An integrated approach to cardioprotection in lymphomas
- PMID: 35512725
- DOI: 10.1016/S2352-3026(22)00082-5
An integrated approach to cardioprotection in lymphomas
Abstract
In potentially curable cancers, long-term survival depends not only on the successful treatment of the malignancy but also on the risks associated with treatment-related toxicity, especially cardiotoxicity. Malignant lymphomas affect patients at any age, with acute and late toxicity risks that could have a severe effect on morbidity, mortality, and quality of life. Although our understanding of chemotherapy-associated and radiotherapy-associated cardiovascular disease has advanced considerably, new drugs with potential cardiotoxicity have been introduced for the treatment of lymphomas. In this Review, we summarise the mechanisms of treatment-related cardiac injury, available clinical data, and protocols for optimising cardioprotection in lymphomas. We discuss ongoing research strategies to advance our knowledge of the molecular basis of drug-induced and radiation-induced toxicity. Additionally, we emphasise the potential for personalised follow-up and early detection, including the role of biomarkers and novel diagnostic tests, highlighting the role of the cardio-oncology team.
Copyright © 2022 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests MCA acknowledges the support of the Engineering and Physical Research Council (grant number EP/T028017/1), Cancer Research UK RadNet Manchester [C1994/A28701], and the charity Friends of Rosie, UK. MVM acknowledges grants from the Danish Cancer Society and Danish Childhood Cancer Foundation. CM is partially supported by the University College London Hospitals and Barts National Institute for Health Research Biomedical Research Centres. AG is cofounder and a board member of Kither Biotech, a pharmaceutical product company developing PI3K inhibitors for the treatment of respiratory diseases not in conflict with statements present in this Review. ARL has received speaker, advisory board, or consultancy fees and/or research grants from Pfizer, Novartis, Servier, AstraZeneca, Bristol Myers Squibb, GlaxoSmithKline, Amgen, Takeda, Roche, Janssens-Cilag, Clinigen Group, Eli Lily, Eisai, Ferring Pharmaceuticals, Boehringer Ingelheim, Akcea Therapeutics, Myocardial Solutions, iOWNA Health, and Heartfelt Technologies. All other authors declare no competing interests.
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