在波斯尼亚和黑塞哥维那的实际环境中,维多珠单抗对炎症性肠病患者的短期疗效。

0 MEDICINE, RESEARCH & EXPERIMENTAL Biomolecules & biomedicine Pub Date : 2024-09-06 DOI:10.17305/bb.2024.10433
Nermin Salkić, Mirela Bašić Denjagić, Nađa Zubčević, Renata Tamburić, Azra Husić Selimović, Emil Babić, Milenko Bevanda, Aida Saray, Predrag Jovanović, Zoran Tošić, Aleksandar Dobrovoljski, Tatjana Barać
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引用次数: 0

摘要

炎症性肠病(IBD)包括克罗恩病(CD)和溃疡性结肠炎(UC),必须采取有效的治疗策略。本研究旨在评估维多珠单抗这种新型生物疗法在治疗波斯尼亚和黑塞哥维那 IBD 方面的实际疗效。这项回顾性观察研究在 6 个医疗中心进行,涉及 139 名 IBD 患者,其中 76 人患有 UC,63 人患有 CD。在维多珠单抗治疗开始后的 26 周,对患者的临床缓解和其他结果进行了评估。26周时,82.9%的UC患者和85.7%的CD患者达到了临床缓解。38.1%的CD患者出现了黏膜愈合。维多珠单抗的疗效并不因患者之前是否接触过抗肿瘤坏死因子(TNF)而有明显差异。值得注意的是,用于预测维多珠单抗反应的临床评分工具在该队列中的适用性有限。在波斯尼亚和黑塞哥维那的真实世界中,维多珠单抗在治疗UC和CD方面都表现出了很高的疗效,这突显了它作为一种重要的IBD治疗选择的潜力。
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Short-term efficacy of vedolizumab in patients with inflammatory bowel disease in real-life settings in Bosnia and Herzegovina.

Inflammatory bowel disease (IBD), encompassing Crohn's disease (CD) and ulcerative colitis (UC), necessitates effective management strategies. This study aims to evaluate the real-world efficacy of vedolizumab, a newer biological therapy, in treating IBD in Bosnia and Herzegovina. A retrospective observational study was conducted across six medical centers, involving 139 IBD patients, 76 with UC and 63 with CD. Patients were assessed for clinical remission and other outcomes at the 26-week mark post vedolizumab treatment initiation. At 26 weeks, clinical remission was achieved in 82.9% of UC patients and 85.7% of CD patients. Mucosal healing was observed in 38.1% of CD patients. The efficacy of vedolizumab did not significantly differ based on prior anti-tumor necrosis factor (anti-TNF) exposure. Notably, the clinical scoring tools for predicting vedolizumab response showed limited applicability in this cohort. Vedolizumab demonstrated high efficacy in treating both UC and CD in real-world settings in Bosnia and Herzegovina, underscoring its potential as a significant therapeutic option in IBD management.

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