Gerriets Valerie, Goyal Amandeep, Khaddour Karam
California Northstate University College of Medicine
University of Kansas Medical Center
Tumor necrosis factor (TNF)-alpha inhibitors, including etanercept (E), infliximab (I), adalimumab (A), certolizumab pegol (C), and golimumab (G), are biologic agents which are FDA-approved to treat ankylosing spondylitis (E, I, A, C, and G), Crohn disease (I, A and C), hidradenitis suppurativa (A), juvenile idiopathic arthritis (A), plaque psoriasis (E, I and A), polyarticular juvenile idiopathic arthritis (E), psoriatic arthritis (E, I, A, C, and G), rheumatoid arthritis (E, I, A, C, and G), ulcerative colitis (I, A and G), and uveitis (A). There are also several off-label indications. This activity outlines the indications, mechanism of action, methods of administration, important adverse effects, contraindications, toxicity, and monitoring, of tumor necrosis factors, so providers can direct patient therapy where they are indicated as part of the interprofessional team.
肿瘤坏死因子(TNF)-α抑制剂,包括依那西普(E)、英夫利昔单抗(I)、阿达木单抗(A)、赛妥珠单抗聚乙二醇化制剂(C)和戈利木单抗(G),是经美国食品药品监督管理局(FDA)批准用于治疗强直性脊柱炎(E、I、A、C和G)、克罗恩病(I、A和C)、化脓性汗腺炎(A)、幼年特发性关节炎(A)、斑块状银屑病(E、I和A)、多关节型幼年特发性关节炎(E)、银屑病关节炎(E、I、A、C和G)、类风湿关节炎(E、I、A、C和G)、溃疡性结肠炎(I、A和G)以及葡萄膜炎(A)的生物制剂。此外还有一些非适应证用药。本活动概述了肿瘤坏死因子的适应证、作用机制、给药方法、重要不良反应、禁忌证、毒性及监测,以便医疗服务提供者在作为跨专业团队一部分的适用情况下指导患者治疗。