Management and treatment of cardiotoxicity due to anticancer drugs: 10 questions and answers
- PMID: 35938306
- DOI: 10.1093/eurjpc/zwac170
Management and treatment of cardiotoxicity due to anticancer drugs: 10 questions and answers
Abstract
Since the introduction of anthracyclines into clinical practice in the 1960s, chemotherapy has always been associated with cardiotoxicity. Patients on cardiotoxic drugs can develop a wide range of cardiovascular diseases, including left ventricular (LV) systolic dysfunction and heart failure (HF), arrhythmias, hypertension, and coronary artery disease (CAD). The rising number of cancer patients, population ageing, and the frequent overlap of cardiovascular and oncological diseases have highlighted the importance of close collaboration between cardiologists and oncologists. As a result, in 1995, cardiologists at the IEO (European Institute of Oncology) coined the term cardioncology, a new discipline focused on the dynamics of cardiovascular disease in cancer patients. Given the complex scenario characterized by a constant dialogue between the oncological condition and cardiovascular comorbidity, it is essential for the clinician to get the knowledge to properly fulfill the needs of the oncological patient under cardiotoxic treatment. Through the answer to 10 questions, we aim to describe the complex issue of cardiotoxicity by addressing the main critical points and current evidence related to the assessment, management, treatment, and surveillance of cancer patients under chemotherapy.
Keywords: Cardiac biomarker; Cardio protection; Cardiotoxic; Chemotherapy; Heart failure; Ventricular function.
© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please email: journals.permissions@oup.com.
Conflict of interest statement
Conflict of interest: None declared.
Similar articles
-
Management of cancer patients at high and very-high risk of cardiotoxicity: Main questions and answers.Curr Probl Cardiol. 2024 Mar;49(3):102229. doi: 10.1016/j.cpcardiol.2023.102229. Epub 2023 Dec 27. Curr Probl Cardiol. 2024. PMID: 38154703 Review.
-
Cardiotoxicity of anticancer treatments: Epidemiology, detection, and management.CA Cancer J Clin. 2016 Jul;66(4):309-25. doi: 10.3322/caac.21341. Epub 2016 Feb 26. CA Cancer J Clin. 2016. PMID: 26919165 Review.
-
Cardiotoxicity associated with cancer therapy: pathophysiology and prevention strategies.Rev Port Cardiol. 2013 May;32(5):395-409. doi: 10.1016/j.repc.2012.11.002. Epub 2013 Apr 24. Rev Port Cardiol. 2013. PMID: 23623503 Review. English, Portuguese.
-
Practices in management of cancer treatment-related cardiovascular toxicity: A cardio-oncology survey.Int J Cardiol. 2017 Aug 15;241:387-392. doi: 10.1016/j.ijcard.2017.02.154. Epub 2017 Mar 21. Int J Cardiol. 2017. PMID: 28365180
-
Pharmacological foundations of cardio-oncology.J Pharmacol Exp Ther. 2010 Jul;334(1):2-8. doi: 10.1124/jpet.110.165860. Epub 2010 Mar 24. J Pharmacol Exp Ther. 2010. PMID: 20335321
Cited by
-
Biochemical Insights into the Effects of a Small Molecule Drug Candidate on Imatinib-Induced Cardiac Inflammation.Int J Mol Sci. 2025 Jul 11;26(14):6661. doi: 10.3390/ijms26146661. Int J Mol Sci. 2025. PMID: 40724911 Free PMC article.
-
Reduced cardiovascular reserve capacity in long-term allogeneic stem cell transplant survivors.Sci Rep. 2023 Feb 6;13(1):2112. doi: 10.1038/s41598-023-28320-w. Sci Rep. 2023. PMID: 36747066 Free PMC article.
-
Endothelin-based markers for endothelial dysfunction in chemotherapy-induced cardiotoxicity.J Mol Cell Cardiol Plus. 2023 Oct 13;6:100053. doi: 10.1016/j.jmccpl.2023.100053. eCollection 2023 Dec. J Mol Cell Cardiol Plus. 2023. PMID: 39802623 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous