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局部和全身药物治疗的疗效和安全性:一项系统文献综述,为 EULAR 干燥综合征管理建议提供信息。

Efficacy and safety of topical and systemic medications: a systematic literature review informing the EULAR recommendations for the management of Sjögren's syndrome.

机构信息

Autoimmune Diseases Unit, Department of Medicine, Hospital CIMA-Sanitas, Barcelona, Spain.

Laboratory of Autoimmune Diseases Josep Font, CELLEX, IDIBAPS, Barcelona, Spain.

出版信息

RMD Open. 2019 Oct 28;5(2):e001064. doi: 10.1136/rmdopen-2019-001064. eCollection 2019.

Abstract

OBJECTIVE

To evaluate current evidence on the efficacy and safety of topical and systemic medications in patients with primary Sjögren syndrome (SjS) to inform European League Against Rheumatism treatment recommendations.

METHODS

The MEDLINE, EMBASE and Cochrane databases were searched for case-control/prospective cohort studies, randomised controlled trials (RCTs) and systematic reviews.

RESULTS

Current evidence in primary SjS patients fulfilling the 2002 criteria is based on the data from 9 RCTs, 18 prospective cohort studies and 5 case-control studies. Two Cochrane systematic literature reviews (SLRs) have reported that topical treatments for dry mouth and dry eye are safe and effective. Ocular cyclosporine A was safe and effective in two RCTs including 1039 patients with dry eye syndrome. Two Cochrane SLRs on serum tear drops and plugs showed inconsistency in possible benefits, both for symptoms and objective measures. Five RCTs reported significant improvements in oral dryness and salivary flow rates for pilocarpine and cevimeline. An RCT showed no significant placebo-differences for hydroxychloroquine 400 mg/day for the primary outcome (visual analogue scale (VAS) composite of dryness, fatigue and pain). We identified seven RCTs carried out in primary SjS patients. RCTs using infliximab, anakinra and baminercept found no placebo-differences for the primary outcomes. The two largest RCTs randomised 255 patients to receive rituximab or placebo and reported no significant results in the primary outcome (VAS composite), while prospective studies suggested efficacy in systemic disease.

CONCLUSION

The current evidence supporting the use of the main topical therapeutic options of primary SjS is solid, while limited data from RCTs are available to guide systemic therapies.

摘要

目的

评估原发性干燥综合征(SjS)患者局部和全身药物治疗的疗效和安全性证据,为欧洲抗风湿病联盟的治疗建议提供信息。

方法

检索 MEDLINE、EMBASE 和 Cochrane 数据库,以获取病例对照/前瞻性队列研究、随机对照试验(RCT)和系统评价。

结果

符合 2002 年标准的原发性 SjS 患者的当前证据基于 9 项 RCT、18 项前瞻性队列研究和 5 项病例对照研究的数据。两项 Cochrane 系统文献综述(SLR)报告称,局部治疗口干和干眼病是安全有效的。环孢素 A 滴眼剂在两项纳入 1039 例干眼综合征患者的 RCT 中安全且有效。两项关于血清泪液和泪点塞的 Cochrane SLR 显示,对于症状和客观测量,可能的益处不一致。五项 RCT 报道了毛果芸香碱和西维美林对口腔干燥和唾液流率的显著改善。一项 RCT 显示羟氯喹 400mg/天对主要结局(干燥、疲劳和疼痛的视觉模拟量表(VAS)综合评分)无显著安慰剂差异。我们确定了 7 项在原发性 SjS 患者中进行的 RCT。使用英夫利昔单抗、阿那白滞素和巴尼单抗的 RCT 发现主要结局无安慰剂差异。两项最大的 RCT 将 255 例患者随机分配至接受利妥昔单抗或安慰剂组,主要结局(VAS 综合评分)无显著结果,而前瞻性研究表明系统性疾病有效。

结论

目前支持原发性 SjS 主要局部治疗选择的证据确凿,而 RCT 提供的有限数据可用于指导全身治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ff/6827762/96f43df08107/rmdopen-2019-001064f01.jpg

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