Real-World Cardiotoxicity in Metastatic Melanoma Patients Treated with Encorafenib and Binimetinib.
Sidsel PedersenMarc Østergaard NielsenMarco DoniaInge Marie SvaneBo ZerahnEva EllebaekPublished in: Cancers (2024)
Modern therapies targeting the BRAF gene mutation in advanced melanoma have significantly improved patient outcomes but pose cardiovascular risks. This retrospective study in Eastern Denmark (2019-2022) assessed 108 melanoma patients treated with encorafenib and binimetinib. Patients were monitored for heart function using multigated acquisition (MUGA) scans. The study defined major cardiotoxicity as a decline in left ventricular ejection fraction (LVEF) by more than 10 percentage points to below 50%, and minor cardiotoxicity as a decrease in LVEF by more than 15 points but remaining above 50%. Results showed that 19 patients (18%) developed minor cardiotoxicity and were asymptomatic, while 7 (6%) experienced major cardiotoxicity, with two requiring intervention. Notably, no significant declines in LVEF were observed after six months of treatment. The study concluded that significant cardiotoxicity occurred in 6% of cases, mostly asymptomatic and reversible, and suggests that monitoring LVEF could potentially be reduced after 6-9 months if no early signs of cardiotoxicity are detected. This provides valuable insights into the cardiac safety of these treatments in real-world settings.
Keyphrases
- ejection fraction
- aortic stenosis
- left ventricular
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- heart failure
- computed tomography
- prognostic factors
- magnetic resonance imaging
- acute myocardial infarction
- coronary artery disease
- drug delivery
- atrial fibrillation
- patient reported outcomes
- cancer therapy
- climate change
- magnetic resonance
- acute coronary syndrome
- aortic valve
- hypertrophic cardiomyopathy
- percutaneous coronary intervention
- patient reported
- left atrial