{"title":"Routine prostate biopsy reports carry grade-specific tumor burden information beyond the highest Grade Group.","authors":"Yoichiro Okubo, Shu Yuguchi, Rika Kasajima, Shinya Sato, Noboru Nakaigawa, Yukihiko Hiroshima, Kota Washimi, Shuka Wada, Yuki Kobayashi, Tatsuma Juichi, Atsuto Suzuki, Kimitsugu Usui, Yohei Miyagi","doi":"10.1016/j.humpath.2026.106285","DOIUrl":null,"url":null,"abstract":"<p><p>Routine prostate biopsy reports contain quantitative information that is lost when a case is reduced to the single highest Grade Group (GG). We examined whether GG-specific tumor burden in routine biopsy reports provides information on radical prostatectomy (RP) pathology beyond the highest biopsy GG. This retrospective single-institution study included 508 analyzable paired biopsy-RP cases from 2014 to 2026. For GG3, GG4, and GG5, burden was reconstructed as the number of positive reporting units and summed cancer length. Firth penalized logistic regression adjusted for highest biopsy GG and non-target GG3-GG5 burden. The focused endpoints were RP GG4-5 for GG4 burden, pT3 or higher disease for GG3 burden, and RP GG5 for GG5 burden. For count models, odds ratios (ORs) were expressed per additional target reporting unit. GG4 count was associated with RP GG4-5 (OR, 1.72; 95% confidence interval [CI], 1.29-2.29), GG3 count with pT3 or higher disease (OR, 1.72; 95% CI, 1.41-2.10; n=473), and GG5 count with RP GG5 (OR, 3.46; 95% CI, 1.40-8.59). Corresponding cancer-length measures showed concordant associations, and the strict 318-case quality-control sensitivity subset yielded similar estimates. Adding target GG burden to models already containing highest biopsy GG and non-target GG burden yielded optimism-corrected area-under-the-curve gains of 0.029 for GG4 count, 0.042 for GG3 count, and 0.010 for GG5 count. Grade-specific burden already present in routine biopsy reports therefore provides complementary information on subsequent RP grade and local stage beyond the highest biopsy GG alone.</p>","PeriodicalId":13062,"journal":{"name":"Human pathology","volume":" ","pages":"106285"},"PeriodicalIF":3.0000,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.humpath.2026.106285","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Routine prostate biopsy reports contain quantitative information that is lost when a case is reduced to the single highest Grade Group (GG). We examined whether GG-specific tumor burden in routine biopsy reports provides information on radical prostatectomy (RP) pathology beyond the highest biopsy GG. This retrospective single-institution study included 508 analyzable paired biopsy-RP cases from 2014 to 2026. For GG3, GG4, and GG5, burden was reconstructed as the number of positive reporting units and summed cancer length. Firth penalized logistic regression adjusted for highest biopsy GG and non-target GG3-GG5 burden. The focused endpoints were RP GG4-5 for GG4 burden, pT3 or higher disease for GG3 burden, and RP GG5 for GG5 burden. For count models, odds ratios (ORs) were expressed per additional target reporting unit. GG4 count was associated with RP GG4-5 (OR, 1.72; 95% confidence interval [CI], 1.29-2.29), GG3 count with pT3 or higher disease (OR, 1.72; 95% CI, 1.41-2.10; n=473), and GG5 count with RP GG5 (OR, 3.46; 95% CI, 1.40-8.59). Corresponding cancer-length measures showed concordant associations, and the strict 318-case quality-control sensitivity subset yielded similar estimates. Adding target GG burden to models already containing highest biopsy GG and non-target GG burden yielded optimism-corrected area-under-the-curve gains of 0.029 for GG4 count, 0.042 for GG3 count, and 0.010 for GG5 count. Grade-specific burden already present in routine biopsy reports therefore provides complementary information on subsequent RP grade and local stage beyond the highest biopsy GG alone.
期刊介绍:
Human Pathology is designed to bring information of clinicopathologic significance to human disease to the laboratory and clinical physician. It presents information drawn from morphologic and clinical laboratory studies with direct relevance to the understanding of human diseases. Papers published concern morphologic and clinicopathologic observations, reviews of diseases, analyses of problems in pathology, significant collections of case material and advances in concepts or techniques of value in the analysis and diagnosis of disease. Theoretical and experimental pathology and molecular biology pertinent to human disease are included. This critical journal is well illustrated with exceptional reproductions of photomicrographs and microscopic anatomy.