Key result
Pretreatment with diltiazem ER 240 mg allowed a patient with previous 5-fluorouracil-induced cardiotoxicity to successfully tolerate continued 5-FU chemotherapy infusion without adverse cardiac events.
Why the study?
Does pretreatment with diltiazem prevent 5-FU-induced cardiotoxicity in a patient with prior 5-FU-induced chest pain?
Case Report (n=1)
No
Does pretreatment with diltiazem prevent 5-FU-induced cardiotoxicity in a patient with prior 5-FU-induced chest pain?
Pretreatment with diltiazem may allow patients with suspected 5-FU-induced coronary vasospasm to safely continue vital chemotherapy.
5-Fluorouracil (5-FU), a known cardiotoxin, is the backbone for the treatment of colorectal cancer. It is associated with arrhythmias, myocardial infarction and sudden cardiac death. Most commonly, it is associated with coronary vasospasm secondary to direct toxic effects on vascular endothelium.A woman with metastatic colon cancer, originally treated with a 5-FU infusion as part of the FOLFIRI (Folinic acid, 5-Fluorouracil, Irinotecan) regimen, was unable to tolerate the chemotherapy due to chest pain. She was transitioned from infusional 5-FU to inferior 1-hour bolus 5-FU, in an attempt to minimise cardiotoxicity, but had disease progression. A multidisciplinary decision was made to again trial 5-FU infusion and pretreat with diltiazem. She tolerated chemotherapy without adverse events. A multidisciplinary discussion is recommended for co-management of reversible 5-FU-associated cardiotoxicity. After coronary artery disease (CAD) risk stratification and treatment, empiric treatment with calcium channel blockers and/or nitrates may allow patients with suspected coronary vasospasm, from 5-FU, to continue this vital chemotherapy.
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Boldig et al. (2022) conducted a case report in Metastatic colon cancer with 5-fluorouracil cardiotoxicity (n=1). Diltiazem extended release (ER) pretreatment was evaluated on Tolerance of 5-FU infusion without angina or abnormal rhythms. Pretreatment with diltiazem ER 240 mg allowed a patient with previous 5-fluorouracil-induced cardiotoxicity to successfully tolerate continued 5-FU chemotherapy infusion without adverse cardiac events.
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