Doxorubicin (adriamycin) cardiomyopathy.
- 1 September 1983
- journal article
- review article
- Vol. 139 (3) , 332-41
Abstract
Despite its vast utility in clinical oncology, the use of doxorubicin hydrochloride (Adriamycin) is limited by a potentially fatal cardiomyopathy. The following critical review, which examines the natural course, histopathologic effects, risk factors and monitoring indicators of this toxicity, also analyzes recent research of proposed mechanisms, including free radical formation with depletion of detoxifying enzymes, inhibition of vital enzyme systems and alterations in relative calcium concentrations. Prevention of the adverse reaction has been attempted by using such agents as alpha-tocopherol, selenium sulfide, coenzyme Q(10), sulfhydryl donors, nucleosides and razoxane, and via liposomal carriage and alternative methods of administration.This publication has 84 references indexed in Scilit:
- Dose-effect and structure-function relationships in doxorubicin cardiomyopathyAmerican Heart Journal, 1981
- Doxorubicin cardiotoxicity in childrenThe Journal of Pediatrics, 1980
- Adriamycin cardiotoxicityAmerican Heart Journal, 1980
- Hepatic irradiation and adriamycin cardiotoxicityThe Journal of Pediatrics, 1979
- Serial Assessment of Doxorubicin Cardiotoxicity with Quantitative Radionuclide AngiocardiographyNew England Journal of Medicine, 1979
- Assessment of Adriamycin cardiotoxicity in children by systolic time intervalsEuropean Journal of Pediatrics, 1979
- Echocardiographic assessment of anthracycline cardiotoxicity in childrenMedical and Pediatric Oncology, 1978
- Doxorubicin cardiotoxicity: possible role of digoxin in its prevention.BMJ, 1977
- Adriamycin stimulated superoxide formation in submitochondrial particlesChemico-Biological Interactions, 1977
- Adriamycin: The Role of Lipid Peroxidation in Cardiac Toxicity and Tumor ResponseScience, 1977