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间歇性环磷酰胺脉冲疗法治疗进展型多发性硬化症:东北多发性硬化症协作治疗组的最终报告

Intermittent cyclophosphamide pulse therapy in progressive multiple sclerosis: final report of the Northeast Cooperative Multiple Sclerosis Treatment Group.

作者信息

Weiner H L, Mackin G A, Orav E J, Hafler D A, Dawson D M, LaPierre Y, Herndon R, Lehrich J R, Hauser S L, Turel A

机构信息

Multiple Sclerosis Unit of the Center for Neurologic Diseases, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.

出版信息

Neurology. 1993 May;43(5):910-8. doi: 10.1212/wnl.43.5.910.

Abstract

Previous studies reported that a 2- to 3-week course of IV cyclophosphamide plus adrenocorticotropic hormone (ACTH) induction can temporarily halt progressive MS for a period of 12 months in the majority of patients treated, after which reprogression occurs. The Northeast Cooperative Multiple Sclerosis Treatment Group was formed to determine whether outpatient pulse cyclophosphamide therapy could affect reprogression and whether there were differences between a modified induction regimen and the previously published regimen. Two hundred fifty-six progressive MS patients were randomized into four groups to receive IV cyclophosphamide/ACTH via the previously published versus a modified induction regimen, with or without outpatient IV cyclophosphamide boosters (700 mg/m2 every other month for 2 years). There were blinded evaluations performed every 6 months. Results demonstrate that (1) there were no differences between the modified and the published induction regimens either in terms of initial stabilization or subsequent progression; (2) without boosters, the majority of patients continued to progress; and (3) in patients receiving boosters, there was a statistically significant benefit at 24 months and 30 months (p = 0.04). Time to treatment failure after 1 year was also significantly prolonged in the booster versus the nonbooster group (p = 0.03). Age was the most important variable that correlated with response to therapy in that amelioration of disease progression occurred primarily in patients 40 years of age or younger. Boosters had a significant benefit on time to treatment failure in patients ages 18 to 40, p = 0.003, but not in patients ages 41 to 55, p = 0.97.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

以往研究报道,静脉注射环磷酰胺加促肾上腺皮质激素(ACTH)进行2至3周的诱导治疗,可使大多数接受治疗的患者的进展性多发性硬化症(MS)暂时停止12个月,之后疾病会再次进展。东北多发性硬化症合作治疗组旨在确定门诊脉冲环磷酰胺疗法是否会影响疾病再次进展,以及改良诱导方案与先前公布的方案之间是否存在差异。256例进展性MS患者被随机分为四组,分别接受先前公布的方案或改良诱导方案静脉注射环磷酰胺/ACTH,同时接受或不接受门诊静脉注射环磷酰胺强化治疗(每两个月700mg/m²,共2年)。每6个月进行一次盲法评估。结果表明:(1)改良诱导方案与公布的诱导方案在初始病情稳定或后续进展方面均无差异;(2)不进行强化治疗时,大多数患者病情继续进展;(3)接受强化治疗的患者在24个月和30个月时具有统计学显著益处(p = 0.04)。强化治疗组与非强化治疗组相比,1年后治疗失败时间也显著延长(p = 0.03)。年龄是与治疗反应相关的最重要变量,因为疾病进展的改善主要发生在40岁及以下的患者中。强化治疗对18至40岁患者的治疗失败时间有显著益处,p = 0.003,但对41至55岁患者无显著益处,p = 0.97。(摘要截选至250字)

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