Optimizing Therapies Using Therapeutic Drug Monitoring: Current Strategies and Future Perspectives

被引:65
作者
Irving, Peter M. [1 ,2 ,4 ]
Gecse, Krisztina B. [3 ]
机构
[1] Guys & St Thomas Hosp, Dept Gastroenterol, IBD Unit, London, England
[2] Kings Coll London, Sch Immunol & Microbial Sci, London, England
[3] Amsterdam UMC, Dept Gastroenterol & Hepatol, Amsterdam, Netherlands
[4] St Thomas Hosp, Dept Gastroenterol, 1st Floor,Coll House,South Wing,Westminster Bridge, London SE1 7EH, England
基金
英国医学研究理事会;
关键词
Crohn's Disease; Inflammatory Bowel Diseases; Therapeutic Drug Monitoring; Ulcerative Colitis; INFLAMMATORY-BOWEL-DISEASE; INDUCTION INFLIXIMAB LEVELS; ULCERATIVE-COLITIS; COMBINATION THERAPY; TROUGH LEVELS; MAINTENANCE THERAPY; CLINICAL-RESPONSE; CROHNS-DISEASE; AZATHIOPRINE; ASSOCIATION;
D O I
10.1053/j.gastro.2022.02.014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Therapeutic drug monitoring (TDM) has emerged as a strategy for treatment optimization in inflammatory bowel diseases to maximize benefit and to reach more stringent, objective end points. Optimal drug concentrations in inflammatory bowel disease vary according to treatment target, disease phenotype, inflammatory burden, and timing of sampling during the treatment cycle. This review provides an update on TDM with biologic and oral small molecules, evaluates the role of reactive vs proactive TDM, and identifies the gaps in current evidence. In the future, adaptations to how we use TDM may contribute further to the goal of personalized treatment in patients with IBD.
引用
收藏
页码:1512 / 1524
页数:13
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