Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
J Gastroenterol Hepatol. 2019 Dec;34(12):2090-2095. doi: 10.1111/jgh.14751. Epub 2019 Jun 28.
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.
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.
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.
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.
维得利珠单抗(VDZ)已被用于抗肿瘤坏死因子(TNF)治疗失败的炎症性肠病(IBD)患者。本研究旨在研究因治疗失败以外的原因而从抗 TNF 药物转换为 VDZ 的 IBD 患者的长期结局。
回顾性分析芝加哥大学 IBD 中心的 IBD 患者,这些患者在接受抗 TNF 治疗时处于临床缓解期,然后因治疗失败以外的原因选择转换为 VDZ。主要结局是通过 Kaplan-Meier 生存分析评估 VDZ 维持的临床缓解的持久性。分析转换为 VDZ 治疗后 6-12 个月时处于临床和内镜缓解的患者比例。
共有 41 名患者(36 名克罗恩病患者和 5 名溃疡性结肠炎患者)符合纳入标准,在转换时处于临床缓解期。大多数患者因不良反应(56.1%)或感染(14.6%)而转换治疗。在 VDZ 治疗的中位 30 个月(范围 7-52)期间,34 名(82.9%)患者处于 VDZ 维持的临床缓解期。1 名(2.4%)和 4 名(9.8%)患者因病情加重和不良反应分别停用 VDZ。25 名接受随访结肠镜检查的患者中有 25 名(83.3%)存在内镜缓解。
对于因治疗失败以外的原因而从抗 TNF 药物转换的 IBD 患者,维得利珠单抗在维持缓解方面是有效且安全的。我们的结果表明,在特定的患者人群中,将抗 TNF 缓解者转换为 VDZ 治疗是一种安全的做法。