Why the study?
Increasing reports indicate cardiovascular complications from androgen deprivation therapy (ADT) lead to worse outcomes in prostate cancer, with ADT-type-specific complications suggesting mechanisms beyond androgen suppression.
Does androgen deprivation therapy increase the risk of cardiovascular complications in patients with prostate cancer?
Does androgen deprivation therapy increase the risk of cardiovascular complications in patients with prostate cancer?
Different classes of androgen deprivation therapy carry distinct cardiovascular risks, highlighting the need for individualized cardiovascular risk assessment and management in prostate cancer patients.
ADT-associated CV complications in prostate cancer warrant monitoring; leaves open type-specific mechanisms and management pending prospective data.
PURPOSE OF THE REVIEW: There have been increasing reports of cardiovascular complications of androgen deprivation therapy (ADT) leading to worse outcomes among patients with prostate cancer. While this may result from the direct effects of androgen suppression in the cardiovascular systems, there are ADT-type-specific distinct cardiovascular complications suggestive of mechanisms beyond androgen-mediated. Thus, it is critical to understand the biological and clinical impact of ADT on the cardiovascular system. RECENT FINDINGS: Gonadotropin-releasing hormone (GnRH) agonists cause increased cardiovascular events compared to GnRH antagonists. Androgen receptor antagonists are linked to an increased risk of long QT syndrome, torsades de pointes, and sudden cardiac death. Androgen synthesis inhibitors are associated with increased rates of hypertension, atrial tachyarrhythmia, and, in rare incidences, heart failure. ADT increases the risk of cardiovascular disease. The risk among ADT drugs differs and must be evaluated to develop a medically optimal plan for prostate cancer patients.
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Kim et al. (2023) studied this question.
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