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Merck

Alternative treatment options in colorectal cancer patients with 5-fluorouracil- or capecitabine-induced cardiotoxicity.

Clinical colorectal cancer (2012-10-30)
Guido Deboever, Nick Hiltrop, Mike Cool, Guy Lambrecht
RESUMEN

Most chemotherapy regimens in colorectal cancer treatment are 5-fluorouracil (5-FU)/leucovorin or capecitabine-based. Cardiotoxicity is a less common but potentially lethal complication of 5-FU or capecitabine treatment, and some physicians might be unfamiliar with treatment alternatives. Rechallenging should be avoided because it carries a high risk of recurrence of the cardiac symptoms and prophylactic treatment is not always protective. Possible alternative treatment options to be considered are to replace the oral capecitabine or intravenous 5-FU by a 5-FU bolus regimen, by uracil-tegafur or tegafur/gimeracil/oteracil, both oral fluoropyrimidines combining a 5-FU prodrug with a dihydropyrimidine dehydrogenase (DPD) inhibitor, or by raltitrexed, a thymidilate synthase inhibitor whose metabolism is independent of DPD. Patients with advanced colorectal cancer and fluoropyrimidine-induced cardiotoxicity can be treated with other non-fluoropyrimidine related chemotherapy, either as a single agent, combined, or in combination with biological agents. In this report we discuss the different alternative treatment options.

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5-Fluorouracil, ≥99% (HPLC), powder
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Capecitabine, ≥98% (HPLC)
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Fluorouracil, meets USP testing specifications
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Fluorouracil, Pharmaceutical Secondary Standard; Certified Reference Material
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5-Fluorouracil, analytical standard
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Fluorouracil, European Pharmacopoeia (EP) Reference Standard
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Capecitabine, European Pharmacopoeia (EP) Reference Standard
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