O'Connor Paul W, Oh Jiwon
Multiple Sclerosis Clinic, St. Michael's Hospital, Toronto, Canada.
Multiple Sclerosis Clinic, St. Michael's Hospital, Toronto, Canada; Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.
Handb Clin Neurol. 2014;122:465-501. doi: 10.1016/B978-0-444-52001-2.00021-2.
Over the past two decades, major advances have been made in the development of disease-modifying agents (DMAs) for multiple sclerosis (MS), and nine agents are now licensed for use in the treatment of MS in the United States. Clinical trials have demonstrated that a number of investigational agents have beneficial effects on clinical and radiographic measures of disease activity, thus the repertoire of available DMAs in MS will likely continue to expand moving forward. Although many of the first-line DMAs have the benefits of established long-term safety and tolerability, in some patients, treatment with one of the more potent novel agents may be appropriate. However, the use of novel agents must be approached with caution, since short-term clinical trials give little information on the long-term efficacy and safety of novel DMAs in MS patients. This chapter will consider the efficacy and safety of both established and investigational agents for the treatment of MS.
在过去二十年中,多发性硬化症(MS)疾病修正药物(DMA)的研发取得了重大进展,目前在美国有九种药物被批准用于治疗MS。临床试验表明,一些研究性药物对疾病活动的临床和影像学指标具有有益作用,因此MS可用的DMA种类可能会在未来继续增加。尽管许多一线DMA具有已确立的长期安全性和耐受性等优点,但在某些患者中,使用一种效力更强的新型药物进行治疗可能是合适的。然而,使用新型药物必须谨慎,因为短期临床试验几乎无法提供关于新型DMA在MS患者中的长期疗效和安全性的信息。本章将探讨已确立的和研究性的MS治疗药物的疗效和安全性。