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Good results for early treatment of clinically isolated syndrome prior to multiple sclerosis with interferon beta-1b and glatiramer

机译:干扰素β-1b和格拉替雷治疗多发性硬化症之前临床分离的综合征的早期治疗效果良好

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摘要

Background: 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 β and glatiramer acetate) to determine whether they prevent progression to definite multiple sclerosis. Results: In the BENEFIT trial, after 2 years, 45% of subjects in the placebo group developed clinically definite multiple sclerosis, and the rate was lower in the interferon β-1b group. Then all subjects were offered interferon β-1b, and the original interferon β-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 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. Conclusions: Interferon β-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.
机译:背景:发展为多发性硬化症的第一个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:目的是回顾两种药物在临床分离的综合症(干扰素β和醋酸格拉替雷)中的临床试验,以确定它们是否可预防发展为明确的多发性硬化症。结果:在BENEFIT试验中,两年后,安慰剂组中45%的受试者发展为临床明确的多发性硬化症,而干扰素β-1b组的发病率更低。然后向所有受试者提供干扰素β-1b,原始干扰素β-1b组成为早期治疗组,而安慰剂组成为延迟治疗组。 5年后,早期治疗的临床确诊多发性硬化症患者的数量仍然低于晚期治疗组。在PreCISe试验中,两年后,格拉替雷组延长了25%的受试者转变为明确的多发性硬化症的时间。结论:干扰素β-1b和醋酸格拉替雷可减缓临床分离综合征发展为明确的多发性硬化症的进程。然而,尚不清楚这种早期治疗是否会减慢多发性硬化症所致身体残疾的进展。

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    Doggrell Sheila;

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  • 年度 2010
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