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卡罗替格拉酯甲基在日本中度活动性溃疡性结肠炎患者中的真实世界有效性和安全性

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

作者信息

Ohmori Toshihide

机构信息

Department of Gastroenterology, Ohmori Toshihide Gastro-intestinal Clinic, Ageo, Saitama, Japan.

出版信息

Inflamm Intest Dis. 2024 Oct 21;9(1):271-282. doi: 10.1159/000541663. eCollection 2024 Jan-Dec.

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) ( = 0.008), the Mayo score decreased significantly from 7.0 (5-9) to 0.0 (0-9) ( = 0.006), and the clinical activity index decreased significantly from 6.0 (1-11) to 0.0 (0-9) ( = 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.

摘要

引言

卡罗替格拉司甲酯(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-氨基水杨酸类药物反应不足或不耐受的中度活动性溃疡性结肠炎(UC)的诱导缓解治疗。

方法

我们对日本中度活动性UC患者进行了一项单中心回顾性观察研究,以评估CGM作为诱导缓解治疗的真实有效性和安全性。

结果

14例患者中,71%(10/14)为女性,年龄中位数(范围)为47(20 - 68)岁。疾病类型为直肠炎7%(1/14),左侧结肠炎50%(7/14),全结肠炎43%(6/14)。治疗持续时间中位数(范围)为8(2 - 26)周,内镜改善率(梅奥内镜亚评分[MES]为0或1)为64%(9/14),内镜缓解率(MES为0)为57%(8/14)。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,大便次数和腹泻频率显著下降,便血和腹痛患者的比例趋于下降。在9例通过CGM实现内镜改善的患者中,第26周的累积无复发率为77.8%(95%置信区间,36.5% - 93.9%)。研究期间未报告包括进行性多灶性白质脑病在内的药物不良反应。

结论

这项对14例日本UC患者的单中心回顾性观察研究表明,在现实环境中,CGM作为对5-氨基水杨酸类药物反应不足的中度活动性UC的诱导缓解治疗是安全有效的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4288/11575925/5db5f9a0871f/iid-2024-0009-0001-541663_F01.jpg

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