Analysis of T1c prostate cancers treated at very low prostate-specific antigen levels

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dc.authoridArda, Ersan/0000-0002-5430-6561
dc.authorwosidKaplan, Mustafa/D-4977-2014
dc.authorwosidArda, Ersan/L-7357-2016
dc.contributor.authorKaplan, Mustafa
dc.contributor.authorArda, Ersan
dc.date.accessioned2024-06-12T11:22:54Z
dc.date.available2024-06-12T11:22:54Z
dc.date.issued2009
dc.departmentTrakya Üniversitesien_US
dc.description.abstractBackground:The Prostate Cancer Prevention Trial (PCPT) has challenged the validity of recommended prostate-specific antigen (PSA) thresholds for prostate biopsy (>2.5 ng/ml) given the 17% prostate cancer (pCA) detection rate at PSA of 1.1-2.0. The outcome of patients treated at PSA is poorly defined, and advantages associated with such an early diagnosis are uncertain. Objective: Compare the outcome of patients with Tlc pCA with pretreatment PSA and 2.6-4.0. Design, setting, and participants: Since 1998, 351 patients with clinical stage Tlc and PSA 4.0 have been treated at our institution; 84 (24%) of those patients had PSA 2.5. Clinical information was obtained from a prospective database. Treatment was radical prostatectomy, brachytherapy, and external-beam radiotherapy in 261 (74%), 67 (19%), and 23 (7%) patients, respectively. Measurements: Progression-free probability and pathological end points. Results and limitations: No significant differences between the groups were observed in terms of biopsy (18% vs 22%) or specimen Gleason score 7-8 (44% vs 56%), non organ-confined cancer (11% vs 13%), indolent cancer (34% vs 24%), or 5-yr progression -free probability (89% vs 93%; p > 0.1 for all). More biologically unimportant cancers (defined as pathologically organ-confined and Gleason were identified among patients with PSA (55% vs 41%, p = 0.050), and indolent cancers were three times more frequent than non organ-confined cancers among these patients (p = 0.003). Conclusions: The pathological features and outcome of patients treated at low PSA levels are favorable and similar for patients with PSA versus 2.6-4.0. However, >50% of the former have potentially biologically unimportant cancer. We failed to identify a therapeutic benefit to the diagnosis of cancers below accepted PSA thresholds for biopsy.en_US
dc.identifier.endpage19en_US
dc.identifier.issn2147-2270
dc.identifier.issue1en_US
dc.identifier.startpage16en_US
dc.identifier.urihttps://hdl.handle.net/20.500.14551/26126
dc.identifier.volume8en_US
dc.identifier.wosWOS:000219365100004en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherGalenos Yayinciliken_US
dc.relation.ispartofUroonkoloji Bulteni-Bulletin Of Urooncologyen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keywords]en_US
dc.titleAnalysis of T1c prostate cancers treated at very low prostate-specific antigen levelsen_US
dc.typeEditorialen_US

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