Quality assessment in multiple sclerosis therapy (QUASIMS) -: A comparison of interferon beta therapies for relapsing-remitting multiple sclerosis

被引:55
作者
Limmroth, Volker
Malessa, Rolf
Zettl, Uwe Klaus
Koehler, Juergen
Japp, Gudrun
Haller, Peter
Elias, Wolfgang
Obhof, Winfried
Viehoever, Andrea
Meier, Uwe
Brosig, Arne
Hasford, Joerg
Putzki, Norman
Kalski, Gabriele
Wernsdoerfer, Colin
机构
[1] Univ Cologne, Cologne City Hosp, Dept Neurol, D-51109 Cologne, Germany
[2] Sophien & Hufeland Klinikum, Weimar, Germany
[3] Univ Hosp Rostock, Dept Neurol, Rostock, Germany
[4] Univ Hosp Mainz, Dept Neurol, Mainz, Germany
[5] Neurol Clin, Konigstein Falkenstein, Germany
[6] Neurol Clin, Osnabruck, Germany
[7] Rehabil Clin, Waldbronn, Germany
[8] Univ Heidelberg, Dept Neurol, Heidelberg, Germany
[9] Rehabil Ctr, Grevenbroich, Germany
[10] Univ Munich, Dept Med Informat & Epidemiol, Munich, Germany
[11] Univ Hosp Essen, Dept Neurol, Essen, Germany
[12] Biogen Idec GmbH, Ismaning, Germany
关键词
interferon beta; multiple sclerosis; disease-modifying therapy;
D O I
10.1007/s00415-006-0281-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Interferon beta (IFN beta) preparations are the most frequently prescribed therapies for patients with relapsing multiple sclerosis (MS). Several open-label observational studies report similar efficacy among IFN beta preparations. The Quality Assessment in Multiple Sclerosis Therapy (QUASIMS) study is a large, open-label observational study designed to compare the effectiveness and tolerability of available IFN beta preparations as disease-modifying therapies for relapsing MS across a wide range of clinical practice settings. This retrospective, controlled cohort study was conducted by chart review at 510 sites in Germany, Austria, and Switzerland. Enrolled patients had received one of the four available IFN beta preparations/dosing regimens (intramuscular IFN beta-1a 30 mu g 1x/week [Avonex (R)], subcutaneous (SC) IFN beta-1a 22 or 44 mu g 3x/week [Rebif (R)], or SC IFN beta-1b 250 mu g 3.5x/week [Betaferon/Betaseron (R)]) for >= 2 years. Preplanned outcomes at 1 and 2 years included change from baseline Expanded Disability Status Scale (EDSS) score, percentage of progression-free patients (< 1.0 EDSS point), annualised relapse rate (RR), percentage of relapse-free patients, and reasons for therapy change. Of 4754 evaluable patients, 3991 (84%) received IFN beta as initial therapy. There were no significant differences among IFN beta s when used as initial or follow-up therapy on almost all outcome variables. Relapse rate was consistently higher and percentage of relapse-free patients consistently lower for all products used as follow-up versus initial therapy. Results of QUASIMS showed similar effectiveness among IFN beta products. Benefits were consistently superior when IFN beta was used as initial rather than follow-up therapy. Our results suggest that patients do not benefit in terms of disease outcome from switching between IFN beta preparations/dosing regimens.
引用
收藏
页码:67 / 77
页数:11
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