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Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis
Patients with highly active relapsing-remitting multiple sclerosis (RRMS) are at greater risk for disease progression and may respond differently to MS therapeutics than those with less active disease. The current post hoc analysis evaluated the effects of daclizumab high-yield process (DAC HYP) vs....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915085/ https://www.ncbi.nlm.nih.gov/pubmed/24375015 http://dx.doi.org/10.1007/s00415-013-7196-4 |
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author | Giovannoni, Gavin Radue, Ernst-Wilhelm Havrdova, Eva Riester, Katherine Greenberg, Steven Mehta, Lahar Elkins, Jacob |
author_facet | Giovannoni, Gavin Radue, Ernst-Wilhelm Havrdova, Eva Riester, Katherine Greenberg, Steven Mehta, Lahar Elkins, Jacob |
author_sort | Giovannoni, Gavin |
collection | PubMed |
description | Patients with highly active relapsing-remitting multiple sclerosis (RRMS) are at greater risk for disease progression and may respond differently to MS therapeutics than those with less active disease. The current post hoc analysis evaluated the effects of daclizumab high-yield process (DAC HYP) vs. placebo in patients with highly active RRMS in the SELECT study. Highly active RRMS was defined as patients with ≥2 relapses in the year before randomization and ≥1 gadolinium-enhancing (Gd(+)) lesion at baseline. Because results were similar in the DAC HYP dose groups, data from the DAC HYP arms were pooled for analysis. Treatment with DAC HYP resulted in similar effects in highly active (n = 88) and less active (n = 506) RRMS patients. DAC HYP reduced the annualized relapse rate by 50 % and 51 % in the highly active (p = 0.0394) and less active (p < 0.0001) groups vs. placebo, respectively (interaction p = 0.82). DAC HYP reduced new/newly-enlarging T2 lesions (highly active RRMS 76 % reduction, p < 0.0001; less active RRMS 73 % reduction, p < 0.0001; interaction p = 0.18), the risk of having more Gd(+) lesions (highly active RRMS 89 % reduction, p < 0.0001; less active RRMS 86 % reduction, p < 0.0001; interaction p = 0.46), and sustained disability progression (highly active RRMS 88 % reduction, p = 0.0574; less active RRMS 46 % reduction, p = 0.0383; interaction p = 0.22) vs. placebo. DAC HYP efficacy was similar across the spectrum of MS disease activity as assessed prior to treatment initiation. |
format | Online Article Text |
id | pubmed-3915085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-39150852014-02-10 Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis Giovannoni, Gavin Radue, Ernst-Wilhelm Havrdova, Eva Riester, Katherine Greenberg, Steven Mehta, Lahar Elkins, Jacob J Neurol Original Communication Patients with highly active relapsing-remitting multiple sclerosis (RRMS) are at greater risk for disease progression and may respond differently to MS therapeutics than those with less active disease. The current post hoc analysis evaluated the effects of daclizumab high-yield process (DAC HYP) vs. placebo in patients with highly active RRMS in the SELECT study. Highly active RRMS was defined as patients with ≥2 relapses in the year before randomization and ≥1 gadolinium-enhancing (Gd(+)) lesion at baseline. Because results were similar in the DAC HYP dose groups, data from the DAC HYP arms were pooled for analysis. Treatment with DAC HYP resulted in similar effects in highly active (n = 88) and less active (n = 506) RRMS patients. DAC HYP reduced the annualized relapse rate by 50 % and 51 % in the highly active (p = 0.0394) and less active (p < 0.0001) groups vs. placebo, respectively (interaction p = 0.82). DAC HYP reduced new/newly-enlarging T2 lesions (highly active RRMS 76 % reduction, p < 0.0001; less active RRMS 73 % reduction, p < 0.0001; interaction p = 0.18), the risk of having more Gd(+) lesions (highly active RRMS 89 % reduction, p < 0.0001; less active RRMS 86 % reduction, p < 0.0001; interaction p = 0.46), and sustained disability progression (highly active RRMS 88 % reduction, p = 0.0574; less active RRMS 46 % reduction, p = 0.0383; interaction p = 0.22) vs. placebo. DAC HYP efficacy was similar across the spectrum of MS disease activity as assessed prior to treatment initiation. Springer Berlin Heidelberg 2013-12-29 2014 /pmc/articles/PMC3915085/ /pubmed/24375015 http://dx.doi.org/10.1007/s00415-013-7196-4 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Communication Giovannoni, Gavin Radue, Ernst-Wilhelm Havrdova, Eva Riester, Katherine Greenberg, Steven Mehta, Lahar Elkins, Jacob Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis |
title | Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis |
title_full | Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis |
title_fullStr | Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis |
title_full_unstemmed | Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis |
title_short | Effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis |
title_sort | effect of daclizumab high-yield process in patients with highly active relapsing-remitting multiple sclerosis |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915085/ https://www.ncbi.nlm.nih.gov/pubmed/24375015 http://dx.doi.org/10.1007/s00415-013-7196-4 |
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