在LUCENT诱导和维持试验方案中用Mirikizumab解决溃疡性结肠炎的组织学炎症。

IF 8.3 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Fernando Magro, Rish K Pai, Taku Kobayashi, Vipul Jairath, Florian Rieder, Isabel Redondo, Trevor Lissoos, Nathan Morris, Mingyang Shan, Meekyong Park, Laurent Peyrin-Biroulet
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引用次数: 0

摘要

背景和目的:评估mirikizumab,一种p19靶向的抗白细胞介素-23,对中度至重度活动性溃疡性结肠炎[UC]的组织学和/或内镜结果的影响,并在第[W]12[LUCENT-1:N周评估组织学内镜下粘膜缓解[HEMR] = 1162,诱导]和W40[LUCENT-2:N = 544,维持]用于随机接受mirikizumab或安慰剂的患者。进行分析以评估以下预测因素:在重新随机分配至皮下[SC]米丽珠单抗的患者中,使用米丽珠珠单抗的W12时的HEMI和W40时的HEMR;在重新随机分配至mirikizumab SC的mirikizimab应答者中,W12组织学/内镜终点与W40结果之间的相关性;以及W40内窥镜正常化[EN]与HR/无HR之间的关系。结果:与安慰剂相比,接受米丽珠单抗治疗的患者明显更多地达到HI、HR、ER、HEMI和HEMR[p 结论:米丽珠单抗早期解决内镜和组织学炎症与更好的UC预后相关。Clinicaltrials.gov:LUCENT-1,NCT03518086;LUCENT-2,nct33524092。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Resolving Histological Inflammation in Ulcerative Colitis With Mirikizumab in the LUCENT Induction and Maintenance Trial Programmes.

Resolving Histological Inflammation in Ulcerative Colitis With Mirikizumab in the LUCENT Induction and Maintenance Trial Programmes.

Resolving Histological Inflammation in Ulcerative Colitis With Mirikizumab in the LUCENT Induction and Maintenance Trial Programmes.

Resolving Histological Inflammation in Ulcerative Colitis With Mirikizumab in the LUCENT Induction and Maintenance Trial Programmes.

Background and aims: To evaluate the effect of mirikizumab, a p19-targeted anti-interleukin-23, on histological and/or endoscopic outcomes in moderately-to-severely active ulcerative colitis [UC].

Methods: Endoscopic remission [ER], histological improvement [HI], histological remission [HR], histological-endoscopic mucosal improvement [HEMI], and histological-endoscopic mucosal remission [HEMR] were assessed at Week [W]12 [LUCENT-1: N = 1162, induction] and W40 [LUCENT-2: N = 544, maintenance] for patients randomised to mirikizumab or placebo. Analyses were performed to evaluate predictors of: HEMI at W12 with mirikizumab and HEMR at W40 in patients re-randomised to subcutaneous [SC] mirikizumab; associations between W12 histological/endoscopic endpoints and W40 outcomes in mirikizumab responders re-randomised to mirikizumab SC; and associations between W40 endoscopic normalisation [EN] with/without HR.

Results: Significantly more patients treated with mirikizumab achieved HI, HR, ER, HEMI, and HEMR vs placebo [p <0.001], irrespective of prior biologic/tofacitinib failure [p <0.05]. Lower clinical baseline disease activity, female sex, no baseline immunomodulator use, and no prior biologic/tofacitinib failure were predictors of HEMI at W12 [p <0.05]. Corticosteroid use and longer disease duration were negative predictors of achieving HEMR at W40 [p <0.05]. W12 HI, HR, or ER was associated with W40 HEMI or HEMR [p <0.05]; ER at W12 was associated with clinical remission [CR] [p <0.05] and corticosteroid-free remission [CSFR] at W40 [p = 0.052]. HR and HEMR at W12 were associated with CSFR, CR, and symptomatic remission at W40. Alternate HEMR [EN + HR] at W40 was associated with bowel urgency remission at W40 [p <0.05].

Conclusions: Early resolution of endoscopic and histological inflammation with mirikizumab is associated with better UC outcomes. Clinicaltrials.gov: LUCENT-1, NCT03518086; LUCENT-2, NCT03524092.

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来源期刊
Journal of Crohns & Colitis
Journal of Crohns & Colitis 医学-胃肠肝病学
CiteScore
15.50
自引率
7.50%
发文量
1048
审稿时长
1 months
期刊介绍: Journal of Crohns and Colitis is concerned with the dissemination of knowledge on clinical, basic science and innovative methods related to inflammatory bowel diseases. The journal publishes original articles, review papers, editorials, leading articles, viewpoints, case reports, innovative methods and letters to the editor.
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