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Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial
BACKGROUND: Natalizumab (NTZ) discontinuation leads to multiple sclerosis reactivation. The objective of this study is to compare disease activity in MS patients who continued on NTZ treatment to those who were switched to subcutaneous interferon 1b (IFNB) treatment. METHODS: 1-year randomized, rate...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750382/ https://www.ncbi.nlm.nih.gov/pubmed/23915113 http://dx.doi.org/10.1186/1471-2377-13-101 |
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author | Gobbi, Claudio Meier, Dominik S Cotton, François Sintzel, Martina Leppert, David Guttmann, Charles R G Zecca, Chiara |
author_facet | Gobbi, Claudio Meier, Dominik S Cotton, François Sintzel, Martina Leppert, David Guttmann, Charles R G Zecca, Chiara |
author_sort | Gobbi, Claudio |
collection | PubMed |
description | BACKGROUND: Natalizumab (NTZ) discontinuation leads to multiple sclerosis reactivation. The objective of this study is to compare disease activity in MS patients who continued on NTZ treatment to those who were switched to subcutaneous interferon 1b (IFNB) treatment. METHODS: 1-year randomized, rater-blinded, parallel-group, pilot study (ClinicalTrial.gov ID: NCT01144052). Relapsing remitting MS patients on NTZ for ≥12 months who had been free of disease activity on this therapy (no relapses and disability progression for ≥6 months, no gadolinium-enhancing lesions on baseline MRI) were randomized to NTZ or IFNB. Primary endpoint was time to first on-study relapse. Additional clinical, MRI and safety parameters were assessed. Analysis was based on intention to treat. RESULTS: 19 patients (NTZ n=10; IFNB n=9) with similar baseline characteristics were included. 78% of IFNB treated patients remained relapse free (NTZ group: 100%), and 25% remained free of new T2 lesions (NTZ group: 62.5%). While time to first on-study relapse was not significantly different between groups (p=0.125), many secondary clinical and radiological endpoints (number of relapses, proportion of relapse free patients, number of new T2 lesions) showed a trend, or were significant (new T2 lesions at month 6) in favoring NTZ. CONCLUSIONS: De-escalation therapy from NTZ to IFNB over 1 year was associated with some clinical and radiological disease recurrence. Overall no major safety concerns were observed. |
format | Online Article Text |
id | pubmed-3750382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37503822013-08-24 Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial Gobbi, Claudio Meier, Dominik S Cotton, François Sintzel, Martina Leppert, David Guttmann, Charles R G Zecca, Chiara BMC Neurol Research Article BACKGROUND: Natalizumab (NTZ) discontinuation leads to multiple sclerosis reactivation. The objective of this study is to compare disease activity in MS patients who continued on NTZ treatment to those who were switched to subcutaneous interferon 1b (IFNB) treatment. METHODS: 1-year randomized, rater-blinded, parallel-group, pilot study (ClinicalTrial.gov ID: NCT01144052). Relapsing remitting MS patients on NTZ for ≥12 months who had been free of disease activity on this therapy (no relapses and disability progression for ≥6 months, no gadolinium-enhancing lesions on baseline MRI) were randomized to NTZ or IFNB. Primary endpoint was time to first on-study relapse. Additional clinical, MRI and safety parameters were assessed. Analysis was based on intention to treat. RESULTS: 19 patients (NTZ n=10; IFNB n=9) with similar baseline characteristics were included. 78% of IFNB treated patients remained relapse free (NTZ group: 100%), and 25% remained free of new T2 lesions (NTZ group: 62.5%). While time to first on-study relapse was not significantly different between groups (p=0.125), many secondary clinical and radiological endpoints (number of relapses, proportion of relapse free patients, number of new T2 lesions) showed a trend, or were significant (new T2 lesions at month 6) in favoring NTZ. CONCLUSIONS: De-escalation therapy from NTZ to IFNB over 1 year was associated with some clinical and radiological disease recurrence. Overall no major safety concerns were observed. BioMed Central 2013-08-02 /pmc/articles/PMC3750382/ /pubmed/23915113 http://dx.doi.org/10.1186/1471-2377-13-101 Text en Copyright © 2013 Gobbi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gobbi, Claudio Meier, Dominik S Cotton, François Sintzel, Martina Leppert, David Guttmann, Charles R G Zecca, Chiara Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial |
title | Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial |
title_full | Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial |
title_fullStr | Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial |
title_full_unstemmed | Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial |
title_short | Interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial |
title_sort | interferon beta 1b following natalizumab discontinuation: one year, randomized, prospective, pilot trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750382/ https://www.ncbi.nlm.nih.gov/pubmed/23915113 http://dx.doi.org/10.1186/1471-2377-13-101 |
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