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Grade Group Underestimation in Prostate Biopsy: Predictive Factors and Outcomes in Candidates for Active Surveillance.
Audenet, François; Rozet, François; Resche-Rigon, Matthieu; Bernard, Rémy; Ingels, Alexandre; Prapotnich, Dominique; Sanchez-Salas, Rafael; Galiano, Marc; Barret, Eric; Cathelineau, Xavier.
Afiliación
  • Audenet F; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
  • Rozet F; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France. Electronic address: francois.rozet@imm.fr.
  • Resche-Rigon M; Department of Biostatistics, Hôpital Saint Louis, Université Paris Diderot, Paris, France.
  • Bernard R; Department of Biostatistics, Hôpital Saint Louis, Université Paris Diderot, Paris, France.
  • Ingels A; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
  • Prapotnich D; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
  • Sanchez-Salas R; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
  • Galiano M; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
  • Barret E; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
  • Cathelineau X; Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
Clin Genitourin Cancer ; 15(6): e907-e913, 2017 12.
Article en En | MEDLINE | ID: mdl-28522288
OBJECTIVE: We intended to analyze the outcomes and predictive factors for underestimating the prostate cancer (PCa) grade group (GG) from prostate biopsies in a large monocentric cohort of patients treated by minimally invasive radical prostatectomy (RP). MATERIALS AND METHODS: Using a monocentric prospectively maintained database, we included 3062 patients who underwent minimally invasive RP between 2006 and 2013. We explored clinicopathologic features and outcomes associated with a GG upgrade from biopsy to RP. Multivariate logistic regression was used to develop and validate a nomogram to predict upgrading for GG1. RESULTS: Biopsy GG was upgraded after RP in 51.5% of cases. Patients upgraded from GG1 to GG2 or GG3 after RP had a longer time to biochemical recurrence than those with GG2 or GG3 respectively, on both biopsy and RP, but a shorter time to biochemical recurrence than those who remained GG1 after RP (P < .0001). In multivariate analyses, variables predicting upgrading for GG1 PCa were age (P = .0014), abnormal digital rectal examination (P < .0001), prostate-specific antigen density (P < .0001), percentage of positive cores (P < .0001), and body mass index (P = .037). A nomogram was generated and validated internally. CONCLUSIONS: Biopsy grading system is misleading in approximately 50% of cases. Upgrading GG from biopsy to RP may have consequences on clinical outcomes. A nomogram using clinicopathologic features could aid the probability of needing to upgrade GG1 patients at their initial evaluation.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Nomogramas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: Clin Genitourin Cancer Asunto de la revista: NEOPLASIAS / UROLOGIA Año: 2017 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Nomogramas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: Clin Genitourin Cancer Asunto de la revista: NEOPLASIAS / UROLOGIA Año: 2017 Tipo del documento: Article