Incidence of Cardiovascular Events in Patients With Prostate Cancer and Treated With Androgen Deprivation Therapy

Urol Pract. 2024 Jan;11(1):154-161. doi: 10.1097/UPJ.0000000000000487. Epub 2023 Nov 1.

Abstract

Introduction: Cardiovascular disease (CVD) is the leading cause of death among prostate cancer (PC) patients. Androgen deprivation therapy (ADT) with a gonadotropin-releasing hormone receptor (GnRH) agonist or antagonist is the standard treatment for advanced PC. Since 2010, the Food and Drug Administration has required labeling for GnRH agonists to include warnings about increased risk for diabetes and some CVDs.

Methods: In this observational, retrospective, real-world study, we evaluated time to a first cardiovascular (CV) event within 3 years postinitiation of ADT in PC patients while controlling for CVD history and risk factors. Data from a large administrative US claims dataset (2010-2019) were analyzed using Kaplan-Meier survival analysis to calculate the HR for time to first CV event and Cox regressions to identify factors associated with time to first CV event.

Results: Of 10,530 patients, 92% had no history of CVD, 8% had history of CVD, and 95% were exposed to a GnRH agonist during follow-up. Kaplan-Meier analysis indicated that patients with a baseline history of CVD had increased risk of CV events within 3 years of ADT initiation vs those without such history (HR, 3.20; 95% CI, 2.58-3.96; P < .0001). Among covariates associated with higher likelihood of CV event, baseline history of CVD yielded the highest HR (2.83; 95% CI, 2.40-3.32, P < .0001).

Conclusions: PC patients with a history of CVD are at increased risk of a CV event within 3 years of ADT initiation compared with those with no history of CVD.

Keywords: androgens; cardiovascular diseases; cardiovascular risk; gonadotropin releasing hormone; prostate cancer.

Publication types

  • Observational Study

MeSH terms

  • Androgen Antagonists / adverse effects
  • Androgens / therapeutic use
  • Cardiovascular Diseases* / chemically induced
  • Gonadotropin-Releasing Hormone / agonists
  • Humans
  • Incidence
  • Male
  • Prostatic Neoplasms* / drug therapy
  • Retrospective Studies
  • Risk Factors
  • United States

Substances

  • Androgen Antagonists
  • Androgens
  • Gonadotropin-Releasing Hormone