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