Key result
Capecitabine therapy linked to rare but reversible takotsubo cardiomyopathy resolving after drug cessation.
Why the study?
Capecitabine is thought to have minimal cardiac toxicity, but rare cases of takotsubo cardiomyopathy related to its use have been reported.
Case Report (n=1)
Capecitabine can rarely induce takotsubo cardiomyopathy, which appears reversible upon drug discontinuation and standard heart failure therapy.
May prompt monitoring for takotsubo cardiomyopathy during capecitabine therapy; leaves open causality with only five cases reported.
Capecitabine is an orally administered chemotherapeutic agent that is metabolized at the tumor site to 5-fluorouracil and thought to be without significant cardiac toxicity. We report a rare case of takotsubo cardiomyopathy that is thought to be related to capecitabine where the patient presented with chest pain, and ST elevation within 48 hours of capecitabine therapy. Workup included cardiac catheterization and coronary angiogram that showed nonobstructive coronary artery disease and anteroapical left ventricular wall motion abnormality with left ventricular ejection fraction of 35%. The drug was stopped, and the patient was treated with beta-blocker and angiotensin-converting enzymes inhibitor. Six weeks later, she had a repeat echocardiogram that was normal. Capecitabine-related cardiomyopathy seems to be very rare because only 5 cases have been reported in the literature (including our case). The condition has to be anticipated and treated to prevent the serious consequence of cardiac dysfunction. All reported cases have eventually recovered after stopping capecitabine.
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Qasem et al. (2014) conducted a case report in Takotsubo cardiomyopathy (n=1). Capecitabine was evaluated on Development of takotsubo cardiomyopathy. Capecitabine therapy can induce rare but reversible takotsubo cardiomyopathy, with 5 total cases reported in the literature recovering after drug cessation.
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