Are Sodium-Glucose Cotransporter-2 Inhibitors the Cherry on Top of Cardio-Oncology Care?
Carlos A GongoraLili ZhangJuan Lopez MatteiEnrique Ruiz-MoriGina Gonzalez-RobledoLeandro SlipczukJoffre LaraJorge E Cossio-ArandaJuan José BadimonPublished in: Cardiovascular drugs and therapy (2024)
The increasing aging of the population combined with improvements in cancer detection and care has significantly improved the survival and quality of life of cancer patients. These benefits are hampered by the increase of cardiovascular diseases being heart failure the most frequent manifestation of cardiotoxicity and becoming the major cause of morbidity and mortality among cancer survivor. Current strategies to prevent cardiotoxicity involves different approaches such as optimal management of CV risk factors, use of statins and/or neurohormonal medications, and, in some cases, even the use of chelating agents. As a class, SGLT2-i have revolutionized the therapeutic horizon of HF patients independently of their ejection fraction or glycemic status. There is an abundance of data from translational and observational clinical studies supporting a potential beneficial role of SGLT2-i in mitigating the cardiotoxic effects of cancer patients receiving anthracyclines. These findings underscore the need for more robust clinical trials to investigate the effect on cardiovascular outcomes of the prophylactic SGLT2-i treatment in patients undergoing cancer treatment.
Keyphrases
- ejection fraction
- papillary thyroid
- heart failure
- clinical trial
- palliative care
- cardiovascular disease
- risk factors
- squamous cell
- patients undergoing
- healthcare
- aortic stenosis
- type diabetes
- quality improvement
- newly diagnosed
- left ventricular
- squamous cell carcinoma
- end stage renal disease
- risk assessment
- lymph node metastasis
- young adults
- microbial community
- coronary artery disease
- atrial fibrillation
- patient reported
- insulin resistance
- big data
- loop mediated isothermal amplification
- aortic valve