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Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies
OBJECTIVE: To assess the effectiveness of glatiramer acetate (GA) compared to other multiple sclerosis (MS) therapies in routine clinical practice. MATERIALS AND METHODS: Observational cohort study carried out in MS patients treated with GA (GA cohort) or other MS therapies –switched from GA– (non-G...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467772/ https://www.ncbi.nlm.nih.gov/pubmed/26085963 http://dx.doi.org/10.1002/brb3.337 |
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author | Izquierdo, Guillermo García-Agua Soler, Nuria Rus, Macarena García-Ruiz, Antonio José |
author_facet | Izquierdo, Guillermo García-Agua Soler, Nuria Rus, Macarena García-Ruiz, Antonio José |
author_sort | Izquierdo, Guillermo |
collection | PubMed |
description | OBJECTIVE: To assess the effectiveness of glatiramer acetate (GA) compared to other multiple sclerosis (MS) therapies in routine clinical practice. MATERIALS AND METHODS: Observational cohort study carried out in MS patients treated with GA (GA cohort) or other MS therapies –switched from GA– (non-GA cohort). Study data were obtained through review of our MS patient database. The primary endpoint was the Expanded Disability Status Scale (EDSS) scores reached at the end of treatment/last check-up. RESULTS: A total of 180 patients were included: GA cohort n = 120, non-GA cohort n = 60. Patients in the GA cohort showed better EDSS scores at the end of treatment/last check-up (mean ± SD, 2.8 ± 1.8 vs. 3.9 ± 2.2; P = 0.001) and were 1.65 times more likely to show better EDSS scores compared to the non-GA cohort (odds ratio, 0.606; 95%CI, 0.436–0.843; P = 0.003). Patients in the GA cohort showed longer mean time to reach EDSS scores of 6 (209.1 [95%CI, 187.6–230.6] vs. 164.3 [95%CI, 137.0–191.6] months; P = 0.004) and slower disability progression (hazard ratio, 0.415 [95%CI, 0.286–0.603]; P < 0.001). The annualized relapse rate was lower in the GA cohort (mean ± SD, 0.5 ± 0.5 vs. 0.8 ± 0.5; P = 0.001) and patients’ quality of life was improved in this study cohort compared to the non-GA cohort (mean ± SD, 0.7 ± 0.1 vs. 0.6 ± 0.2; P = 0.01). CONCLUSIONS: GA may slow down the progression of EDSS scores to a greater extent than other MS therapies, as well as achieving a greater reduction in relapses and a greater improvement in patients’ quality of life. Switching from GA to other MS therapies has not proved to entail a better response to treatment. |
format | Online Article Text |
id | pubmed-4467772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44677722015-06-17 Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies Izquierdo, Guillermo García-Agua Soler, Nuria Rus, Macarena García-Ruiz, Antonio José Brain Behav Original Research OBJECTIVE: To assess the effectiveness of glatiramer acetate (GA) compared to other multiple sclerosis (MS) therapies in routine clinical practice. MATERIALS AND METHODS: Observational cohort study carried out in MS patients treated with GA (GA cohort) or other MS therapies –switched from GA– (non-GA cohort). Study data were obtained through review of our MS patient database. The primary endpoint was the Expanded Disability Status Scale (EDSS) scores reached at the end of treatment/last check-up. RESULTS: A total of 180 patients were included: GA cohort n = 120, non-GA cohort n = 60. Patients in the GA cohort showed better EDSS scores at the end of treatment/last check-up (mean ± SD, 2.8 ± 1.8 vs. 3.9 ± 2.2; P = 0.001) and were 1.65 times more likely to show better EDSS scores compared to the non-GA cohort (odds ratio, 0.606; 95%CI, 0.436–0.843; P = 0.003). Patients in the GA cohort showed longer mean time to reach EDSS scores of 6 (209.1 [95%CI, 187.6–230.6] vs. 164.3 [95%CI, 137.0–191.6] months; P = 0.004) and slower disability progression (hazard ratio, 0.415 [95%CI, 0.286–0.603]; P < 0.001). The annualized relapse rate was lower in the GA cohort (mean ± SD, 0.5 ± 0.5 vs. 0.8 ± 0.5; P = 0.001) and patients’ quality of life was improved in this study cohort compared to the non-GA cohort (mean ± SD, 0.7 ± 0.1 vs. 0.6 ± 0.2; P = 0.01). CONCLUSIONS: GA may slow down the progression of EDSS scores to a greater extent than other MS therapies, as well as achieving a greater reduction in relapses and a greater improvement in patients’ quality of life. Switching from GA to other MS therapies has not proved to entail a better response to treatment. BlackWell Publishing Ltd 2015-06 2015-05-01 /pmc/articles/PMC4467772/ /pubmed/26085963 http://dx.doi.org/10.1002/brb3.337 Text en © 2015 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Izquierdo, Guillermo García-Agua Soler, Nuria Rus, Macarena García-Ruiz, Antonio José Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies |
title | Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies |
title_full | Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies |
title_fullStr | Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies |
title_full_unstemmed | Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies |
title_short | Effectiveness of glatiramer acetate compared to other multiple sclerosis therapies |
title_sort | effectiveness of glatiramer acetate compared to other multiple sclerosis therapies |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467772/ https://www.ncbi.nlm.nih.gov/pubmed/26085963 http://dx.doi.org/10.1002/brb3.337 |
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