期刊
CLINICAL COLORECTAL CANCER
卷 9, 期 4, 页码 224-228出版社
CIG MEDIA GROUP, LP
DOI: 10.3816/CCC.2010.n.033
关键词
5-FU catabolism; Methylenetetrahydrofolate; Thymidylate synthase
类别
资金
- Association pour la Recherche contre le Cancer [1093]
- Groupe des Entreprises Financant la Lutte contre le Cancer (GEFLUC)
5-Fluorouracil (5-FU) is a mainstay for treating colorectal cancer, alone or more frequently as part of combination therapies. However, its efficacy/toxicity balance is often limited by the occurrence of severe toxicities, showing in about 15%-20% of patients. Several clinical reports have shown the deleterious effect of dihydropyrimidine dehydrogenase (DPD) genetic polymorphism, a condition that reduces the liver detoxification step of standard dosages of 5-FU, in patients undergoing fluoropyrimidine-based therapy. Admittedly, DPD deficiency accounts for 50%-75% of the severe and sometimes life-threatening toxicities associated with 5-FU (or oral 5-FU). However, technical consensus on the best way to identify patients with DPD deficiency before administrating 5-FU is far from being achieved. Consequently, no regulatory step has been undertaken yet to recommend DPD testing as part of routine clinical practice for securing the administration of 5-FU. This review covers the limits and achievements of the various strategies proposed so far for determining DPD status in patients scheduled for 5-FU therapy.
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