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Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience

Teriflunomide is an oral disease-modifying therapy for relapsing–remitting multiple sclerosis patients. A decline in physical and cognitive functions, which negatively impacts their quality of life (QoL), is observed in relapsing–remitting multiple sclerosis patients. The aim of this study was to ch...

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Autores principales: Nunes, Carla Cecília, Abreu, Pedro, Correia, Filipe, Mendes, Irene, da Silva, Ana Martins
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363901/
https://www.ncbi.nlm.nih.gov/pubmed/37492519
http://dx.doi.org/10.1177/23982128231185290
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author Nunes, Carla Cecília
Abreu, Pedro
Correia, Filipe
Mendes, Irene
da Silva, Ana Martins
author_facet Nunes, Carla Cecília
Abreu, Pedro
Correia, Filipe
Mendes, Irene
da Silva, Ana Martins
author_sort Nunes, Carla Cecília
collection PubMed
description Teriflunomide is an oral disease-modifying therapy for relapsing–remitting multiple sclerosis patients. A decline in physical and cognitive functions, which negatively impacts their quality of life (QoL), is observed in relapsing–remitting multiple sclerosis patients. The aim of this study was to characterise adult Portuguese relapsing–remitting multiple sclerosis patients treated with teriflunomide in routine clinical practice concerning their quality of life, comorbidities, treatment effectiveness, satisfaction, compliance and safety. TeriLIVE-QoL was a multicentre, non-interventional, prospective cohort study that collected demographic and clinical characteristics, patient-reported outcomes and adverse events from patients treated with teriflunomide of 14 mg over 2 years. Notably, around 18 months of this period occurred during the COVID-19 pandemic. Of the 99 participants, 25% were treatment-naïve. Annualised relapse rate and the score for the Hospital Anxiety and Depression Scale decreased after 1 (p = 0.01) and 2 years of treatment (p < 0.001), respectively. Convenience (p = 0.001), effectiveness (p = 0.002) and global satisfaction scores (p < 0.001) presented high values (up to 95.6) and continued to improve along the study. Treatment persistence was 77%, and compliance reached 82% 2 years after initiation. Three patients experienced serious adverse events. TeriLIVE-QoL provides real-world evidence of clinical effectiveness, high treatment satisfaction, consistent safety and improved psychiatric outcomes, associated with elevated treatment persistence and compliance in patients treated with teriflunomide.iance reached 82% 2 years after initiation. Three patients experienced serious adverse events.
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spelling pubmed-103639012023-07-25 Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience Nunes, Carla Cecília Abreu, Pedro Correia, Filipe Mendes, Irene da Silva, Ana Martins Brain Neurosci Adv Research Paper Teriflunomide is an oral disease-modifying therapy for relapsing–remitting multiple sclerosis patients. A decline in physical and cognitive functions, which negatively impacts their quality of life (QoL), is observed in relapsing–remitting multiple sclerosis patients. The aim of this study was to characterise adult Portuguese relapsing–remitting multiple sclerosis patients treated with teriflunomide in routine clinical practice concerning their quality of life, comorbidities, treatment effectiveness, satisfaction, compliance and safety. TeriLIVE-QoL was a multicentre, non-interventional, prospective cohort study that collected demographic and clinical characteristics, patient-reported outcomes and adverse events from patients treated with teriflunomide of 14 mg over 2 years. Notably, around 18 months of this period occurred during the COVID-19 pandemic. Of the 99 participants, 25% were treatment-naïve. Annualised relapse rate and the score for the Hospital Anxiety and Depression Scale decreased after 1 (p = 0.01) and 2 years of treatment (p < 0.001), respectively. Convenience (p = 0.001), effectiveness (p = 0.002) and global satisfaction scores (p < 0.001) presented high values (up to 95.6) and continued to improve along the study. Treatment persistence was 77%, and compliance reached 82% 2 years after initiation. Three patients experienced serious adverse events. TeriLIVE-QoL provides real-world evidence of clinical effectiveness, high treatment satisfaction, consistent safety and improved psychiatric outcomes, associated with elevated treatment persistence and compliance in patients treated with teriflunomide.iance reached 82% 2 years after initiation. Three patients experienced serious adverse events. SAGE Publications 2023-07-21 /pmc/articles/PMC10363901/ /pubmed/37492519 http://dx.doi.org/10.1177/23982128231185290 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Paper
Nunes, Carla Cecília
Abreu, Pedro
Correia, Filipe
Mendes, Irene
da Silva, Ana Martins
Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience
title Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience
title_full Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience
title_fullStr Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience
title_full_unstemmed Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience
title_short Teriflunomide treatment outcomes in multiple sclerosis: A Portuguese real-life experience
title_sort teriflunomide treatment outcomes in multiple sclerosis: a portuguese real-life experience
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363901/
https://www.ncbi.nlm.nih.gov/pubmed/37492519
http://dx.doi.org/10.1177/23982128231185290
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