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Published on: May 16, 2020
Anthracycline-induced cardiotoxicity: course, pathophysiology, prevention and management
Elly Barry1, Jorge A Alvarez, Rebecca E Scully
1Department of Pediatric Oncology, Dana-Farber Cancer Institute/Children's Hospital, Boston/Harvard Medical School, 44 Binney Street, 3rd Floor, Boston, MA 02115, USA.
Anthracycline chemotherapy can cause heart damage, but strategies like dose limitation and cardioprotectants such as dexrazoxane can minimize risks. Managing anthracycline-induced cardiotoxicity involves standard heart failure treatments.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- Anthracyclines are vital anti-cancer drugs but cause significant cardiotoxicity.
- Cardiovascular disease is a major concern for long-term cancer survivors treated with anthracyclines, potentially leading to heart failure.
Purpose of the Study:
- To review current strategies for minimizing anthracycline-induced cardiotoxicity.
- To discuss methods for monitoring and managing cardiac dysfunction in cancer patients and survivors.
Main Methods:
- Literature review of strategies to mitigate anthracycline cardiotoxicity.
- Examination of cardioprotective agents, including dexrazoxane.
- Overview of monitoring techniques (echocardiography, radionuclide scans, biomarkers).
- Analysis of current management approaches for established cardiotoxicity.
Main Results:
- Several strategies exist to reduce cardiotoxicity, such as dose capping, controlled infusion rates, liposomal formulations, and novel analogues.
- Dexrazoxane shows promise as a cardioprotectant.
- Monitoring cardiotoxicity involves functional and biochemical assessments.
- Management of anthracycline-induced cardiotoxicity mirrors standard heart failure treatments.
Conclusions:
- Minimizing anthracycline cardiotoxicity requires a multi-faceted approach involving drug administration modifications and cardioprotective agents.
- Effective monitoring and management are crucial for long-term cancer survivors.
- Further research is needed on systematic treatment protocols for anthracycline-related cardiac dysfunction.
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