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首页> 外文期刊>Journal of gastroenterology and hepatology >Outcome of elective switching to vedolizumab in inflammatory bowel disease patients under tumor necrosis factor antagonist-maintained clinical remission
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Outcome of elective switching to vedolizumab in inflammatory bowel disease patients under tumor necrosis factor antagonist-maintained clinical remission

机译:在肿瘤坏死因子拮抗剂维持临床缓解下肿瘤坏死因子患者炎症性肠病患者的选修症的结果

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Background and Aim Vedolizumab (VDZ) has been used in inflammatory bowel disease (IBD) patients who failed anti-tumor necrosis factor (TNF) therapy. This study was to examine long-term outcome of IBD patients switching to VDZ from anti-TNF agents for reasons other than failure of therapy. Methods Inflammatory bowel disease patients at the University of Chicago IBD center who were in clinical remission with anti-TNF therapy and then electively changed to VDZ due to reasons other than loss of response were retrospectively analyzed. The primary outcome was the durability of clinical remission maintained by VDZ as assessed by Kaplan-Meier survival analysis. The proportion of patients in clinical and endoscopic remission at 6-12 months after switching to VDZ therapy was analyzed. Results A total of 41 patients (36 with Crohn's disease and 5 with ulcerative colitis) met the inclusion criteria and were in clinical remission at the time of switch. The majority of patients switched therapy due to adverse effects (56.1%) or infections (14.6%). During a median duration of 30 months (range 7-52) of VDZ therapy, 34 (82.9%) were in VDZ-maintained clinical remission. One (2.4%) and four (9.8%) patients discontinued VDZ due to flare and adverse effects, respectively. Endoscopic remission was present in 25 of 30 patients (83.3%) who had a follow-up colonoscopy. Conclusions Vedolizumab was effective and safe in maintaining remission in IBD patients who switched from anti-TNF agents due to reasons other than failure of therapy. Our results suggest that switching anti-TNF remitters to VDZ treatment is a safe practice in specific patient populations.
机译:背景和AIM Vedolizumab(VDZ)已用于炎症性肠病(IBD)患者,失败抗肿瘤坏死因子(TNF)治疗。本研究是检查IBD患者的长期结果,从抗TNF药剂切换到VDZ,原因是治疗失败的原因。方法回顾性分析了抗TNF疗法临床缓解临床缓解的芝加哥IBD中心炎症患者,临床缓解,然后临床缓解到VDZ。主要结果是VDZ维持的临床缓解耐久性,如Kaplan-Meier生存率分析评估。分析了切换到VDZ治疗后6-12个月临床和内镜缓解患者的比例。结果共有41名患者(36例患克罗恩病和溃疡性结肠炎)达到了纳入标准,并在开关时临床缓解。大多数患者由于不良反应(56.1%)或感染(14.6%)而转换治疗。在VDZ疗法的30个月(范围7-52)的中位持续时间(范围7-52)期间,34(82.9%)在VDZ保持的临床缓解中。一种(2.4%)和四个(9.8%)患者分别停止VDZ,分别因耀斑和不良反应而停止。内镜下缓解存在于30名患者中的25个(83.3%)中存在后续结肠镜检查。结论Vedolizumab在维持从抗TNF药剂的IBD患者中维持缓解的安全性和安全的安全性是有效和安全的。我们的研究结果表明,切换抗TNF炼乳剂至VDZ治疗是特定患者人口的安全实践。

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