Upadacitinib for the treatment of radiographic axial spondyloarthritis - case series and review of the literature.

Q2 Pharmacology, Toxicology and Pharmaceutics
Drugs in Context Pub Date : 2025-05-12 eCollection Date: 2025-01-01 DOI:10.7573/dic.2024-12-3
Giuseppe Lopalco, Arianna D'Antonio, Maria Sole Chimenti, Florenzo Iannone
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引用次数: 0

Abstract

Upadacitinib is a Janus kinase (JAK) inhibitor approved for the treatment of different rheumatic diseases, including axial spondyloarthritis (axSpA). In phase III clinical trials, upadacitinib was associated with rapid and significant improvement in disease parameters, including scores for pain, function and mobility, signs of structural damage, and patient-reported outcomes, and had an overall incidence of adverse events similar to that in the placebo group. Improvement in axSpA disease severity was observed in both biologic-naive patients and those with prior biologic exposure, and this improvement was sustained during open-label treatment. Indirect comparisons with other agents suggest that upadacitinib is more effective than biologics and other JAK inhibitors in patients with axSpA and is associated with the lowest number-needed-to-treat. Long-term safety data indicate that upadacitinib is well tolerated in patients with axSpA, with a low rate of infections, malignancies, major adverse cardiovascular events and thromboembolism. Four case studies described here illustrate the effectiveness of upadacitinib in a range of real-world patients with axSpA, including patients with early disease and those who have been pre-treated with biologics.

Upadacitinib治疗影像学中轴性脊柱性关节炎-病例系列及文献回顾。
Upadacitinib是一种Janus激酶(JAK)抑制剂,被批准用于治疗不同的风湿性疾病,包括轴性脊柱炎(axSpA)。在III期临床试验中,upadacitinib与疾病参数的快速和显著改善相关,包括疼痛评分、功能和活动能力、结构损伤迹象和患者报告的结果,并且不良事件的总体发生率与安慰剂组相似。在未接受生物制剂治疗的患者和有过生物制剂暴露的患者中,axSpA疾病严重程度均有改善,并且这种改善在开放标签治疗期间持续。与其他药物的间接比较表明,upadacitinib在axSpA患者中比生物制剂和其他JAK抑制剂更有效,并且需要治疗的数量最少。长期安全性数据表明,upadacitinib在axSpA患者中耐受性良好,感染、恶性肿瘤、主要不良心血管事件和血栓栓塞发生率低。本文描述的四个案例研究说明了upadacitinib在一系列现实世界axSpA患者中的有效性,包括早期疾病患者和已接受生物制剂预处理的患者。
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
Drugs in Context
Drugs in Context Medicine-Medicine (all)
CiteScore
5.90
自引率
0.00%
发文量
63
审稿时长
9 weeks
期刊介绍: Covers all phases of original research: laboratory, animal and human/clinical studies, health economics and outcomes research, and postmarketing studies. Original research that shows positive or negative results are welcomed. Invited review articles may cover single-drug reviews, drug class reviews, latest advances in drug therapy, therapeutic-area reviews, place-in-therapy reviews, new pathways and classes of drugs. In addition, systematic reviews and meta-analyses are welcomed and may be published as original research if performed per accepted guidelines. Editorials of key topics and issues in drugs and therapeutics are welcomed. The Editor-in-Chief will also consider manuscripts of interest in areas such as technologies that support diagnosis, assessment and treatment. EQUATOR Network reporting guidelines should be followed for each article type. GPP3 Guidelines should be followed for any industry-sponsored manuscripts. Other Editorial sections may include Editorial, Case Report, Conference Report, Letter-to-the-Editor, Educational Section.
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