Does SGLT2i prevent cardiac events and improve survival in oncological patients with preexisting cardiovascular risk or receiving cardiotoxic therapies?
Oncological patients with preexisting cardiovascular risk and/or candidates to receive cardiotoxic therapies
Sodium-glucose cotransporter 2 inhibitors (SGLT2i)
SGLT2 inhibitors represent a promising therapeutic option in cardio-oncology to mitigate cardiotoxicity and potentially attenuate tumor growth and cytopenias.
Sodium-glucose cotransporter 2 inhibitors (SGLT2i), a new drug class initially designed and approved for treatment of diabetes mellitus, have been shown to exert pleiotropic metabolic and direct cardioprotective and nephroprotective effects that extend beyond their glucose-lowering action. These properties prompted their use in two frequently intertwined conditions, heart failure and chronic kidney disease. Their unique mechanism of action makes SGLT2i an attractive option also to lower the rate of cardiac events and improve overall survival of oncological patients with preexisting cardiovascular risk and/or candidate to receive cardiotoxic therapies. This review will cover biological foundations and clinical evidence for SGLT2i modulating myocardial function and metabolism, with a focus on their possible use as cardioprotective agents in the cardio-oncology settings. Furthermore, we will explore recently emerged SGLT2i effects on hematopoiesis and immune system, carrying the potential of attenuating tumor growth and chemotherapy-induced cytopenias.
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Massimiliano Camilli
Marcello Viscovo
Luca Maggio
Basic Research in Cardiology
Istituti di Ricovero e Cura a Carattere Scientifico
Università Cattolica del Sacro Cuore
Semmelweis University
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Camilli et al. (Thu,) studied this question.
www.synapsesocial.com/papers/69effa2d4f6a06657c21deae — DOI: https://doi.org/10.1007/s00395-024-01059-9