5-fluorouracil and cardiotoxicity: a review

Author:

Sara Jaskanwal D.1,Kaur Jasvinder2,Khodadadi Ryan3,Rehman Muneeb3,Lobo Ronstan3,Chakrabarti Sakti4,Herrmann Joerg5,Lerman Amir5,Grothey Axel4

Affiliation:

1. Department of Cardiovascular Diseases, Mayo College of Medicine, 200 First Street SW, Rochester, MN 55905-0001, USA

2. Kent Oncology Centre, Maidstone and Tunbridge Wells NHS Trust, Maidstone, Kent, UK

3. Department of Internal Medicine, Mayo College of Medicine, Rochester, MN, USA

4. Department of Medical Oncology, Mayo College of Medicine, Rochester, MN, USA

5. Department of Cardiovascular Diseases, Mayo College of Medicine, Rochester, MN, USA

Abstract

Fluoropyrimidines such as 5-fluorouracil (5-FU) form the foundation of a wide variety of chemotherapy regimens. 5-FU is in fact the third most commonly used chemotherapeutic agent in the treatment of solid malignancies across the world. As with all chemotherapy, balancing the potential benefits of therapy against the risks of drug-related toxicity is crucial when clinicians and patients make shared decisions about treatment. 5-FU is the second most common chemotherapeutic drug associated with cardiotoxicity after anthracyclines, which can manifest as chest pain, acute coronary syndrome/myocardial infarction or death. Nevertheless a widespread appreciation of 5-FU-related cardiotoxicity and its implications is lacking amongst clinicians. In this review, we outline the incidence, possible risk factors, and likely pathophysiological mechanisms that may account for 5-FU-related cardiotoxicity and also highlight potential management strategies for this poorly understood clinical entity.

Publisher

SAGE Publications

Subject

Oncology

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