New outlook for the treatment of secondary progressive multiple sclerosis

被引:0
|
作者
Noga, Magdalena [1 ]
Bartosik-Psujek, Halina [1 ]
机构
[1] Klin Szpital Wojewodzki 2 Rzeszowie, Klin Neurol Pododdzialem Leczenia Udaru Mozgu, Rzeszowie, Poland
来源
AKTUALNOSCI NEUROLOGICZNE | 2015年 / 15卷 / 03期
关键词
multiple sclerosis; immunosuppression; mitoxantrone; interferon beta-1a; interferon beta-1b;
D O I
10.15557/AN.2015.0018
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple sclerosis is a chronic autoimmune disease of the central nervous system which has an unknown origin and variable course. In about 85% of cases it starts as the relapsing-remitting form that, in different periods of time depending on the patient, turns into the secondary progressive form with constant progression of disability, sometimes with preserved relapse and magnetic resonance imaging activity at the beginning. The treatment options for the secondary progressive form of multiple sclerosis are still limited. Based on the results of Mitoxantrone in Multiple Sclerosis Study, mitoxantrone has been registered for the treatment of secondary progressive multiple sclerosis. In addition, the drugs that have received registration in Europe are interferon beta-1b and interferon beta-1a given subcutaneously. These drugs have a proven effect in slowing the progression of disability (interferon beta-1b, mitoxantrone) as well as reducing the annualised relapse rate (interferon beta-1b, interferon beta-1a, mitoxantrone) and the number of new outbreaks in magnetic resonance imaging (interferon beta-1a, interferon beta-1b). The study of North American Study Group on Interferon a-1b in Secondary Progressive MS showed no effect of the therapy with interferon beta-1b on the inhibition of disability progression and as a result, the drug has not obtained registration for the treatment of secondary progressive multiple sclerosis in the United States. The patients who benefit most from the therapy which modifies the course of the progressive form of multiple sclerosis are younger, with a shorter history of the disease, preserved relapse activity and rapidly increasing disability.
引用
收藏
页码:130 / 134
页数:5
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