Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, China.
Key Laboratory of Hubei Province for Digestive System Disease, Renmin Hospital of Wuhan University, Wuhan, China.
Clin Transl Gastroenterol. 2024 Nov 1;15(11):e00759. doi: 10.14309/ctg.0000000000000759.
Despite increasing studies confirming the efficacy of vedolizumab (VDZ) in Crohn's disease (CD), improving the responses to this biologic agent remains challenging in clinical practice. In this article, we investigated the efficacy of combined treatment of VDZ and 16-week exclusive enteral nutrition (EEN) in moderately to severely active CD.
From October 2020 to October 2023, 81 patients with moderately to severely active CD treated with VDZ from 2 inflammatory bowel disease centers were retrospectively selected. Forty-one patients received treatment of VDZ with concomitant 16-week EEN (VDZ + EEN cohort), and 40 patients received VDZ treatment alone (VDZ cohort). Clinical and biological outcomes were evaluated. Endoscopic response and mucosal healing were assessed by colonoscopy at weeks 16 and 52.
There was no statistically significant difference between 2 groups at baseline for demographic and clinical characteristics. Compared with patients treated with VDZ alone, patients in the VDZ + EEN cohort achieved higher rates of clinical response (84.2% vs 40.0%), clinical remission (81.6% vs 30.0%), endoscopic response (91.4% vs 34.6%), including mucosal healing (85.7% vs 26.9%) at week 16. The superiority of VDZ + EEN treatment sustained in maintenance, with 76.7% (vs 33.3%) clinical response, 70.0% (vs 26.7%) clinical remission, 76.9% (vs 33.3%) endoscopic response, and 61.5% (vs 26.7%) mucosal healing at week 52. None of the patients experienced severe adverse events.
VDZ with concomitant 16-week EEN might be an effective and optimized approach with solid efficacy in the induction and maintenance treatment of active CD.
尽管越来越多的研究证实了维得利珠单抗(VDZ)在克罗恩病(CD)中的疗效,但在临床实践中,提高对这种生物制剂的反应仍然具有挑战性。在本文中,我们研究了 VDZ 联合 16 周肠内营养(EEN)在中重度活动期 CD 中的疗效。
2020 年 10 月至 2023 年 10 月,我们从 2 个炎症性肠病中心回顾性选择了 81 例接受 VDZ 治疗的中重度活动期 CD 患者。41 例患者接受 VDZ 联合 16 周 EEN 治疗(VDZ+EEN 队列),40 例患者接受 VDZ 单药治疗(VDZ 队列)。评估临床和生物学结局。第 16 周和第 52 周通过结肠镜检查评估内镜缓解和黏膜愈合。
两组患者在基线时的人口统计学和临床特征无统计学差异。与单独接受 VDZ 治疗的患者相比,VDZ+EEN 队列的患者在第 16 周时获得更高的临床缓解率(84.2% vs. 40.0%)、临床缓解率(81.6% vs. 30.0%)、内镜缓解率(91.4% vs. 34.6%),包括黏膜愈合率(85.7% vs. 26.9%)。在维持治疗中,VDZ+EEN 治疗的优势持续存在,第 52 周时的临床缓解率为 76.7%(vs. 33.3%)、临床缓解率为 70.0%(vs. 26.7%)、内镜缓解率为 76.9%(vs. 33.3%)和黏膜愈合率为 61.5%(vs. 26.7%)。所有患者均未发生严重不良事件。
VDZ 联合 16 周 EEN 可能是一种有效的方法,在诱导和维持活动期 CD 的治疗中具有坚实的疗效。