van de Wyngaert F A, Beguin C, D'Hooghe M B, Dooms G, Lissoir F, Carton H, Sindic C J
Department of Neurology, Cliniques Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.
Acta Neurol Belg. 2001 Dec;101(4):210-6.
A double-blind clinical trial of mitoxantrone versus methylprednisolone was performed in 49 patients with relapsing, secondary multiple sclerosis. Patients were randomized to receive 13 infusions of mitoxantrone 12 mg/m2 (n = 28), or 13 infusions of 1 g of methylprednisolone (n = 21), over 32 months. Twenty-four patients completed the trial. There were no statistical differences between the two groups of patients at study entry. A significant improvement in the Expanded Disability Scale Score (EDSS) was observed in the mitoxantrone group after one year of treatment (p < 0.0022). The total number of relapses, the mean number of relapses/patient/year, and the total number of gadolinium-enhanced lesions on bi-annual MRI scans were significantly decreased in the mitoxantrone group throughout the study period. Nausea, vomiting, and alopecia were more frequent in the mitoxantrone-treated patients. Mitoxantrone has a role in the treatment of MS patients with frequent exacerbations and rapid disease progression.
对49例复发型继发进展型多发性硬化患者进行了米托蒽醌与甲泼尼龙的双盲临床试验。患者被随机分为两组,在32个月内接受13次静脉输注,其中一组接受米托蒽醌12mg/m²(n = 28),另一组接受1g甲泼尼龙(n = 21)。24例患者完成了试验。两组患者在研究开始时无统计学差异。治疗一年后,米托蒽醌组的扩展残疾状态量表评分(EDSS)有显著改善(p < 0.0022)。在整个研究期间,米托蒽醌组的复发总数、平均每年每位患者的复发次数以及每半年MRI扫描时钆增强病灶总数均显著减少。米托蒽醌治疗的患者中恶心、呕吐和脱发更为常见。米托蒽醌在频繁发作和疾病进展迅速的MS患者治疗中具有一定作用。