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Alemtuzumab: a review of efficacy and risks in the treatment of relapsing remitting multiple sclerosis

机译:Alemtuzumab:复发缓解型多发性硬化症的疗效和风险评估

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摘要

Alemtuzumab is a selective humanized monoclonal antibody directed against the CD52 antigen, and has been found to be a powerful treatment for relapsing remitting multiple sclerosis. Alemtuzumab demonstrated high efficacy in several clinical studies. The risk of relapse and sustained accumulation of disability showed significant reduction in the Phase II CAMMS223 and the Phase III clinical trials CARE MS I and CARE MS II. The data presented at the 32nd Congress of the European Committee for Treatment and Research in Multiple Sclerosis confirmed these results. After completion of a 1-year treatment cycle, alemtuzumab showed a sustained effect. Although the efficacy of alemtuzumab has been widely proven, several severe adverse effects have been reported with its use. Infusion-associated reactions, increased risk of infections, and secondary autoimmunity have been associated with alemtuzumab. Autoimmune disease – mainly of the thyroid – has been reported. Immune thrombocytopenic purpura and autoimmune nephropathies have been observed less frequently. These adverse effects, given the short period of alemtuzumab marketing for relapsing remitting multiple sclerosis, require strict monitoring.
机译:Alemtuzumab是针对CD52抗原的选择性人源化单克隆抗体,已发现是复发缓解型多发性硬化症的有效治疗方法。 Alemtuzumab在多项临床研究中显示出高疗效。复发风险和持续残疾累积表明,II期CAMMS223和III期临床试验CARE MS I和CARE MS II显着降低。欧洲多发性硬化症治疗和研究委员会第32届代表大会上提交的数据证实了这些结果。在完成1年的治疗周期后,Alemtuzumab表现出持续的作用。尽管已经证明了alemtuzumab的功效,但已报道了使用Alemtuzumab会产生严重的不良反应。输注相关反应,感染风险增加和继发性自身免疫与阿仑单抗相关。据报道,自身免疫疾病-主要是甲状腺疾病。免疫性血小板减少性紫癜和自身免疫性肾病的发生率较低。考虑到阿仑单抗用于复发缓解型多发性硬化症的短期营销,这些不良反应需要严格监控。

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