Pharmacokinetics and pharmacogenomics in esophageal cancer chemoradiotherapy

被引:31
作者
Sakaeda, Toshiyuki [1 ]
Yamamori, Motohiro
Kuwahara, Akiko
Nishiguchi, Kohshi
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Ctr Integrat Educ Pharm Frontier, Kyoto, Japan
关键词
Esophageal cancer; Chemoradiotherapy; 5-fluorouracil; Cisplatin; Pharmacokinetically guided administration; Genotype-guided administration; SQUAMOUS-CELL CARCINOMA; ENDOTHELIAL GROWTH-FACTOR; S-TRANSFERASE P1; THYMIDYLATE-SYNTHASE GENE; PHASE-II TRIAL; VASCULAR-PERMEABILITY FACTOR; ADVANCED COLORECTAL-CANCER; COMBINED-MODALITY THERAPY; METHYLENETETRAHYDROFOLATE-REDUCTASE C677T; SINGLE NUCLEOTIDE POLYMORPHISMS;
D O I
10.1016/j.addr.2008.10.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Esophageal cancer is one of the most lethal malignancies. Surgical resection of the tumor from the primary site has been the standard treatment, especially for localized squamous cell carcinoma, but considerable clinical efforts during the last decade have resulted in novel courses of treatment. These options include chemoradiotherapy, consisting of a continuous infusion of 5-fluorouracil (5-FU), cisplatin (CDDP), and concurrent radiation. Given the substantial inter- and/or intra-individual variation in clinical outcome, future improvements will likely require the incorporation of a novel anticancer drug, pharmacokinetically guided administration of CDDP or 5-FU, and identification of potential responders by patient genetic profiling prior to treatment. In this review, the latest information on incidence, risk factors, biomarkers, therapeutic strategies, and the pharmacokinetically guided or genotype-guided administration of CDDP and 5-FU is summarized for future individualization of esophageal cancer treatment. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:388 / 401
页数:14
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