Long-term (up to 22 years), open-label, compassionate-use study of glatiramer acetate in relapsing-remitting multiple sclerosis

被引:27
作者
Miller, Aaron [1 ]
Spada, Vincent [2 ]
Beerkircher, Dorothy [2 ]
Kreitman, Rivka Riven [2 ]
机构
[1] Mt Sinai Sch Med, New York, NY 10029 USA
[2] Teva Neurosci Inc, Horsham, PA USA
来源
MULTIPLE SCLEROSIS | 2008年 / 14卷 / 04期
关键词
disability; disease modifying therapy; EDSS; glatiramer acetate; immunomodulator; relapse; relapsing-remitting multiple sclerosis;
D O I
10.1177/1352458507085029
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
To evaluate the safety and efficacy of long-term glatiramer acetate (GA) therapy, 46 patients with relapsing-remitting multiple sclerosis (RRMS) were treated for up to 22 years in an ongoing, open-label study. Kurtzke expanded disability status scale (EDSS) was measured every six months, relapses were reported at occurrence and patients self-reported adverse events (AEs). At GA initiation, disease durations ranged from 0-20 years (median 6.0 years) and at data cut-off (October 2004), GA therapy duration ranged from 1-22 years (median 12.0 years). Mean EDSS score increased 0.9 +/- 1.9 from the pretreatment score (3.0 +/- 1.8; P = 0.076). Only 10/28 (36%) patients with baseline EDSS < 4.0 had a last observed value >= 4.0 and 8/34 (24%) with entry EDSS < 6.0 reached EDSS >= 6.0. A majority (57%) maintained improved or unchanged EDSS scores. Annualized relapse rate decreased to 0.1 +/- 0.2 from 2.9 +/- 1.4 prestudy (P < 0.0001). Of the 18 remaining patients in October 2004 (average disease duration 23 years), 17% with baseline EDSS scores < 4.0 reached EDSS >= 4.0 and 28% with baseline scores < 6.0 reached EDSS >= 6.0. Adverse events were similar to those reported in short-term clinical trials. This study shows a low rate of relapses and EDSS progression in RRMS patients on GA for up to 22 years.
引用
收藏
页码:494 / 499
页数:6
相关论文
共 17 条
  • [1] BORNSTEIN MB, 1988, NEUROLOGY, V38, P66
  • [2] A PILOT TRIAL OF COP-1 IN EXACERBATING REMITTING MULTIPLE-SCLEROSIS
    BORNSTEIN, MB
    MILLER, A
    SLAGLE, S
    WEITZMAN, M
    CRYSTAL, H
    DREXLER, E
    KEILSON, M
    MERRIAM, A
    WASSERTHEILSMOLLER, S
    SPADA, V
    WEISS, W
    ARNON, R
    JACOBSOHN, I
    TEITELBAUM, D
    SELA, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (07) : 408 - 414
  • [3] MULTIPLE-SCLEROSIS - TRIAL OF A SYNTHETIC POLYPEPTIDE
    BORNSTEIN, MB
    MILLER, AI
    TEITELBAUM, D
    ARNON, R
    SELA, M
    [J]. ANNALS OF NEUROLOGY, 1982, 11 (03) : 317 - 319
  • [4] BORNSTEIN MB, 1984, ANN NY ACAD SCI, V436, P366, DOI 10.1111/j.1749-6632.1984.tb14807.x
  • [5] Relapses and progression of disability in multiple sclerosis.
    Confavreux, C
    Vukusic, S
    Moreau, T
    Adeleine, P
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (20) : 1430 - 1438
  • [6] EBERS G, 2006, 58 ANN M AM AC NEUR
  • [7] Eight-year follow-up study of brain atrophy in patients with MS
    Fisher, E
    Rudick, RA
    Simon, JH
    Cutter, G
    Baier, M
    Lee, JC
    Miller, D
    Weinstock-Guttman, B
    Mass, MK
    Dougherty, DS
    Simonian, NA
    [J]. NEUROLOGY, 2002, 59 (09) : 1412 - 1420
  • [8] A prospective open-label study of glatiramer acetate: over a decade of continuous use in multiple sclerosis patients
    Ford, CC
    Johnson, KP
    Lisak, RP
    Panitch, HS
    Shifroni, G
    Wolinsky, JS
    [J]. MULTIPLE SCLEROSIS JOURNAL, 2006, 12 (03) : 309 - 320
  • [9] Benign multiple sclerosis? Clinical course, long term follow up, and assessment of prognostic factors
    Hawkins, SA
    McDonnell, GV
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 67 (02) : 148 - 152
  • [10] Defining the clinical course of multiple sclerosis: Results of an international survey
    Lublin, FD
    Reingold, SC
    [J]. NEUROLOGY, 1996, 46 (04) : 907 - 911