Optimizing 6-mercaptopurine and azathioprine therapy in the management of inflammatory bowel disease

被引:66
作者
Bradford, Kara [2 ]
Shih, David Q. [1 ]
机构
[1] Cedars Sinai Med Ctr, Inflammatory Bowel & Immunobiol Res Inst, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
关键词
Azathioprine; Drug levels; Inflammatory bowel disease; 6-Mercaptopurine; Thiopurine; 6-THIOGUANINE NUCLEOTIDE LEVELS; T-CELL LYMPHOMA; CROHNS-DISEASE; IBD PATIENTS; SUCCESSFUL DESENSITIZATION; ORAL; 6-THIOGUANINE; COST-EFFECTIVENESS; ALLERGIC REACTIONS; METABOLITE LEVELS; CONTROLLED-TRIAL;
D O I
10.3748/wjg.v17.i37.4166
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The thiopurine drugs, 6-mercaptopurine (6-MP) and azathioprine, are efficacious in the arsenal of inflammatory bowel disease (IBD) therapy. Previous reports indicate that 6-thioguanine nucleotide (6-TGN) levels correlate with therapeutic efficacy, whereas high 6-methylmercaptopurine (6-MMP) levels are associated with hepatotoxicity and myelotoxicity. Due to their complex metabolism, there is wide individual variation in patient response therein, both in achieving therapeutic drug levels as well as in developing adverse reactions. Several strategies to optimize 6-TGN while minimizing 6-MMP levels have been adopted to administer the thiopurine class of drugs to patients who otherwise would not tolerate these drugs due to side-effects. In this report, we will review different approaches to administer the thiopurine medications, including the administration of 6-mercaptopurine in those unsuccessfully treated with azathioprine; co-administration of thiopurine with allopurinol; co-administration of thiopurine with anti-tumor necrosis factor a; 6-TGN administration; desensitization trials; and split dosing of 6-MP. (C) 2011 Baishideng. All rights reserved.
引用
收藏
页码:4166 / 4173
页数:8
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