Effectiveness of upadacitinib in ulcerative colitis patients with prior tofacitinib exposure: a systematic review and meta-analysis.

IF 2.2 Q3 GASTROENTEROLOGY & HEPATOLOGY
Annals of Gastroenterology Pub Date : 2025-09-01 Epub Date: 2025-08-14 DOI:10.20524/aog.2025.0991
Fariha Hasan, Ayesha Liaquat, Ahmed Raza, Zain Ali Nadeem, Fatima Farooqi, Hassam Ali, Dushyant Singh Dahiya, Zeina Issa, Bhanu Siva Mohan Pinnam, Saqr Alsakarneh, Islam Mohamad, Gursimran S Kocchar
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引用次数: 0

Abstract

Background: Upadacitinib, a selective Janus kinase (JAK) inhibitor, is a recently approved therapy for moderate-to-severe ulcerative colitis (UC). Limited data are available on its efficacy in patients previously exposed to tofacitinib, a non-selective JAK inhibitor. Therefore, we conducted a systematic review and meta-analysis to evaluate the efficacy of upadacitinib in UC patients with prior tofacitinib treatment.

Methods: PubMed, Embase, Web of Science, and Cochrane Library were queried for studies evaluating the effectiveness of upadacitinib in UC patients with prior tofacitinib treatment. Primary outcomes included clinical remission, steroid-free clinical remission (SFCR), and clinical response. Secondary outcomes were the mean decrease in fecal calprotectin, and adverse events. Statistical analyses were performed using R, calculating pooled proportions with 95% confidence intervals (CI) for dichotomous outcomes and mean differences with 95%CI for continuous outcomes using a random-effects model.

Results: Five studies, with 127 patients, were included in the final analysis. Upadacitinib increased pooled clinical remission rates by 57% (95%CI 0.32-0.80), SFCR rates by 52% (95%CI 0.26-0.78), and clinical response rates by 75% (95%CI 0.44-0.96). Upadacitinib reduced mean fecal calprotectin levels by 597.59% (95%CI 350.94-844.324). Adverse events, such as headache, acne vulgaris, rash, nasopharyngitis and infections, were reported in 34% of patients (95%CI 0.11-0.62).

Conclusions: Our meta-analysis indicates that upadacitinib may be an effective treatment for patients with prior tofacitinib exposure, demonstrating significant clinical remission, SFCR, and clinical response. Larger clinical trials are needed to establish long-term outcomes.

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upadacitinib对先前暴露于托法替尼的溃疡性结肠炎患者的有效性:一项系统评价和荟萃分析。
背景:Upadacitinib是一种选择性Janus激酶(JAK)抑制剂,最近被批准用于治疗中重度溃疡性结肠炎(UC)。对于先前暴露于非选择性JAK抑制剂tofacitinib的患者,其疗效的数据有限。因此,我们进行了系统回顾和荟萃分析,以评估upadacitinib对既往接受过托法替尼治疗的UC患者的疗效。方法:对PubMed、Embase、Web of Science和Cochrane Library进行查询,以评估upadacitinib对既往接受过托法替尼治疗的UC患者的有效性。主要结局包括临床缓解、无类固醇临床缓解(SFCR)和临床反应。次要结局是粪钙保护蛋白的平均减少和不良事件。使用R进行统计分析,使用随机效应模型计算二分结果95%置信区间(CI)的合并比例和连续结果95%置信区间(CI)的平均差异。结果:5项研究,127例患者被纳入最终分析。Upadacitinib使合并临床缓解率提高57% (95%CI 0.32-0.80), SFCR率提高52% (95%CI 0.26-0.78),临床缓解率提高75% (95%CI 0.44-0.96)。Upadacitinib降低粪钙保护蛋白水平597.59% (95%CI 350.94-844.324)。34%的患者报告了头痛、寻常痤疮、皮疹、鼻咽炎和感染等不良事件(95%CI 0.11-0.62)。结论:我们的荟萃分析表明,upadacitinib可能是先前暴露于托法替尼的患者的有效治疗方法,表现出显著的临床缓解、SFCR和临床反应。需要更大规模的临床试验来确定长期结果。
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
Annals of Gastroenterology
Annals of Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.30
自引率
0.00%
发文量
58
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