The distribution of magnetic resonance imaging response to interferonβ-1b in multiple sclerosis

被引:19
作者
Sormani, MP
Bruzzi, P
Beckmann, K
Kappos, L
Miller, DH
Polman, C
Pozzilli, C
Thompson, AJ
Wagner, K
Filippi, M
机构
[1] Inst Sci, Neuroimaging Res Unit, Dept Neurol, I-20132 Milan, Italy
[2] Univ Osped San Raffaele, I-20132 Milan, Italy
[3] Natl Inst Canc Res, Unit Clin Epidemiol & Trials, Genoa, Italy
[4] Schering AG, Berlin, Germany
[5] Univ Spital Basel, Neurol Poliklin, Basel, Switzerland
[6] UCL, NMR Res Unit, Dept Neuroinflammat, Inst Neurol, London, England
关键词
multiple sclerosis; IFN beta-1b; MRI response;
D O I
10.1007/s00415-005-0885-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Whereas the effect of interferons (IFNs) on magnetic resonance imaging (MRI) outcome measures in patients with multiple sclerosis (MS) has been convincingly shown, little work has been done to define the between-patient heterogeneity of treatment response. Our aim was to assess the distribution of the effect of IFN beta-1b in terms of reduction of active T2 lesions in patients with MS. Using a fixed and a random effects model, we investigated the distribution of active T2 lesions reduction over a three-year follow up in response to treatment with 250mcg IFN beta-1b every other day in 695 patients with a complete MRI data-set of the 718 (97%) enrolled in the European, multicenter, randomised, double-blind, placebo-controlled trial of secondary progressive MS. The two statistical models consistently showed that the between patient response to IFN beta-1b, in terms of reduction of active T2 lesions, is highly heterogeneous. Whereas treated patients have a high probability (more than 65%) of showing an active T2 lesion reduction equal to or greater than 60%, there is also a 7% probability for treated patients not to show any reduction of MRI-detected disease activity during the course of the trial or even to have an increase of T2 active lesions. This study might be regarded as a first step toward the definition of markers potentially useful to identify IFN beta treatment responders and non-responders with regard to T2 lesion activity.
引用
收藏
页码:1455 / 1458
页数:4
相关论文
共 9 条
[1]   Placebo-controlled multicentre randomised trial of interferon β-1b in treatment of secondary progressive multiple sclerosis [J].
Kappos, L ;
Polman, C ;
Pozzilli, C ;
Thompson, A ;
Dahlke, F ;
Knight, R ;
Hern, J ;
Coleman, R ;
Gerrie, L ;
Cooper, G ;
Moore, J ;
Boringa, J ;
van Oosten, B ;
Ronner, H ;
Schrijver, H ;
Truyen, L ;
Montalbán, J ;
Río, J ;
Tintoré, M ;
Jacas, C ;
Marzo, E ;
Lechner-Scott, J ;
Huber, S ;
Lienert, C ;
Brunnschweiler, H ;
Hawkins, S ;
Droogan, A ;
McDonnell, G ;
Duddy, M ;
McKinstry, S ;
Altenkirch, H ;
Baum, K ;
Einhäupl, K ;
Marx, P ;
Poewe, W ;
Walter, G ;
Akman, H ;
Brockmeier, B ;
Scherer, P ;
Zschenderlein, R ;
Schmierer, K ;
Gelderblom, H ;
Hartmann, A ;
Stapf, C ;
Lüschow, A ;
Mackert, B ;
Schumacher, H ;
Masuhr, F ;
Hempel, T ;
Zimmermann, R .
LANCET, 1998, 352 (9139) :1491-1497
[2]   Final analysis of the European multicenter trial on IFNβ-1b in secondary-progressive MS [J].
Kappos, L ;
Polman, C ;
Pozzilli, C ;
Thompson, A ;
Beckmann, K ;
Dahlke, F .
NEUROLOGY, 2001, 57 (11) :1969-1975
[3]  
Kuhle J, 2004, NEUROLOGY, V62, pA489
[4]  
Miller DH, 1999, ANN NEUROL, V46, P850, DOI 10.1002/1531-8249(199912)46:6<850::AID-ANA7>3.0.CO
[5]  
2-Q
[6]   New and emerging treatment options for multiple sclerosis [J].
Polman, CH ;
Uitdehaag, BMJ .
LANCET NEUROLOGY, 2003, 2 (09) :563-566
[7]   Modelling MRI enhancing lesion counts in multiple sclerosis using a negative binomial model: implications for clinical trials [J].
Sormani, MP ;
Bruzzi, P ;
Miller, DH ;
Gasperini, C ;
Barkhof, F ;
Filippi, L .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 163 (01) :74-80
[8]  
Spiegelhalter DJ, 1999, WINBUGS VERSION 1 2
[9]   Characterization of MRI response to treatment with interferon beta-1b: Contrast-enhancing MRI lesion frequency as a primary outcome measure [J].
Stone, LA ;
Frank, JA ;
Albert, PS ;
Bash, CN ;
Calabresi, PA ;
Maloni, H ;
McFarland, HF .
NEUROLOGY, 1997, 49 (03) :862-869