Bech E, Lycke J, Gadeberg P, Hansen H J, Malmeström C, Andersen O, Christensen T, Ekholm S, Haahr S, Höllsberg P, Bergström T, Svennerholm B, Jakobsen J
Department of Neurology, Aarhus University Hospital, Denmark.
Neurology. 2002 Jan 8;58(1):31-6. doi: 10.1212/wnl.58.1.31.
To evaluate the effect of treatment with the antiherpes drug valacyclovir on MRI-evident lesions in patients with relapsing-remitting MS in a phase 2, randomized, double-blind, placebo-controlled study.
It has been postulated from virologic studies that herpesvirus infection could play a role in the progression of MS.
Patients were eligible for the study if they had had two or more MS relapses in the 2-year period before enrollment. Seventy patients with Expanded Disability Status Scale scores of 0 to 5.5 were randomly assigned to receive 1 gram of valacyclovir (n = 36) or placebo (n = 34) three times daily for 24 weeks. Patients underwent MRI every fourth week for 32 weeks: twice during pretreatment, six times during treatment, and once after treatment. Scoring of neurologic disability was performed at the start and end of the treatment period. The primary endpoint was the number of new active MRI-evident lesions over 24 weeks of treatment. Secondary endpoints included other MRI measures and clinical endpoints.
The mean number of new active lesions +/- SD per patient during 24 weeks of treatment with valacyclovir was 11.9 +/- 17.6 and that during placebo treatment was 14.5 +/- 21.4. A protocol-planned exploratory analysis stratified patients according to baseline activity; this analysis showed that patients with high levels of disease activity in the valacyclovir treatment group (n = 17) developed fewer new active lesions per scan than did those in the placebo treatment group (n = 11). The median number (Q(1), Q(3) range) of active lesions was 2.0 (1.38, 3.96) in the valacyclovir treatment group and 6.5 (2.63, 9.0) in the placebo treatment group.
Valacyclovir treatment did not reduce the formation of active lesions in patients with relapsing-remitting MS who had two or more relapses during the previous 2-year period. In a subgroup of patients with high levels of disease activity who had more than one active MRI-evident lesion during 4 weeks, valacyclovir treatment was associated with a reduced number of new active MRI-evident lesions and with an increase in the number of scans free of new active lesions. The results of the exploratory subgroup analysis provide support for further studies of antiherpes therapy for patients with MS and high levels of MRI-evident disease activity.
在一项2期随机双盲安慰剂对照研究中,评估抗疱疹药物伐昔洛韦治疗对复发缓解型多发性硬化症(MS)患者MRI可见病灶的影响。
病毒学研究推测,疱疹病毒感染可能在MS的进展中起作用。
入选前2年内有两次或更多次MS复发的患者符合研究条件。70例扩展残疾状态量表评分在0至5.5之间的患者被随机分配,分别接受每日3次、每次1克伐昔洛韦治疗(n = 36)或安慰剂治疗(n = 34),疗程24周。患者在32周内每4周接受一次MRI检查:治疗前2次,治疗期间6次,治疗后1次。在治疗期开始和结束时进行神经功能残疾评分。主要终点是治疗24周内新出现的MRI可见活动性病灶数量。次要终点包括其他MRI测量指标和临床终点。
伐昔洛韦治疗24周期间,每位患者新出现的活动性病灶平均数±标准差为11.9±17.6,安慰剂治疗期间为14.5±21.4。一项方案计划的探索性分析根据基线活动情况对患者进行分层;该分析显示,伐昔洛韦治疗组中疾病活动水平高的患者(n = 17)每次扫描出现的新活动性病灶比安慰剂治疗组患者(n = 11)少。伐昔洛韦治疗组活动性病灶的中位数(四分位数间距)为2.0(1.38,3.96),安慰剂治疗组为6.5(2.63,9.0)。
伐昔洛韦治疗未能减少在前2年内有两次或更多次复发的复发缓解型MS患者活动性病灶的形成。在疾病活动水平高且在4周内有一个以上MRI可见活动性病灶的亚组患者中,伐昔洛韦治疗与新出现的MRI可见活动性病灶数量减少以及无新活动性病灶扫描次数增加有关。探索性亚组分析结果为进一步研究针对MRI可见疾病活动水平高的MS患者的抗疱疹治疗提供了支持。