Survival, and time to an advanced disease state or progression, of untreated patients with moderately severe multiple sclerosis in a multicenter observational database: relevance for design of a clinical trial for high dose immunosuppressive therapy with autologous hematopoietic stem cell transplantation

被引:23
作者
Daumer, M
Griffith, LM
Meister, W
Nash, RA
Wolinsky, JS
机构
[1] Sylvia Lawry Ctr MS Res, D-81677 Munich, Germany
[2] NIAID, Div Allergy Immunol & Transplantat, NIH, Bethesda, MD 20892 USA
[3] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[4] Univ Washington, Seattle, WA 98195 USA
[5] Univ Texas, Hlth Sci Ctr, Dept Neurol, Houston, TX 77225 USA
来源
MULTIPLE SCLEROSIS | 2006年 / 12卷 / 02期
关键词
autologous hematopoietic cell transplantation; immunosuppressive therapy; multiple; sclerosis; survival; time-to-progression;
D O I
10.1191/135248506ms1256oa
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Despite prolonged survival, patients with multiple sclerosis ( MS) experience considerable morbidity, which adversely impacts quality of life. To assess the risk - benefit of a clinical trial of high dose immunosuppressive therapy with autologous hematopoietic stem cell transplantation for MS, we sought to determine the natural history of the disease in a comparison group of untreated patients. We identified 285 individuals with 2132 combined observation years ( median: 5.6 years; 5th to 95th percentile: 1 - 21 years), with Expanded Disability Status Scale (EDSS) scores of 3.0 - 5.5 at baseline observation. Disease-related mortality was zero at five years, 5.4% at 10 years, and 22% at 15 years ( 40 patients contributing to the data point; 95% confidence interval: 4 - 32%). Risk for progression to advanced disability, defined as an EDSS score of 8, was very low for the subgroup with a baseline EDSS score of 3 - 3.5; however, for those with a baseline EDSS score of 4 - 5.5, 3% had advanced disability after two years, 5% after three years, 6% after four years, 12% after five years, and 40% after 10 years. The estimated probability of disease progression, defined as an increase in EDSS score by >= 1.0 sustained for at least 180 days, was 5% after one year, 14% after two years, 22% after three years, 38% after five years, 57% after 10 years, and > 80% after 20 years of observation. The relevance of these features to the design of the clinical trial is discussed.
引用
收藏
页码:174 / 179
页数:6
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