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Updated: Nov 18, 2025

A Doxorubicin-induced Cardiomyopathy Model in Adult Zebrafish
Published on: June 7, 2018
5-FU Cardiotoxicity: Vasospasm, Myocarditis, and Sudden Death
Luis Alberto More1, Sarah Lane1, Aarti Asnani2,3,4
1CardioVascular Institute, Beth Israel Deaconess Medical Center, Boston, MA, USA.
5-fluorouracil (5-FU) chemotherapy can cause diverse cardiotoxicity. This review guides clinicians on managing 5-FU cardiotoxicity, highlighting genetic testing and the antidote uridine triacetate.
Area of Science:
- Cardiology
- Oncology
- Pharmacology
Background:
- 5-fluorouracil (5-FU) is a widely used chemotherapy agent.
- 5-FU is a common cause of chemotherapy-induced cardiotoxicity.
- Clinical guidelines for diagnosing and managing 5-FU cardiotoxicity are lacking.
Purpose of the Study:
- To summarize mechanistic and clinical data on 5-FU cardiotoxicity.
- To guide clinicians in the diagnosis and management of patients with suspected 5-FU cardiotoxicity.
Main Methods:
- Review of existing mechanistic and clinical data.
- Synthesis of information to inform clinical practice.
Main Results:
- 5-FU cardiotoxicity presents with diverse manifestations.
- Resuming 5-FU treatment after cardiotoxicity is challenging.
- Genetic variant testing may aid in risk assessment.
- Uridine triacetate is an approved antidote for severe cases.
Conclusions:
- 5-FU cardiotoxicity is poorly understood with limited data.
- Individualized risk-benefit assessment is crucial for treatment decisions.
- Management strategies require further research and prospective trials.
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