DPYD*5 gene mutation contributes to the reduced DPYD enzyme activity and chemotherapeutic toxicity of 5-FU
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology,Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF02698048.pdf
Reference24 articles.
1. Ciccolini J, et al. Toxic death-case after capecitabine+ oxaliplatin (XELOX) administration: probable implication of dihydropyrimidine dehydrogenase deficiency.Cancer Chemother Pharmacol 2006;58: 272–275.
2. Lazar A, et al. Multiple organ fail due to 5-fluorouracil chemotherapy in a patient with a rare dihydropyrimidine dehydrogenase gene variant.Onkologie 2004;27: 559–562.
3. van Kuilenburg AB, De Abreu RA, van Gennip AH. Pharmacogenetic and clinical aspects of dihydropyrimidine dehydrogenase deficiency.Ann Clin Biochem 2003;40: 41–45.
4. Ciccolini J, et al. A simple and rapid high-performance liquid chromatographic (HPLC) method for 5-fluorouracil (5-FU) assay in plasma and possible detection of patients with impaired dihydropyrimidine dehydrogenase (DPYD) activity.J Clin Pharm Ther 200429: 307–315.
5. Ritschel, W.A.Handbook of Basic Pharmacokinetics, 2nd ed. Drug Intelligence Publications, 1980, pp 413–426. http://www.boomer.org/c/p3/c02/c0204.html
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