# Real-world analyses of major adverse cardiovascular events and mortality risk after androgen deprivation therapy initiation in black vs. white prostate cancer patients

**Authors:** Judd W. Moul, Deborah M. Boldt-Houle, Mack Roach

PMC · DOI: 10.1038/s41391-025-00963-y · Prostate Cancer and Prostatic Diseases · 2025-04-18

## TL;DR

Black prostate cancer patients on androgen deprivation therapy have lower risk of heart issues and better survival than white patients.

## Contribution

Identified racial differences in cardiovascular risks and mortality after androgen deprivation therapy in prostate cancer patients using real-world data.

## Key findings

- White patients had higher MACE risk (4.0% vs. 2.4% at one year) and mortality (11.7% vs. 18.1% at four years) compared to Black patients.
- Black race was associated with lower MACE rates and improved survival during androgen deprivation therapy.
- Study used real-world data encompassing a broader patient scope than prior studies.

## Abstract

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.

Historical, longitudinal patient-level were collected from the Decision Resources Group (DRG, now Clarivate) Real World Evidence repository. The analysis included PCa patients receiving ≥1 ADT 1991–2020. Multivariable regression model accounted for baseline metastasis, BMI (<18.5 vs. ≥18.5 kg/m2), 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.

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.

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.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}
- **Diseases:** diabetes (MESH:D003920), hypertension (MESH:D006973), cardiovascular (MESH:D002318), Prostate cancer (MESH:D011471), metastasis (MESH:D009362), castration-resistant (MESH:D064129)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12643916/full.md

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Source: https://tomesphere.com/paper/PMC12643916