Klinik für Innere Medizin, Rheumatologie und Immunologie, Medius Kliniken, Akademisches Lehrkrankenhaus der Universität Tübingen, Kirchheim unter Teck, Germany
Nephrology Department, Hospital Universitario del Sureste, Arganda del Rey, Spain.
Ann Rheum Dis. 2024 Jan 2;83(1):30-47. doi: 10.1136/ard-2022-223764.
Since the publication of the EULAR recommendations for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) in 2016, several randomised clinical trials have been published that have the potential to change clinical care and support the need for an update.
Using EULAR standardised operating procedures, the EULAR task force undertook a systematic literature review and sought opinion from 20 experts from 16 countries. We modified existing recommendations and created new recommendations.
Four overarching principles and 17 recommendations were formulated. We recommend biopsies and ANCA testing to assist in establishing a diagnosis of AAV. For remission induction in life-threatening or organ-threatening AAV, we recommend a combination of high-dose glucocorticoids (GCs) in combination with either rituximab or cyclophosphamide. We recommend tapering of the GC dose to a target of 5 mg prednisolone equivalent/day within 4-5 months. Avacopan may be considered as part of a strategy to reduce exposure to GC in granulomatosis with polyangiitis (GPA) or microscopic polyangiitis (MPA). Plasma exchange may be considered in patients with rapidly progressive glomerulonephritis. For remission maintenance of GPA/MPA, we recommend rituximab. In patients with relapsing or refractory eosinophilic GPA, we recommend the use of mepolizumab. Azathioprine and methotrexate are alternatives to biologics for remission maintenance in AAV.
In the light of recent advancements, these recommendations provide updated guidance on AAV management. As substantial data gaps still exist, informed decision-making between physicians and patients remains of key relevance.
自 2016 年发布 EULAR 关于抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)管理的建议以来,已经发表了几项可能改变临床护理并支持更新的随机临床试验。
EULAR 工作组使用 EULAR 标准操作程序进行了系统的文献回顾,并征求了来自 16 个国家的 20 名专家的意见。我们修改了现有的建议并制定了新的建议。
制定了四项总体原则和 17 项建议。我们建议进行活检和 ANCA 检测以协助诊断 AAV。对于危及生命或危及器官的 AAV,我们建议联合使用大剂量糖皮质激素(GC)联合利妥昔单抗或环磷酰胺进行缓解诱导。我们建议在 4-5 个月内将 GC 剂量逐渐减少至 5mg 泼尼松等效剂量/天的目标剂量。阿伐考帕可能被视为减少 GPA 或显微镜下多血管炎患者 GC 暴露的策略的一部分。在快速进展性肾小球肾炎患者中可考虑血浆置换。为了维持 GPA/MPA 的缓解,我们建议使用利妥昔单抗。对于复发或难治性嗜酸性粒细胞 GPA 患者,我们建议使用美泊利珠单抗。对于缓解期的 AAV,硫唑嘌呤和甲氨蝶呤是生物制剂的替代药物。
鉴于最近的进展,这些建议为 AAV 管理提供了更新的指导。由于仍然存在大量数据空白,医生和患者之间的知情决策仍然至关重要。