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风湿性疾病中 JAK 抑制剂的新兴安全性特征。

The Emerging Safety Profile of JAK Inhibitors in Rheumatic Diseases.

机构信息

Medicine Service, VA Medical Center, 700 19th St S, Birmingham, AL, 35233, USA.

Department of Medicine at the School of Medicine, University of Alabama at Birmingham (UAB), Faculty Office Tower 805B, 510 20th Street S, Birmingham, AL, 35294-0022, USA.

出版信息

BioDrugs. 2023 Sep;37(5):625-635. doi: 10.1007/s40259-023-00612-7. Epub 2023 Jun 23.

Abstract

Janus kinase inhibitor (JAKi) medications are small-molecule drugs that affect intracellular signal transduction. They are highly effective oral medications that have been approved for the treatment of various rheumatic diseases, with rheumatoid arthritis being a key example of an autoimmune rheumatic disease. JAKi are oral-route medications that are alternatives to injectable biologic therapies, launched in the late 1990s. While most safety concerns with JAKi are similar to the biologics, there are many differences. New data on comparative safety of JAKi versus tumor necrosis factor inhibitors (TNFi) were recently published that led to new black box warnings by the US Food and Drug Administration (FDA) about cardiovascular and cancer risks and a label change for JAKi. This review summarizes the current published data with regards to the safety of JAKi, focused on rheumatic diseases. Specifically, any risk differences between agents or across different indications are discussed, as well as the risk factors for these adverse outcomes.

摘要

Janus 激酶抑制剂 (JAKi) 药物是影响细胞内信号转导的小分子药物。它们是高效的口服药物,已被批准用于治疗各种风湿性疾病,类风湿关节炎是一种自身免疫性风湿性疾病的典型例子。JAKi 是 1990 年代后期推出的口服药物,替代了注射用生物疗法。虽然 JAKi 的大多数安全性问题与生物制剂相似,但也有许多不同之处。最近公布了关于 JAKi 与肿瘤坏死因子抑制剂 (TNFi) 比较安全性的新数据,导致美国食品和药物管理局 (FDA) 发布了关于心血管和癌症风险的新黑框警告,并对 JAKi 进行了标签更改。这篇综述总结了目前已发表的关于 JAKi 安全性的研究数据,重点关注风湿性疾病。具体而言,讨论了不同药物或不同适应症之间的任何风险差异,以及这些不良结果的风险因素。

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