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炎症性肠病的治疗药物监测。西班牙克罗恩病和溃疡性结肠炎工作组的立场声明。

Therapeutic drug monitoring in inflammatory bowel diseases. Position statement of the Spanish Working Group on Crohn's Disease and Ulcerative Colitis.

机构信息

Servicio de Aparato Digestivo, Hospital Universitario de Bellvitge, IDIBELL, L'Hospitalet de Llobregat, Barcelona, España.

Servicio de Aparato Digestivo, Hospital Universitario Virgen Macarena, Sevilla, España; Facultad de Medicina, Universidad de Sevilla, Sevilla, España.

出版信息

Gastroenterol Hepatol. 2024 May;47(5):522-552. doi: 10.1016/j.gastrohep.2024.01.007. Epub 2024 Feb 2.

Abstract

The treatment of inflammatory bowel disease has undergone a significant transformation following the introduction of biologic drugs. Thanks to these drugs, treatment goals have evolved from clinical response and remission to more ambitious objectives, such as endoscopic or radiologic remission. However, even though biologics are highly effective, a significant percentage of patients will not achieve an initial response or may lose it over time. We know that there is a direct relationship between the trough concentrations of the biologic and its therapeutic efficacy, with more demanding therapeutic goals requiring higher drug levels, and inadequate exposure being common. Therapeutic drug monitoring of biologic medications, along with pharmacokinetic models, provides us with the possibility of offering a personalized approach to treatment for patients with IBD. Over the past few years, relevant information has accumulated regarding its utility during or after induction, as well as in the maintenance of biologic treatment, in reactive or proactive strategies, and prior to withdrawal or treatment de-escalation. The aim of this document is to establish recommendations regarding the utility of therapeutic drug monitoring of biologics in patients with inflammatory bowel disease, in different clinical practice scenarios, and to identify areas where its utility is evident, promising, or controversial.

摘要

生物制剂的问世使炎症性肠病的治疗发生了重大转变。这些药物的出现使治疗目标从临床缓解和缓解期进一步提升,例如内镜或影像学缓解期。然而,尽管生物制剂非常有效,但仍有相当一部分患者初始治疗无应答或应答逐渐丧失。我们知道生物制剂的谷浓度与其治疗效果之间存在直接关系,更具挑战性的治疗目标需要更高的药物水平,而药物暴露不足则较为常见。生物制剂的治疗药物监测以及药代动力学模型为我们提供了为 IBD 患者提供个体化治疗的可能性。在过去几年中,人们积累了相关信息,涉及诱导期、维持期、反应性或主动策略以及停药或治疗降级前使用生物制剂治疗药物监测的疗效。本文件旨在制定炎症性肠病患者生物制剂治疗药物监测的临床应用推荐意见,并确定其疗效明确、有前景或有争议的临床应用场景。

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