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Development and Validation of a Prostate Biopsy Risk Calculator in Black Men.
Mistry, Neil A; Sun, Zequn; Sweis, Jamila; McCall, Cordero; Marshall, Norma; Ofori, Bernice; Hollowell, Courtney M P; Kittles, Rick A; Schaeffer, Edward M; Abern, Michael; Gann, Peter; Murphy, Adam B.
Afiliación
  • Mistry NA; Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Sun Z; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Sweis J; Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • McCall C; Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Marshall N; Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Ofori B; Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Hollowell CMP; Division of Urology, Department of Surgery, Cook County Health, Chicago, Illinois.
  • Kittles RA; Morehouse School of Medicine, Atlanta, Georgia.
  • Schaeffer EM; Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Abern M; Department of Urology, University of Illinois at Chicago, Chicago, Illinois.
  • Gann P; Department of Pathology, University of Illinois at Chicago, Chicago, Illinois.
  • Murphy AB; Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
J Urol ; 211(2): 223-233, 2024 Feb.
Article en En | MEDLINE | ID: mdl-37917725
ABSTRACT

PURPOSE:

We sought to develop and validate a prostate biopsy risk calculator for Black men and compare it with the Prostate Cancer Prevention Trial version 2.0, Prostate Biopsy Collaborative Group, and Kaiser Permanente Prostate Cancer Risk Calculators for the detection of Gleason Grade Group (GG) ≥ 2 prostate cancer (PCa). MATERIALS AND

METHODS:

We prospectively recruited 2 cohorts of men undergoing prostate biopsy from 5 facilities in Chicago. The first cohort was split into development (70%) and internal validation (30%) groups. The second was used for external validation. Iterative logistic regression was used to develop 3 models for predicting GG ≥ 2 PCa. Models were compared for discrimination using the C statistics, calibration curves, and net benefit curves. The frequency of unnecessary biopsies and missed PCas was compared at 10% and 30% risk thresholds.

RESULTS:

The 2 cohorts included 393 and 292 Black men, respectively. Our first model, Mistry-Sun 1, used serum PSA and prior negative biopsy. Mistry-Sun 2 added abnormal digital rectal exam (DRE) and an interaction term with abnormal DRE and PSA to Mistry-Sun 1. Mistry-Sun 3 added prostate volume, abnormal DRE, and age to Mistry-Sun 1. The C statistics were 0.74, 0.74, and 0.78, respectively, and were similar to or higher than established calculators. At the 10% and 30% risk thresholds our models had the fewest unnecessary biopsies and an appropriate proportion of missed GG ≥ 2 PCas.

CONCLUSIONS:

Tailoring a risk calculator to detect clinically significant PCa in Black men may improve biopsy decision-making and outcomes compared to tools developed in non-Black populations.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Próstata / Neoplasias de la Próstata Límite: Humans / Male Idioma: En Revista: J Urol Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Próstata / Neoplasias de la Próstata Límite: Humans / Male Idioma: En Revista: J Urol Año: 2024 Tipo del documento: Article