Suppr超能文献

低剂量利妥昔单抗治疗常规治疗抵抗的活动期中重度格雷夫斯眼病。

Low-Dose Rituximab for Active Moderate to Severe Graves' Orbitopathy Resistant to Conventional Treatment.

机构信息

a Department of Internal Medicine, Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts , Paris Cedex 12 , France.

b Department of Ophthalmology 4, Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts , Paris Cedex 12 , France.

出版信息

Ocul Immunol Inflamm. 2019;27(5):844-850. doi: 10.1080/09273948.2018.1453078. Epub 2018 Apr 13.

Abstract

: To report low-dose rituximab effect in Graves' orbitopathy (GO) resistant to conventional treatment. : Retrospective analysis of medical records, filled in according to the European Group on Graves' Orbitopathy (EUGOGO) standards, of patients with active moderate-to-severe GO who received low-dose rituximab after failure of conventional treatment. Efficacy was defined by a decrease of the clinical activity score of 2 points or <4/10. : Among 219 patients treated between 2012 and 2016 by pulse methylprednisolone, possibly followed by oral steroids and/or orbital radiotherapy, 15 (6.8%) finally received 100 mg rituximab doses (cumulative dose, 100-400 mg) owing to persistent active disease. Rituximab showed efficacy within 2 months in 13 of 15 (87%), stable at 1 year. No significant effect was observed on proptosis, lid fissure width, and eye motility. : Low-dose rituximab showed sustained anti-inflammatory effect in most patients with active GO resistant to conventional treatment.

摘要

报告对常规治疗抵抗的 Graves 眼病(GO)的低剂量利妥昔单抗疗效。

根据欧洲 Graves 眼病专家组(EUGOGO)标准,对接受常规治疗失败后接受低剂量利妥昔单抗治疗的活动期中重度 GO 患者的病历进行回顾性分析。疗效定义为临床活动评分降低 2 分或<4/10。

在 2012 年至 2016 年期间,219 例患者接受了脉冲甲基强的松龙治疗,可能随后接受了口服类固醇和/或眼眶放射治疗,其中 15 例(6.8%)由于持续的活动期疾病而最终接受了 100mg 利妥昔单抗剂量(累积剂量为 100-400mg)。利妥昔单抗在 15 例中的 13 例(87%)中在 2 个月内显示出疗效,在 1 年内稳定。对眼球突出度、睑裂宽度和眼球运动无明显影响。

低剂量利妥昔单抗在大多数对常规治疗抵抗的活动期 GO 患者中显示出持续的抗炎作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验