医学
炎症性肠病
重症监护医学
临床实习
药品
炎症性肠病
英夫利昔单抗
克罗恩病
内科学
治疗药物监测
溃疡性结肠炎
维多利祖马布
生物制剂
肿瘤坏死因子α
疾病
阿达木单抗
药物治疗
乌斯特基努马
评论文章
梅德林
肿瘤坏死因子α
外科
妥珠单抗
临床试验
胃肠病学
作者
Kenneth Ernest-Suárez,Bella Ungar,Konstantinos H Katsanos,Triana Lobatón,Iago Rodríguez–Lago,Henit A. Yanai,Manuel Barreiro‐de Acosta,Ferdinando D’Amico,Jurij Hanžel,Željko Krznarić,Viviana Parra-Izquierdo,Nikolas Plevris,Helena Tavares de Sousa,Natália Sousa Freitas Queiroz,Uri Kopylov
标识
DOI:10.1093/ecco-jcc/jjag117
摘要
Abstract Background: Advanced therapies have revolutionized inflammatory bowel disease (IBD) management, but primary non-response and secondary loss of response remain clinical challenges across all mechanisms of action. This topical review aims to offer evidence-based current practice positions for therapy optimization across all available advanced therapies. Methods: A panel of gastroenterologists performed a literature review on optimization of IBD advanced therapies (anti-tumour necrosis factor agents, vedolizumab, anti-IL-12/23 and anti-IL-23 agents, and small molecules) and formulated current practice positions that were approved in consensus. Conclusions: Strategies to reduce treatment failures, maximize drug persistence, and achieve optimal clinical benefit, including therapeutic drug monitoring and dose optimization, have become standard components of modern IBD care; however, this may vary according to the current evidence for each specific drug.
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