A safety evaluation of canakinumab for the treatment of systemic onset juvenile idiopathic arthritis

被引:13
作者
Wulffraat, Nico M. [1 ]
机构
[1] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Pediat, Sect Pediat Rheumatol, NL-3508 AB Utrecht, Netherlands
关键词
IL-1; family; auto-inflammatory syndromes; systemic onset juvenile idiopathic arthritis; inflammasome; safety; registry; INTERLEUKIN-1 RECEPTOR ANTAGONIST; OPEN-LABEL; AUTOINFLAMMATORY DISEASE; MULTICENTER; ANAKINRA; ACTIVATION; MALIGNANCY; IL-1-BETA; EFFICACY; THERAPY;
D O I
10.1517/14740338.2016.1112377
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Interleukin-1 (IL-1) is the key molecule of a strong pro-inflammatory pathway in the innate immune system. The IL-1 family harbors components with pro- and anti-inflammatory effects essential for the regulation of the inflammation process. Auto-inflammatory diseases and systemic onset juvenile idiopathic arthritis (JIA) are examples of chronic inflammatory diseases that are IL-1 dependent. IL-1 blockade has proven to be very effective and has greatly improved the outcome of these disorders.Areas covered: This review describes the components of the IL-1 family and the available IL-1 blocking agents for clinical practice. Among them, canakinumab was more recently introduced. Based on the published clinical trials one can conclude that the clinical efficacy in auto-inflammatory diseases is at least as good as other IL-1 blocking agents. The safety data are limited to those registration studies (Phase 2 and 3). In short term the adverse events described are not very different from the other IL-1 blockers.Expert opinion: Longer term use in larger numbers of patients and adequate data collection using large-scale registries are necessary to provide us with a well-balanced overview of safety issues of canakinumab. Registration studies and open label extension studies show an acceptable safety profile so far.
引用
收藏
页码:1961 / 1967
页数:7
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