Wong Limy, Harper Lorraine, Little Mark A
Trinity Health Kidney Centre, Tallaght Hospital and Trinity College, Dublin, Ireland.
Division of Medical Sciences, University of Birmingham, Birmingham, UK.
Nephrol Dial Transplant. 2015 Apr;30 Suppl 1:i164-70. doi: 10.1093/ndt/gfu406. Epub 2015 Jan 12.
Antineutrophil cytoplasm antibody associated systemic vasculitides (AASV) have traditionally been managed with a combination of cyclophosphamide and glucocorticoids during the induction phase, followed by azathioprine in the maintenance phase. Whilst these therapies have markedly improved the prognosis in AASV, treatment related adverse events remain a major challenge and include complications such as infection, glucocorticoid related side effects, malignancy, cardiovascular disease, infertility and death. Newer biologic therapies have been shown to demonstrate equivalent efficacy as cyclophosphamide for remission but the hoped for reduction in adverse events has yet to be realised. More recent efforts have been focused on refining existing therapeutic regimens and strategies, tailoring individual treatment to disease severity, patient age and kidney function to derive maximum treatment efficacy while minimising treatment toxicity. In particular, current interventional trials are targeting a reduction in corticosteroid exposure in an effort to make induction and maintenance regimens safer.
抗中性粒细胞胞浆抗体相关性系统性血管炎(AASV)传统上在诱导期采用环磷酰胺和糖皮质激素联合治疗,随后在维持期使用硫唑嘌呤。虽然这些疗法显著改善了AASV的预后,但治疗相关不良事件仍然是一个重大挑战,包括感染、糖皮质激素相关副作用、恶性肿瘤、心血管疾病、不孕和死亡等并发症。新型生物疗法已被证明在诱导缓解方面与环磷酰胺具有同等疗效,但减少不良事件的期望尚未实现。最近的努力集中在优化现有治疗方案和策略,根据疾病严重程度、患者年龄和肾功能调整个体化治疗,以在最小化治疗毒性的同时获得最大治疗效果。特别是,目前的干预试验旨在减少糖皮质激素的使用,以使诱导和维持方案更安全。