Focus on Filgotinib in Rheumatoid Arthritis: A Trial-Based Review.

Q4 Medicine Mediterranean Journal of Rheumatology Pub Date : 2024-03-30 eCollection Date: 2024-03-01 DOI:10.31138/mjr.281123.fof
Elpida Skouvaklidou, Dimitrios Deligeorgakis, Anastasia Skalkou, Vasileios Skepastianos, Konstantinos Tsafis, Evdokia Papadimitriou, Eleni Pagkopoulou, Paraskevi Avgerou, Maria G Mytilinaiou, Maria Tzitiridou-Chatzopoulou, Nikolaos Kougkas, Christina Adamichou
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Abstract

Janus kinases (JAK)/Signal Transducer and Activator of Transcription (STAT) pathway is involved in pathophysiologic cascade of a notable number of rheumatic diseases. The development of JAK inhibitors has expanded treatment choices in rheumatoid arthritis (RA) with a sustained class-effect efficacy. Filgotinib is a novel selective inhibitor of JAK1 isoform licensed for use in RA and ulcerative colitis. In this review we aim to present an analysis of filgotinib's efficacy and drug-specific safety warnings. Patients with RA with or without concomitant conventional synthetic Disease-Modifying Antirheumatic Drugs (csDMARDs) (naïve or experienced) and those who have failed biologic Disease-Modifying Antirheumatic Drugs (bDMARDs) were examined in randomised clinical trials. Filgotinib was also tested against placebo, methotrexate, or adalimumab. Long-term extension trials provide insights for up to four years of continuous filgotinib administration. Beneficial effects are depicted in both disease activity parameters and quality of life indexes in moderate or severe RA with a longitudinal efficacy. In head-to-head comparison with adalimumab, filgotinib 200 mg was non-inferior. Adverse effects alerts are marked by the elevated risk of infectious adverse effects with the exception of herpes zoster infection, which has a low incidence.

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聚焦类风湿关节炎中的 Filgotinib:基于试验的综述。
Janus 激酶(JAK)/信号转导和转录激活因子(STAT)通路参与了大量风湿性疾病的病理生理过程。JAK 抑制剂的开发扩大了类风湿性关节炎(RA)的治疗选择,具有持续的类药物疗效。Filgotinib是一种新型的JAK1同工酶选择性抑制剂,获准用于治疗RA和溃疡性结肠炎。在这篇综述中,我们将对菲戈替尼的疗效和特定药物的安全性警告进行分析。在随机临床试验中,我们对同时服用或未服用传统合成改善病情抗风湿药(csDMARDs)(新药或经验药)的RA患者以及服用生物改善病情抗风湿药(bDMARDs)失败的患者进行了研究。菲洛替尼还与安慰剂、甲氨蝶呤或阿达木单抗进行了对比试验。长期延长试验为连续服用菲戈替尼长达四年的时间提供了见解。中度或重度RA患者的疾病活动参数和生活质量指数均显示出有益效果,并具有纵向疗效。在与阿达木单抗的头对头比较中,菲戈替尼200毫克不具劣效。不良反应警报的特点是感染性不良反应风险升高,但带状疱疹感染除外,其发生率较低。
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CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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