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Optimizing detection of clinically significant prostate cancer through nomograms incorporating mri, clinical features, and advanced serum biomarkers in biopsy naïve men.
Siddiqui, Mohammad R; Li, Eric V; Kumar, Sai K S R; Busza, Anna; Lin, Jasmine S; Mahenthiran, Ashorne K; Aguiar, Jonathan A; Shah, Parth V; Ansbro, Brandon; Rich, Jordan M; Moataz, Soliman A S; Keeter, Mary-Kate; Mai, Quan; Mi, Xinlei; Tosoian, Jeffrey J; Schaeffer, Edward M; Patel, Hiten D; Ross, Ashley E.
Afiliación
  • Siddiqui MR; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. mohammad.siddiqui2@northwestern.edu.
  • Li EV; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Kumar SKSR; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Busza A; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Lin JS; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Mahenthiran AK; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Aguiar JA; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Shah PV; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Ansbro B; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Rich JM; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Moataz SAS; Department of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Keeter MK; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Mai Q; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Mi X; Department of Preventative Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Tosoian JJ; Department of Urology, Vanderbilt University, Nashville, TN, USA.
  • Schaeffer EM; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Patel HD; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Ross AE; Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Prostate Cancer Prostatic Dis ; 26(3): 588-595, 2023 09.
Article en En | MEDLINE | ID: mdl-36973367
ABSTRACT

PURPOSE:

To develop nomograms that predict the detection of clinically significant prostate cancer (csPCa, defined as ≥GG2 [Grade Group 2]) at diagnostic biopsy based on multiparametric prostate MRI (mpMRI), serum biomarkers, and patient clinicodemographic features. MATERIALS AND

METHODS:

Nomograms were developed from a cohort of biopsy-naïve men presenting to our 11-hospital system with prostate specific antigen (PSA) of 2-20 ng/mL who underwent pre-biopsy mpMRI from March 2018-June 2021 (n = 1494). The outcomes were the presence of csPCa and high-grade prostate cancer (defined as ≥GG3 prostate cancer). Using significant variables on multivariable logistic regression, individual nomograms were developed for men with total PSA, % free PSA, or prostate health index (PHI) when available. The nomograms were both internally validated and evaluated in an independent cohort of 366 men presenting to our hospital system from July 2021-February 2022.

RESULTS:

1031 of 1494 men (69%) underwent biopsy after initial evaluation with mpMRI, 493 (47.8%) of whom were found to have ≥GG2 PCa, and 271 (26.3%) were found to have ≥GG3 PCa. Age, race, highest PIRADS score, prostate health index when available, % free PSA when available, and PSA density were significant predictors of ≥GG2 and ≥GG3 PCa on multivariable analysis and were used for nomogram generation. Accuracy of nomograms in both the training cohort and independent cohort were high, with areas under the curves (AUC) of ≥0.885 in the training cohort and ≥0.896 in the independent validation cohort. In our independent validation cohort, our model for ≥GG2 prostate cancer with PHI saved 39.1% of biopsies (143/366) while only missing 0.8% of csPCa (1/124) with a biopsy threshold of 20% probability of csPCa.

CONCLUSIONS:

Here we developed nomograms combining serum testing and mpMRI to help clinicians risk stratify patients with elevated PSA of 2-20 ng/mL who are being considered for biopsy. Our nomograms are available at https//rossnm1.shinyapps.io/MynMRIskCalculator/ to aid with biopsy decisions.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: Prostate Cancer Prostatic Dis Asunto de la revista: ENDOCRINOLOGIA / NEOPLASIAS / UROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: Prostate Cancer Prostatic Dis Asunto de la revista: ENDOCRINOLOGIA / NEOPLASIAS / UROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos