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复发型多发性硬化症治疗的诱导疗法与强化疗法:证据

Induction vs. escalation of therapy for relapsing multiple sclerosis: the evidence.

作者信息

Freedman Mark S

机构信息

Multiple Sclerosis Research Unit, The Ottawa Hospital General Campus, University of Ottawa, Ottawa, Canada.

出版信息

Neurol Sci. 2008 Sep;29 Suppl 2:S250-2. doi: 10.1007/s10072-008-0953-y.

DOI:10.1007/s10072-008-0953-y
PMID:18690508
Abstract

Not all patients presenting with their first attack of multiple sclerosis (MS) or early thereafter are necessarily in the same phase of disease; some truly present early with minimal disease, whereas others present late, having accumulated already considerable damage to the central nervous system (CNS). This beckons a different approach to therapy depending on "where" a patient may be in the course of disease. If early, then any of the current first line immunomodulating agents may be appropriate, whereas later disease calls for a more aggressive approach entailing either induction with a more powerful but riskier treatment or an escalation approach, moving through first line agents and stepping up to more aggressive treatments. This paper discusses the rationale for either regimen.

摘要

并非所有首次出现多发性硬化症(MS)发作或在此后不久发病的患者都必然处于疾病的同一阶段;一些患者确实在疾病早期表现为轻微症状,而另一些患者则在晚期发病,此时中枢神经系统(CNS)已积累了相当程度的损伤。这就需要根据患者在疾病进程中所处的“位置”采取不同的治疗方法。如果是早期,那么目前任何一种一线免疫调节药物可能都是合适的,而对于晚期疾病,则需要采取更积极的治疗方法,要么采用更强大但风险更高的治疗进行诱导,要么采用逐步升级的方法,从一线药物开始,逐步升级到更积极的治疗。本文讨论了这两种治疗方案的依据。

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High serum neurofilament light chain normalizes after hematopoietic stem cell transplantation for MS.多发性硬化症患者接受造血干细胞移植后,血清神经丝轻链会恢复正常。

本文引用的文献

1
Canadian treatment optimization recommendations (TOR) as a predictor of disease breakthrough in patients with multiple sclerosis treated with interferon beta-1a: analysis of the PRISMS study.加拿大治疗优化建议(TOR)作为预测接受β-1a干扰素治疗的多发性硬化症患者疾病突破的指标:PRISMS研究分析
Mult Scler. 2008 Nov;14(9):1234-41. doi: 10.1177/1352458508093892. Epub 2008 Jul 16.
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Efficacy of disease-modifying therapies in relapsing remitting multiple sclerosis: a systematic comparison.疾病修饰疗法在复发缓解型多发性硬化症中的疗效:一项系统比较。
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Predictive nature of IgM anti-α-glucose serum biomarker for relapse activity and EDSS progression in CIS patients: a BENEFIT study analysis.IgM 抗-α-葡萄糖血清生物标志物对 CIS 患者复发活动和 EDSS 进展的预测性质:BENEFIT 研究分析。
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米托蒽醌诱导治疗后使用醋酸格拉替雷治疗复发型多发性硬化症。
Mult Scler. 2008 Jun;14(5):663-70. doi: 10.1177/1352458507085759. Epub 2008 Apr 18.
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Intense immunosuppression in patients with rapidly worsening multiple sclerosis: treatment guidelines for the clinician.快速进展型多发性硬化患者的强化免疫抑制:临床医生治疗指南
Lancet Neurol. 2008 Feb;7(2):173-83. doi: 10.1016/S1474-4422(08)70020-6.
5
Mitoxantrone as induction treatment in aggressive relapsing remitting multiple sclerosis: treatment response factors in a 5 year follow-up observational study of 100 consecutive patients.米托蒽醌作为侵袭性复发缓解型多发性硬化症的诱导治疗:对100例连续患者进行5年随访观察研究中的治疗反应因素
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New natural history of interferon-beta-treated relapsing multiple sclerosis.干扰素β治疗复发型多发性硬化症的新自然史。
Ann Neurol. 2007 Apr;61(4):300-6. doi: 10.1002/ana.21102.
7
A randomized, placebo-controlled trial of natalizumab for relapsing multiple sclerosis.那他珠单抗治疗复发型多发性硬化症的随机安慰剂对照试验。
N Engl J Med. 2006 Mar 2;354(9):899-910. doi: 10.1056/NEJMoa044397.
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Induction versus escalation therapy.诱导治疗与强化治疗
Neurol Sci. 2005 Dec;26 Suppl 4:S193-9. doi: 10.1007/s10072-005-0519-1.
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Enhanced benefit of increasing interferon beta-1a dose and frequency in relapsing multiple sclerosis: the EVIDENCE Study.增加干扰素β-1a剂量和给药频率对复发型多发性硬化症的增效作用:EVIDENCE研究
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Stabilization of rapidly worsening multiple sclerosis for 36 months in patients treated with interferon beta plus cyclophosphamide followed by interferon beta.接受干扰素β加环磷酰胺治疗后再用干扰素β治疗的患者中,快速进展型多发性硬化症病情稳定长达36个月。
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