A US real-world study of treatment patterns and outcomes in localized or locally advanced prostate cancer patients.


Journal

World journal of urology
ISSN: 1433-8726
Titre abrégé: World J Urol
Pays: Germany
ID NLM: 8307716

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 17 05 2023
accepted: 07 10 2023
medline: 4 12 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: ppublish

Résumé

Men with localized or locally advanced prostate cancer (LPC/LAPC) are at risk of progression after radiotherapy (RT) or radical prostatectomy (RP). Using real-world data, we evaluated patient characteristics, treatment patterns, and outcomes in LPC/LAPC. Optum claims and electronic health records (EHR) data from January 2010 to December 2021 were queried for men with LPC/LAPC who received primary RT, RP, or androgen deprivation therapy alone within 180 days after diagnosis. Survival outcomes were analyzed using descriptive statistics and Kaplan-Meier curves. Real-world overall survival (rwOS) was compared in patients with and without evidence of disease (i.e., disease recurrence, metastasis, diagnosis of castration-resistant PC) at defined time points. 61,772 and 62,361 men in claims and EHR cohorts met the inclusion criteria. Median follow-up was 719 and 901 days, respectively. Most men received primary RT (51.0% claims, 35.0% EHR) or RP (39.4% claims, 53.8% EHR). Survival was greatest among men treated with RP, followed by RT. Adjusted for age and comorbidity, rwOS was shorter among men with evidence of disease within 1, 3, 4, and 5 years after primary treatment than those without at the same time points. Real-world claims and EHR data show that survival among men with LPC/LAPC differs by primary treatment and time point of disease recurrence thereafter. Poor outcomes in men with LPC/LAPC who progress early indicate an unmet medical need for more effective primary treatment. If validated for surrogacy, no evidence of disease at specific time points could represent an intermediate efficacy endpoint in future trials.

Identifiants

pubmed: 37966506
doi: 10.1007/s00345-023-04680-w
pii: 10.1007/s00345-023-04680-w
pmc: PMC10693516
doi:

Substances chimiques

Androgen Antagonists 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3535-3542

Informations de copyright

© 2023. The Author(s).

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Auteurs

Stephen J Freedland (SJ)

Cedars-Sinai Medical Center, Los Angeles, CA, USA. Stephen.Freedland@cshs.org.
Durham VA Medical Center, Durham, NC, USA. Stephen.Freedland@cshs.org.

Sandhya Nair (S)

Janssen Pharmaceutica NV, Beerse, Belgium.

Xiwu Lin (X)

Janssen Global Services, Horsham, PA, USA.

Lawrence Karsh (L)

The Urology Center of Colorado, Denver, CO, USA.

Christopher Pieczonka (C)

Associated Medical Professionals of NY, Syracuse, NY, USA.

Ravi Potluri (R)

Putnam Associates, HEOR & RWE, New York, NY, USA.

Sabine D Brookman-May (SD)

Janssen Research & Development, Spring House, PA, USA.
Department of Urology, Ludwig-Maximilians-University, Munich, Germany.

Suneel D Mundle (SD)

Janssen Global Services, Raritan, NJ, USA.

Sarah Fleming (S)

Janssen Global Services, Titusville, NJ, USA.

Neeraj Agarwal (N)

Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

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Classifications MeSH