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Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study
In the Phase 3 DEFINE study, delayed-release dimethyl fumarate (DMF) 240 mg twice (BID) and three times daily (TID) significantly reduced the mean number of new or enlarging T2-hyperintense lesions and gadolinium-enhancing (Gd+) lesion activity at 2 years in patients (MRI cohort; n = 540) with relap...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155185/ https://www.ncbi.nlm.nih.gov/pubmed/24989666 http://dx.doi.org/10.1007/s00415-014-7412-x |
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author | Arnold, Douglas L. Gold, Ralf Kappos, Ludwig Bar-Or, Amit Giovannoni, Gavin Selmaj, Krzysztof Yang, Minhua Zhang, Ray Stephan, Monica Sheikh, Sarah I. Dawson, Katherine T. |
author_facet | Arnold, Douglas L. Gold, Ralf Kappos, Ludwig Bar-Or, Amit Giovannoni, Gavin Selmaj, Krzysztof Yang, Minhua Zhang, Ray Stephan, Monica Sheikh, Sarah I. Dawson, Katherine T. |
author_sort | Arnold, Douglas L. |
collection | PubMed |
description | In the Phase 3 DEFINE study, delayed-release dimethyl fumarate (DMF) 240 mg twice (BID) and three times daily (TID) significantly reduced the mean number of new or enlarging T2-hyperintense lesions and gadolinium-enhancing (Gd+) lesion activity at 2 years in patients (MRI cohort; n = 540) with relapsing–remitting MS. The analyses described here expand on these results by considering additional MRI measures (number of T1-hypointense lesions; volume of T2-hyperintense, Gd+, and T1-hypointense lesions; brain atrophy), delineating the time course of the effects, and examining the generality of the effects across a diverse patient population. Reductions in lesion counts with delayed-release DMF BID and TID, respectively, vs. placebo were apparent by the first MRI assessment at 6 months [T2-hyperintense: 80 and 69 % reduction (both P < 0.0001); Gd+, 94 and 81 % reduction (both P < 0.0001); T1-hypointense: 58 % (P < 0.0001) and 48 % (P = 0.0005) reduction] and maintained at 1 and 2 years. Reductions in lesion volume were statistically significant beginning at 6 months for T2-hyperintense [P = 0.0002 (BID) and P = 0.0035 (TID)] and Gd+ lesions [P = 0.0059 (BID) and P = 0.0176 (TID)] and beginning at 1 year [P = 0.0126 (BID)] to 2 years [P = 0.0063 (TID)] for T1-hypointense lesions. Relative reductions in brain atrophy from baseline to 2 years (21 % reduction; P = 0.0449) and 6 months to 2 years (30 % reduction; P = 0.0214) were statistically significant for delayed-release DMF BID. The effect of delayed-release DMF on mean number of new or enlarging T2-hyperintense lesions and Gd+ lesion activity was consistent across pre-specified patient subpopulations. Collectively, these results suggest that delayed-release DMF favorably affects multiple aspects of MS pathophysiology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00415-014-7412-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4155185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-41551852014-09-08 Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study Arnold, Douglas L. Gold, Ralf Kappos, Ludwig Bar-Or, Amit Giovannoni, Gavin Selmaj, Krzysztof Yang, Minhua Zhang, Ray Stephan, Monica Sheikh, Sarah I. Dawson, Katherine T. J Neurol Original Communication In the Phase 3 DEFINE study, delayed-release dimethyl fumarate (DMF) 240 mg twice (BID) and three times daily (TID) significantly reduced the mean number of new or enlarging T2-hyperintense lesions and gadolinium-enhancing (Gd+) lesion activity at 2 years in patients (MRI cohort; n = 540) with relapsing–remitting MS. The analyses described here expand on these results by considering additional MRI measures (number of T1-hypointense lesions; volume of T2-hyperintense, Gd+, and T1-hypointense lesions; brain atrophy), delineating the time course of the effects, and examining the generality of the effects across a diverse patient population. Reductions in lesion counts with delayed-release DMF BID and TID, respectively, vs. placebo were apparent by the first MRI assessment at 6 months [T2-hyperintense: 80 and 69 % reduction (both P < 0.0001); Gd+, 94 and 81 % reduction (both P < 0.0001); T1-hypointense: 58 % (P < 0.0001) and 48 % (P = 0.0005) reduction] and maintained at 1 and 2 years. Reductions in lesion volume were statistically significant beginning at 6 months for T2-hyperintense [P = 0.0002 (BID) and P = 0.0035 (TID)] and Gd+ lesions [P = 0.0059 (BID) and P = 0.0176 (TID)] and beginning at 1 year [P = 0.0126 (BID)] to 2 years [P = 0.0063 (TID)] for T1-hypointense lesions. Relative reductions in brain atrophy from baseline to 2 years (21 % reduction; P = 0.0449) and 6 months to 2 years (30 % reduction; P = 0.0214) were statistically significant for delayed-release DMF BID. The effect of delayed-release DMF on mean number of new or enlarging T2-hyperintense lesions and Gd+ lesion activity was consistent across pre-specified patient subpopulations. Collectively, these results suggest that delayed-release DMF favorably affects multiple aspects of MS pathophysiology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00415-014-7412-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-07-03 2014 /pmc/articles/PMC4155185/ /pubmed/24989666 http://dx.doi.org/10.1007/s00415-014-7412-x Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ 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 Arnold, Douglas L. Gold, Ralf Kappos, Ludwig Bar-Or, Amit Giovannoni, Gavin Selmaj, Krzysztof Yang, Minhua Zhang, Ray Stephan, Monica Sheikh, Sarah I. Dawson, Katherine T. Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study |
title | Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study |
title_full | Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study |
title_fullStr | Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study |
title_full_unstemmed | Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study |
title_short | Effects of delayed-release dimethyl fumarate on MRI measures in the Phase 3 DEFINE study |
title_sort | effects of delayed-release dimethyl fumarate on mri measures in the phase 3 define study |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155185/ https://www.ncbi.nlm.nih.gov/pubmed/24989666 http://dx.doi.org/10.1007/s00415-014-7412-x |
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