Azienda USL-IRCCS di Reggio Emilia, Università di Modena e Reggio Emilia, Modena, Italy.
Department of Internal Medicine, Division of Rheumatology, School of Medicine, Istanbul University - Cerrahpasa, Istanbul, Turkey.
Curr Opin Rheumatol. 2019 Jan;31(1):25-31. doi: 10.1097/BOR.0000000000000561.
Glucocorticoids are the mainstay of therapy for large-vessel vasculitis, but potential toxicity and frequent relapses led to studies with nonbiologic and biologic glucocorticoid-sparing agents. The aim of this review is to discuss the recent evidence for the management of giant cell arteritis (GCA) and Takayasu arteritis (TAK).
Tocilizumab proved to be a powerful glucocorticoid-sparing agent for GCA in a randomized placebo-controlled trial, whereas the trials with tocilizumab and abatacept failed to show a significant difference from placebo in relapse-free survival rate in TAK. Further trials are awaiting for establishing the role of abatacept and ustekinumab for GCA, and rituximab and tumor necrosis factor inhibitors, including certolizumab for TAK, as well as nonbiologic agents for both indications.
Despite recent randomized controlled trials with biologic agents, management of large-vessel vasculitis largely depends on observational studies. Well designed controlled trials using validated outcome measures in large number of patients, identification of biologic markers that could guide the choice of targeted treatments, and standardization of disease assessment including imaging modalities are unmet needs for the management of large-vessel vasculitis.
糖皮质激素是大血管血管炎治疗的主要药物,但潜在的毒性和频繁复发促使人们研究非生物和生物糖皮质激素节约药物。本文旨在讨论巨细胞动脉炎(GCA)和 Takayasu 动脉炎(TAK)治疗的最新证据。
托珠单抗在一项随机安慰剂对照试验中被证明是 GCA 的一种有效的糖皮质激素节约药物,而托珠单抗和阿巴西普治疗 TAK 的试验未能显示与安慰剂在无复发生存率方面有显著差异。进一步的试验正在等待确定阿巴西普和乌司奴单抗在 GCA 中的作用,以及利妥昔单抗和肿瘤坏死因子抑制剂,包括培塞利珠单抗在 TAK 中的作用,以及这两种适应证的非生物制剂。
尽管最近有生物制剂的随机对照试验,但大血管血管炎的治疗在很大程度上仍依赖于观察性研究。需要设计使用验证后的疗效指标、在大量患者中进行的、识别能够指导靶向治疗选择的生物标志物的、以及包括成像方式在内的疾病评估标准化的、良好的对照试验。