Gastroenterology Unit, Medical Department, Capio St Göran Hospital.
Division of Gastroenterology, Medical Department, Karolinska University Hospital, Stockholm.
Eur J Gastroenterol Hepatol. 2024 Dec 1;36(12):1419-1425. doi: 10.1097/MEG.0000000000002854. Epub 2024 Sep 20.
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.
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.
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%).
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.
乌司奴单抗(UST)是一种用于治疗炎症性肠病的抗白细胞介素-12/23 抗体。本研究纳入了斯德哥尔摩四家医院治疗的患者,以提供长期的真实世界数据。
本回顾性研究纳入了 2019 年至 2021 年期间接受乌司奴单抗治疗的溃疡性结肠炎患者。患者接受治疗直至停药或 2021 年 7 月 31 日研究结束。采用医师总体评估(PGA)评估疾病活动度;采用溃疡性结肠炎内镜严重指数(UCEIS)、实验室参数和药物持续时间评估疾病活动度。主要结局指标分别为治疗 3 个月和 12 个月时无激素缓解(PGA=0)和应答(PGA 较基线下降≥1)。
共纳入 96 例患者,其中女性 44 例,男性 52 例。患者结肠炎类型包括广泛结肠炎(69%)、左半结肠炎(29%)或直肠炎(3%)。除 2 例患者外,其余患者均为抗 TNF 治疗失败,94 例(98%)患者至少 1 种、59 例(61%)患者至少 2 种、34 例(35%)患者至少 3 种抗 TNF 药物治疗失败。此外,28 例(29%)患者抗 vedolizumab 治疗失败。纳入时,96 例患者中有 92 例(96%)患者存在疾病活动,4 例患者处于缓解期。在接受乌司奴单抗治疗的患者中,治疗 3 个月时,9 例(13%)患者达到无激素缓解,12 个月时 26 例(78%)患者达到无激素缓解。3 个月和 12 个月的停药率分别为 12%和 26%,主要原因为疾病持续活动(20%)。
在这组治疗困难的溃疡性结肠炎患者中,乌司奴单抗显示出有效性,大多数患者在 12 个月时药物持续有效,且安全性良好。