Leuchten Nicolai, Aringer Martin
Division of Rheumatology, Department of Medicine III, University Medical Center & Faculty of Medicine Carl Gustav Carus at the TU Dresden, Dresden, Germany.
Immunotherapy. 2018 Mar 1;10(6):465-472. doi: 10.2217/imt-2017-0182. Epub 2018 Mar 5.
Giant cell arteritis is a systemic vasculitis of large vessels, manifesting mainly as temporal arteritis or large vessel vasculitis of the aorta and its branches. Glucocorticoid therapy is essential and so far had to be continued over a period of 1.5-2 years, resulting in relevant morbidity through adverse effects. With the approval of tocilizumab, an effective glucocorticoid sparing option is now available. In two randomized controlled trials, a profound reduction of cumulative glucocorticoid dose, prolonged relapse-free remission and reduced number of adverse events in the treatment groups have been demonstrated. Therefore, tocilizumab constitutes a novel therapeutic option in giant cell arteritis. Its differential role in different subgroups, timing of tocilizumab therapy and optimal treatment duration remain to be determined.
巨细胞动脉炎是一种大血管的系统性血管炎,主要表现为颞动脉炎或主动脉及其分支的大血管血管炎。糖皮质激素治疗至关重要,迄今为止必须持续1.5至2年,这会因不良反应导致相关发病率。随着托珠单抗的获批,现在有了一种有效的糖皮质激素节约方案。在两项随机对照试验中,已证明治疗组的累积糖皮质激素剂量大幅降低、无复发缓解期延长且不良事件数量减少。因此,托珠单抗构成了巨细胞动脉炎的一种新型治疗选择。其在不同亚组中的差异作用、托珠单抗治疗的时机和最佳治疗持续时间仍有待确定。