Key result
Capecitabine therapy for colon cancer was associated with severe cardiotoxicity, presenting as symptomatic bradycardia and sinus arrest that ultimately required a pacemaker.
Why the study?
Does capecitabine cause severe cardiotoxicity such as symptomatic bradycardia and sinus arrest in patients with colon cancer?
Case Report (n=1)
Does capecitabine cause severe cardiotoxicity such as symptomatic bradycardia and sinus arrest in patients with colon cancer?
Capecitabine can induce severe cardiotoxicity, including symptomatic bradycardia and sinus arrest requiring pacemaker implantation.
Alerts clinicians to possible capecitabine cardiotoxicity; leaves open incidence, mechanisms, and management strategies.
Capecitabine, an oral prodrug of 5-fluorouracil (5FU), has been integrated into the management of multiple cancer types because of convenience of administration and efficacy comparable with 5fu. Cardiotoxicity induced by 5FU-in particular angina-has been well described in the literature, but reports of adverse cardiac events with capecitabine are also emerging. The mechanism underlying 5FU cardiotoxicity has long been thought to result from coronary vasospasm, but animal-model studies and patient echocardiographic findings both suggest a cardiomyopathic picture. Although 5FU cardiotoxicity is often reversible and can be managed supportively, presentations that are more severe-including arrhythmias, acute ischemic events, and cardiogenic shock-have been documented. In this report, we describe the case of a patient who ultimately required a pacemaker after developing symptomatic bradycardia and sinus arrest while receiving capecitabine for colon cancer.
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Ang et al. (2010) conducted a case report in Colon cancer (n=1). Capecitabine was evaluated on Symptomatic bradycardia and sinus arrest requiring a pacemaker. Capecitabine therapy for colon cancer was associated with severe cardiotoxicity, presenting as symptomatic bradycardia and sinus arrest that ultimately required a pacemaker.
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