Schreiner Teri L, Miravalle Augusto
Department of Neurology, University of Colorado, Denver, CO, USA.
J Cent Nerv Syst Dis. 2012 Jan 3;4:1-14. doi: 10.4137/JCNSD.S5128. Print 2012.
Multiple Sclerosis (MS) is a chronic inflammatory, immune-mediated, demyelinating disorder of the central nervous system with a heterogeneous clinical presentation and pathology in which activated lymphocytes play an important role in mediating tissue damage. Until recently, all first line therapies for MS were injectable. Several oral medications have been studied for preventative treatment of MS. Cladribine (2-chlorodeoxyadenosine) is a purine nucleoside analog that has been used for the treatment of several hematologic neoplasms, with a unique lymphcytotoxic mechanism of action. Cladribine has been investigated as treatment of MS for more than 15 years. A recent placebo-controlled, double-blind study of cladribine, CLARITY, showed decreased relapse rates, risk of disability progression and MRI measures of disease activity at 96 weeks. Cladribine's strengths included high efficacy and convenient, biannual oral dosing. However, concerns about safety prevented the FDA from approving cladribine in 2011. Thus, use of cladribine for treatment of relapsing and remitting multiple sclerosis will remain off-label.
多发性硬化症(MS)是一种慢性炎症性、免疫介导的中枢神经系统脱髓鞘疾病,临床表现和病理具有异质性,其中活化淋巴细胞在介导组织损伤中起重要作用。直到最近,所有用于MS的一线治疗方法都是注射剂。已经对几种口服药物进行了MS预防性治疗的研究。克拉屈滨(2-氯脱氧腺苷)是一种嘌呤核苷类似物,已用于治疗多种血液系统肿瘤,具有独特的淋巴细胞毒性作用机制。克拉屈滨作为MS的治疗药物已被研究了15年以上。最近一项关于克拉屈滨的安慰剂对照、双盲研究CLARITY显示,在96周时复发率、残疾进展风险和疾病活动的MRI指标均有所降低。克拉屈滨的优点包括高效和方便的半年一次口服给药。然而,对安全性的担忧阻止了美国食品药品监督管理局(FDA)在2011年批准克拉屈滨。因此,克拉屈滨用于复发缓解型多发性硬化症的治疗仍属于超说明书用药。