倾向评分匹配真实世界的比较治疗结果,在有和没有事先暴露于抗肿瘤坏死因子α抗体的溃疡性结肠炎患者中使用Janus激酶抑制剂。

IF 3.4 Q2 GASTROENTEROLOGY & HEPATOLOGY
Maiko Ikenouchi, Hirokazu Fukui, Soichi Yagi, Akira Nogami, Koji Kaku, Toshiyuki Sato, Mikio Kawai, Koji Kamikozuru, Yoko Yokoyama, Tetsuya Takagawa, Toshihiko Tomita, Taku Kobayashi, Shinichiro Shinzaki
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We compared the efficacy and safety of 3 JAK inhibitors in patients with UC, considering their prior aTNF exposure.</p><p><strong>Methods: </strong>A retrospective study was conducted in patients with UC who started TFB, FIL, or UPA at 2 academic centers. This propensity score-matched cohort study assessed the effectiveness of the 3 JAK inhibitors for UC in patients with and without prior aTNF exposure, comparing steroid-free clinical remission and response rates after 8 weeks.</p><p><strong>Results: </strong>Among 274 patients who met the inclusion criteria, 145 experienced aTNF exposure (TFB: 59.2%, 100/169; FIL: 34.5%, 20/58; UPA: 53.2%, 25/47). Based on propensity score-matching, UPA led to a higher steroid-free clinical remission rates than TFB (adjusted odds ratio [aOR], 5.57; 95% confidence interval [CI], 1.42-21.90) or FIL (aOR, 9.00; 95% CI, 1.42-57.10) in patients exposed to aTNF. 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引用次数: 0

摘要

背景/目的:Tofacitinib (TFB), filgotinib (FIL)和upadacitinib (UPA)是Janus激酶(JAK)抑制剂,已被批准用于中重度溃疡性结肠炎(UC)。然而,每种JAK抑制剂在治疗算法中的适当定位尚不清楚。此外,JAK抑制剂对UC患者和既往抗肿瘤坏死因子α抗体(aTNF)治疗的实际疗效尚未得到充分研究。我们比较了3种JAK抑制剂在UC患者中的疗效和安全性,考虑到他们之前的aTNF暴露。方法:在2个学术中心对开始TFB、FIL或UPA治疗的UC患者进行回顾性研究。这项倾向评分匹配的队列研究评估了3种JAK抑制剂对有和没有aTNF暴露的UC患者的有效性,比较了8周后无类固醇临床缓解和反应率。结果:274例符合纳入标准的患者中,145例出现aTNF暴露(TFB: 59.2%, 100/169;Fil: 34.5%, 20/58;Upa: 53.2%, 25/47)。基于倾向评分匹配,UPA导致的无类固醇临床缓解率高于TFB(调整优势比[aOR], 5.57;95%置信区间[CI], 1.42-21.90)或FIL (aOR, 9.00;95% CI, 1.42-57.10)。在未暴露于aTNF的患者中,各组无类固醇临床缓解和临床缓解率无显著差异。UPA组不良事件发生率略高于TFB或FIL组。结论:UPA治疗UC可能比TFB或FIL更有效,特别是对于先前有aTNF暴露的患者,尽管应考虑不良事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Propensity score-matched real-world comparative treatment outcomes of Janus kinase inhibitors for ulcerative colitis in patients with and without prior exposure to anti-tumor necrosis factor α antibody.

Background/aims: Tofacitinib (TFB), filgotinib (FIL), and upadacitinib (UPA) are Janus kinase (JAK) inhibitors approved for moderate-to-severe ulcerative colitis (UC). The appropriate positioning of each JAK inhibitor in the treatment algorithm, however, is unclear. Furthermore, real-world efficacy of JAK inhibitors for patients with UC and prior anti-tumor necrosis factor α antibody (aTNF) treatment are not fully investigated. We compared the efficacy and safety of 3 JAK inhibitors in patients with UC, considering their prior aTNF exposure.

Methods: A retrospective study was conducted in patients with UC who started TFB, FIL, or UPA at 2 academic centers. This propensity score-matched cohort study assessed the effectiveness of the 3 JAK inhibitors for UC in patients with and without prior aTNF exposure, comparing steroid-free clinical remission and response rates after 8 weeks.

Results: Among 274 patients who met the inclusion criteria, 145 experienced aTNF exposure (TFB: 59.2%, 100/169; FIL: 34.5%, 20/58; UPA: 53.2%, 25/47). Based on propensity score-matching, UPA led to a higher steroid-free clinical remission rates than TFB (adjusted odds ratio [aOR], 5.57; 95% confidence interval [CI], 1.42-21.90) or FIL (aOR, 9.00; 95% CI, 1.42-57.10) in patients exposed to aTNF. Steroid-free clinical remission and clinical response rates did not differ significantly between each group in patients non-exposed to aTNF. The incidence of adverse events was slightly higher with UPA than TFB or FIL.

Conclusions: UPA may be more effective for UC than TFB or FIL, especially in patients with previous aTNF exposure, although consideration should be given to adverse events.

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来源期刊
Intestinal Research
Intestinal Research GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
7.40
自引率
10.20%
发文量
69
审稿时长
38 weeks
期刊介绍: Intestinal Research (Intest Res) is the joint official publication of the Asian Organization for Crohn''s and Colitis (AOCC), Chinese Society of IBD (CSIBD), Japanese Society for IBD (JSIBD), Korean Association for the Study of Intestinal Diseases (KASID), Taiwan Society of IBD (TSIBD) and Colitis Crohn''s Foundation (India) (CCF, india). The aim of the Journal is to provide broad and in-depth analysis of intestinal diseases, especially inflammatory bowel disease, which shows increasing tendency and significance. As a Journal specialized in clinical and translational research in gastroenterology, it encompasses multiple aspects of diseases originated from the small and large intestines. The Journal also seeks to propagate and exchange useful innovations, both in ideas and in practice, within the research community. As a mode of scholarly communication, it encourages scientific investigation through the rigorous peer-review system and constitutes a qualified and continual platform for sharing studies of researchers and practitioners. Specifically, the Journal presents up-to-date coverage of medical researches on the physiology, epidemiology, pathophysiology, clinical presentations, and therapeutic interventions of the intestinal diseases. General topics of interest include inflammatory bowel disease, colon and small intestine cancer or polyp, endoscopy, irritable bowel syndrome and other motility disorders, infectious enterocolitis, intestinal tuberculosis, and so forth. The Journal publishes diverse types of academic materials such as editorials, clinical and basic reviews, original articles, case reports, letters to the editor, brief communications, perspective, statement or commentary, and images that are useful to clinicians and researchers.
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