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米托蒽醌治疗快速进展型多发性硬化症。

Mitoxantrone therapy in rapidly worsening multiple sclerosis.

作者信息

Benesova Y, Stourac P, Beranek M, Kadanka Z

机构信息

Department of Neurology, University Hospital, Brno, Czech Republic.

出版信息

Bratisl Lek Listy. 2005;106(3):141-3.

Abstract

BACKGROUND

This study evaluates mitoxantrone (MX) therapy in patients with relapsing remitting and secondary progressive multiple sclerosis (MS).

OBJECTIVES

Evaluation of the disability progression and side effects of MX.

METHODS

There were studied 33 patients (10 males, 23 females), average age 48.5+/-9.9 SD) with relapsing remitting and secondary progressive MS. The disability was evaluated using Expanded Disability Status Scale (EDSS). Time period from the onset to secondary progressive course of the disease was 9.3 years. Patients, whose disability progression increased by one or more EDSS point per one year, and not responding to other therapy, were treated with mitoxantrone. Patients were treated once monthly with intravenous administration of mitoxantrone 12 mg/m2, not exceeding the maximum cumulative dose of 14 mg/m2 and Solu-Medrol 1000 mg. Six pulses were done in each patient. EDSS score was measured at the beginning of the treatment and after twelwe month. Disability progression was evaluated. Nonparametric Wilcoxon matched pair test was used for statistical analysis. (Tab. 1, Fig. 3, Ref: 5.)

摘要

背景

本研究评估米托蒽醌(MX)治疗复发缓解型和继发进展型多发性硬化症(MS)患者的疗效。

目的

评估MX的残疾进展情况和副作用。

方法

研究了33例复发缓解型和继发进展型MS患者(10例男性,23例女性),平均年龄48.5±9.9标准差。使用扩展残疾状态量表(EDSS)评估残疾情况。从疾病发作到继发进展期的时间为9.3年。残疾进展每年增加一个或多个EDSS评分点且对其他治疗无反应的患者接受米托蒽醌治疗。患者每月静脉注射一次米托蒽醌12 mg/m²,不超过最大累积剂量14 mg/m²,同时静脉注射甲泼尼龙1000 mg。每位患者进行6次脉冲治疗。在治疗开始时和12个月后测量EDSS评分。评估残疾进展情况。采用非参数Wilcoxon配对检验进行统计分析。(表1,图3,参考文献:5)

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