Artigo Revisado por pares

Prostate Biopsy Tumor Extent but Not Location Predicts Recurrence After Radical Prostatectomy: Results From CaPSURE

2005; Lippincott Williams & Wilkins; Volume: 175; Issue: 1 Linguagem: Inglês

10.1016/s0022-5347(05)00056-x

ISSN

1527-3792

Autores

Kirsten L. Greene, Eric P. Elkin, Armine Karapetian, Janeen DuChane, Peter R. Carroll, Christopher J. Kane,

Tópico(s)

Statistical Methods in Clinical Trials

Resumo

No AccessJournal of UrologyAdult urology1 Jan 2006Prostate Biopsy Tumor Extent but Not Location Predicts Recurrence After Radical Prostatectomy: Results From CaPSUREis accompanied byThe Continuing Search for Meaningful Prognostic Information From Prostate Biopsy Kirsten L. Greene, Eric P. Elkin, Armine Karapetian, Janeen DuChane, Peter R. Carroll, Christopher J. Kane, and CaPSURE™ Investigators Kirsten L. GreeneKirsten L. Greene Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco More articles by this author , Eric P. ElkinEric P. Elkin Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco More articles by this author , Armine KarapetianArmine Karapetian Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco More articles by this author , Janeen DuChaneJaneen DuChane TAP Pharmaceutical Products, Inc., Lake Forest, Illinois Financial interest and/or other relationship with TAP Pharmaceuticals, Inc. More articles by this author , Peter R. CarrollPeter R. Carroll Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco Financial interest and/or other relationship with AstraZeneca, Steba Biotech N.V., Predicant Biosciences Inc., Watson Pharmaceuticals, National Cancer Institute, TAP Pharmaceuticals and ICPME. More articles by this author , Christopher J. KaneChristopher J. Kane San Francisco Veterans Affairs Medical Center, San Francisco, California Financial interest and/or other relationship with TAP Pharmaceuticals, Merck and AstraZeneca. More articles by this author , and CaPSURE™ Investigators More articles by this author View All Author Informationhttps://doi.org/10.1016/S0022-5347(05)00056-XAboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract Purpose: Prostate cancer biopsy information is important for patient risk assessment. Although the number and extent of positive biopsies have been used to predict recurrence, the impact of positive biopsy location and contiguity is less clear. We compared the ability of positive prostate biopsy location and pattern with number and percent positive biopsies to predict recurrence after RP. Materials and Methods: From CaPSURE we identified 2,037 men treated with RP from 1992 to 2002 for whom detailed biopsy information and 2 or more followup PSA values were available. Treatment failure was defined as 2 consecutive PSA values of 0.2 ng/ml or higher, or a second treatment delivered more than 6 months after RP. Biopsy tumor volume (number and percent positive sites), location of disease (anatomical site, laterality), and contiguity of positive biopsies were entered into Cox proportional hazards models to predict risk of disease recurrence while controlling for Gleason grade, PSA and T stage. Results: Higher number and percent of positive biopsy cores were associated with prostate cancer recurrence, risk stratification category and Gleason grade, p <0.0001, HR 1.09 (CI 1.02 to 1.16) and 1.01 (CI 1.00 to 1.01), respectively. Number of biopsy cores taken, laterality, contiguity and positive biopsy location were not associated with disease recurrence. Conclusions: The number and the percentage of biopsies positive for cancer correlated with treatment failure after radical prostatectomy. Contiguity, laterality and location were not associated with recurrence. References 1 : Time trends in clinical risk stratification for prostate cancer: implications for outcomes (data from CaPSURE). J Urol2003; 170: S21. Link, Google Scholar 2 : Cancer statistics, 2004. CA Cancer J Clin2004; 54: 8. Google Scholar 3 : Assessment of the enhancement in predictive accuracy provided by systematic biopsy in predicting outcome for clinically localized prostate cancer. J Urol2004; 171: 200. Link, Google Scholar 4 : Under staging and under grading in a contemporary series of patients undergoing radical prostatectomy: results from the Cancer of the Prostate Strategic Urologic Research Endeavor database. J Urol2001; 165: 851. 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Link, Google Scholar © 2006 by American Urological AssociationFiguresReferencesRelatedDetailsCited byPloussard G, Salomon L, Xylinas E, Allory Y, Vordos D, Hoznek A, Abbou C and de la Taille A (2018) Pathological Findings and Prostate Specific Antigen Outcomes After Radical Prostatectomy in Men Eligible for Active Surveillance—Does the Risk of Misclassification Vary According to Biopsy Criteria?Journal of Urology, VOL. 183, NO. 2, (539-545), Online publication date: 1-Feb-2010.Eskicorapci S and Tuncay L (2018) Re: Diagnostic Value of Systematic Biopsy Methods in the Investigation of Prostate Cancer: A Systematic ReviewJournal of Urology, VOL. 176, NO. 6, (2745-2746), Online publication date: 1-Dec-2006.Related articlesJournal of Urology9 Nov 2018The Continuing Search for Meaningful Prognostic Information From Prostate Biopsy Volume 175Issue 1January 2006Page: 125-129 Advertisement Copyright & Permissions© 2006 by American Urological AssociationKeywordsbiopsyrecurrenceprostatectomyprostatic neoplasmsMetricsAuthor Information Kirsten L. Greene Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco More articles by this author Eric P. Elkin Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco More articles by this author Armine Karapetian Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco More articles by this author Janeen DuChane TAP Pharmaceutical Products, Inc., Lake Forest, Illinois Financial interest and/or other relationship with TAP Pharmaceuticals, Inc. More articles by this author Peter R. Carroll Department of Urology, University of California, San Francisco Comprehensive Cancer Center, University of California, San Francisco Financial interest and/or other relationship with AstraZeneca, Steba Biotech N.V., Predicant Biosciences Inc., Watson Pharmaceuticals, National Cancer Institute, TAP Pharmaceuticals and ICPME. More articles by this author Christopher J. Kane San Francisco Veterans Affairs Medical Center, San Francisco, California Financial interest and/or other relationship with TAP Pharmaceuticals, Merck and AstraZeneca. More articles by this author CaPSURE™ Investigators More articles by this author Expand All Advertisement PDF downloadLoading ...

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