| Literature DB >> 31382864 |
Dimitra Ioanna Lampropoulou1, Konstantinos Laschos1, Anna-Lea Amylidi1, Ariadni Angelaki1, Nikolaos Soupos1, Sotirios Boumpoucheropoulos1, Eirini Papadopoulou2, Evgenia Nanou3,4, Vasilios Zidianakis3,4, George Nasioulas2, George Fildissis3,4, Gerasimos Aravantinos1.
Abstract
Fluoropyrimidine-based regimens are among the most commonly used chemotherapy combinations for the treatment of solid tumors. Several genetic polymorphisms that are implicated with fluoropyrimidine anabolism and catabolism have been associated with the development of life-threatening toxicities. Uridine triacetate is an FDA-approved antidote for 5-fluorouracil or capecitabine overdose and early-onset, life-threatening toxicity within 96 h of last chemotherapy dose. To date, it is not accessible for Greek patients as per the current summary of product characteristic's time restrictions. We report and discuss the course and outcome of capecitabine toxicity in a 66-year-old female colorectal cancer patient with heterozygous dihydropyrimidine dehydrogenase deficiency. This paper highlights the difficulty in timely access of this lifesaving medication for Greek and possibly other European patients.Entities:
Keywords: Cardiotoxicity; dihydropyrimidine dehydrogenase deficiency; early-onset capecitabine toxicity; uridine triacetate indications
Year: 2019 PMID: 31382864 DOI: 10.1177/1078155219865597
Source DB: PubMed Journal: J Oncol Pharm Pract ISSN: 1078-1552 Impact factor: 1.809