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mirikizumab对中度至重度活动性溃疡性结肠炎患者疾病清除的影响:一项预先设定的LUCENT试验终点分析

Mirikizumab impact on disease clearance in patients with moderately to severely active ulcerative colitis: analysis of a pre-specified LUCENT trial endpoint.

作者信息

Colombel Jean-Frederic, Wu Jianmin, Kobayashi Taku, Zhu Baojin, Paulissen Jerome, Dhanabal Agni, Jairath Vipul, Siegel Corey, Siegmund Britta, Redondo Isabel, Moses Richard, Magro Fernando

机构信息

Henry D. Janowitz Division of Gastroenterology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Eli Lilly and Company, Indianapolis, IN, USA.

出版信息

J Crohns Colitis. 2025 Jul 12. doi: 10.1093/ecco-jcc/jjaf124.

Abstract

BACKGROUND AND AIMS

Concurrent achievement of symptomatic, endoscopic, and histologic remission, known as disease clearance, has been proposed as a treatment target in ulcerative colitis. Mirikizumab, an anti-interleukin-23 p19 antibody, has demonstrated long-term efficacy and safety, as reported in the LUCENT Phase 3 trials (NCT03518086, NCT03524092, and NCT03519945). The current analysis evaluates the impact of mirikizumab on disease clearance and the association with other clinical and patient-reported outcomes (PROs).

METHODS

LUCENT methods have previously been reported. The proportion of patients achieving disease clearance was determined through week (W)104. Association analyses were assessed between disease clearance and PROs (IBDQ, SF-36, WPAI:UC, PGRS, and PGRC), and early disease clearance and subsequent clinical outcomes (clinical, corticosteroid-free, endoscopic, histological, histologic-endoscopic, bowel urgency, stool frequency, and rectal bleeding).

RESULTS

The proportions of patients achieving disease clearance with mirikizumab at W12, W52, and W104 were 16.0%, 36.4%, and 51.3%, respectively. Mirikizumab-treated patients with disease clearance showed greater PRO improvements through W52 than those without. Early clearance at W12 was associated with significantly better clinical outcomes at later time points, except for bowel urgency remission at W52. This trend was repeated for clinical outcomes at W104 in patients who achieved disease clearance at W52.

CONCLUSIONS

Mirikizumab consistently demonstrated disease clearance across induction, maintenance, and long-term studies. The attainment of disease clearance was associated with greater improvement in PROs, and early achievement of disease clearance was associated with better long-term outcomes, including clinical remission, corticosteroid-free remission, endoscopic and histological outcomes, reduced stool frequency, and rectal bleeding.

摘要

背景与目的

同时实现症状缓解、内镜缓解和组织学缓解,即疾病清除,已被提议作为溃疡性结肠炎的治疗目标。如LUCENT 3期试验(NCT03518086、NCT03524092和NCT03519945)所报道,抗白细胞介素-23 p19抗体mirikizumab已证明具有长期疗效和安全性。本分析评估了mirikizumab对疾病清除的影响以及与其他临床和患者报告结局(PROs)的关联。

方法

LUCENT试验方法先前已报道。通过第104周确定达到疾病清除的患者比例。评估疾病清除与PROs(IBDQ、SF-36、WPAI:UC、PGRS和PGRC)之间以及早期疾病清除与随后临床结局(临床、无皮质类固醇、内镜、组织学、组织学-内镜、排便急迫感、大便频率和直肠出血)之间的关联分析。

结果

在第12周、第52周和第104周使用mirikizumab实现疾病清除的患者比例分别为16.0%、36.4%和51.3%。接受mirikizumab治疗且实现疾病清除的患者在第52周之前的PRO改善程度高于未实现疾病清除的患者。第12周的早期清除与后期时间点显著更好的临床结局相关,但第52周的排便急迫感缓解除外。在第52周实现疾病清除的患者中,第104周的临床结局也出现了同样的趋势。

结论

在诱导、维持和长期研究中,mirikizumab始终显示出疾病清除效果。实现疾病清除与PROs的更大改善相关,早期实现疾病清除与更好的长期结局相关,包括临床缓解、无皮质类固醇缓解、内镜和组织学结局、大便频率降低以及直肠出血。

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