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英夫利昔单抗治疗难治性或不耐受性溃疡性结肠炎的临床疗效。

Clinical outcomes with ustekinumab as rescue treatment in therapy-refractory or therapy-intolerant ulcerative colitis.

机构信息

IBD Center Munich, Munich, Germany.

Synesis IBD Research Center, Munich, Germany.

出版信息

United European Gastroenterol J. 2020 Feb;8(1):91-98. doi: 10.1177/2050640619895361. Epub 2019 Dec 12.

Abstract

BACKGROUND

Recently, ustekinumab a monoclonal antibody targeting interleukin-12 and -23 and successfully used in Crohn's disease also has been shown to be effective in induction and maintaining remission in patients with moderate to severe ulcerative colitis in a large phase 3 trial. However, no observational data on the use of ustekinumab in ulcerative colitis in daily clinical practice is available.

AIM

The purpose of this study was to assess the clinical outcomes achieved with ustekinumab as rescue treatment in therapy-refractory or -intolerant ulcerative colitis in a real-life setting.

METHODS

A retrospective data analysis was performed in 19 ulcerative colitis patients who were intolerant or refractory to all of the following drugs: steroids, purine-analogues, tumour necrosis factor antibodies and vedolizumab. To all patients ustekinumab was provided as a rescue treatment (intravenous induction with 6 mg/kg, followed by week subcutaneous injection once every eight weeks of 90 mg). The primary outcome was achievement of clinical remission at one year, defined as score of ≤ 3 points in the Lichtiger score (colitis activity index). Patients were evaluated regularly and a colonoscopy was performed before the start and at the end of the observation. Ethical approval was provided by Ethikkommission Ärztekammer Hamburg (PV 5539).

RESULTS

In five patients, therapy was stopped due to refractory disease or side effects. In all remaining 14 patients the median colitis activity index dropped from 8.5 points (range 1-12) at start to 2.0 points at one year (range 0-5.5) and Mayo endoscopy scores fell from a median of two points (range 1-3, mean of 2.3) at start to a median of one point (range 1-3, mean of 1.4) at one year. Including the five drop-outs, clinical remission was achieved in 53% of the 19 patients at one year.

CONCLUSIONS

In accordance with the UNIFI (A Study to Evaluate the Safety and Efficacy of Ustekinumab Induction and Maintenance Therapy in Participants With Moderately to Severely Active Ulcerative Colitis) trial our real-life data support ustekinumab as an effective and safe treatment option in therapy refractory moderate to severe ulcerative colitis with a history of biological therapies.

摘要

背景

乌司奴单抗是一种针对白细胞介素-12 和 -23 的单克隆抗体,已成功用于克罗恩病,在一项大型 3 期试验中也显示出在诱导和维持中重度溃疡性结肠炎缓解方面的有效性。然而,在日常临床实践中,尚无乌司奴单抗治疗溃疡性结肠炎的观察性数据。

目的

本研究旨在评估乌司奴单抗作为补救治疗在难治性或不耐受性溃疡性结肠炎患者中的临床疗效。

方法

对 19 例对所有以下药物均不耐受或耐药的溃疡性结肠炎患者进行回顾性数据分析:类固醇、嘌呤类似物、肿瘤坏死因子抗体和维得利珠单抗。所有患者均接受乌司奴单抗作为补救治疗(静脉诱导 6mg/kg,随后每 8 周皮下注射 90mg 一次)。主要结局是在一年内达到临床缓解,定义为 Lichtiger 评分(结肠炎活动指数)≤3 分。患者定期接受评估,并在开始和观察结束时进行结肠镜检查。汉堡医师协会伦理委员会(PV 5539)提供了伦理批准。

结果

在 5 例患者中,由于疾病难治或出现副作用而停止治疗。在所有其余 14 例患者中,中位数结肠炎活动指数从开始时的 8.5 分(范围 1-12)降至 1 年时的 2.0 分(范围 0-5.5),Mayo 内镜评分从开始时的中位数 2 分(范围 1-3,平均 2.3)降至 1 年时的中位数 1 分(范围 1-3,平均 1.4)。包括 5 例退出者,19 例患者中有 53%在 1 年内达到临床缓解。

结论

与 UNIFI(评估乌司奴单抗在中重度活动性溃疡性结肠炎参与者中的诱导和维持治疗的安全性和有效性的研究)试验一致,我们的真实数据支持乌司奴单抗作为一种有效的、安全的治疗选择,用于治疗生物治疗史的难治性中重度溃疡性结肠炎。

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