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
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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