Publication:
Efficacy of alemtuzumab in relapsing-remitting MS patients who received additional courses after the initial two courses: Pooled analysis of the CARE-MS, extension, and TOPAZ studies.

dc.contributor.authorComi, Giancarlo
dc.contributor.authorAlroughani, Raed
dc.contributor.authorBoster, Aaron L
dc.contributor.authorBass, Ann D
dc.contributor.authorBerkovich, Regina
dc.contributor.authorFernández, Óscar
dc.contributor.authorKim, Ho Jin
dc.contributor.authorLimmroth, Volker
dc.contributor.authorLycke, Jan
dc.contributor.authorMacdonell, Richard Al
dc.contributor.authorSharrack, Basil
dc.contributor.authorSinger, Barry A
dc.contributor.authorVermersch, Patrick
dc.contributor.authorWiendl, Heinz
dc.contributor.authorZiemssen, Tjalf
dc.contributor.authorJacobs, Alan
dc.contributor.authorDaizadeh, Nadia
dc.contributor.authorRodriguez, Claudio E
dc.contributor.authorTraboulsee, Anthony
dc.contributor.authorCARE-MS I, CARE-MS II, CAMMS03409, and TOPAZ Investigators
dc.date.accessioned2024-02-10T20:02:33Z
dc.date.available2024-02-10T20:02:33Z
dc.date.issued2019-11-25
dc.description.abstractAlemtuzumab is given as two annual courses. Patients with continued disease activity may receive as-needed additional courses. To evaluate efficacy and safety of additional alemtuzumab courses in the CARE-MS (Comparison of Alemtuzumab and Rebif® Efficacy in Multiple Sclerosis) studies and their extensions. Subgroups were based on the number of additional alemtuzumab courses received. Exclusion criteria: other disease-modifying therapy (DMT); In the additional-courses groups, Courses 3 and 4 reduced annualized relapse rate (12 months before: 0.73 and 0.74, respectively; 12 months after: 0.07 and 0.08). For 36 months after Courses 3 and 4, 89% and 92% of patients were free of 6-month confirmed disability worsening, respectively, with 20% and 26% achieving 6-month confirmed disability improvement. Freedom from magnetic resonance imaging (MRI) disease activity increased after Courses 3 and 4 (12 months before: 43% and 53%, respectively; 12 months after: 73% and 74%). Safety was similar across groups; serious events occurred irrespective of the number of courses. Additional alemtuzumab courses significantly improved outcomes, without increased safety risks, in CARE-MS patients with continued disease activity after Course 2. How this compares to outcomes if treatment is switched to another DMT instead remains unknown.
dc.format.number14es_ES
dc.format.page1866-1876es_ES
dc.format.volume26es_ES
dc.identifier.doi10.1177/1352458519888610
dc.identifier.e-issn1477-0970es_ES
dc.identifier.journalMultiple sclerosis (Houndmills, Basingstoke, England)es_ES
dc.identifier.otherhttp://hdl.handle.net/10668/14739
dc.identifier.pubmedID31762387es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17936
dc.language.isoeng
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectAlemtuzumab
dc.subjectEfficacy
dc.subjectMultiple sclerosis
dc.subjectRelapse
dc.subjectRetreatment
dc.subjectsafety
dc.subject.meshAlemtuzumab
dc.subject.meshHumans
dc.subject.meshInterferon beta-1a
dc.subject.meshMultiple Sclerosis
dc.subject.meshMultiple Sclerosis, Relapsing-Remitting
dc.subject.meshRecurrence
dc.titleEfficacy of alemtuzumab in relapsing-remitting MS patients who received additional courses after the initial two courses: Pooled analysis of the CARE-MS, extension, and TOPAZ studies.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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