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dc.contributor.authorRebecca C. Czajaen_US
dc.contributor.authorSergey Tarimaen_US
dc.contributor.authorRuizhe Wuen_US
dc.contributor.authorWatchareepohn Palagnmonthipen_US
dc.contributor.authorKenneth A. Iczkowskien_US
dc.date.accessioned2022-10-16T07:22:52Z-
dc.date.available2022-10-16T07:22:52Z-
dc.date.issued2021-06-01en_US
dc.identifier.issn15328198en_US
dc.identifier.issn10929134en_US
dc.identifier.other2-s2.0-85101399112en_US
dc.identifier.other10.1016/j.anndiagpath.2021.151725en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85101399112&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/77103-
dc.description.abstractThe International Society of Urological Pathology endorses specifying presence of cribriform architecture in Gleason (G)4 prostate cancer because of cribriform's aggressiveness. The relative effect of cribriform presence versus percentage G4 within grade group (GG)2 or 3 was uncertain. 194 men's biopsies with GG2 with or without cribriform (excluding glomeruloid from cribriform) and GG3 without cribriform (controls) from 4 years were reviewed. 173 cases had follow-up including 147 GG2 (15/147 or 10% had cribriform) and 26 GG3. Effects of total tumor specimen involvement, %Gleason 4, and cribriform were stratified into prostatectomy (n = 90), radiotherapy (n = 61), and watching waiting (n = 22) groups. Median follow-up duration was 3.32 years (range 1.90–6.18). Biochemical failures in the above 3 cohorts numbered 9 (9/90; 10%), 5 (5/61; 8%), and 13 (13/22; 59%) respectively. In all groups, (GG2+ GG3, n = 173), the HR for C pattern was 1.64. In GG2, cribriform presence (considering glomeruloid as non-cribriform) conferred a hazard ratio (HR) of 1.51 (p = 0.48). It was 1.38, excluding glomeruloid. In watchful waiting cohort only, presence of C conferred a HR of 2.62 (p = 0.086). All remaining comparisons including percent G4, remained not significant. Thus, only in WW group did cribriform pattern presence approach significance. Detection of differences otherwise was not feasible, probably because: 1) biochemical failure is too rare in GG2 cancer; 2) cribriform frequency was only 10% in GG2 (in current study), less than in higher-grade cancer. 3) Use of biopsy tissue is subject to sampling variation which may undersample cribriform pattern, though biopsy forms the basis of treatment decisions.en_US
dc.subjectMedicineen_US
dc.titleComparative influence of cribriform growth and percent Gleason 4 in prostatic biopsies with Gleason 3+4 canceren_US
dc.typeJournalen_US
article.title.sourcetitleAnnals of Diagnostic Pathologyen_US
article.volume52en_US
article.stream.affiliationsMedical College of Wisconsinen_US
article.stream.affiliationsChiang Mai Universityen_US
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