Richez Christophe, Truchetet Marie-Elise, Kostine Marie, Schaeverbeke Thierry, Bannwarth Bernard
a Département de Rhumatologie , FHU ACRONIM CHU Bordeaux , Bordeaux , France.
b UMR-CNRS 5164 , ImmunoConcept Université de Bordeaux , Bordeaux , France.
Expert Opin Pharmacother. 2017 Sep;18(13):1399-1407. doi: 10.1080/14656566.2017.1359256. Epub 2017 Jul 27.
although the outcome for patients with rheumatoid arthritis (ra) has improved in the past decades, adequate disease control cannot be achieved in a substantial proportion of patients. new drugs with a novel mechanism of action, may represent a valuable addition to the current armamentarium. Areas covered: This review focuses on the pharmacodynamics and pharmacokinetics of baricitinib. Furthermore, the article summarizes and comments the drug's efficacy and safety profile in RA patients. Expert opinion: Baricitinib is an oral targeted synthetic (ts) disease-modifying antirheumatic drug (DMARD) that mainly inhibits JAK1 and JAK2. Baricitinib monotherapy, or in combination with conventional synthetic (cs) DMARDs, has demonstrated its efficacy while having an acceptable safety profile in early active RA naive to DMARDs, and active RA with an inadequate response to csDMARDs and/or biologic (b)DMARDs. The future place of baricitinib in the management of RA patients will depend on several factors. However, baricitinib offer few advantages: oral administration, rapidity of action, efficacy in monotherapy and over adalimumab in one study and non-immunization. However, pending further safety data, current practice would be to start a bDMARD when the treatment target is not achieved with csDMARDs. Availability of additional long-term safety data may influence prescribing decisions.
尽管在过去几十年中类风湿关节炎(RA)患者的治疗结果有所改善,但仍有相当一部分患者无法实现充分的疾病控制。具有新作用机制的新药可能是现有治疗手段的宝贵补充。涵盖领域:本综述聚焦于巴瑞替尼的药效学和药代动力学。此外,本文总结并评论了该药在RA患者中的疗效和安全性。专家观点:巴瑞替尼是一种口服靶向合成(TS)抗风湿药物(DMARD),主要抑制JAK1和JAK2。巴瑞替尼单药治疗,或与传统合成(CS)DMARD联合使用,已在初治的早期活动性RA患者以及对CS DMARD和/或生物(B)DMARD反应不足的活动性RA患者中显示出疗效,且安全性可接受。巴瑞替尼在RA患者管理中的未来地位将取决于多个因素。然而,巴瑞替尼具有一些优势:口服给药、起效迅速、单药治疗有效,在一项研究中优于阿达木单抗,且无需免疫。然而,在获得更多安全性数据之前,当前的做法是当CS DMARD未达到治疗目标时启动B DMARD。更多长期安全性数据的可得性可能会影响处方决策。