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停止非复发性多发性硬化症的疾病修饰治疗:临床实践经验

Stopping Disease-Modifying Therapy in Nonrelapsing Multiple Sclerosis: Experience from a Clinical Practice.

作者信息

Birnbaum Gary

出版信息

Int J MS Care. 2017 Jan-Feb;19(1):11-14. doi: 10.7224/1537-2073.2015-032.

Abstract

BACKGROUND

Current disease-modifying therapies (DMTs) are of benefit only in people with relapsing forms of multiple sclerosis (RMS). Thus, safely stopping DMTs in people with secondary progressive MS may be possible.

METHODS

Two groups of patients with MS were studied. Group A consisted of 77 patients with secondary progressive MS and no evidence of acute central nervous system inflammation for 2 to 20 years. These patients were advised to stop DMTs. Group B consisted of 17 individuals with RMS who stopped DMTs on their own. Both groups were evaluated at treatment cessation and for a minimum of 1 year thereafter. Multiple variables were assessed to determine those that predicted recurrent acute disease.

RESULTS

Nine patients in group A (11.7%) and ten patients in group B (58.8%) had recurrent acute disease, almost always within 1 to 2 years of stopping treatment. The only variable of significance in group A distinguishing stable and relapsing patients was age (P = .0003), with relapsing patients being younger. Group B patients were younger and had significantly lower Expanded Disability Status Scale scores than group A, with no significant differences in age between relapsed and stable patients.

CONCLUSIONS

The DMTs can be stopped safely in older patients with MS (≥7 decades) with no evidence of acute disease for 2 years or longer, with an almost 90% probability of remaining free of acute recurrence. The high proportion of untreated patients with RMS experiencing recurrent acute disease is consistent with published data.

摘要

背景

目前的疾病修正疗法(DMTs)仅对复发型多发性硬化症(RMS)患者有益。因此,对于继发进展型多发性硬化症患者,安全停用DMTs可能是可行的。

方法

对两组多发性硬化症患者进行了研究。A组由77例继发进展型多发性硬化症患者组成,这些患者在2至20年期间无急性中枢神经系统炎症证据。建议这些患者停用DMTs。B组由17例自行停用DMTs的复发型多发性硬化症患者组成。两组患者均在停药时及之后至少1年进行评估。评估了多个变量以确定那些可预测复发性急性疾病的变量。

结果

A组中有9例患者(11.7%)和B组中有10例患者(58.8%)出现复发性急性疾病,几乎总是在停药后1至2年内出现。在A组中,区分稳定和复发患者的唯一显著变量是年龄(P = .0003),复发患者更年轻。B组患者比A组患者更年轻,扩展残疾状态量表评分显著更低,复发患者和稳定患者之间年龄无显著差异。

结论

对于年龄≥70岁、2年或更长时间无急性疾病证据的多发性硬化症患者,可以安全停用DMTs,几乎有90%的概率不会出现急性复发。复发型多发性硬化症未治疗患者中复发性急性疾病的高比例与已发表的数据一致。

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本文引用的文献

1
Evaluation of no evidence of disease activity in a 7-year longitudinal multiple sclerosis cohort.
JAMA Neurol. 2015 Feb;72(2):152-8. doi: 10.1001/jamaneurol.2014.3537.
2
Relapses and disability accumulation in progressive multiple sclerosis.
Neurology. 2015 Jan 6;84(1):81-8. doi: 10.1212/WNL.0000000000001094. Epub 2014 Nov 14.
3
MS disease activity in RESTORE: a randomized 24-week natalizumab treatment interruption study.
Neurology. 2014 Apr 29;82(17):1491-8. doi: 10.1212/WNL.0000000000000355. Epub 2014 Mar 28.
4
Immunology of relapse and remission in multiple sclerosis.
Annu Rev Immunol. 2014;32:257-81. doi: 10.1146/annurev-immunol-032713-120227. Epub 2014 Jan 15.
5
Interferon β for secondary progressive multiple sclerosis: a systematic review.
J Neurol Neurosurg Psychiatry. 2013 Apr;84(4):420-6. doi: 10.1136/jnnp-2012-303291. Epub 2012 Sep 5.
6
Interferon beta for secondary progressive multiple sclerosis.
Cochrane Database Syst Rev. 2012 Jan 18;1(1):CD005181. doi: 10.1002/14651858.CD005181.pub3.
7
Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria.
Ann Neurol. 2011 Feb;69(2):292-302. doi: 10.1002/ana.22366.
8
Discontinuing disease-modifying therapy in progressive multiple sclerosis: can we stop what we have started?
Mult Scler. 2009 Dec;15(12):1528-31. doi: 10.1177/1352458509351730. Epub 2009 Dec 7.
9
The relation between inflammation and neurodegeneration in multiple sclerosis brains.
Brain. 2009 May;132(Pt 5):1175-89. doi: 10.1093/brain/awp070. Epub 2009 Mar 31.
10
Multiple sclerosis.
Lancet. 2008 Oct 25;372(9648):1502-17. doi: 10.1016/S0140-6736(08)61620-7.

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