Efficacy and Safety of Vedolizumab in Patients with Inflammatory Bowel Disease in Association with Vedolizumab Drug Levels

被引:2
|
作者
Huettemann, Eva [1 ,2 ]
Muzalyova, Anna [1 ]
Groehl, Katharina [1 ]
Nagl, Sandra [1 ]
Fleischmann, Carola [1 ,3 ]
Ebigbo, Alanna [1 ]
Classen, Johanna [1 ]
Wanzl, Julia [1 ]
Prinz, Friederike [1 ]
Mayr, Patrick [4 ,5 ]
Schnoy, Elisabeth [1 ]
机构
[1] Univ Hosp Augsburg, Internal Med 3, D-86156 Augsburg, Germany
[2] Kantonsspital St Gallen, Internal Med, CH-9007 St Gallen, Switzerland
[3] Klinikum Nurnberg, Dept Gastroenterol Hepatol & Endocrinol, D-90419 Nurnberg, Germany
[4] Univ Hosp Augsburg, Internal Med 2, D-86156 Augsburg, Germany
[5] Kantonsspital St Gallen, Dept Oncol & Hematol, CH-9007 St Gallen, Switzerland
关键词
inflammatory bowel disease; vedolizumab; drug level; ulcerative colitis; Crohn's disease; TROUGH LEVELS; ULCERATIVE-COLITIS; INDUCTION THERAPY; MAINTENANCE THERAPY; CLINICAL REMISSION;
D O I
10.3390/jcm13010140
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Vedolizumab (VDZ) is a well-established and important therapeutic option in the treatment of patients with inflammatory bowel disease (IBD). However, the significance of therapeutic drug monitoring (TDM) with VDZ remains a contradictory field in daily clinical practice. Our study aims to clarify the predictive impact of VDZ drug levels in long-term clinical outcomes in a real-world cohort. Methods: Patients with moderate to severe ulcerative colitis (UC) and Crohn's disease (CD) from a tertiary IBD referral center at the University Hospital Augsburg, Germany, were enrolled in this single-center retrospective data analysis. Clinical and endoscopic data were collected at month 6, month 12, and at the last time of follow-up, and outcomes were correlated with VDZ levels at week 6. Results: This study included 95 patients, 68.4% (n = 65) with UC, 24.2% (n = 23) with CD, and 7.4% (n = 7) with indeterminate colitis (CI). Patients with a mean VDZ treatment time of 17.83 months +/- 14.56 showed clinical response in 29.5% (n = 28) and clinical remission in 45.3% (n = 43) at the end of the study. Endoscopic response occurred in 20.0% (n = 19) and endoscopic remission in 29.5% (n = 28) at the end of the study. The sustained beneficial effect of VDZ was also reflected in a significant change in biomarker levels. VDZ trough level at week 6 was determined in 48.4% (n = 46) with a mean of 41.79 mu g/mL +/- 24.58. A significant association between VDZ level at week 6 and both short and long-term outcomes could not be demonstrated. However, numerically higher VDZ levels were seen in patients with endoscopic and clinical improvement at month 6 and at the time of last follow-up. Conclusions: This study demonstrated efficacy and safety for VDZ in a real-world cohort. Although, for some parameters, a clear trend for higher VDZ levels at week 6 was seen, the efficacy of VDZ was not significantly correlated to VDZ level at week 6, which questions the predictive value of VDZ levels in the real world.
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页数:17
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