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Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion

Multiple sclerosis (MS) is a chronic and progressive neurological disease that is characterized by neuroinflammation, demyelination and neurodegeneration occurring from the earliest phases of the disease and that may be underestimated. MS patients accumulate disability through relapse-associated wor...

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Autores principales: Filippi, Massimo, Amato, Maria Pia, Centonze, Diego, Gallo, Paolo, Gasperini, Claudio, Inglese, Matilde, Patti, Francesco, Pozzilli, Carlo, Preziosa, Paolo, Trojano, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489547/
https://www.ncbi.nlm.nih.gov/pubmed/35608658
http://dx.doi.org/10.1007/s00415-022-11193-w
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author Filippi, Massimo
Amato, Maria Pia
Centonze, Diego
Gallo, Paolo
Gasperini, Claudio
Inglese, Matilde
Patti, Francesco
Pozzilli, Carlo
Preziosa, Paolo
Trojano, Maria
author_facet Filippi, Massimo
Amato, Maria Pia
Centonze, Diego
Gallo, Paolo
Gasperini, Claudio
Inglese, Matilde
Patti, Francesco
Pozzilli, Carlo
Preziosa, Paolo
Trojano, Maria
author_sort Filippi, Massimo
collection PubMed
description Multiple sclerosis (MS) is a chronic and progressive neurological disease that is characterized by neuroinflammation, demyelination and neurodegeneration occurring from the earliest phases of the disease and that may be underestimated. MS patients accumulate disability through relapse-associated worsening or progression independent of relapse activity. Early intervention with high-efficacy disease-modifying therapies (HE-DMTs) may represent the best window of opportunity to delay irreversible central nervous system damage and MS-related disability progression by hindering underlying heterogeneous pathophysiological processes contributing to disability progression. In line with this, growing evidence suggests that early use of HE-DMTs is associated with a significant greater reduction not only of inflammatory activity (clinical relapses and new lesion formation at magnetic resonance imaging) but also of disease progression, in terms of accumulation of irreversible clinical disability and neurodegeneration compared to delayed HE-DMT use or escalation strategy. These beneficial effects seem to be associated with acceptable long-term safety risks, thus configuring this treatment approach as that with the most positive benefit/risk profile. Accordingly, it should be mandatory to treat people with MS early with HE-DMTs in case of prognostic factors suggestive of aggressive disease, and it may be advisable to offer an HE-DMT to MS patients early after diagnosis, taking into account drug safety profile, disease severity, clinical and/or radiological activity, and patient-related factors, including possible comorbidities, family planning, and patients’ preference in agreement with the EAN/ECTRIMS and AAN guidelines. Barriers for an early use of HE-DMTs include concerns for long-term safety, challenges in the management of treatment initiation and monitoring, negative MS patients’ preferences, restricted access to HE-DMTs according to guidelines and regulatory rules, and sustainability. However, these barriers do not apply to each HE-DMT and none of these appear insuperable.
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spelling pubmed-94895472022-09-22 Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion Filippi, Massimo Amato, Maria Pia Centonze, Diego Gallo, Paolo Gasperini, Claudio Inglese, Matilde Patti, Francesco Pozzilli, Carlo Preziosa, Paolo Trojano, Maria J Neurol Original Communication Multiple sclerosis (MS) is a chronic and progressive neurological disease that is characterized by neuroinflammation, demyelination and neurodegeneration occurring from the earliest phases of the disease and that may be underestimated. MS patients accumulate disability through relapse-associated worsening or progression independent of relapse activity. Early intervention with high-efficacy disease-modifying therapies (HE-DMTs) may represent the best window of opportunity to delay irreversible central nervous system damage and MS-related disability progression by hindering underlying heterogeneous pathophysiological processes contributing to disability progression. In line with this, growing evidence suggests that early use of HE-DMTs is associated with a significant greater reduction not only of inflammatory activity (clinical relapses and new lesion formation at magnetic resonance imaging) but also of disease progression, in terms of accumulation of irreversible clinical disability and neurodegeneration compared to delayed HE-DMT use or escalation strategy. These beneficial effects seem to be associated with acceptable long-term safety risks, thus configuring this treatment approach as that with the most positive benefit/risk profile. Accordingly, it should be mandatory to treat people with MS early with HE-DMTs in case of prognostic factors suggestive of aggressive disease, and it may be advisable to offer an HE-DMT to MS patients early after diagnosis, taking into account drug safety profile, disease severity, clinical and/or radiological activity, and patient-related factors, including possible comorbidities, family planning, and patients’ preference in agreement with the EAN/ECTRIMS and AAN guidelines. Barriers for an early use of HE-DMTs include concerns for long-term safety, challenges in the management of treatment initiation and monitoring, negative MS patients’ preferences, restricted access to HE-DMTs according to guidelines and regulatory rules, and sustainability. However, these barriers do not apply to each HE-DMT and none of these appear insuperable. Springer Berlin Heidelberg 2022-05-24 2022 /pmc/articles/PMC9489547/ /pubmed/35608658 http://dx.doi.org/10.1007/s00415-022-11193-w Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Communication
Filippi, Massimo
Amato, Maria Pia
Centonze, Diego
Gallo, Paolo
Gasperini, Claudio
Inglese, Matilde
Patti, Francesco
Pozzilli, Carlo
Preziosa, Paolo
Trojano, Maria
Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion
title Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion
title_full Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion
title_fullStr Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion
title_full_unstemmed Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion
title_short Early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion
title_sort early use of high-efficacy disease‑modifying therapies makes the difference in people with multiple sclerosis: an expert opinion
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489547/
https://www.ncbi.nlm.nih.gov/pubmed/35608658
http://dx.doi.org/10.1007/s00415-022-11193-w
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