_authors>Kreipe H</pubmed_authors><pubmed_authors>Schlack K</pubmed_authors><pubmed_authors>Hartmann W</pubmed_authors><pubmed_authors>Abbas M</pubmed_authors><pubmed_authors>Hommerding O</pubmed_authors><pubmed_authors>Lopez-Cotarelo C</pubmed_authors><pubmed_authors>Scherping A</pubmed_authors><pubmed_authors>Dressler FF</pubmed_authors><pubmed_authors>Hartmann A</pubmed_authors><pubmed_authors>Saar M</pubmed_authors><pubmed_authors>Weber F</pubmed_authors><pubmed_authors>Ellinger J</pubmed_authors><pubmed_authors>Lafos M</pubmed_authors><pubmed_authors>Sailer V</pubmed_authors><pubmed_authors>Tischler V</pubmed_authors><pubmed_authors>Bernhardt M</pubmed_authors><pubmed_authors>Kreft T</pubmed_authors><pubmed_authors>Sommer U</pubmed_authors><pubmed_authors>Breyer J</pubmed_authors><pubmed_authors>Heitplatz B</pubmed_authors><pubmed_authors>Erber R</pubmed_authors><pubmed_authors>Wullich B</pubmed_authors></additional><is_claimable>false</is_claimable><name>High interobserver variability of PTEN immunohistochemistry defining PTEN status in low- to intermediate-risk prostate cancer: results of the first German ring trial.</name><description>The prognostication of individual disease trajectory and selection of optimal therapy in patients with localized, low-grade prostate cancer often presents significant difficulty. The phosphatase and tensin homolog on chromosome 10 (PTEN) has emerged as a potential novel biomarker in this clinical context, based on its demonstrated prognostic significance in multiple retrospective studies. Incorporation into standard clinical practice necessitates exceptional diagnostic accuracy, and PTEN's binary readout-retention or loss-suggests its suitability as a biomarker. This multi-institutional ring trial aimed to validate the diagnostic precision of PTEN immunohistochemistry in localized, low- to intermediate-risk prostate cancer, across ten university pathology institutes in Germany. The trial i</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-03-17T13:41:58.906Z</modification><creation>2025-08-28T03:04:47.073Z</creation></dates><accession>S-EPMC12289804</accession><cross_references><pubmed>39653828</pubmed><doi>10.1007/s00428-024-03999-y</doi></cross_references></HashMap>