Rheumatology Department, Hospital Universitario de Guadalajara, Guadalajara, Spain.
Institute for Musculoskeletal Health, Madrid, Spain.
Semin Arthritis Rheum. 2014 Feb;43(4):542-57. doi: 10.1016/j.semarthrit.2013.07.010. Epub 2013 Aug 24.
Relapses and failure are frequent in systemic vasculitis (SV) patients. Biological agents have been prescribed as rescue therapies. The aim of this systematic review is to analyze the current evidence on the therapeutic use of biological agents for SV.
MEDLINE, EMBASE, the Cochrane Database of Systematic Reviews, and the Cochrane Central Register of Controlled Trials were searched up to the end of April 2013. Systematic reviews and meta-analysis, clinical trials, cohort studies, and case series with >3 patients were included. Independent article review and study quality assessment was done by 2 investigators with consensus resolution of discrepancies.
Of 3447 citations, abstracts, and hand-searched studies screened, 90 were included. Most of the studies included ANCA-associated vasculitis (AAV) patients and only a few included large vessel vasculitis (LVV) patients. Rituximab was the most used agent, having demonstrated efficacy for remission induction in patients with AAV. A number of studies used different anti-TNFα agents with contrasting results. A few uncontrolled studies on the use of abatacept, alemtuzumab, mepolizumab, and tocilizumab were found.
Current evidence on the use of biological therapies for SV is mainly based on uncontrolled, observational data. Rituximab is not inferior to cyclophosphamide for remission induction in AAV and might be superior in relapsing disease. Infliximab and adalimumab are effective as steroid-sparing agents. Etanercept is not effective to maintain remission in patients with granulomatosis with polyangiitis, and serious adverse events have been reported. For LVV, both infliximab and etanercept had a role as steroid-sparing agents, and tocilizumab might be effective also for remission induction in LVV.
系统性血管炎(SV)患者常出现复发和治疗失败。生物制剂已被作为挽救疗法来开具。本系统综述的目的是分析生物制剂治疗 SV 的现有证据。
检索 MEDLINE、EMBASE、Cochrane 系统评价数据库和 Cochrane 对照试验中心注册库,检索截至 2013 年 4 月底。纳入系统性综述和荟萃分析、临床试验、队列研究和超过 3 例患者的病例系列研究。由 2 位研究者独立进行文献评价和研究质量评估,并对存在分歧的内容达成共识。
在筛选的 3447 篇引文、摘要和手工检索的研究中,有 90 篇被纳入。大多数研究纳入了抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)患者,只有少数研究纳入了大血管血管炎(LVV)患者。利妥昔单抗是应用最广泛的药物,已被证明对 AAV 患者诱导缓解有效。多项研究使用了不同的抗 TNF-α 药物,结果存在差异。还发现了一些关于阿巴西普、阿仑单抗、美泊利珠单抗和托珠单抗的非对照研究。
目前关于生物治疗 SV 的证据主要基于非对照、观察性数据。利妥昔单抗在诱导 AAV 缓解方面并不逊于环磷酰胺,在复发性疾病中可能更具优势。英夫利昔单抗和阿达木单抗作为激素保留剂有效。依那西普在肉芽肿性多血管炎患者中维持缓解无效,且已报告严重不良事件。对于 LVV,英夫利昔单抗和依那西普都可作为激素保留剂,托珠单抗也可能对 LVV 的缓解诱导有效。