De Stefano Nicola, Filippi Massimo, Hawkins Clive
Department of Neurological and Behavioral Sciences, University of Siena, Italy.
J Neurol Sci. 2008 Mar 15;266(1-2):44-50. doi: 10.1016/j.jns.2007.08.036. Epub 2007 Sep 25.
To assess if short-term combination of glatiramer acetate (GA) and i.v. steroid in patients with relapsing-remitting multiple sclerosis (RRMS) is safe and sustains the effect of GA treatment on MRI-disease activity.
RRMS patients with >or=2 gadolinium (Gd)-enhancing lesions on screening MRI and EDSS score <or=4.0 received GA injection (20 mg subcutaneously once daily) and monthly 1 g i.v. Methylprednisolone (IVMP) for 6 months. Afterwards, all subjects received GA injections daily alone for additional 6 months. Neurological evaluations were performed at screening, baseline and every 3 months. Laboratory tests for safety were performed at screening, baseline, months 1, 6 and 12. Brain MRIs were performed at screening, baseline, months 5, 6, 11, and 12 to assess the change in the number of Gd-enhancing lesions i) from baseline to month 6, and ii) from baseline to month 12 compared with the change from baseline to month 6.
89 subjects were eligible for the study. In this group, GA in combination with IVMP resulted in 65% (95% CI=0.25-0.49, p<0.0001) reduction in the number of Gd-enhancing lesions. This reduction was sustained for additional 6 months when patients received GA alone. The analysis for change achieved in the second 6 month period showed no difference from the change achieved in the first six months (ratio 0.75, 90% CI=0.468-1.197). Overall, treatment was well tolerated and adverse events reported were similar to the known safety profile of GA.
Short-term combination of GA with 1 g monthly IVMP, preceding treatment with GA alone, is safe. MRI data suggest that this combination therapy may result in an early and sustained reduction of disease activity in RRMS patients.
评估复发缓解型多发性硬化症(RRMS)患者短期联合使用醋酸格拉替雷(GA)和静脉注射类固醇是否安全,以及是否能维持GA治疗对MRI疾病活动的效果。
在筛查MRI上有≥2个钆(Gd)增强病灶且扩展残疾状态量表(EDSS)评分≤4.0的RRMS患者接受GA注射(每日皮下注射20mg),并每月静脉注射1g甲泼尼龙(IVMP),共6个月。之后,所有受试者单独每日接受GA注射,持续6个月。在筛查、基线及每3个月进行神经学评估。在筛查、基线、第1、6和12个月进行安全性实验室检查。在筛查、基线、第5、6、11和12个月进行脑部MRI检查,以评估Gd增强病灶数量的变化:i)从基线到第6个月,以及ii)从基线到第12个月,并与从基线到第6个月的变化进行比较。
89名受试者符合研究条件。在该组中,GA联合IVMP使Gd增强病灶数量减少了65%(95%可信区间=0.25-0.49,p<0.0001)。当患者单独接受GA治疗时,这种减少持续了另外6个月。对第二个6个月期间实现的变化分析显示,与前6个月实现的变化无差异(比值0.75,90%可信区间=0.468-1.197)。总体而言,治疗耐受性良好,报告的不良事件与GA已知的安全性特征相似。
在单独使用GA治疗之前,GA与每月1g IVMP短期联合是安全的。MRI数据表明,这种联合治疗可能会使RRMS患者的疾病活动早期且持续减少。