Biologic Therapies for Giant Cell Arteritis

被引:9
|
作者
Harrington, Robert [1 ]
Al Nokhatha, Shamma Ahmad [1 ]
Conway, Richard [1 ]
机构
[1] St James Hosp, Dept Rheumatol, James St, Dublin 8, Ireland
关键词
giant cell arteritis; biologics; glucocorticoids; PLACEBO-CONTROLLED TRIAL; COMPLICATION AORTIC-ANEURYSM; TERM-FOLLOW-UP; DOUBLE-BLIND; POLYMYALGIA-RHEUMATICA; MONOCLONAL-ANTIBODY; CYCLOSPORINE-A; VISUAL-LOSS; METHOTREXATE; INTERLEUKIN-6;
D O I
10.2147/BTT.S229662
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Glucocorticoids have been the mainstay of treatment in giant cell arteritis (GCA) for the past 70 years. Conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) have largely failed to show significant clinical efficacy or reduction of the glucocorticoid burden in GCA. Tocilizumab is the first biologic to make a substantial impact in GCA treatment. With the current understanding of GCA pathogenesis implicating multiple cytokines, notably interleukin (IL) 6, IL-12, IL-23, IL-1 beta, and the role of janus kinases (JAKs) and the signal transducer and activator of transcription (STAT) pathway in these cytokines, many biologics are currently being investigated in GCA. This review article looks at the existing evidence for biologic agents in GCA. In addition to tocilizumab, the potential role of ustekinumab, abatacept, JAK inhibitors and other promising biologics in GCA are discussed in detail. A treatment algorithm based on the best evidence to date is also presented.
引用
收藏
页码:17 / 29
页数:13
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