{"id":"bdcc8ad43963","type":"article","url":"https://hartvaat.nl/2026/06/01/cardiovasculair-risico-van-adt-en-arpi-s-bij-prostaatkanker-narrative-review/","title":"Cardiovasculair risico van ADT en ARPI's bij prostaatkanker — narrative review","title_en":"Androgen Deprivation Therapy and Cardiovascular Health: Challenges and Opportunities in Prostate Cancer Care.","category":"preventie","category_label":"Preventie","professions":["cardioloog","internist"],"tags":[],"journal":"Archivos espanoles de urologia","doi":"10.56434/j.arch.esp.urol.20267905.87","source_url":"https://doi.org/10.56434/j.arch.esp.urol.20267905.87","authors":["Sandra Fernández Alonso","Fernando López Campos","David Büchser","Sandra Guardado","Jon Andreescu","Walter Vásquez","Ana Castaño","Javier Gil Moradillo","Lucía García González","Andrew Loblaw","Felipe Couñago"],"significance":5,"published":"2026-08-13","source_date":"2026-06-01","image":"","kennis":["https://hartvaat.nl/kennis/cardiometabool/cardiometabool-spreekuur/","https://hartvaat.nl/kennis/lipiden/lpa-meten-wanneer-waarom/"],"congress":"","summary_en":"A narrative review examines the cardiovascular toxicity of androgen deprivation therapy (ADT) and androgen receptor pathway inhibitors (ARPIs) in patients with prostate cancer. ADT induces metabolic and vascular alterations that promote a proatherogenic state; GnRH antagonists appear to carry a lower early risk of major adverse cardiovascular events compared to agonists, while darolutamide demonstrates a more favorable cardiovascular safety profile than abiraterone or apalutamide. Routine cardiovascular risk assessment, aggressive management of modifiable risk factors, and a multidisciplinary cardio-oncology approach are essential to optimize long-term outcomes in this population.","created":"2026-08-07T00:54:42Z","updated":"2026-08-10T10:35:49Z","licence":"Citeer vrij, met bronvermelding en een link naar hartvaat.nl (de url van het record). Samenvattingen zijn redactioneel werk van HartVaat; de oorspronkelijke publicaties blijven van hun uitgevers (doi). Geen medisch advies.","body_markdown":"Een narrative review onderzoekt de cardiovasculaire toxiciteit van androgeendeprivétherapie (ADT) en androgen receptor pathway inhibitors (ARPI's) bij patiënten met prostaatkanker. ADT veroorzaakt metabole en vasculaire veranderingen die een proatherogene staat bevorderen; GnRH-antagonisten lijken een lager vroeg risico op MACE te hebben dan agonisten, terwijl darolutamide een gunstiger veiligheidsprofiel vertoont dan abiraterone of apalutamide. Systematische cardiovasculaire risicoschatting, preventie van modificeerbare risicofactoren en een multidisciplinaire aanpak zijn essentieel om de lange termijn uitkomsten van deze patiënten te optimaliseren.","abstract_original":"BACKGROUND: Androgen deprivation therapy (ADT) and androgen receptor pathway inhibitors (ARPIs) improve advanced prostate cancer (PCa) outcomes but increase cardiovascular (CV) toxicity, making cardiovascular disease (CVD) a major competing cause of morbidity, and mortality. To review the current evidence on CV toxicity related to ADT and ARPIs in PCa focusing on the magnitude of CV risk, strategies for CV risk assessment and prevention in clinical practice. METHODS: A narrative review of the English-language literature was conducted using PubMed, Scopus, the Cochrane Library, and ScienceDirect. The search included studies through December 2025 on ADT- and ARPI-associated cardiovascular toxicity. Search terms combined keywords and Medical Subject Headings (MeSH) terms such as \"prostate cancer\", \"androgen deprivation therapy\", \"androgen receptor pathway inhibitors\", \"cardiovascular toxicity\", and \"cardio-oncology\". Eligible studies included prospective clinical trials, systematic reviews, meta-analyses, and clinically relevant retrospective or real-world studies. Reference snowballing was not performed. RESULTS: ADT induces metabolic, vascular, inflammatory, and endocrine alterations that promote a proatherogenic and prothrombotic state. CV risk appears to vary across hormonal therapies. Gonadotropin-releasing hormone (GnRH) antagonists appear to be associated with lower early rates of major adverse cardiovascular events (MACE)-as defined in each included study-than GnRH agonists, particularly in patients with pre-existing CVD, although evidence from meta-analyses and realworld studies remains heterogeneous. ARPIs show distinct CV safety profiles, with higher rates of hypertension and CV events reported with abiraterone and apalutamide, whereas darolutamide appears to have a more favorable profile. CONCLUSIONS: Systematic CV risk assessment, preventive management of modifiable risk factors, and individualized treatment strategies within a multidisciplinary cardio-oncology framework are essential to optimize long-term outcomes in patients with PCa receiving ADT and ARPIs."}