Cardiovascular toxicity induced by chemotherapy, targeted agents and radiotherapy: ESMO Clinical Practice Guidelines
- PMID: 22997448
- DOI: 10.1093/annonc/mds293
Cardiovascular toxicity induced by chemotherapy, targeted agents and radiotherapy: ESMO Clinical Practice Guidelines
Abstract
Cardiovascular (CV) toxicity is a potential short- or long-term complication of various anticancer therapies. Some drugs, such as anthracyclines or other biological agents, have been implicated in causing potentially irreversible clinically important cardiac dysfunction. Although targeted therapies are considered less toxic and better tolerated by patients compared with classic chemotherapy agents, rare but serious complications have been described, and longer follow-up is needed to determine the exact profile and outcomes of related cardiac side-effects. Some of these side-effects are irreversible, leading to progressive CV disease, and some others induce reversible dysfunction with no long-term cardiac damage to the patient. Assessment of the prevalence, type and severity of cardiac toxicity caused by various cancer treatments is a breakthrough topic for patient management. Guidelines for preventing, monitoring and treating cardiac side-effects are a major medical need. Efforts are needed to promote strategies for cardiac risk prevention, detection and management, avoiding unintended consequences that can impede development, regulatory approval and patient access to novel therapy. These new ESMO Clinical Practice Guidelines are the result of a multidisciplinary cardio-oncology review of current evidence with the ultimate goal of providing strict criteria-based recommendations on CV risk prevention, assessment, monitoring and management during anticancer treatment.
Similar articles
-
Cardiac toxicity from systemic cancer therapy: a comprehensive review.Prog Cardiovasc Dis. 2010 Sep-Oct;53(2):94-104. doi: 10.1016/j.pcad.2010.05.006. Prog Cardiovasc Dis. 2010. PMID: 20728696 Review.
-
Management of cardiac disease in cancer patients throughout oncological treatment: ESMO consensus recommendations.Ann Oncol. 2020 Feb;31(2):171-190. doi: 10.1016/j.annonc.2019.10.023. Ann Oncol. 2020. PMID: 31959335 Free PMC article.
-
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.
-
Cardiotoxicity induced by tyrosine kinase inhibitors.Acta Oncol. 2009;48(7):964-70. doi: 10.1080/02841860903229124. Acta Oncol. 2009. PMID: 19734999 Review.
-
Detection and prevention of cardiac complications of cancer chemotherapy.Arch Cardiovasc Dis. 2012 Nov;105(11):593-604. doi: 10.1016/j.acvd.2012.04.008. Epub 2012 Oct 4. Arch Cardiovasc Dis. 2012. PMID: 23177488 Review.
Cited by
-
Breast Radiotherapy-Related Cardiotoxicity. When, How, Why. Risk Prevention and Control Strategies.Cancers (Basel). 2021 Apr 4;13(7):1712. doi: 10.3390/cancers13071712. Cancers (Basel). 2021. PMID: 33916644 Free PMC article. Review.
-
Cardio-oncology care in the era of the coronavirus disease 2019 (COVID-19) pandemic: An International Cardio-Oncology Society (ICOS) statement.CA Cancer J Clin. 2020 Nov;70(6):480-504. doi: 10.3322/caac.21635. Epub 2020 Sep 10. CA Cancer J Clin. 2020. PMID: 32910493 Free PMC article. Review.
-
Is there a window of opportunity to optimize trastuzumab cardiac monitoring?World J Cardiol. 2022 Jul 26;14(7):403-410. doi: 10.4330/wjc.v14.i7.403. World J Cardiol. 2022. PMID: 36161060 Free PMC article.
-
Establishing an oncocardiology service.Herz. 2020 Nov;45(7):626-631. doi: 10.1007/s00059-020-04952-w. Herz. 2020. PMID: 32572500 Free PMC article. Review.
-
Benefits of antihypertensive medications for anthracycline- and trastuzumab-induced cardiotoxicity in patients with breast cancer: Insights from recent clinical trials.Indian J Pharmacol. 2016 Sep-Oct;48(5):490-497. doi: 10.4103/0253-7613.190719. Indian J Pharmacol. 2016. PMID: 27721532 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical