Why the study?
Current cardiotoxicity guidelines rely mainly on monitoring LVEF, whereas imaging microvascular and metabolic dysfunction could enable earlier detection before overt LVEF impairment.
Does myocardial perfusion and metabolic imaging improve early detection of anticancer drug-related cardiotoxicity compared to LVEF monitoring?
Does myocardial perfusion and metabolic imaging improve early detection of anticancer drug-related cardiotoxicity compared to LVEF monitoring?
Advanced imaging techniques focusing on myocardial perfusion and metabolism may enable earlier detection of anticancer drug-induced cardiotoxicity than standard LVEF monitoring.
May support earlier cardiotoxicity detection before LVEF decline; leaves open prospective validation before clinical adoption.
Cardio-oncology requires a good knowledge of the cardiotoxicity of anticancer drugs, their mechanisms, and their diagnosis for better management. Anthracyclines, anti-vascular endothelial growth factor (VEGF), alkylating agents, antimetabolites, anti-human epidermal growth factor receptor (HER), and receptor tyrosine kinase inhibitors (RTKi) are therapeutics whose cardiotoxicity involves several mechanisms at the cellular and subcellular levels. Current guidelines for anticancer drugs cardiotoxicity are essentially based on monitoring left ventricle ejection fraction (LVEF). However, knowledge of microvascular and metabolic dysfunction allows for better imaging assessment before overt LVEF impairment. Early detection of anticancer drug-related cardiotoxicity would therefore advance the prevention and patient care. In this review, we provide a comprehensive overview of the cardiotoxic effects of anticancer drugs and describe myocardial perfusion, metabolic, and mitochondrial function imaging approaches to detect them before over LVEF impairment.
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Cadour et al. (2022) studied this question.
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