The Utility of Infliximab Therapeutic Drug Monitoring among Patients with Inflammatory Bowel Disease and Concerns for Loss of Response: A Retrospective Analysis of a Real-World Experience

被引:13
作者
Mitchell, Robert A. [1 ]
Shuster, Constantin [1 ]
Shahidi, Neal [1 ]
Galorport, Cherry [1 ]
DeMarco, Mari L. [2 ]
Rosenfeld, Gregory [1 ]
Enns, Robert A. [1 ]
Bressler, Brian [1 ]
机构
[1] Univ British Columbia, St Pauls Hosp, Div Gastroenterol, Dept Med, Vancouver, BC, Canada
[2] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC, Canada
关键词
CROHNS-DISEASE; ULCERATIVE-COLITIS; DOSE INTENSIFICATION; FECAL CALPROTECTIN; INDUCTION THERAPY; RANDOMIZED-TRIAL; CLINICIAN GUIDE; ADALIMUMAB; ANTIBODIES; ARTICLE;
D O I
10.1155/2016/5203898
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background. Infliximab (IFX) therapeutic drug monitoring (TDM) allows for objective decision making in patients with inflammatory bowel disease (IBD) and loss of response. Questions remain about whether IFX TDM improves outcomes. Methods. Patients with IBD who had IFX TDM due to concerns for loss of response were considered for inclusion. Serum IFX trough concentration and anti-drug antibody (ADA) concentrations were measured. Patients were grouped by TDM results: group 1, low IFX/high ADA; group 2, low IFX/ low ADA; group 3, therapeutic IFX. Changes in management were analyzed according to groupings; remission rates were assessed at 6 months. Results. 71 patients were included of whom 37% underwent an appropriate change in therapy. Groups 1 (67%) and 2 (83%) had high adherence compared to only 9% in group 3. At 6 months, 57% had achieved remission. More patients who underwent an appropriate change in therapy achieved remission, though this did not reach statistical significance (69% versus 49%; p = 0.098). Conclusions. A trend towards increased remission rates was associated with appropriate changes in management following TDM results. Many patients with therapeutic IFX concentrations did not undergo an appropriate change in management, potentially reflecting a lack of available out-of-class options at the time of TDM or due to uncertainty of the meaning of the reported therapeutic range.
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页数:7
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