De-escalating and discontinuing disease-modifying therapies in multiple sclerosis
The development of disease-modifying therapies (DMTs) for the treatment of multiple sclerosis (MS) has been highly successful in recent decades. It is now widely accepted that early initiation of DMTs after disease onset is associated with a better long-term prognosis. However, the question of when...
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creator | Androdias, Géraldine Lünemann, Jan D Maillart, Elisabeth Amato, Maria Pia Audoin, Bertrand Bruijstens, Arlette L Bsteh, Gabriel Butzkueven, Helmut Ciccarelli, Olga Cobo-Calvo, Alvaro Derfuss, Tobias Di Pauli, Franziska Edan, Gilles Enzinger, Christian Geraldes, Ruth Granziera, Cristina Hacohen, Yael Hartung, Hans-Peter Hynes, Sinéad Inglese, Matilde Kappos, Ludwig Kuusisto, Hanna Langer-Gould, Annette Magyari, Melinda Marignier, Romain Montalban, Xavier Mycko, Marcin P Nourbakhsh, Bardia Oh, Jiwon Oreja-Guevara, Celia Piehl, Fredrik Prosperini, Luca Sastre-Garriga, Jaume Sellebjerg, Finn Selmaj, Krzysztof Siva, Aksel Tallantyre, Emma van Pesch, Vincent Vukusic, Sandra Weinstock-Guttman, Bianca Zipp, Frauke Tintoré, Mar Iacobaeus, Ellen Stankoff, Bruno |
description | The development of disease-modifying therapies (DMTs) for the treatment of multiple sclerosis (MS) has been highly successful in recent decades. It is now widely accepted that early initiation of DMTs after disease onset is associated with a better long-term prognosis. However, the question of when and how to de-escalate or discontinue DMTs remains open and critical. This topic was discussed during an international focused workshop organized by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) in 2023. The aim was to review the current evidence on the rationale for, but also the potential pitfalls of, treatment de-escalation in MS. Several clinical scenarios emerged, mainly driven by a change in the benefit-risk ratio of DMTs over the course of the disease and with aging. The workshop also addressed the issue of de-escalation by the type of DMT used and in specific situations including pregnancy and paediatric onset MS. Finally, we provide practical guidelines for selecting appropriate patients, defining de-escalation and monitoring modalities, and outline unmet needs in this field. |
doi_str_mv | 10.1093/brain/awae409 |
format | Article |
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It is now widely accepted that early initiation of DMTs after disease onset is associated with a better long-term prognosis. However, the question of when and how to de-escalate or discontinue DMTs remains open and critical. This topic was discussed during an international focused workshop organized by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) in 2023. The aim was to review the current evidence on the rationale for, but also the potential pitfalls of, treatment de-escalation in MS. Several clinical scenarios emerged, mainly driven by a change in the benefit-risk ratio of DMTs over the course of the disease and with aging. The workshop also addressed the issue of de-escalation by the type of DMT used and in specific situations including pregnancy and paediatric onset MS. Finally, we provide practical guidelines for selecting appropriate patients, defining de-escalation and monitoring modalities, and outline unmet needs in this field.</description><identifier>ISSN: 1460-2156</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/awae409</identifier><identifier>PMID: 39707906</identifier><language>eng</language><publisher>England</publisher><ispartof>Brain (London, England : 1878), 2024-12</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-8490-9657 ; 0000-0002-9631-4674 ; 0000-0002-3007-708X ; 0000-0002-1589-2254 ; 0000-0002-1231-1928 ; 0000-0002-2574-0721 ; 0009-0002-1016-0828 ; 0000-0002-4917-8761 ; 0000-0002-0825-0851 ; 0000-0002-7990-5894</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39707906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Androdias, Géraldine</creatorcontrib><creatorcontrib>Lünemann, Jan D</creatorcontrib><creatorcontrib>Maillart, Elisabeth</creatorcontrib><creatorcontrib>Amato, Maria Pia</creatorcontrib><creatorcontrib>Audoin, Bertrand</creatorcontrib><creatorcontrib>Bruijstens, Arlette L</creatorcontrib><creatorcontrib>Bsteh, Gabriel</creatorcontrib><creatorcontrib>Butzkueven, Helmut</creatorcontrib><creatorcontrib>Ciccarelli, Olga</creatorcontrib><creatorcontrib>Cobo-Calvo, Alvaro</creatorcontrib><creatorcontrib>Derfuss, Tobias</creatorcontrib><creatorcontrib>Di Pauli, Franziska</creatorcontrib><creatorcontrib>Edan, Gilles</creatorcontrib><creatorcontrib>Enzinger, Christian</creatorcontrib><creatorcontrib>Geraldes, Ruth</creatorcontrib><creatorcontrib>Granziera, Cristina</creatorcontrib><creatorcontrib>Hacohen, Yael</creatorcontrib><creatorcontrib>Hartung, Hans-Peter</creatorcontrib><creatorcontrib>Hynes, Sinéad</creatorcontrib><creatorcontrib>Inglese, Matilde</creatorcontrib><creatorcontrib>Kappos, Ludwig</creatorcontrib><creatorcontrib>Kuusisto, Hanna</creatorcontrib><creatorcontrib>Langer-Gould, Annette</creatorcontrib><creatorcontrib>Magyari, Melinda</creatorcontrib><creatorcontrib>Marignier, Romain</creatorcontrib><creatorcontrib>Montalban, Xavier</creatorcontrib><creatorcontrib>Mycko, Marcin P</creatorcontrib><creatorcontrib>Nourbakhsh, Bardia</creatorcontrib><creatorcontrib>Oh, Jiwon</creatorcontrib><creatorcontrib>Oreja-Guevara, Celia</creatorcontrib><creatorcontrib>Piehl, Fredrik</creatorcontrib><creatorcontrib>Prosperini, Luca</creatorcontrib><creatorcontrib>Sastre-Garriga, Jaume</creatorcontrib><creatorcontrib>Sellebjerg, Finn</creatorcontrib><creatorcontrib>Selmaj, Krzysztof</creatorcontrib><creatorcontrib>Siva, Aksel</creatorcontrib><creatorcontrib>Tallantyre, Emma</creatorcontrib><creatorcontrib>van Pesch, Vincent</creatorcontrib><creatorcontrib>Vukusic, Sandra</creatorcontrib><creatorcontrib>Weinstock-Guttman, Bianca</creatorcontrib><creatorcontrib>Zipp, Frauke</creatorcontrib><creatorcontrib>Tintoré, Mar</creatorcontrib><creatorcontrib>Iacobaeus, Ellen</creatorcontrib><creatorcontrib>Stankoff, Bruno</creatorcontrib><title>De-escalating and discontinuing disease-modifying therapies in multiple sclerosis</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>The development of disease-modifying therapies (DMTs) for the treatment of multiple sclerosis (MS) has been highly successful in recent decades. 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It is now widely accepted that early initiation of DMTs after disease onset is associated with a better long-term prognosis. However, the question of when and how to de-escalate or discontinue DMTs remains open and critical. This topic was discussed during an international focused workshop organized by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) in 2023. The aim was to review the current evidence on the rationale for, but also the potential pitfalls of, treatment de-escalation in MS. Several clinical scenarios emerged, mainly driven by a change in the benefit-risk ratio of DMTs over the course of the disease and with aging. The workshop also addressed the issue of de-escalation by the type of DMT used and in specific situations including pregnancy and paediatric onset MS. 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title | De-escalating and discontinuing disease-modifying therapies in multiple sclerosis |
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