Short- and Long-Term Outcomes of Mirikizumab for Ulcerative Colitis: A Real-World Multicenter Retrospective Cohort Study from the INSIGHT study

医学 溃疡性结肠炎 回顾性队列研究 内科学 临床试验 不利影响 队列研究 临床终点 队列 多中心研究 炎症性肠病 皮质类固醇 儿科 前瞻性队列研究 年轻人 结肠炎 随机对照试验 疾病严重程度 自发缓解 临床实习 外科 入射(几何)
作者
Tsunaki Sawada,Takeshi Yamamura,Keiko Maeda,Eri Ishikawa,Kentaro Murate,Nobuyuki Miyake,Rinzaburo Matsuura,Toshihisa Fujiyoshi,Genta Uchida,Hiroto Suzuki,Takahiro Nishikawa,Takeshi Kuno,Shun Hattori,Noboru Urata,Ayako Ohashi,Issei Hasegawa,Masanao Nakamura,Hiroki Kawashima
出处
期刊:Digestion [Karger Publishers]
卷期号:: 1-25
标识
DOI:10.1159/000551500
摘要

INTRODUCTION: Mirikizumab (MIR), a selective IL-23p19 inhibitor, has shown efficacy in clinical trials for ulcerative colitis (UC). However, real-world data, especially on long-term outcomes and in treatment-experienced populations, remain limited. METHODS: We conducted a multicenter retrospective cohort study involving 85 patients with moderate-to-severe UC who initiated MIR between July 2023 and December 2024 across 12 Japanese centers. Co-primary endpoints were clinical remission (Simple Clinical Colitis Activity Index [SCCAI] ≤2 and with no rectal bleeding) at weeks 12 and 52. Secondary outcomes included corticosteroid (CS)-free remission, CRP normalization, treatment persistence, and safety. RESULTS: Clinical remission was achieved in 62.4% at week 12 and 55.3% at week 52. CS-free remission rates were identical to overall remission at both time points. MIR maintained effectiveness regardless of prior exposure to biologics or JAK inhibitors. Early clinical response at week 4 independently predicted week 52 remission, while steroid dependence was a predictor at week 12. Among patients receiving extended induction, 27.3% of initial nonresponders achieved remission by week 24. Treatment was generally well tolerated, with 17.6% experiencing adverse events and 9.4% discontinuing due to these events. No serious infections or hospitalizations occurred. CONCLUSION: MIR demonstrated durable effectiveness and a favorable safety profile over 52 weeks in a real-world UC population, including those with prior treatment failures. These findings support MIR as a viable long-term therapeutic option in routine clinical practice.
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