Fluoropyrimidine-induced toxicity and DPD deficiency.. A case report of early onset, lethal capecitabine-induced toxicity and mini review of the literature. Uridine triacetate: Efficacy and safety as an antidote. Is it accessible outside USA?
Dimitra Ioanna LampropoulouKonstantinos LaschosAnna-Lea AmylidiAriadni AngelakiNikolaos SouposSotirios BoumpoucheropoulosEirini PapadopoulouEvgenia NanouVasilios ZidianakisGeorge NasioulasGeorge FildissisGerasimos AravantinosPublished in: Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners (2019)
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.
Keyphrases
- early onset
- late onset
- locally advanced
- end stage renal disease
- oxidative stress
- ejection fraction
- newly diagnosed
- prognostic factors
- healthcare
- high glucose
- randomized controlled trial
- phase ii study
- squamous cell carcinoma
- patient reported outcomes
- case report
- phase iii
- metastatic breast cancer
- replacement therapy
- rectal cancer
- radiation therapy