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Managing life-threatening 5-fluorouracil cardiotoxicity
Kimberly Boldig1, Anupriya Ganguly2, Meet Kadakia3
1Department of Internal Medicine, University of Florida Health at Jacksonville, Jacksonville, Florida, USA kimberly.boldig@jax.ufl.edu.
5-Fluorouracil (5-FU) chemotherapy can cause cardiotoxicity, often presenting as coronary vasospasm. Pre-treatment with diltiazem allowed a patient with colon cancer to safely continue 5-FU infusion, managing this adverse event.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- 5-Fluorouracil (5-FU) is a cornerstone chemotherapy for colorectal cancer.
- 5-FU is associated with significant cardiotoxicity, including coronary vasospasm, arrhythmias, myocardial infarction, and sudden cardiac death.
- Direct toxic effects on vascular endothelium are the common mechanism for 5-FU-induced coronary vasospasm.
Observation:
- A patient with metastatic colon cancer experienced intolerable chest pain during 5-FU infusion chemotherapy.
- Transitioning to bolus 5-FU led to disease progression.
- A multidisciplinary team decided to re-challenge with 5-FU infusion, incorporating pre-treatment with diltiazem.
Findings:
- The patient tolerated the 5-FU infusion with diltiazem pre-treatment without cardiotoxic adverse events.
- This case demonstrates the potential for managing 5-FU-associated cardiotoxicity.
- Multidisciplinary discussion is crucial for co-managing reversible 5-FU-induced cardiotoxicity.
Implications:
- Empiric treatment with calcium channel blockers and/or nitrates may enable patients to continue 5-FU chemotherapy after coronary artery disease risk stratification.
- This approach could preserve a vital treatment option for patients with colorectal cancer.
- Further research into proactive management strategies for 5-FU cardiotoxicity is warranted.
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