Start RA treatment – Biologics or JAK-inhibitors?

托法替尼 医学 生物仿制药 类风湿性关节炎 贾纳斯激酶 Janus激酶抑制剂 鲁索利替尼 不利影响 重症监护医学 内科学 细胞因子 骨髓 骨髓纤维化
作者
Roberto Caporali,Sabino Germinario,Dorottya Kacsándi,Ernest Choy,Zoltán Szekanecz
出处
期刊:Autoimmunity Reviews [Elsevier BV]
卷期号:23 (1): 103429-103429 被引量:10
标识
DOI:10.1016/j.autrev.2023.103429
摘要

Janus Kinase inhibitors (JAKi) have been approved for the treatment of Rheumatoid Arthritis (RA) for several years. They are the first oral advanced treatment with efficacy similar to, if not greater than, biologic agents. Recently, concerns over their safety was raised by the results from Oral Surveillance trial suggesting that tofacitinib, one of the JAKi, was associated with higher cardiovascular adverse events and malignancies than TNF inhibitors (TNFi). Since then, regulatory authorities have added warnings to the labels of JAKi. On this purpose, whether rheumatologists should use JAKi as first line advance treatment has become a controversial topic. Some rheumatologists have argued that biologics should be first line advance treatment since there are extensive effectiveness and safety data. In addition, with the advent of biosimilar drugs, they are the most cost-effective treatment. On the other hand, JAKi are very efficacious and are generally safe apart from older and high-risk patients. When TNFi are contraindicated and in certain RA patients ,especially when an oral drug is preferable, JAKi have significant advantage providing patients are involved in the decision-making process.
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