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大剂量环磷酰胺治疗中重度难治性多发性硬化症:2 年随访(研究性新药编号:65863)。

High-dose cyclophosphamide for moderate to severe refractory multiple sclerosis: 2-year follow-up (investigational new drug No. 65863).

机构信息

Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD 21287, USA.

出版信息

Am J Ther. 2011 Jan;18(1):23-30. doi: 10.1097/MJT.0b013e3181b3ad95.

DOI:10.1097/MJT.0b013e3181b3ad95
PMID:19770795
Abstract

High-dose cyclophosphamide (HDC) is a chemotherapy treatment designed to eradicate autoreative B- and T-cells responsible for lymphocyte-mediated autoimmune illness while sparing the pluripotent blood stem cell of any ill effects. Multiple sclerosis (MS) is the most common inflammatory and demyelinating immune-mediated disorder of the central nervous system in young adults. Patients with moderate to severe, refractory MS, defined as an Expanded Disability Status Scale (EDSS) score of 3.5 or higher after two or more Food and Drug Administration-approved disease-modifying agents, received 200 mg/kg of cyclophosphamide over 4 days. For the next 2 years, quarterly EDSS score evaluations and biannual brain magnetic resonance imaging and neuro-ophthalmologic evaluations were obtained. Fifteen patients were evaluated for clinical response. During follow-up, one patient increased their baseline EDSS score by 1.0. EDSS score stability of decrease was realized in five of seven (71%) patients with relapsing-remitting MS and six of eight (75%) patients with secondary progressive MS. Four patients required additional immunomodulatory treatment after treatment. Treatment response was seen regardless of the baseline presence or absence of contrast lesion activity. HDC can effectively decrease symptoms, stop disease progression, and allow for disability regression in relapsing-remitting MS and secondary progressive MS patients. The most appropriate candidates for HDC, its duration of benefit, and the potential need for prophylactic preventative immune manipulation after HDC all require further investigation.

摘要

高剂量环磷酰胺(HDC)是一种化疗治疗方法,旨在消除自身反应性 B 和 T 细胞,这些细胞负责淋巴细胞介导的自身免疫性疾病,同时使多能造血干细胞免受任何不良影响。多发性硬化症(MS)是年轻人中最常见的中枢神经系统炎症性和脱髓鞘性免疫介导性疾病。中重度、难治性 MS 患者,定义为在两种或多种经食品和药物管理局批准的疾病修饰药物后,扩展残疾状态量表(EDSS)评分达到 3.5 或更高,接受 200mg/kg 的环磷酰胺治疗 4 天。在接下来的 2 年内,每季度进行 EDSS 评分评估,每半年进行一次脑磁共振成像和神经眼科评估。对 15 名患者进行了临床反应评估。在随访期间,有 1 名患者的 EDSS 评分基线增加了 1.0。在 7 名复发性缓解型 MS 患者中有 5 名(71%)和 8 名继发性进展型 MS 患者中有 6 名(75%)实现了 EDSS 评分稳定下降。4 名患者在治疗后需要额外的免疫调节治疗。无论基线是否存在对比病变活动,治疗均有反应。HDC 可有效降低症状、停止疾病进展,并使复发性缓解型 MS 和继发性进展型 MS 患者的残疾状况逆转。HDC 最适合的候选者、其受益持续时间以及 HDC 后预防性免疫干预的潜在需求都需要进一步研究。

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Stem Cell-Based Therapies for Multiple Sclerosis: Current Perspectives.基于干细胞的多发性硬化症治疗:当前观点
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Curr Treat Options Neurol. 2015 Jan;17(1):324. doi: 10.1007/s11940-014-0324-3.
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