Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22217
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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 A L-
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.date2019-11-25-
dc.date.accessioned2019-12-04T05:00:32Z-
dc.date.available2019-12-04T05:00:32Z-
dc.date.issued2020-12-
dc.identifier.citationMultiple Sclerosis 2020; 26(14): 1866-1876en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22217-
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); <12-month follow-up after last alemtuzumab course. 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.en_US
dc.language.isoeng-
dc.subjectAlemtuzumaben_US
dc.subjectefficacyen_US
dc.subjectmultiple sclerosisen_US
dc.subjectrelapseen_US
dc.subjectretreatmenten_US
dc.subjectsafetyen_US
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.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleMultiple sclerosis (Houndmills, Basingstoke, England)en_US
dc.identifier.affiliationDivision of Neurology, Department of Medicine, The University of British Columbia, Vancouver, BC, Canadaen_US
dc.identifier.affiliationDepartment of Neurology, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationMS Center for Innovations in Care, Missouri Baptist Medical Center, St Louis, MO, USAen_US
dc.identifier.affiliationUniv. Lille, INSERM U995, CHU Lille, FHU Imminent, F-59000 Lille, Franceen_US
dc.identifier.affiliationDepartment of Neurology, University of Münster, Münster, Germanyen_US
dc.identifier.affiliationCenter of Clinical Neuroscience, Carl Gustav Carus University Hospital, Dresden, Germanyen_US
dc.identifier.affiliationSanofi, Cambridge, MA, USAen_US
dc.identifier.affiliationDepartment of Neurology, University Vita-Salute San Raffaele, Milan, Italyen_US
dc.identifier.affiliationDepartment of Medicine, Amiri Hospital, Sharq, Kuwaiten_US
dc.identifier.affiliationOhioHealth Neurological Physicians, Columbus, OH, USAen_US
dc.identifier.affiliationNeurology Center of San Antonio, San Antonio, TX, USAen_US
dc.identifier.affiliationKeck School of Medicine, University of Southern California, Los Angeles, CA, USA/Regina Berkovich, MD, PhD, Inc., West Hollywood, CA, USAen_US
dc.identifier.affiliationInstituto de Investigación Biomédica de Málaga (IBIMA), Málaga, Spainen_US
dc.identifier.affiliationResearch Institute and Hospital, National Cancer Center, Goyang, South Koreaen_US
dc.identifier.affiliationKlinik für Neurologie und Palliativmedizin, Cologne, Germanyen_US
dc.identifier.affiliationInstitute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Swedenen_US
dc.identifier.affiliationNIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals, University of Sheffield, Sheffield, UKen_US
dc.identifier.doi10.1177/1352458519888610en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-5436-5804en_US
dc.identifier.orcid0000-0002-7891-8466en_US
dc.identifier.orcid0000-0001-8799-8202en_US
dc.identifier.pubmedid31762387-
dc.type.austinJournal Article-
local.name.researcherMacdonell, Richard A L
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptNeurology-
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