Therapeutic drug monitoring with vedolizumab in inflammatory bowel disease.

被引:5
作者
Pugliese, Daniela [1 ,2 ]
Privitera, Giuseppe [3 ]
Pizzolante, Fabrizio [1 ,2 ]
Gasbarrini, Antonio [2 ,3 ,4 ]
Guidi, Luisa [1 ,2 ,3 ]
Armuzzi, Alessandro [1 ,2 ,3 ]
机构
[1] A Gemelli Univ Hosp Fdn, Columbus Hosp, Unit Inflammatory Bowel Dis, Via Moscati 31, I-00168 Rome, Italy
[2] IRCCS, Via Moscati 31, I-00168 Rome, Italy
[3] Sacred Heart Catholic Univ, Rome, Italy
[4] A Gemelli Univ Hosp Fdn, Unit Internal Med & Gastroenterol, Rome, Italy
关键词
Vedolizumab; Inflammatory bowel diseases; Drug monitoring; Vaccine immunogenicity; ANTI-TNF THERAPY; CROHNS-DISEASE; ULCERATIVE-COLITIS; INDUCTION THERAPY; TROUGH LEVELS; MAINTENANCE THERAPY; CLINICAL REMISSION; PHARMACOKINETICS; INFLIXIMAB; ANTIBODIES;
D O I
10.23736/S1121-421X.19.02625-4
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) is a useful tool for decision-making process in patients with inflammatory bowel disease (IBD) treated with anti TNF-alpha drugs, especially when experiencing loss of response. Growing evidences support the existence of exposure-response relationship with vedolizumab, but the utility and the appropriate use of TDM in clinical practice is still under debate. In this review, we summarize all evidences supporting a TDM-guided approach for patients treated with vedolizumab, suggesting three potential scenarios: 1) early prediction of long-term outcomes; 2) verifying the best strategy in case of loss of response; 3) maximizing therapeutic efficacy during maintenance treatment. Vedolizumab through concentrations <20 mu g/mL at week 6 and >12 mu g/mL seem to be associated with more favorable outcomes. No comparative studies have been conducted so far to demonstrate the advantage of adopting a TDM-guided versus an empirical approach for managing primary or secondary nonresponses. The frequency of antibodies to vedolizumab detection is quite low (up to 4% in pivotal trials), suggesting, unlike of anti TNF-alpha agents, a low probability of experiencing an immune-mediated pharmacokinetic failure in clinical practice. Future prospective and controlled studies are warranted to establish the guidance on the use of a TDM-guided approach with vedolizumab in clinical practice.
引用
收藏
页码:280 / 290
页数:11
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