Real-World Clinical Effectiveness and Safety of Vedolizumab and Ustekinumab in Biologic-Naive Patients With Crohn's Disease By Disease Location: Results from the EVOLVE Expansion Study.

IF 2.8 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Michael Scharl, Britt Christensen, Brian Bressler, Neil R Brett, Lauren Gianchetti, Celine Gisler, Pravin Kamble, Shashi Adsul, Zeinab Farhat, Marc Ferrante
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引用次数: 0

Abstract

Goals: This analysis compared the real-world effectiveness and safety of vedolizumab versus ustekinumab in biologic-naive patients by CD location.

Background: Crohn's disease (CD) location may affect disease course and treatment decisions.

Study: Medical charts of biologic-naive patients with CD aged 18 years or older initiating vedolizumab or ustekinumab were analyzed in the multicenter, observational, retrospective EVOLVE Expansion study. Outcomes with vedolizumab versus ustekinumab over 36 months were compared in patients with baseline isolated ileal, ileocolonic, and isolated colonic CD (Montreal classification).

Results: This analysis included 293 patients with ileal (vedolizumab, n=158, ustekinumab, n=135), 185 with ileocolonic (vedolizumab, n=91, ustekinumab, n=94), and 121 with colonic (vedolizumab, n=84, ustekinumab, n=37) CD. Cumulative rates over 36 months were similar between vedolizumab and ustekinumab in ileal, ileocolonic, and colonic CD subgroups for clinical response, remission, mucosal healing, and treatment persistence. There were no differences in risks of serious adverse events, serious infections, CD exacerbations, and CD-related hospitalizations between cohorts across disease location; the risk of CD-related surgeries was similar in patients with ileocolonic and colonic CD, and higher with vedolizumab versus ustekinumab in patients with ileal CD. CD-related surgeries for ileal CD were reported in 12 of 158 (7.6%) vedolizumab-treated patients and 3 of 135 (2.2%) ustekinumab-treated patients.

Conclusions: Effectiveness, safety, and health care resource utilization outcomes over 36 months were similar between treatment cohorts regardless of baseline disease location. The number of patients requiring CD-related surgeries was low. Both vedolizumab and ustekinumab can be used as first-line biologics in patients with CD, regardless of disease location.

Vedolizumab和Ustekinumab在生物初治克罗恩病患者中的临床有效性和安全性:来自EVOLVE扩展研究的结果
目的:该分析比较了vedolizumab与ustekinumab在生物初治患者中的实际有效性和安全性。背景:克罗恩病(CD)的发病部位可能影响病程和治疗决策。研究:在多中心、观察性、回顾性的EVOLVE扩展研究中,分析了18岁或以上的生物初治CD患者启动vedolizumab或ustekinumab的医学图表。在基线分离性回肠、回肠结肠和分离性结肠CD(蒙特利尔分类)患者中,比较了vedolizumab和ustekinumab治疗36个月的结果。结果:该分析包括293例回肠(vedolizumab, n=158, ustekinumab, n=135), 185例回肠(vedolizumab, n=91, ustekinumab, n=94)和121例结肠(vedolizumab, n=84, ustekinumab, n=37) CD患者。在回肠、回肠和结肠CD亚组中,在临床反应、缓解、粘膜愈合和治疗持续性方面,vedolizumab和ustekinumab在36个月内的累积率相似。在不同疾病部位的队列中,严重不良事件、严重感染、CD恶化和CD相关住院的风险没有差异;回肠和结肠CD患者发生CD相关手术的风险相似,而vedolizumab与ustekinumab相比,回肠CD患者发生CD相关手术的风险更高。158例vedolizumab治疗患者中有12例(7.6%)进行了CD相关手术,135例ustekinumab治疗患者中有3例(2.2%)进行了CD相关手术。结论:无论基线疾病位置如何,36个月内治疗队列之间的有效性、安全性和卫生保健资源利用结果相似。需要cd相关手术的患者数量很低。无论疾病部位如何,vedolizumab和ustekinumab都可以作为CD患者的一线生物制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of clinical gastroenterology
Journal of clinical gastroenterology 医学-胃肠肝病学
CiteScore
5.60
自引率
3.40%
发文量
339
审稿时长
3-8 weeks
期刊介绍: Journal of Clinical Gastroenterology gathers the world''s latest, most relevant clinical studies and reviews, case reports, and technical expertise in a single source. Regular features include cutting-edge, peer-reviewed articles and clinical reviews that put the latest research and development into the context of your practice. Also included are biographies, focused organ reviews, practice management, and therapeutic recommendations.
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