Low risk is low risk, regardless of race or ethnicity: Outcomes of prostate cancer active surveillance and factors associated with reclassification in a racially diverse cohort.


Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
04 2023
Historique:
received: 26 07 2022
revised: 04 12 2022
accepted: 09 01 2023
medline: 18 4 2023
pubmed: 6 2 2023
entrez: 5 2 2023
Statut: ppublish

Résumé

Active surveillance (AS) is the standard for very low- and low-risk prostate cancer. Although risk factors for pathologic reclassification while on AS have been identified, results are mixed for non-Hispanic Black (NHB) and Hispanic ethnicity. We aim to further explore how race and ethnicity may be affecting AS participation and outcomes in a primarily urban, diverse, and vulnerable population. Patients eligible for AS from 2005-2020 were reviewed. Demographics, race/ethnicity, prostate specific antigen (PSA), prostate volume, and pathologic characteristics were analyzed between patients enrolled in AS and those that underwent immediate therapy. Kaplan-Meier survival analysis was used to compare biochemical recurrence (BCR) rates. Cox proportional hazards models were used to develop prediction models for clinical reclassification. A total of 471 men were eligible for AS. Of those, 188 (39.9%) enrolled in AS while 283 (60.1%) underwent immediate radical therapy. No significant differences were found in racial/ethnic composition between the AS and immediate treatment groups. In our AS cohort, 79 (42.0%) experienced clinical reclassification and underwent deferred treatment. BCR rates were similar between treatment groups. Race/ethnicity were not found to be predictors of clinical reclassification, while metrics at diagnostic biopsy such as elevated PSA, higher PSA density, and lower prostate volume increased reclassification odds. In our diverse population, NHB race and Hispanic ethnicity were not significant predictors of adverse reclassification while on AS. Our findings support utilizing other metrics taken at initial biopsy to identify high-risk patients such as PSA, prostate volume, and PSA density.

Identifiants

pubmed: 36740489
pii: S1078-1439(23)00007-8
doi: 10.1016/j.urolonc.2023.01.007
pii:
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

204.e7-204.e15

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest None of the authors have relevant conflicts of interest, financial or otherwise, to declare.

Auteurs

Kevin Labagnara (K)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY.

Denzel Zhu (D)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY; Department of Urology, University of Rochester Medical Center, Rochester, NY.

Justin Loloi (J)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY.

Evan Shreck (E)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY.

Marnie Abeshouse (M)

Department of Surgery, Mt. Sinai Hospital, New York, NY.

Kara L Watts (KL)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY.

Alex Sankin (A)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY.

Ahmed A Aboumohamed (AA)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY.

Evan Kovac (E)

Department of Urology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY; Division of Urology, Department of Surgery, Rutgers New Jersey Medical School, Newark, NJ; Cancer Institute of New Jersey, Newark, NJ. Electronic address: evan.kovac@rutgers.edu.

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Classifications MeSH