Long-term real-world data of ustekinumab in ulcerative colitis: the Stockholm Ustekinumab Study (STOCUSTE).

IF 2.3 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Haider Sabhan, Francesca Bello, Samer Muhsen, Alexandra Borin, Fredrik Johansson, Charlotte Höög, Ole Forsberg, Christina Wennerström, Mikael Lördal, Sven Almer, Charlotte Söderman
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引用次数: 0

Abstract

Background: Ustekinumab (UST) is an anti-interleukin-12/23 antibody used in the treatment of inflammatory bowel disease. This study includes patients treated at four hospitals in Stockholm to provide long-term real-world data.

Methods: Retrospective study including patients diagnosed with ulcerative colitis and treated with UST between the years 2019 and 2021. Patients were followed until withdrawal of treatment, or until a predefined end of study, 31 July 2021. Disease activity was assessed with Physician Global Assessment (PGA); Ulcerative Colitis Endoscopic Index of Severity (UCEIS), laboratory parameters, and drug persistence. The primary outcome was steroid-free remission (PGA = 0) and response (decrease PGA ≥ 1 from baseline) at 3 and 12 months, respectively.

Results: A total of 96 patients, 44 women and 52 men were included. The patients had either extensive colitis (69%), left-sided colitis (29%), or proctitis (3%). All but two patients were anti-TNF-experienced; 94 (98%) had failed ≥1, 59 (61%) ≥ 2, and 34 (35%) had failed ≥ 3 anti-TNF drugs. In addition, 28 (29%) had failed vedolizumab. At inclusion, 92/96 patients (96%) had active disease and four patients were in remission. Among patients who were treated with UST, 9/71 (13%) were in steroid-free remission at 3 months, and 26/33 (78%) were at 12 months. Withdrawal rates at 3 and 12 months, were 12 and 26%, respectively, mainly due to persisting disease activity (20%).

Conclusion: In this group of patients with difficult-to-treat ulcerative colitis, UST was shown to be effective in the majority, with high drug persistence at 12 months in combination with a favorable safety profile.

乌司珠单抗治疗溃疡性结肠炎的长期真实数据:斯德哥尔摩乌司珠单抗研究(STOCUSTE)。
背景:优思明单抗(UST)是一种用于治疗炎症性肠病的抗白细胞介素-12/23抗体。这项研究包括在斯德哥尔摩四家医院接受治疗的患者,以提供长期的真实世界数据:回顾性研究包括 2019 年至 2021 年期间诊断为溃疡性结肠炎并接受 UST 治疗的患者。对患者进行随访,直至停止治疗,或直至 2021 年 7 月 31 日预定的研究结束。疾病活动性通过医生全球评估(PGA)、溃疡性结肠炎内镜下严重程度指数(UCEIS)、实验室参数和药物持续性进行评估。主要结果分别为3个月和12个月时的无类固醇缓解(PGA=0)和应答(PGA较基线下降≥1):共纳入 96 名患者,其中女性 44 名,男性 52 名。患者患有广泛结肠炎(69%)、左侧结肠炎(29%)或直肠炎(3%)。除两人外,所有患者都有抗肿瘤坏死因子治疗经验;94人(98%)服用过≥1种、59人(61%)服用过≥2种、34人(35%)服用过≥3种抗肿瘤坏死因子药物。此外,28 人(29%)曾使用过维多利珠单抗。纳入研究时,92/96 名患者(96%)的病情处于活动期,4 名患者病情缓解。在接受 UST 治疗的患者中,9/71(13%)的患者在 3 个月时达到无类固醇缓解,26/33(78%)的患者在 12 个月时达到无类固醇缓解。3个月和12个月时的停药率分别为12%和26%,主要原因是疾病持续活动(20%):结论:在这群难以治疗的溃疡性结肠炎患者中,UST 对大多数患者有效,12 个月的药物持续率高,且安全性良好。
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来源期刊
CiteScore
4.40
自引率
4.80%
发文量
269
审稿时长
1 months
期刊介绍: European Journal of Gastroenterology & Hepatology publishes papers reporting original clinical and scientific research which are of a high standard and which contribute to the advancement of knowledge in the field of gastroenterology and hepatology. The journal publishes three types of manuscript: in-depth reviews (by invitation only), full papers and case reports. Manuscripts submitted to the journal will be accepted on the understanding that the author has not previously submitted the paper to another journal or had the material published elsewhere. Authors are asked to disclose any affiliations, including financial, consultant, or institutional associations, that might lead to bias or a conflict of interest.
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