An inverse probability of treatment weighted comparison between vedolizumab, ustekinumab, and tofacitinib in anti-TNF-experienced ulcerative colitis patients.

IF 3.8 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Therapeutic Advances in Gastroenterology Pub Date : 2026-06-15 eCollection Date: 2026-01-01 DOI:10.1177/17562848261455563
Antonio Tursi, Andrea Pasta, Walter Elisei, Brigida Barberio, Luisa Bertin, Giammarco Mocci, Giovanni Maconi, Antonietta Gerarda Gravina, Raffaele Pellegrino, Giorgia Bodini, Alfredo Papa, Edoardo Vincenzo Savarino
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引用次数: 0

Abstract

Background: Biologics and small-molecule therapies are widely used for ulcerative colitis (UC), but their comparative effectiveness in anti-tumor necrosis factor (TNF)-exposed patients is unclear.

Objectives: To compare the effectiveness and safety of vedolizumab, ustekinumab, and tofacitinib in anti-TNF-experienced patients with UC.

Design: Multicenter retrospective observational cohort study.

Methods: A multicenter retrospective cohort of anti-TNF-experienced UC patients treated with vedolizumab (n = 260), tofacitinib (n = 149), or ustekinumab (n = 193) was analyzed. Partial Mayo Score (pMayo), endoscopic remission, and biomarker response were assessed at baseline, 12, 24, and 52 weeks, respectively. Inverse Probability of Treatment Weighting (IPTW) was applied to balance baseline characteristics, and longitudinal changes were analyzed using repeated-measures general linear models with post hoc corrections.

Results: After IPTW adjustment, at week 52, clinical remission was highest with tofacitinib compared with ustekinumab (p < 0.001) and vedolizumab (p = 0.002). Steroid-free clinical remission showed a similar pattern (tofacitinib vs ustekinumab: p = 0.006; tofacitinib vs vedolizumab: p < 0.001). No significant differences in biochemical remission were found across groups at week 52 (p = 0.931). Endoscopic remission favored vedolizumab over ustekinumab and tofacitinib (p < 0.001). Subgroup analyses revealed superior tofacitinib performance in extensive colitis and in patients with ⩾2 prior biologic classes (vs vedolizumab: p = 0.089; vs ustekinumab: p < 0.001). Adverse events were infrequent and similar across groups.

Conclusion: In anti-TNF-experienced UC patients, tofacitinib was associated with higher long-term clinical and steroid-free remission rates, ustekinumab showed intermediate effectiveness with a favorable safety profile, while vedolizumab was associated with higher endoscopic remission. These findings may help inform individualized, outcome-oriented treatment strategies, but they should be interpreted with caution and confirmed in prospective head-to-head studies.

vedolizumab, ustekinumab和tofacitinib在抗tnf经历的溃疡性结肠炎患者中的治疗加权比较的逆概率。
背景:生物制剂和小分子治疗被广泛用于溃疡性结肠炎(UC),但它们在抗肿瘤坏死因子(TNF)暴露患者中的相对疗效尚不清楚。目的:比较vedolizumab、ustekinumab和tofacitinib在抗tnf -经历的UC患者中的有效性和安全性。设计:多中心回顾性观察队列研究。方法:对接受维多单抗(260例)、托法替尼(149例)或乌斯特金单抗(193例)治疗的抗tnf -经历的UC患者进行多中心回顾性队列分析。分别在基线、12周、24周和52周评估部分Mayo评分(pMayo)、内窥镜缓解和生物标志物反应。应用治疗加权逆概率(IPTW)来平衡基线特征,并使用具有事后修正的重复测量一般线性模型分析纵向变化。结果:调整IPTW后,在第52周,与ustekinumab相比,托法替尼组的临床缓解最高(p p = 0.002)。无类固醇临床缓解表现出类似的模式(托法替尼vs ustekinumab: p = 0.006;托法替尼vs vedolizumab: p = 0.931)。与ustekinumab和tofacitinib相比,内镜下缓解倾向于vedolizumab (p = 0.089; vs ustekinumab: p): p结论:在抗tnf经历的UC患者中,tofacitinib具有较高的长期临床和无类固醇缓解率,ustekinumab具有中等疗效和良好的安全性,而vedolizumab具有较高的内镜下缓解率。这些发现可能有助于提供个性化的、以结果为导向的治疗策略,但它们应该谨慎解释,并在前瞻性的头对头研究中得到证实。
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来源期刊
Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.70
自引率
2.40%
发文量
103
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area. The editors welcome original research articles across all areas of gastroenterology and hepatology. The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.
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