Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26803
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dc.contributor.authorHunter, Samuel F-
dc.contributor.authorAburashed, Rany A-
dc.contributor.authorAlroughani, Raed-
dc.contributor.authorChan, Andrew-
dc.contributor.authorDive, Dominique-
dc.contributor.authorEichau, Sara-
dc.contributor.authorKantor, Daniel-
dc.contributor.authorKim, Ho Jin-
dc.contributor.authorLycke, Jan-
dc.contributor.authorMacdonell, Richard A L-
dc.contributor.authorPozzilli, Carlo-
dc.contributor.authorScott, Thomas-
dc.contributor.authorSharrack, Basil-
dc.contributor.authorWiendl, Heinz-
dc.contributor.authorChung, Luke-
dc.contributor.authorDaizadeh, Nadia-
dc.contributor.authorBaker, Darren P-
dc.contributor.authorVermersch, Patrick-
dc.date2021-
dc.date.accessioned2021-06-28T06:12:05Z-
dc.date.available2021-06-28T06:12:05Z-
dc.date.issued2021-06-24-
dc.identifier.citationNeurology and Therapy 2021; online first: 24 Juneen
dc.identifier.issn2193-8253
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26803-
dc.description.abstractIn the 2-year CARE-MS trials (NCT00530348; NCT00548405) in patients with relapsing-remitting multiple sclerosis, alemtuzumab showed superior efficacy versus subcutaneous interferon beta-1a. Efficacy was maintained in two consecutive extensions (NCT00930553; NCT02255656). This post hoc analysis compared disability outcomes over 9 years among alemtuzumab-treated patients according to whether they experienced confirmed disability improvement (CDI) or worsening (CDW) or neither CDI nor CDW. CARE-MS patients were randomized to receive two alemtuzumab courses (12 mg/day; 5 days at baseline; 3 days at 12 months), with additional as-needed 3-day courses in the extensions. CDI or CDW were defined as ≥ 1.0-point decrease or increase, respectively, in Expanded Disability Status Scale (EDSS) score from core study baseline confirmed over 6 months, assessed in patients with baseline EDSS score ≥ 2.0. Improved or stable EDSS scores were defined as ≥ 1-point decrease or ≤ 0.5-point change (either direction), respectively, from core study baseline. Functional systems (FS) scores were also assessed. Of 511 eligible patients, 43% experienced CDI and 34% experienced CDW at any time through year 9 (patients experiencing both CDI and CDW were counted in each individual group); 29% experienced neither CDI nor CDW. At year 9, patients with CDI had a -0.58-point mean EDSS score change from baseline; 88% had stable or improved EDSS scores. Improvements occurred across all FS, primarily in sensory, pyramidal, and cerebellar domains. Patients with CDW had a +1.71-point mean EDSS score change; 16% had stable or improved EDSS scores. Patients with neither CDI nor CDW had a -0.10-point mean EDSS score change; 98% had stable or improved EDSS scores. CDI achievement at any point during the CARE-MS studies was associated with improved disability at year 9, highlighting the potential of alemtuzumab to change the multiple sclerosis course. Conversely, CDW at any point was associated with worsened disability at year 9.en
dc.language.isoeng
dc.subjectAlemtuzumaben
dc.subjectConfirmed disability improvementen
dc.subjectConfirmed disability worseningen
dc.subjectDisease-modifying therapyen
dc.subjectExpanded Disability Status Scaleen
dc.subjectFunctional systemsen
dc.subjectMultiple sclerosisen
dc.titleConfirmed 6-Month Disability Improvement and Worsening Correlate with Long-term Disability Outcomes in Alemtuzumab-Treated Patients with Multiple Sclerosis: Post Hoc Analysis of the CARE-MS Studies.en
dc.typeJournal Articleen
dc.identifier.journaltitleNeurology and Therapyen
dc.identifier.affiliationUniv. Lille, INSERM U1172 LilNCog, CHU Lille, FHU Precise, Lille, Franceen
dc.identifier.affiliationPenn Center for Global Health, Philadelphia, PA, USAen
dc.identifier.affiliationDepartment of Human Neuroscience, Sapienza University, Rome, Italyen
dc.identifier.affiliationAllegheny General Hospital, Drexel University College of Medicine, Pittsburgh, PA, USAen
dc.identifier.affiliationSanofi, Cambridge, MA, USAen
dc.identifier.affiliationUniversity of Münster, Münster, Germanyen
dc.identifier.affiliationResearch Institute and Hospital of National Cancer Center, Goyang, Koreaen
dc.identifier.affiliationAdvanced Neurosciences Institute, 101 Forrest Crossing Blvd., Franklin, TN, 37064, USAen
dc.identifier.affiliationInstitute for Neurosciences and Multiple Sclerosis, Owosso, MI, USAen
dc.identifier.affiliationSheffield NIHR Neuroscience BRC and Sheffield Teaching Hospitals, Sheffield, UKen
dc.identifier.affiliationDepartment of Neurology, Inselspital Bern, Bern University Hospital, University of Bern, Bern, Switzerlanden
dc.identifier.affiliationFlorida Atlantic University, Boca Raton, FL, USAen
dc.identifier.affiliationNova Southeastern University, Fort Lauderdale, FL, USAen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen
dc.identifier.affiliationDivision of Neurology, Department of Medicine, Amiri Hospital, Sharq, Kuwait..en
dc.identifier.affiliationUniversity Hospital Centre of Liège, Liège, Belgium..en
dc.identifier.affiliationHospital Universitario Virgen Macarena, Seville, Spain..en
dc.identifier.affiliationDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology at Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden..en
dc.identifier.affiliationNeurologyen
dc.identifier.doi10.1007/s40120-021-00262-3en
dc.type.contentTexten
dc.identifier.orcid0000-0002-0542-1176en
dc.identifier.pubmedid34165694
local.name.researcherMacdonell, Richard A L
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptNeurology-
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