2009
DOI: 10.1007/bf03086265
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Capecitabine-induced cardiotoxicity mimicking myocardial infarction

Abstract: Capecitabine, a fluoropyrimidine derivative, is an orally administered drug that delivers 5-fluorouracil (5-FU) selectively to the tumour. The drug has demonstrated activity in metastatic colorectal cancer. We describe a male patient receiving capecitabine therapy with typical chest pain and electrocardiographic changes consistent with STsegment elevation myocardial infarction. Capecitabine-induced cardiotoxicity may develop in patients who have had a previous episode of 5-FU-induced cardiotoxicity. Capecitabi… Show more

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Cited by 18 publications
(9 citation statements)
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References 14 publications
(12 reference statements)
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“…The risk of HF remains higher for patients who receive anthracyclines compared with those who receive other agents, even after excluding elderly patients and those with relevant comorbidities . Cancer treatment‐induced HF occurs with several other traditional chemotherapeutic agents, including cyclophosphamide (7%‐28%)and docetaxel (2.3%‐8%) (Table ) . The potential for permanent cardiac damage with exposure to anthracyclines has led to the adoption, in some clinical settings (ie, early stage breast cancer), of chemotherapy regimens with lower cumulative anthracycline exposure.…”
Section: Common CV Adverse Eventsmentioning
confidence: 99%
“…The risk of HF remains higher for patients who receive anthracyclines compared with those who receive other agents, even after excluding elderly patients and those with relevant comorbidities . Cancer treatment‐induced HF occurs with several other traditional chemotherapeutic agents, including cyclophosphamide (7%‐28%)and docetaxel (2.3%‐8%) (Table ) . The potential for permanent cardiac damage with exposure to anthracyclines has led to the adoption, in some clinical settings (ie, early stage breast cancer), of chemotherapy regimens with lower cumulative anthracycline exposure.…”
Section: Common CV Adverse Eventsmentioning
confidence: 99%
“…Prior case reports reveal disease-free coronary arteries on angiography [24]. Other studies note the efficacy of vasodilator therapy, including nitrates and calcium channel blockers, in resolving chest pain and dynamic ECG changes in the setting of 5-FU administration [24,25]. 5-FU also has been shown in vitro to induce vasoconstriction of vascular smooth muscle cells via the activation of protein kinase C, which resolves with administration of protein kinase inhibitors [4].…”
Section: Coronary Vasospasmmentioning
confidence: 99%
“…Several studies have utilized oral capecitabine, an oral pro-drug of 5-FU, as an alternative agent to mitigate the adverse effects of 5-FU. Unfortunately, several reports still demonstrate drug-induced cardiotoxicity, albeit delayed until significant metabolite accumulation occurred [1,25]. Eskilsson et al [48] attempted to prevent vasospasm-induced 5-FU cardiotoxicity via preadministration of verapamil without significant clinical effect.…”
Section: Treatment and Prophylaxismentioning
confidence: 99%
“…Endothelin-1 is a potent vasoconstrictor that has a known regulatory role in vascular vasomotor tone in coronary artery disease [39,40]. The efficacy of vasodilator therapy including non-dihydropyridine calcium channel blockers such as verapamil and nitrates were noted to be effective in resolving chest pain and dynamic ECG changes in the setting of 5-FU induced cardiotoxicity [41,42]. These data support that theory of coronary vasoconstriction as part of the pathophysiology of fluoropyrimidine-induced cardiotoxicity.…”
Section: Coronary Vasospasmmentioning
confidence: 59%