影响溃疡性结肠炎患者停用生物疗法的因素。

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Arisa Fukuyama, Akio Nakashima, Motoyasu Miyazaki, Masakatsu Fujiki, Hideki Kakimoto, Takashi Hisabe, Osamu Imakyure
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引用次数: 0

摘要

背景:最近,溃疡性结肠炎(UC)的治疗范围已扩大到抗肿瘤坏死因子α、抗整合素和抗IL-12/23p40抗体药物。这些生物制剂是根据患者的个体情况量身定制的。然而,有些患者会停止生物治疗。本研究探讨了影响 UC 患者停止生物治疗的因素:这项回顾性单队列研究涵盖了2019年4月至2022年3月期间开始接受英夫利西单抗、阿达木单抗、戈利木单抗、维妥珠单抗和乌司替尼等生物制剂治疗的UC患者。根据患者一年的治疗情况,将其分为继续治疗组和停止治疗组。对两组患者的基线特征进行了比较:在 116 名 UC 患者中,102 人被纳入研究。其中,74 人(72.5%)继续接受生物治疗,28 人(27.5%)中断治疗。英夫利西单抗、阿达木单抗、戈利木单抗、维妥珠单抗和乌司他单抗的停药率分别为33.3%、25.0%、50.0%、30.2%和15.6%。停药的主要原因是缺乏疗效(85.7%),其次是不良事件(7.1%)、妊娠(3.6%)和死亡(3.6%)。与继续用药组相比,停药组同时使用硫嘌呤的比例明显较低(28.6% 对 56.8%,P = 0.0132)。多变量分析显示,同时服用硫嘌呤与继续治疗独立相关(p = 0.0075):该研究表明,同时使用硫嘌呤与 UC 患者继续使用生物疗法有显著相关性,强调了同时使用硫嘌呤对维持生物疗法的重要性。有必要开展进一步研究,以评估联合疗法的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors influencing the discontinuation of biologic therapies in patients with ulcerative colitis.

Background: The therapeutic landscape for ulcerative colitis (UC) has recently broadened to include anti-TNFα, anti-integrin, and anti-IL-12/23p40 antibody agents. These biological agents are tailored to individual patient profiles. However, some patients cease biological treatment. This study investigates factors influencing the discontinuation of biological treatment in UC patients.

Methods: This retrospective single-cohort study encompasses UC patients who commenced treatment with biological agents like infliximab, adalimumab, golimumab, vedolizumab, and ustekinumab from April 2019 to March 2022. Patients were categorized into continuation and discontinuation groups based on their one-year treatment status. Baseline characteristics were compared between the groups.

Results: Of the 116 UC patients, 102 were included in the study. Among these, 74 (72.5%) continued and 28 (27.5%) discontinued biological therapy. Discontinuation rates for infliximab, adalimumab, golimumab, vedolizumab, and ustekinumab were 33.3%, 25.0%, 50.0%, 30.2%, and 15.6%, respectively. The primary discontinuation reason was lack of efficacy (85.7%), followed by adverse events (7.1%), pregnancy (3.6%), and death (3.6%). The discontinuation group had a significantly lower rate of concomitant thiopurine compared to the continuation group (28.6% vs. 56.8%, p = 0.0132). Multivariable analysis revealed that concomitant thiopurine was independently associated with therapy continuation (p = 0.0075).

Conclusion: The study indicates that concomitant thiopurine significantly correlates with the continuation of biological therapies in UC patients, underscoring the importance of concomitant thiopurine in sustaining biological therapy. Further studies are warranted to assess the efficacy of combination therapy.

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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
29
审稿时长
8 weeks
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