Queensland University of Technology, School of Life Sciences, Faculty of Science and Technology, GPO 2343, QLD 4001, Brisbane, Australia.
Expert Opin Pharmacother. 2010 May;11(7):1225-30. doi: 10.1517/14656561003677390.
The first sign of developing multiple sclerosis is a clinically isolated syndrome that resembles a multiple sclerosis relapse.
OBJECTIVE/METHODS: The objective was to review the clinical trials of two medicines in clinically isolated syndromes (interferon beta and glatiramer acetate) to determine whether they prevent progression to definite multiple sclerosis. In the BENEFIT trial, after 2 years, 45% of subjects in the placebo group developed clinically definite multiple sclerosis; the rate was lower in the interferon beta-1b group. All subjects were then offered interferon beta-1b, and the original interferon beta-1b group became the early-treatment group and the placebo group became the delayed-treatment group. After 5 years, the number of subjects with clinical definite multiple sclerosis remained lower in the early-treatment than in the late-treatment group. In the PreCISe trial, after 2 years, the time for 25% of the subjects to convert to definite multiple sclerosis was prolonged in the glatiramer group. Interferon beta-1b and glatiramer acetate slow the progression of clinically isolated syndromes to definite multiple sclerosis. However, it is not known whether this early treatment slows the progression to the physical disabilities experienced in multiple sclerosis.
多发性硬化症的最初迹象是类似于多发性硬化症复发的临床孤立综合征。
目的/方法:本研究旨在回顾两种药物(干扰素 β 和醋酸格拉替雷)在临床孤立综合征中的临床试验,以确定它们是否能预防进展为明确的多发性硬化症。在 BENEFIT 试验中,2 年后,安慰剂组 45%的受试者发展为临床明确的多发性硬化症;干扰素 β-1b 组的发病率较低。所有受试者随后均接受干扰素 β-1b 治疗,原干扰素 β-1b 组成为早期治疗组,安慰剂组成为延迟治疗组。5 年后,早期治疗组临床明确多发性硬化症的受试者数量仍低于晚期治疗组。在 PreCISe 试验中,2 年后,格拉替雷组有 25%的受试者转化为明确多发性硬化症的时间延长。干扰素 β-1b 和醋酸格拉替雷可减缓临床孤立综合征向明确多发性硬化症的进展。然而,目前尚不清楚这种早期治疗是否会减缓向多发性硬化症所经历的身体残疾的进展。