Benefit of interferon β-1a on MSFC progression in secondary progressive MS

被引:305
作者
Cohen, JA
Cutter, GR
Fischer, JS
Goodman, AD
Heidenreich, FR
Kooijmans, MF
Sandrock, AW
Rudick, RA
Simon, JH
Simonian, NA
Tsao, EC
Whitaker, JN
机构
[1] Cleveland Clin Fdn, Mellen Ctr Multiple Sclerosis Treatment & Res, Dept Neurol, Cleveland, OH 44195 USA
[2] AMC Canc Ctr, Ctr Res Methodol & Biometr, Lakewood, CO USA
[3] Univ Rochester, Dept Neurol, Rochester, NY 14627 USA
[4] Hannover Med Sch, Dept Neurol, D-3000 Hannover, Germany
[5] Biogen Inc, Cambridge, MA 02142 USA
[6] Univ Colorado, Dept Radiol, Denver, CO 80202 USA
[7] Univ Alabama Birmingham, Dept Neurol, Birmingham, AL 35294 USA
关键词
D O I
10.1212/WNL.59.5.679
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Interferon beta-1a (IFNbeta-1a, Avonex) is efficacious in relapsing forms of MS. Studies of other IFNbeta preparations in secondary progressive MS (SPMS) yielded conflicting results. This study was undertaken to determine whether IFNbeta-1a slowed disease progression in SP-MS. Methods: A total of 436 subjects with SPMS and Expanded Disability Status Scale (EDSS) score 3.5 to 6.5 were randomized to receive IFNbeta-1a (60 mug) or placebo by weekly intramuscular injection for 2 years. The primary outcome measure, used for the first time in a large-scale MS trial, was baseline to month 24 change in the MS Functional Composite (MSFC), comprising quantitative tests of ambulation Timed 25-Foot Walk), arm function (Nine-Hole Peg Test [9HPT]), and cognition (Paced Auditory Serial Addition Test [PASAT]). Results: Median MSFC Z-score change was reduced 40.4% in IFNbeta-1a subjects (-0.096 vs -0.161 in placebo subjects, p = 0.033), an effect driven mainly by the 9HPT and PASAT. There was no discernible benefit on the EDSS, which in this range principally reflects walking ability. IFNbeta-1a subjects had 33% fewer relapses p = 0.008). There was significant benefit on eight of 11 MS Quality of Life Inventory subscales. New or enlarging T2-hyperintense brain MRI lesions and gadolinium-enhancing lesions were reduced at months 12 and 24 (both p < 0.001). IFNbeta-1a was well tolerated by the majority of subjects. Neutralizing antibodies developed in 3.3% of IFNbeta-1a-treated subjects. Conclusions: IFNbeta-1a demonstrated benefit on MSFC progression, relapses, quality of life, and MRI activity in SPMS.
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收藏
页码:679 / 687
页数:9
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