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本文引用的文献

1
Systematic Literature Review of Real-World Evidence on Baricitinib for the Treatment of Rheumatoid Arthritis.巴瑞替尼治疗类风湿关节炎的真实世界证据的系统文献综述
Rheumatol Ther. 2023 Dec;10(6):1417-1457. doi: 10.1007/s40744-023-00591-9. Epub 2023 Sep 16.
2
Efficacy and Safety Outcomes Up to ~4 Years of Treatment With Filgotinib 200 mg Among Patients With Ulcerative Colitis: Results From the SELECTIONLTE Study.溃疡性结肠炎患者使用200mg非戈替尼治疗长达约4年的疗效和安全性结果:SELECTION LTE研究结果
Gastroenterol Hepatol (N Y). 2023 Apr;19(4 Suppl 1):10-11.
3
Filgotinib for the Treatment of Small Bowel Crohn's Disease: The DIVERGENCE 1 Trial.非戈替尼治疗小肠克罗恩病:DIVERGENCE 1试验
Gastroenterology. 2023 Jul;165(1):289-292.e3. doi: 10.1053/j.gastro.2023.03.234. Epub 2023 Apr 11.
4
Filgotinib Improved Health-Related Quality of Life and Led to Comprehensive Disease Control in Individuals with Ulcerative Colitis: Data from the SELECTION Trial.Filgotinib 改善了溃疡性结肠炎患者的健康相关生活质量,并实现了全面的疾病控制:SELECTION 试验的数据。
J Crohns Colitis. 2023 Jun 16;17(6):863-875. doi: 10.1093/ecco-jcc/jjad018.
5
Management of Axial Spondyloarthritis - Insights into Upadacitinib.中轴型脊柱关节炎的治疗——乌帕替尼的见解。
Drug Des Devel Ther. 2022 Oct 19;16:3609-3620. doi: 10.2147/DDDT.S330413. eCollection 2022.
6
Safety and efficacy of filgotinib for Japanese patients with RA and inadequate response to MTX: FINCH 1 52-week results and FINCH 4 48-week results.在对甲氨蝶呤反应不足的日本类风湿关节炎患者中,Filgotinib 的安全性和疗效:FINCH1 的 52 周结果和 FINCH4 的 48 周结果。
Mod Rheumatol. 2023 Jul 4;33(4):668-679. doi: 10.1093/mr/roac084.
7
Efficacy and safety of filgotinib in combination with methotrexate in Japanese patients with active rheumatoid arthritis who have an inadequate response to methotrexate: Subpopulation analyses of 24-week data of a global phase 3 study (FINCH 1).在对甲氨蝶呤应答不足的日本活动性类风湿关节炎患者中,联合使用非戈替尼和甲氨蝶呤的疗效和安全性:一项全球 3 期研究(FINCH 1)24 周数据的亚组分析。
Mod Rheumatol. 2022 Feb 28;32(2):263-272. doi: 10.1093/mr/roab030.
8
Integrated safety analysis of filgotinib in patients with moderately to severely active rheumatoid arthritis receiving treatment over a median of 1.6 years.接受治疗中位数为 1.6 年的中重度活动性类风湿关节炎患者的 filgotinib 的综合安全性分析。
Ann Rheum Dis. 2022 Feb;81(2):184-192. doi: 10.1136/annrheumdis-2021-221051. Epub 2021 Nov 5.
9
JAK selectivity and the implications for clinical inhibition of pharmacodynamic cytokine signalling by filgotinib, upadacitinib, tofacitinib and baricitinib.JAK 选择性及其对 filgotinib、upadacitinib、tofacitinib 和 baricitinib 抑制药效细胞因子信号的临床意义。
Ann Rheum Dis. 2021 Jul;80(7):865-875. doi: 10.1136/annrheumdis-2020-219012. Epub 2021 Mar 19.
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Safety and Efficacy of Filgotinib: Up to 4-year Results From an Open-label Extension Study of Phase II Rheumatoid Arthritis Programs.安全性和有效性的 Filgotinib:高达 4 年的结果从一个开放标签扩展研究的二期类风湿关节炎计划。
J Rheumatol. 2021 Aug;48(8):1230-1238. doi: 10.3899/jrheum.201183. Epub 2021 Feb 1.

聚焦类风湿关节炎中的非戈替尼:基于试验的综述。

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

作者信息

Skouvaklidou Elpida, Deligeorgakis Dimitrios, Skalkou Anastasia, Skepastianos Vasileios, Tsafis Konstantinos, Papadimitriou Evdokia, Pagkopoulou Eleni, Avgerou Paraskevi, Mytilinaiou Maria G, Tzitiridou-Chatzopoulou Maria, Kougkas Nikolaos, Adamichou Christina

机构信息

Department of Rheumatology, 4th Department of Internal Medicine, Hippokration Hospital, Thessaloniki, Greece.

School of Healthcare Sciences, Department of Midwifery, University of Western Macedonia, Kozani, Greece.

出版信息

Mediterr J Rheumatol. 2024 Mar 30;35(Suppl 1):1-9. doi: 10.31138/mjr.281123.fof. eCollection 2024 Mar.

DOI:10.31138/mjr.281123.fof
PMID:38756936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11094443/
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.

摘要

Janus激酶(JAK)/信号转导子和转录激活子(STAT)通路参与了许多风湿性疾病的病理生理级联反应。JAK抑制剂的开发扩大了类风湿关节炎(RA)的治疗选择,具有持续的类效应疗效。非戈替尼是一种新型的JAK1亚型选择性抑制剂,已获许可用于治疗RA和溃疡性结肠炎。在本综述中,我们旨在对非戈替尼的疗效和药物特异性安全警告进行分析。在随机临床试验中,对患有或未患有传统合成抗风湿药物(csDMARDs)(初治或经治)的RA患者以及生物抗风湿药物(bDMARDs)治疗失败的患者进行了研究。非戈替尼还与安慰剂、甲氨蝶呤或阿达木单抗进行了对照试验。长期扩展试验提供了长达四年持续使用非戈替尼的相关见解。在中度或重度RA患者中,非戈替尼在疾病活动参数和生活质量指标方面均显示出有益效果,具有纵向疗效。在与阿达木单抗的头对头比较中,200mg非戈替尼不劣于阿达木单抗。除带状疱疹感染发病率较低外,感染性不良反应风险升高是不良反应的警示标志。