a Arthritis Unit, Rheumatology Department , Hospital Clinic, and IDIBAPs , Barcelona , Spain.
Expert Opin Drug Saf. 2018 Jul;17(7):727-732. doi: 10.1080/14740338.2018.1486819. Epub 2018 Jun 14.
The anti-interleukin-1 receptor antagonist, anakinra, was approved for the treatment of rheumatoid arthritis (RA) more than 12 years ago. However, its adverse effects are not well known. Areas covered: We review the safety profile of anakinra, analyzing clinical trials, observational studies, and registry data. Expert opinion: Due to its lower efficacy compared with other biological therapies approved for RA and its daily subcutaneous administration, anakinra is used only marginally for the treatment of RA. This has limited the experience with this drug in RA, with a lack of data from long-term observational studies or registries. From the five clinical trials performed, and given the unfeasibility of developing new studies of anakinra in RA, it may be concluded that site injection reactions, infections at higher doses (>100 mg), and immunogenicity are the most frequent adverse events related to anakinra administration.
抗白细胞介素-1 受体拮抗剂阿那白滞素在 12 年前就已被批准用于治疗类风湿关节炎(RA)。然而,其不良反应尚不清楚。
我们回顾了阿那白滞素的安全性概况,分析了临床试验、观察性研究和注册数据。
由于与其他批准用于 RA 的生物疗法相比,阿那白滞素的疗效较低,且需要每天皮下注射,因此仅将其作为 RA 的治疗药物。这限制了该药在 RA 中的应用经验,缺乏来自长期观察性研究或注册的数据。从进行的五项临床试验来看,并且由于在 RA 中开展新的阿那白滞素研究不可行,因此可以得出结论,注射部位反应、高剂量(>100mg)时的感染和免疫原性是与阿那白滞素给药相关的最常见不良事件。