Key result
Radiation therapy increases major coronary events ~7% per Gy mean heart dose across modern cancer regimens.
Why the study?
Improved cancer survival has made cardiovascular disease a major determinant of long-term morbidity and mortality in cancer survivors, establishing cancer therapy-related cardiovascular toxicity as a central challenge requiring a comprehensive clinician-oriented, mechanism-based resource for prevention, detection, and management.
This review provides a mechanism-based framework and practical clinical guidance aligned with ESC-ICOS guidelines for the risk assessment, surveillance, prevention, and management of cardiovascular toxicities associated with contemporary cancer therapies.
Answers are grounded in this paper and cite their sources.
May warrant mechanism-based cardio-oncology surveillance in cancer care; leaves open prospective validation of strategies.
Advances in cancer therapy have substantially improved survival, resulting in a rapidly growing population of cancer survivors. Consequently, cardiovascular disease has emerged as a major determinant of long-term morbidity and mortality, establishing cancer therapy-related cardiovascular toxicity as a central challenge in contemporary cardio-oncology. Modern oncologic therapies produce a broad spectrum of cardiovascular complications, including heart failure, arrhythmias, myocarditis, vascular toxicity, thromboembolic disease, valvular abnormalities, pulmonary hypertension, and autonomic dysfunction. These toxicities arise through diverse mechanisms, including direct myocardial injury, endothelial dysfunction, immune-mediated inflammation, cytokine excess, metabolic derangements, and neurohormonal alterations. This review provides a clinician-oriented, mechanism-based overview of cancer therapy-related cardiovascular toxicity in the modern era. Major therapeutic classes are discussed, including anthracyclines, human epidermal growth factor receptor 2 (HER2)-targeted therapies, tyrosine kinase inhibitors, immune checkpoint inhibitors (ICIs), chimeric antigen receptor T cell therapies, radiation therapy, endocrine therapies, and emerging targeted agents. The review also highlights evolving cardiovascular toxicity phenotypes, radiation-induced heart disease, and the growing relevance of cardiac amyloidosis within the cardio-oncology spectrum. Moreover, contemporary strategies for cardiovascular risk assessment, imaging and biomarker surveillance, cardioprotection, and therapy-specific management are reviewed, with an emphasis on practical clinical application. Finally, current knowledge gaps, survivorship considerations, and future directions are discussed, including artificial intelligence-assisted risk stratification. Overall, by integrating mechanistic understanding with practical management frameworks, this review aims to provide clinicians with a comprehensive resource for the prevention, detection, and treatment of cardiovascular complications associated with modern cancer therapies.
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Mukul Bhattarai (2026) conducted a review in Cancer therapy-related cardiovascular toxicity. Antineoplastic therapies (anthracyclines, HER2 inhibitors, TKIs, ICIs, CAR-T, radiation, endocrine therapies) and cardio-oncology management was evaluated. Modern cancer therapies cause diverse cardiovascular toxicities—including a 7% relative increase in major coronary events per 1 Gy mean heart dose—requiring mechanism-based surveillance and treatment.
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