Holle Julia U, Moosig Frank
Rheumazentrum Schleswig-Holstein Mitte, Kuhberg 5a-7, 24534, Neumünster, Deutschland.
Rheumazentrum Schleswig-Holstein Mitte, Sophienblatt 13-17, 24103, Kiel, Deutschland.
Z Rheumatol. 2024 Dec;83(10):787-799. doi: 10.1007/s00393-024-01548-1. Epub 2024 Aug 28.
This article summarizes the current guidelines and recommendations published by the European Alliance of Associations for Rheumatology (EULAR), the Kidney Disease Improving Global Outcomes (KDIGO) and the American College of Rheumatology (ACR). In addition to glucocorticoids (GC), treatment with biologics is nowadays an established option to treat Anti-Neutrophil Cytoplasmic Antibody (ANCA)-associated vasculitis (AAV). Rituximab (RTX) is used for remission induction and maintenance in organ-threatening and non-organ-threatening granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA). For eosinophilic GPA (EGPA) anti-interleukin 5 (IL5) strategies are an important component of treatment for remission induction and maintenance of refractory or relapsing non-organ-threatening diseases in conjunction with GC. The dosing of GC for remission induction in GPA and MPA is now lower than was previously used and additionally, avacopan is approved as a new GC-sparing medication for GPA and MPA over 52 weeks. Conventional strategies, such as cyclophosphamide (CYC) are important for remission induction in severe or refractory organ-threatening disease for all AAVs. The use of methotrexate (MTX) and azathioprine (AZA) is becoming less prominent. The most important unanswered questions in the treatment of AAVs are with respect to the duration of remission maintenance treatment and the individualized treatment guidance based on biomarkers.
本文总结了欧洲风湿病协会联盟(EULAR)、改善全球肾脏病预后组织(KDIGO)和美国风湿病学会(ACR)发布的现行指南及建议。除糖皮质激素(GC)外,生物制剂治疗如今是治疗抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)的既定选择。利妥昔单抗(RTX)用于器官威胁性和非器官威胁性肉芽肿性多血管炎(GPA)及显微镜下多血管炎(MPA)的诱导缓解和维持治疗。对于嗜酸性粒细胞性GPA(EGPA),抗白细胞介素5(IL5)策略是联合GC诱导难治性或复发性非器官威胁性疾病缓解和维持治疗的重要组成部分。目前,GPA和MPA诱导缓解时GC的剂量低于以往使用剂量,此外,阿伐考泮被批准作为一种新的节省GC的药物用于GPA和MPA超过52周的治疗。传统策略,如环磷酰胺(CYC),对于所有AAV严重或难治性器官威胁性疾病的诱导缓解很重要。甲氨蝶呤(MTX)和硫唑嘌呤(AZA)的使用正变得不那么突出。AAV治疗中最重要的未解决问题是缓解维持治疗的持续时间以及基于生物标志物的个体化治疗指导。