Advanced Combination Therapy with Biologics and Upadacitinib in Refractory Inflammatory Bowel Disease: A Retrospective Study from Taiwan.

IF 4.1 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2025-02-26 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S511309
Ming-Jung Meng, Chia-Jung Kuo, Ming-Wei Lai, Cheng-Tang Chiu, Ming-Yao Su, Ming-Ling Chang, Puo-Hsien Le
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Abstract

Background: Refractory inflammatory bowel disease (IBD) remains challenging despite the availability of various biologics. Advanced combination therapy (ACT) with biologics and Upadacitinib (UPA), a rapid-onset oral selective Janus kinase inhibitor, has shown promise in managing refractory IBD. However, its use in Asia has not been explored. This study aims to fill that gap by providing data from Taiwan.

Materials and methods: This retrospective study included refractory IBD patients who received ACT with biologics and UPA, followed up at the Chang Gung Inflammatory Bowel Disease Center from July 2020 to August 2024. Patients were assessed for clinical response and remission at weeks 4, 12, and 24. Safety profiles were monitored throughout the follow-up period to evaluate the risk of adverse events.

Results: Sixteen refractory IBD patients were enrolled. The median disease duration was 4.5 years [IQR 2.25-9.50]. The most common regimen was Ustekinumab plus UPA (63%). Clinical response rates at weeks 4, 12, and 24 were 88%, 83%, and 100%, respectively, while remission rates were 31%, 50%, and 80%. One patient (6.25%) experienced a minor adverse event (acne), with no major events like herpes zoster reactivation or major cardiac complications.

Conclusion: This is the first study in Asia to demonstrate that UPA-based ACT is both effective and safe in treating refractory IBD. However, the limitations of this retrospective, single-center study with a relatively small sample size highlight the need for future larger-scale, multi-center prospective studies to confirm these findings, identify predictors of treatment response, and evaluate long-term outcomes.

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生物制剂与厄帕他替尼联合治疗难治性炎症性肠病:台湾回顾性研究。
背景:尽管有各种生物制剂,难治性炎症性肠病(IBD)仍然具有挑战性。生物制剂和Upadacitinib (UPA,一种快速起效的口服选择性Janus激酶抑制剂)的高级联合治疗(ACT)在治疗难治性IBD方面显示出希望。然而,它在亚洲的应用尚未得到探索。本研究旨在通过提供台湾的数据来填补这一空白。材料和方法:本回顾性研究纳入了2020年7月至2024年8月在长庚炎症性肠病中心接受ACT联合生物制剂和UPA治疗的难治性IBD患者。在第4周、第12周和第24周评估患者的临床反应和缓解。在整个随访期间监测安全性概况,以评估不良事件的风险。结果:16例难治性IBD患者入组。中位病程为4.5年[IQR 2.25-9.50]。最常见的方案是Ustekinumab加UPA(63%)。第4、12和24周的临床缓解率分别为88%、83%和100%,而缓解率分别为31%、50%和80%。1例患者(6.25%)出现轻微不良事件(痤疮),无带状疱疹再激活或主要心脏并发症等重大事件。结论:这是亚洲第一个证明基于upa的ACT治疗难治性IBD既有效又安全的研究。然而,这项回顾性、单中心、样本量相对较小的研究存在局限性,因此需要未来更大规模、多中心的前瞻性研究来证实这些发现,确定治疗反应的预测因素,并评估长期结果。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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