首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >Combination of cyclophosphamide and interferon-β haltsprogression in patients with rapidly transitional multiple sclerosis
【2h】

Combination of cyclophosphamide and interferon-β haltsprogression in patients with rapidly transitional multiple sclerosis

机译:环磷酰胺和干扰素-β停药的组合移行性多发性硬化症患者的病情发展

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The effects of combined treatment with cyclophosphamide (CTX) and interferon-β (IFN-β) are described in selected patients with "rapidly transitional" multiple sclerosis. This form of multiple sclerosis is extremely active with very frequent and severe attacks which produce a dramatic increase on the expanded disability status scale (EDSS). Ten patients with rapidly transitional multiple sclerosis were previously treated with interferon-β, but none benefited by this treatment. Monthly treatment with intravenous CTX, from 500 mg/m2 to 1500 mg/m2 to obtain a chronic lymphocytopenia (600/mm3 to 900/mm3) produced a marked and significant reduction in the number of relapses (p<0.0001), disability previously accumulated (p<0.0001), and a reduction of T2 MRI burden of lesion. This particular group of patients benefited by combining cyclophosphamide and IFN-β. The possibility is considered of carrying out further studies to test the efficacy of the association between the two drugs for patients who are not responsive to IFN-β or other active disease modifying therapies.

机译:在选定的“快速过渡性”多发性硬化患者中描述了环磷酰胺(CTX)和干扰素-β(IFN-β)联合治疗的效果。这种形式的多发性硬化症在非常频繁和严重的发作中非常活跃,这会导致扩展的残疾状态量表(EDSS)急剧增加。先前曾用干扰素-β治疗10例快速过渡性多发性硬化症患者,但无一受益。静脉CTX每月治疗,范围从500 mg / m 2 至1500 mg / m 2 ,以获得慢性淋巴细胞减少症(600 / mm 3 至900 / mm 3 )可显着显着降低复发次数(p <0.0001),先前累积的残疾(p <0.0001)和减轻T2 MRI病变负担。这组特定的患者受益于环磷酰胺和IFN-β的联合使用。考虑对进一步治疗以测试两种药物之间的关联对不响应IFN-β或其他活性疾病修饰疗法的患者的疗效的可能性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号