Real-World Effectiveness and Safety of Carotegrast Methyl in Japanese Patients with Moderately Active Ulcerative Colitis.

Q2 Medicine
Inflammatory Intestinal Diseases Pub Date : 2024-10-21 eCollection Date: 2024-01-01 DOI:10.1159/000541663
Toshihide Ohmori
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引用次数: 0

Abstract

Introduction: Carotegrast methyl (CGM) is an oral, small-molecule α4-integrin antagonist, which became clinically available in Japan in May 2022. CGM is approved for remission induction treatment for moderately active ulcerative colitis (UC) with an inadequate response or intolerance to 5-aminosalicylates.

Methods: We performed a single-center, retrospective, observational study of Japanese patients with moderately active UC to assess the real-world effectiveness and safety of CGM as remission induction treatment.

Results: Of 14 patients, 71% (10/14) were women, and the median (range) age was 47 (20-68) years. Disease types were proctitis in 7% (1/14), left-sided colitis in 50% (7/14), and total colitis in 43% (6/14). With a median (range) treatment duration of 8 (2-26) weeks, the rate of endoscopic improvement (Mayo endoscopic subscore [MES] of 0 or 1) was 64% (9/14), and the rate of endoscopic remission (MES of 0) was 57% (8/14). After treatment with CGM, the median (range) MES decreased significantly from 3.0 (2-3) to 0.0 (0-3) (p = 0.008), the Mayo score decreased significantly from 7.0 (5-9) to 0.0 (0-9) (p = 0.006), and the clinical activity index decreased significantly from 6.0 (1-11) to 0.0 (0-9) (p = 0.015). Stool and diarrhea frequencies decreased significantly after initiating CGM, and the percentage of patients with bloody stool and abdominal pain tended to decrease. The cumulative relapse-free rate at week 26 among 9 patients who achieved endoscopic improvement with CGM was 77.8% (95% confidence interval, 36.5%-93.9%). No adverse drug reactions, including progressive multifocal leukoencephalopathy, were reported during the study period.

Conclusion: This single-center, retrospective, observational study of 14 Japanese patients with UC showed that CGM was safe and effective as a remission induction treatment for moderately active UC with an inadequate response to 5-aminosalicylates in real-world settings.

在日本中度活动性溃疡性结肠炎患者中使用 Carotegrast Methyl 的实际效果和安全性。
简介Carotegrast methyl(CGM)是一种口服小分子α4-整合素拮抗剂,于2022年5月在日本上市。CGM被批准用于对5-氨基水杨酸盐反应不充分或不耐受的中度活动性溃疡性结肠炎(UC)的缓解诱导治疗:我们对日本中度活动性溃疡性结肠炎患者进行了一项单中心、回顾性、观察性研究,以评估 CGM 作为缓解诱导治疗的实际有效性和安全性:14名患者中,71%(10/14)为女性,年龄中位数(范围)为47(20-68)岁。7%的患者(1/14)患有直肠炎,50%的患者(7/14)患有左侧结肠炎,43%的患者(6/14)患有全结肠炎。治疗时间中位数(范围)为 8(2-26)周,内镜改善率(梅奥内镜子评分 [MES] 为 0 或 1)为 64%(9/14),内镜缓解率(MES 为 0)为 57%(8/14)。使用 CGM 治疗后,MES 中位数(范围)从 3.0(2-3)显著降至 0.0(0-3)(p = 0.008),梅奥评分从 7.0(5-9)显著降至 0.0(0-9)(p = 0.006),临床活动指数从 6.0(1-11)显著降至 0.0(0-9)(p = 0.015)。开始使用 CGM 后,大便和腹泻次数明显减少,出现血便和腹痛的患者比例也呈下降趋势。9 名患者在使用 CGM 后内镜症状得到改善,第 26 周的累计无复发率为 77.8%(95% 置信区间,36.5%-93.9%)。研究期间未报告药物不良反应,包括进行性多灶性白质脑病:这项对14名日本UC患者进行的单中心、回顾性、观察性研究表明,CGM作为一种缓解诱导治疗方法,在现实世界中对5-氨基水杨酸类药物反应不充分的中度活动性UC患者是安全有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Inflammatory Intestinal Diseases
Inflammatory Intestinal Diseases Medicine-Gastroenterology
CiteScore
4.50
自引率
0.00%
发文量
6
审稿时长
20 weeks
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