European Heart Journal Advance Access originally published online on April 12, 2006
European Heart Journal 2006 27(10):1137-1138; doi:10.1093/eurheartj/ehi702
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© The European Society of Cardiology 2006. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Anthracycline cardiotoxicity
1 Regional Medical Cardiology Centre, Royal Victoria Hospital, Belfast, Northern Ireland, UK
2 Department of Haematology, Queen's University Belfast, Northern Ireland, UK
3 Department of Medicine, Institute of Clinical Science, Queen's University Belfast, Grosvenor Road, Belfast BT12 6BJ, Northern Ireland, UK
* Corresponding author. Tel: +44 28 9063 4825; fax: +44 28 9031 2907. E-mail address: p.p.mckeown@qub.ac.uk
This editorial refers to Iloprost attenuates doxorubicin-induced cardiac injury in a murine model without compromising tumour suppression
by T.G. Neilan et al., on page 1251
| The first 10% of the full text of this article appears below. |
Anthracycline drugs have been widely used as chemotherapeutic agents against a range of cancers, including sarcomas, carcinomas, leukaemias, and lymphomas. However, cardiotoxic effects, in particular the development of cardiomyopathy, have limited their clinical use. The observation of dose-dependent cardiotoxicity has resulted in a recommended empirical dose limit of 450 mg/m2 of body surface area. Age, gender, pre-existing heart disease, hypertension, and mediastinal irradiation have also been implicated as factors contributing to the development of doxorubicin-associated cardiomyopathy. However, cardiotoxicity may still occur at relatively low levels of drug administration, even in individuals with no additional risk factors, and the onset may be delayed by many years.1 More recently, the use of trastuzumab, a monoclonal antibody directed against the HER2 receptor, has been
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EHJ 2006 27: 1251-1256.[Abstract] [Full Text]