Use of Vedolizumab in Inflammatory Bowel Disease: A Single-Center Experience

被引:3
作者
Erdogan, Cagdas [1 ]
Yesil, Bayram [1 ]
Bacaksiz, Ferhat [1 ]
Ari, Derya [1 ]
Gokbulut, Volkan [1 ]
Yuksel, Mahmut [1 ]
Ozin, Yasemin Ozderin [1 ]
Kayacetin, Ertugrul [1 ]
机构
[1] Ankara City Hosp, Dept Gastroenterol, Ankara, Turkey
关键词
Crohn's disease; inflammatory bowel disease; ulcerative colitis; vedolizumab; MAINTENANCE THERAPY; INDUCTION; EFFICACY;
D O I
10.5152/tjg.2022.21684
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Vedolizumab, which is a monoclonal antibody that selectively binds to alpha 4 beta 7 integrin in the gastrointestinal system, may be an effective and safe treatment alternative in those with anti-tumor necrosis factor-resistant inflammatory bowel disease. Methods: Patients administered vedolizumab due to anti-tumor necrosis factor resistant or anti-tumor necrosis factor side effects between August 2017 and November 2020 were included in the study. Crohn's patients were evaluated using the Harvey-Bradshaw index and Simple Endoscopic Score for Crohn's Disease, whereas ulcerative colitis patients were evaluated with the Partial Mayo Score Index and Rachmilewitz score. All patients were followed up for 3 months and their blood samples were taken every 3 months. Hemoglobin, white blood cell, leukocyte, lymphocyte, and platelet counts of the patients were performed. Albumin, C-reactive protein, and erythrocye sedimentation rate values were recorded. The side effect profile for vedolizumab was evaluated for all patients. Among the side effects, arthralgia and flu-like symptoms were observed. Results: A total of 48 patients (18 ulcerative colitis and 30 Crohn's disease) were included in the study. Vedolizumab therapy was initiated in the patients due to anti-tumor necrosis factor resistance (17 ulcerative colitis and 26 Crohn's disease) or anti-tumor necrosis factor side effects (1 ulcerative colitis and 4 Crohn's disease). A total of 30 (63%) patients, including 15 (83%) ulcerative colitis and 15 (50%) Crohn's disease, responded to treatment (both response and remission). The mean duration of response to treatment was 4.5 +/- 1.5 months. A total of 20 (42%) patients in the vedolizumab therapy subgroup (10/10, ulcerative colitis/Crohn's disease) went into remission. The mean Harvey-Bradshaw Index value was 9.8 +/- 2.8 in the Crohn's disease patients at the time of initial treatment. The mean Simple Endoscopic Score for Crohn's disease value was 11.2 +/- 3.1 at the time of initial treatment. The mean Harvey-Bradshaw Index value was 6.5 +/- 3.0 and the mean Simple Endoscopic Score for Crohn's disease value was 4.9 +/- 3.6 at 6 months post-treatment. The mean Ulcerative Colitis Endoscopic Index (Rachmilewitz) value was 9.3 +/- 1.2 at the time of initial treatment. In addition, the mean Partial Mayo Scoring Index was 6.4 +/- 1.5 at the time of initial treatment. The mean Ulcerative Colitis Endoscopic Index (Rachmilewitz) value was 0 (0-6.0), and the mean Partial Mayo Scoring Index was 1.5 (0.3-4.0) at 6 months post-treatment. Conclusion: Vedolizumab therapy is effective in both induction and maintenance of remission in inflammatory bowel disease patients who are resistant to anti-tumor necrosis factor or who can not receive anti-tumor necrosis factor therapy due to side effects. No significant side effect was observed in the patients during follow-up.
引用
收藏
页码:831 / 837
页数:7
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