Cited by 542Prostate Cancer Treatment and ResearchHormonal and reproductive studiesChemotherapy-induced cardiotoxicity and mitigation

Androgen deprivation therapy increases cardiovascular morbidity in men with prostate cancer

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Saigal, Christopher S., Gore, John L., Krupski, Tracey L., Hanley, Janet, Schonlau, Matthias, Litwin, Mark S.·2007·Cancer

Abstract

BACKGROUND.: The use of androgen deprivation therapy (ADT) in the treatment of men with prostate cancer has risen sharply. Although cardiovascular disease is the most common reason for death among men with prostate cancer who do not die of the disease itself, data regarding the effect of ADT on cardiovascular morbidity and mortality in men with prostate cancer are limited. In the current study, the authors attempted to measure the risk for subsequent cardiovascular morbidity in men with prostate cancer who received ADT. METHODS.: A cohort of newly diagnosed men in a population‐based registry who were diagnosed between 1992 and 1996 were identified retrospectively. A total of 22,816 subjects were identified after exclusion criteria were applied. Using a multivariate model, the authors calculated the risk of subsequent cardiovascular morbidity in men with prostate cancer who were treated with ADT, as defined using Medicare claims. RESULTS.: Newly diagnosed prostate cancer patients who received ADT for at least 1 year were found to have a 20% higher risk of serious cardiovascular morbidity compared with similar men who did not receive ADT. Subjects began incurring this higher risk within 12 months of treatment. However, Hispanic men were found to have a lowered risk for cardiovascular morbidity. CONCLUSIONS.: ADT is associated with significantly increased cardiovascular morbidity in men with prostate cancer and may lower overall survival in men with low‐risk disease. These data have particular relevance to decisions regarding the use of ADT in men with prostate cancer in settings in which the benefit has not been clearly established. For men with metastatic disease, focused efforts to reduce cardiac risk factors through diet, exercise, or the use of lipid‐lowering agents may mitigate some of the risks of ADT. Cancer 2007. © 2007 American Cancer Society.

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  1. [5]5. Satariano WA, Ragland KE, Van Den Eeden SK. Cause of death in men diagnosed with prostate carcinoma. Cancer. 1998;83:1180-1188.

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Authors
Saigal, C. S., Gore, J. L., Krupski, T. L., Hanley, J., Schonlau, M., & Litwin, M. S.
Affiliations
  • University of California, Los Angeles (US)
  • Duke University (US)
  • RAND Corporation (US)
Corresponding author
Saigal, Christopher S.
Venue
Cancer
Publisher
Wiley
Published
2007-07-26
Volume
110
Issue
7
Pages
1493-1500
ISSN
  • 0008-543X (ISSN-L)
  • 1097-0142
OpenAlex
W2105310697
Cited by
542
References
37
Citations by year
2026: 6 · 2025: 12 · 2024: 15 · 2023: 17 · 2022: 19 · 2021: 20 · 2020: 20 · 2019: 15 · 2018: 17 · 2017: 28 · 2016: 28 · 2015: 25 · 2014: 27 · 2013: 32 · 2012: 65
FWCI
39.17
Type
journal article
Language
en
Open access
Locations
  • Cancer (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Cancer Institute
  • National Institute of Diabetes and Digestive and Kidney Diseases
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Prostate Cancer Treatment and Research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Chemotherapy-induced cardiotoxicity and mitigation
Keywords
androgen deprivation therapy, prostate cancer, cardiovascular morbidity, cardiovascular risk, Hispanic men, low-risk prostate cancer, metastatic prostate cancer, overall survival, lipid-lowering drugs, cardiovascular risk factors
MeSH terms
Aged, Aged, 80 and over, Androgen Antagonists, Cardiovascular Diseases, Educational Status, Medicare, Hispanic or Latino, Humans, Male, Prostatic Neoplasms, Retrospective Studies, Risk Factors, Socioeconomic Factors, United States, Cohort Studies, Multivariate Analysis, SEER Program, Risk Assessment, Antineoplastic Agents, Hormonal, Kaplan-Meier Estimate

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