Key result
White race was associated with a significantly higher risk of major adverse cardiovascular events (adjusted HR 1.30) and all-cause mortality compared to Black race in men with prostate cancer receiving androgen deprivation therapy.
Why the study?
Prostate cancer patients treated with ADT may experience MACE, and prior studies showing longer overall survival in Black vs. White patients were limited to CRPC.
Does White race compared to Black race increase the risk of MACE and all-cause mortality in prostate cancer patients receiving androgen deprivation therapy?
Cohort (n=34,762)
Yes
Does White race compared to Black race increase the risk of MACE and all-cause mortality in prostate cancer patients receiving androgen deprivation therapy?
Hazard Ratio: 1.3 (95% CI 1.09–1.56)
Absolute Event Rate: 21% vs 13.3%
p-value: p=<0.05
In a real-world cohort of prostate cancer patients receiving androgen deprivation therapy, White patients had a significantly higher risk of major adverse cardiovascular events and all-cause mortality compared to Black patients.
Black patients had lower MACE rates after ADT; observational data leaves open whether race modifies cardiovascular risk stratification.
BACKGROUND: Prostate cancer(PCa) patients treated with androgen deprivation therapy(ADT) may experience major adverse cardiovascular events(MACE) [1]. Racial disparities in PCa incidence and outcomes have been noted. In contrast to older studies, three recent studies found significantly longer overall survival in Black vs. White patients: 2019 meta-analysis of nine phase III trials in men with metastatic castration-resistant PCa(CRPC) (n = 8820) [2]; 2020 registry study in men with metastatic CRPC (n = 1902) [3]; and 2023 study in men with non-metastatic CRPC (n = 12,992) [4]. Our "real-world" data study compared MACE and all-cause mortality risk for Black vs. White PCa patients. Compared to prior studies [1-4], our study encompassed a broader scope and was not exclusive to CRPC patients. METHODS: ), oncology vs. urology setting, antagonist vs. agonist, personal MACE history, tobacco history, baseline prostate-specific antigen (>4 vs. ≤4 ng/mL), race (White vs. Black), statin use, increasing age per year, ethnicity (non-Hispanic vs. Hispanic), increasing ADT exposure per year, diabetes, hypertension, and family MACE history. RESULTS: MACE risk was higher for White patients than Black (4.0% vs. 2.4% at one year after ADT initiation; 21.0% vs. 13.3% at four years). Mortality risk after ADT initiation was 1.6% and 2.6% at 1 year and 11.7% and 18.1% at 4 years for Black and White patients, respectively. CONCLUSIONS: Our analysis reveals a unique finding that MACE and all-cause mortality incidence were higher in White vs. Black patients. Black race is associated with lower MACE rates and improved survival for men undergoing ADT treatment. Whether selection bias, underlying biology or other factors are responsible for these differences remains unknown.
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Moul et al. (2025) conducted a cohort in Prostate cancer (n=34,762). White race vs. Black race was evaluated on Major adverse cardiovascular events (MACE) at 4 years (HR 1.30, 95% CI 1.09-1.56, p=<0.05). White race was associated with a significantly higher risk of major adverse cardiovascular events (adjusted HR 1.30) and all-cause mortality compared to Black race in men with prostate cancer receiving androgen deprivation therapy.
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