Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/1060
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dc.contributor.authorMurphy, Declan-
dc.contributor.otherVan den Bergh, Roderick-
dc.contributor.otherZargar, Homayoun-
dc.contributor.otherHeijmink, Stijn-
dc.contributor.otherBozin, Mike-
dc.contributor.othervan der Poel, Henk-
dc.date2017-01-
dc.date.accessioned2017-05-05T00:57:11Z-
dc.date.available2017-05-05T00:57:11Z-
dc.date.issued2017-01-
dc.identifier.citationMinerva Urol Nefrol. 2017 Jan 26en_US
dc.identifier.issn0393-2249en_US
dc.identifier.urihttp://hdl.handle.net/11434/1060-
dc.description.abstractBACKGROUND: To explore the impact of improved risk stratification on biochemical recurrence (BCR) rates after surgery in prostate cancer (PC) patients also suitable for active surveillance (AS). Patients with Gleason upgrading were compared to those who were correctly graded with biopsy. Also, to analyze whether AS criteria may be expanded, by comparing patients outside the AS criteria without Gleason upgrading, to men eligible for AS. METHODS: Low-risk PC was widely defined as clinically organ-confined and biopsy Gleason score =<3+3=6. Within this group, additional AS eligibility criteria were PSA =<10 ng/ml, PSA density <0.2 ng/ml/cc, and 1-2 positive biopsies. RESULTS: Of 755 clinically organ-confined low-grade patients, 181 (24%) were suitable for AS, 324 (44%) had Gleason upgrading after surgery, and 132 (18%) showed BCR after a median follow-up of 1.8 years (25-75p 0.7-3.4). Gleason upgrading between biopsy and surgery score was significantly associated with unfavorable BCR rates (p<0.01) in clinically organ-confined low-grade patients, but it did not impact BCR in AS-suitable patients (p=0.936). Clinically organ-confined low-grade patients without Gleason score upgrading showed BCR rates similar to patients who did fulfill all AS criteria (p=0.187). CONCLUSIONS: These results may be used to guide application of novel diagnostic (imaging) modalities in selection for AS. The added value of improved Gleason grading may be limited in AS-suitable patients, as Gleason upgrading does not impact BCR. However, in patients outside of the AS criteria in whom Gleason upgrading is excluded, BCR rates are not significantly different from AS- suitable patients, suggesting opportunities to expand AS criteria.en_US
dc.publisherEdizioni Minerva Medicaen_US
dc.subjectGleason Scoreen_US
dc.subjectRisk Stratificationen_US
dc.subjectBiochemical Recurrenceen_US
dc.subjectBCRen_US
dc.subjectProstate Canceren_US
dc.subjectPCen_US
dc.subjectNeoplasmsen_US
dc.subjectImproved Risk Stratificationen_US
dc.subjectRecurrenceen_US
dc.subjectBiopsiesen_US
dc.subjectOrgan-Confined Low-Grade Patientsen_US
dc.subjectDiagnostic Imaging Modalitiesen_US
dc.subjectASen_US
dc.subjectActive Surveillanceen_US
dc.subjectAustralian Prostate Cancer Research Centre, Epworth Healthcare, Victoria, Australia.en_US
dc.titleReducing the rate of biopsy Gleason undergrading may not improve biochemical recurrence rates in active surveillance candidates.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.23736/S0393-2249.17.02749-7en_US
dc.identifier.journaltitleMinerva Urologica e Nefrologica.; The Italian journal of urology and nephrology.en_US
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/28124869en_US
dc.description.affiliatesDepartment of Urology, Royal Melbourne Hospital, Melbourne, Australia.en_US
dc.description.affiliatesDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Australiaen_US
dc.description.affiliatesDepartment of Urology, Royal Melbourne Hospital, Melbourne, Australia.en_US
dc.description.affiliatesDepartment of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.en_US
dc.description.affiliatesDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Australia.en_US
dc.type.studyortrialComparative Studyen_US
dc.type.contenttypeTexten_US
Appears in Collections:Cancer Services
Epworth Prostate Centre
UroRenal, Vascular

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