Suppr超能文献

干扰素与醋酸格拉替雷联合治疗复发缓解型多发性硬化症的CombiRx试验:设计与基线特征

The CombiRx trial of combined therapy with interferon and glatiramer acetate in relapsing remitting MS: Design and baseline characteristics.

作者信息

Lindsey J W, Scott T F, Lynch S G, Cofield S S, Nelson F, Conwit R, Gustafson T, Cutter G R, Wolinsky J S, Lublin F D

机构信息

Department of Neurology, University of Texas Health Science Center at Houston, 6431 Fannin St, Suite 7.044, Houston, TX 77030, USA.

Department of Neurology, Drexel College of Medicine, Pittsburgh, PA, USA.

出版信息

Mult Scler Relat Disord. 2012 Apr;1(2):81-6. doi: 10.1016/j.msard.2012.01.006. Epub 2012 Feb 23.

Abstract

BACKGROUND

Interferon-β1a (IFNB) and glatiramer acetate (GA) are distinct therapies which are both partially effective for relapsing MS. It is not known if combining the two treatments would be more effective.

OBJECTIVE

To review the rationale, design, and baseline characteristics of the CombiRx study of combined treatment with IFNB and GA.

METHODS

The key inclusion criteria included a diagnosis of relapsing MS, at least 2 episodes of MS activity in the previous 3 years, expanded disability status scale of 0-5.5, and no prior treatment with either IFNB or GA. Subjects were randomized to IFNB+GA, IFNB monotherapy, or GA monotherapy in a 2:1:1 ratio.

RESULTS

From 2005 to 2009, we enrolled 1008 subjects. The participants were 72.4% female and 87.6% Caucasian with a mean age of 37.7 years. The median duration of symptoms was 2 years at entry into the study, and the mean EDSS was 2.1. On the baseline MRI, the mean total lesion load was 12.2ml, and 40% of the participants had enhancing lesions.

CONCLUSION

We have recruited a population of patients with clinical and MRI characteristics typical for early MS. The study results will aid in deciding on the optimum early treatment. This trial should serve as a model for future studies of combination therapy.

摘要

背景

干扰素-β1a(IFNB)和醋酸格拉替雷(GA)是两种不同的疗法,对复发型多发性硬化症(MS)均有一定疗效。目前尚不清楚联合使用这两种疗法是否会更有效。

目的

回顾IFNB与GA联合治疗的CombiRx研究的基本原理、设计和基线特征。

方法

关键纳入标准包括复发型MS的诊断、过去3年中至少有2次MS活动发作、扩展残疾状态量表评分为0 - 5.5,且既往未接受过IFNB或GA治疗。受试者按2:1:1的比例随机分为IFNB + GA组、IFNB单药治疗组或GA单药治疗组。

结果

2005年至2009年,我们招募了1008名受试者。参与者中72.4%为女性,87.6%为白种人,平均年龄为37.7岁。进入研究时症状的中位持续时间为2年,平均扩展残疾状态量表评分为2.1。在基线MRI检查中,平均总病灶负荷为12.2ml,40%的参与者有强化病灶。

结论

我们招募了一群具有早期MS典型临床和MRI特征的患者。研究结果将有助于确定最佳的早期治疗方案。该试验应作为未来联合治疗研究的一个范例。

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