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抗中性粒细胞胞质抗体相关性血管炎治疗的进展。

Advances in therapy for ANCA-associated vasculitis.

机构信息

Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Curr Rheumatol Rep. 2012 Dec;14(6):509-15. doi: 10.1007/s11926-012-0284-0.

Abstract

The anti-neutrophil cytoplasmic antibody-associated vasculitides include granulomatosis with polyangiitis (Wegener's granulomatosis) and microscopic polyangiitis. The introduction of therapy with cytotoxic agents such as cyclophosphamide transformed these diseases from fatal diagnoses to chronic conditions characterized by cycles of relapse and remission. Modern treatment strategies have focused on minimizing cyclophosphamide exposure or eliminating its use altogether. Two randomized clinical trials have shown that rituximab is not inferior to cyclophosphamide for induction of remission in patients with severe granulomatosis with polyangiitis (Wegener's) or microscopic polyangiitis. For patients with non-life threatening disease, methotrexate may be used to induce and maintain remission, although some patients may have a higher long-term risk of relapse as a result. For patients with life-threatening disease, plasma exchange may be an effective adjuvant therapy. This article reviews seminal studies from the past decade that have contributed to the current standard of care.

摘要

抗中性粒细胞胞浆抗体相关性血管炎包括肉芽肿性多血管炎(韦格纳肉芽肿病)和显微镜下多血管炎。细胞毒性药物(如环磷酰胺)治疗的引入,将这些疾病从致命性诊断转变为以复发和缓解为特征的慢性疾病。现代治疗策略侧重于最大限度地减少环磷酰胺的暴露或完全消除其使用。两项随机临床试验表明,利妥昔单抗在诱导重症肉芽肿性多血管炎(韦格纳肉芽肿病)或显微镜下多血管炎患者缓解方面并不逊于环磷酰胺。对于非危及生命的疾病患者,甲氨蝶呤可用于诱导和维持缓解,尽管一些患者可能因此而有更高的长期复发风险。对于危及生命的疾病患者,血浆置换可能是一种有效的辅助治疗方法。本文综述了过去十年中对当前治疗标准有贡献的重要研究。

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