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利妥昔单抗治疗甲状腺相关性眼病。

Rituximab for thyroid-associated ophthalmopathy.

作者信息

Minakaran Neda, Ezra Daniel G

机构信息

Department of Ophthalmology, Moorfields Eye Hospital NHS Foundation Trust, London, UK.

出版信息

Cochrane Database Syst Rev. 2013 May 31(5):CD009226. doi: 10.1002/14651858.CD009226.pub2.

DOI:10.1002/14651858.CD009226.pub2
PMID:23728689
Abstract

BACKGROUND

Thyroid associated ophthalmopathy (TAO) is the most frequent extrathyroidal manifestation of Graves' disease, affecting up to 50% of patients, and has a great impact on quality of life. Rituximab is a human/murine chimeric monoclonal antibody that targets CD20, a transmembrane protein expressed on the surface of pre-B and mature B lymphocytes, but not on stem cells, pro-B lymphocytes or plasma cells. Preliminary work has shown that blocking the CD20 receptor on B-lymphocytes with rituximab affects the clinical course of TAO, by reducing inflammation and the degree of proptosis.

OBJECTIVES

The aim of this review was to investigate the effectiveness and safety of rituximab for the treatment of TAO.

SEARCH METHODS

We searched CENTRAL (which contains the Cochrane Eyes and Vision Group Trials Register) (The Cochrane Library 2013, Issue 3), Ovid MEDLINE, Ovid MEDLINE In-Process and Other Non-Indexed Citations, Ovid MEDLINE Daily, Ovid OLDMEDLINE, (January 1950 to April 2013), EMBASE (January 1980 to April 2013), Latin American and Caribbean Literature on Health Sciences (LILACS) (January 1982 to April 2013), OpenGrey (System for Information on Grey Literature in Europe) (www.opengrey.eu/), the metaRegister of Controlled Trials (mRCT) (www.controlled-trials.com), ClinicalTrials.gov (www.clinicaltrials.gov), the WHO International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en) and the EU Clinical Trials Register (www.clinicaltrialsregister.eu). We did not use any date or language restrictions in the electronic searches for trials. We last searched the electronic databases on 15 April 2013. We manually searched references of review articles and used the Science Citation Index to identify additional studies citing trials. We contacted the lead investigators of relevant trials on ClinicalTrials.gov and the WHO ICTRP for information and data from as yet unpublished clinical trials. We contacted experts in the field for information about any ongoing trials. We contacted the manufacturers of rituximab for details of any sponsored trials.

SELECTION CRITERIA

We sought to include randomised controlled trials (RCTs) of rituximab treatment by intravenous infusion for the treatment of patients with TAO, compared with placebo or intravenous glucocorticoid treatment.

DATA COLLECTION AND ANALYSIS

Two review authors independently scanned titles and abstracts, as well as independently screened the full reports of the potentially relevant studies. At each stage, the results were compared and disagreements were solved by discussion.

MAIN RESULTS

No studies were identified that met the inclusion criteria. There are three ongoing studies which are likely to meet inclusion criteria once published, and thus be included in future updates of this review.

AUTHORS' CONCLUSIONS: There is currently insufficient evidence to support the use of rituximab in patients with TAO. There is a need for large RCTs, investigating rituximab versus placebo or corticosteroids in patients with active TAO to make adequate judgement on the efficacy and safety of this novel therapy for this condition.

摘要

背景

甲状腺相关眼病(TAO)是格雷夫斯病最常见的甲状腺外表现,影响高达50%的患者,对生活质量有很大影响。利妥昔单抗是一种人/鼠嵌合单克隆抗体,靶向CD20,这是一种在前B淋巴细胞和成熟B淋巴细胞表面表达的跨膜蛋白,但在干细胞、前B淋巴细胞或浆细胞上不表达。初步研究表明,用利妥昔单抗阻断B淋巴细胞上的CD20受体可通过减轻炎症和眼球突出程度来影响TAO的临床病程。

目的

本综述的目的是研究利妥昔单抗治疗TAO的有效性和安全性。

检索方法

我们检索了Cochrane中心对照试验注册库(CENTRAL)(其中包含Cochrane眼科和视觉组试验注册库)(《Cochrane图书馆》2013年第3期)、Ovid MEDLINE、Ovid MEDLINE在研及其他未索引引文、Ovid MEDLINE每日更新、Ovid OLDMEDLINE(1950年1月至2013年4月)、EMBASE(1980年1月至2013年4月)、拉丁美洲和加勒比地区健康科学文献数据库(LILACS)(1982年1月至2013年4月)、OpenGrey(欧洲灰色文献信息系统)(www.opengrey.eu/)、对照试验元注册库(mRCT)(www.controlled-trials.com)、ClinicalTrials.gov(www.clinicaltrials.gov)、世界卫生组织国际临床试验注册平台(ICTRP)(www.who.int/ictrp/search/en)以及欧盟临床试验注册库(www.clinicaltrialsregister.eu)。在电子检索试验时,我们未使用任何日期或语言限制。我们最后一次检索电子数据库是在2013年4月15日。我们手动检索了综述文章的参考文献,并使用科学引文索引来识别引用试验的其他研究。我们联系了ClinicalTrials.gov和世界卫生组织ICTRP上相关试验的主要研究者,以获取尚未发表的临床试验的信息和数据。我们联系了该领域的专家以获取任何正在进行的试验的信息。我们联系了利妥昔单抗的制造商以获取任何赞助试验的详细信息。

选择标准

我们试图纳入利妥昔单抗静脉输注治疗TAO患者的随机对照试验(RCT),并与安慰剂或静脉糖皮质激素治疗进行比较。

数据收集与分析

两位综述作者独立扫描标题和摘要,并独立筛选潜在相关研究的完整报告。在每个阶段,对结果进行比较,分歧通过讨论解决。

主要结果

未发现符合纳入标准的研究。有三项正在进行的研究一旦发表可能符合纳入标准,因此将被纳入本综述的未来更新版本。

作者结论

目前没有足够的证据支持在TAO患者中使用利妥昔单抗。需要进行大型RCT来研究利妥昔单抗与安慰剂或皮质类固醇在活动性TAO患者中的疗效,以便对这种新疗法在该疾病中的疗效和安全性做出充分判断。

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