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Observational Study
. 2023 Oct 2;6(10):e2337272.
doi: 10.1001/jamanetworkopen.2023.37272.

Survival Outcomes by Race and Ethnicity in Veterans With Nonmetastatic Castration-Resistant Prostate Cancer

Affiliations
Observational Study

Survival Outcomes by Race and Ethnicity in Veterans With Nonmetastatic Castration-Resistant Prostate Cancer

Kelli M Rasmussen et al. JAMA Netw Open. .

Erratum in

  • Error in Byline.
    [No authors listed] [No authors listed] JAMA Netw Open. 2023 Nov 1;6(11):e2343869. doi: 10.1001/jamanetworkopen.2023.43869. JAMA Netw Open. 2023. PMID: 37910109 Free PMC article. No abstract available.

Abstract

Importance: Racial and ethnic disparities in prostate cancer are poorly understood. A given disparity-related factor may affect outcomes differently at each point along the highly variable trajectory of the disease.

Objective: To examine clinical outcomes by race and ethnicity in patients with nonmetastatic castration-resistant prostate cancer (nmCRPC) within the US Veterans Health Administration.

Design, setting, and participants: A retrospective, observational cohort study using electronic health care records (January 1, 2006, to December 31, 2021) in a nationwide equal-access health care system was conducted. Mean (SD) follow-up time was 4.3 (3.3) years. Patients included in the analysis were diagnosed with prostate cancer from January 1, 2006, to December 30, 2020, that progressed to nmCRPC defined by (1) increasing prostate-specific antigen levels, (2) ongoing androgen deprivation, and (3) no evidence of metastatic disease. Patients with metastatic disease or death within the landmark period (3 months after the first nmCRPC evidence) were excluded.

Main outcomes and measures: The primary outcome was time from the landmark period to death or metastasis; the secondary outcome was overall survival. A multivariate Cox proportional hazards model, Kaplan-Meier estimates, and adjusted survival curves were used to evaluate outcome differences by race and ethnicity.

Results: Of 12 992 patients in the cohort, 826 patients identified as Hispanic (6%), 3671 as non-Hispanic Black (28%; henceforth Black), 7323 as non-Hispanic White (56%; henceforth White), and 1172 of other race and ethnicity (9%; henceforth other, including American Indian or Alaska Native, Asian, Native Hawaiian or Other Pacific Islander, unknown by patient, and patient declined to answer). Median time elapsed from nmCRPC to metastasis or death was 5.96 (95% CI, 5.58-6.34) years for Black patients, 5.62 (95% CI, 5.11-6.67) years for Hispanic patients, 4.11 (95% CI, 3.96-4.25) years for White patients, and 3.59 (95% CI, 3.23-3.97) years for other patients. Median unadjusted overall survival was 6.26 (95% CI, 6.03-6.46) years among all patients, 8.36 (95% CI, 8.0-8.8) years for Black patients, 8.56 (95% CI, 7.3-9.7) years for Hispanic patients, 5.48 (95% CI, 5.2-5.7) years for White patients, and 4.48 (95% CI, 4.1-5.0) years for other patients.

Conclusions and relevance: The findings of this cohort study of patients with nmCRPC suggest that differences in outcomes by race and ethnicity exist; in addition, Black and Hispanic men may have considerably improved outcomes when treated in an equal-access setting.

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Conflict of interest statement

Conflict of Interest Disclosures: Ms Appukkutan reported being an employee of Bayer Pharmaceuticals. Dr Grossman reported being an employee of Bayer Pharmaceuticals. Dr Jhaveri reported being an employee of Bayer Pharmaceuticals. Dr Halwani reported receiving grants from AbbVie, Pharmacyclics, Genentech, Kyowa Kirin LLS, and the Leukemia and Lymphoma Society outside the submitted work. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Patient Cohort Flow Diagram
CDW indicates Corporate Data Warehouse; CRPC, castration-resistant prostate cancer; ICD-9, International Classification of Diseases, Ninth Revision; ICD-10, International Statistical Classification of Diseases and Related Health Problems, Tenth Revision; ICD-10-CM, International Statistical Classification of Diseases and Related Health Problems, Tenth Revision–Clinical Modification; nmCRPC, nonmetastatic CRPC; and VACRS, Veterans Affairs Cancer Registry System.
Figure 2.
Figure 2.. Adjusted Survival Curves for Survival by Race and Ethnicity
Metastasis-free (A) and overall (B) survival. The numbers at risk are not available for adjusted survival curves, because the survival curves are adjusted proportionally with the confounders. The original numbers at risk would not correctly reflect the curves. The same algorithm we used to create survival curves does not provide numbers at risk, because the scaling is working on survival probabilities. To our knowledge, there are no existing algorithms to scale the number of people in such cases. Other includes American Indian or Alaska Native, Asian, Native Hawaiian or Other Pacific Islander, unknown by patient, and patient declined to answer.

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