dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Jones, Joanne |
dc.contributor.author | Vermersch, Patrick |
dc.contributor.author | Bass, Ann D |
dc.contributor.author | Boster, Aaron |
dc.contributor.author | Montalban Gairín, Xavier |
dc.contributor.author | Coles, Alasdair |
dc.contributor.author | Traboulsee, Anthony |
dc.date.accessioned | 2022-06-09T07:23:29Z |
dc.date.available | 2022-06-09T07:23:29Z |
dc.date.issued | 2022-04-01 |
dc.identifier.citation | Coles AJ, Jones JL, Vermersch P, Traboulsee A, Bass AD, Boster A, et al. Autoimmunity and long-term safety and efficacy of alemtuzumab for multiple sclerosis: Benefit/risk following review of trial and post-marketing data. Mult Scler J. 2022 Apr 1;28(5):842–846. |
dc.identifier.issn | 1477-0970 |
dc.identifier.uri | https://hdl.handle.net/11351/7650 |
dc.description | Alemtuzumab; Product surveillance; Risk assessment |
dc.description.abstract | Does preexisting or treatment-emergent autoimmunity increase the risk of subsequent autoimmune disease in individuals with relapsing-remitting multiple sclerosis (MS) after alemtuzumab? In the extended phase 2/3 trials, 34/96 (35.4%) patients with and 395/1120 (35.3%) without preexisting autoimmunity developed non-MS autoimmunity. Thyroid autoimmunity after alemtuzumab courses 1 or 2 did not increase subsequent non-thyroid autoimmune adverse events. Therefore, autoimmune disease before or after alemtuzumab treatment does not predict autoimmunity after further courses, so should not preclude adequate alemtuzumab dosing to control MS. Finally, post-marketing safety data contribute toward a full record of the alemtuzumab benefit/risk profile for the MS field. |
dc.language.iso | eng |
dc.publisher | SAGE Publications |
dc.relation.ispartofseries | Multiple Sclerosis Journal;28(5) |
dc.rights | Attribution-NonCommercial 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ |
dc.source | Scientia |
dc.subject | Esclerosi múltiple - Tractament |
dc.subject | Avaluació de resultats (Assistència sanitària) |
dc.subject | Autoimmunitat |
dc.subject.mesh | Multiple Sclerosis |
dc.subject.mesh | /drug therapy |
dc.subject.mesh | Autoimmunity |
dc.subject.mesh | Treatment Outcome |
dc.title | Autoimmunity and long-term safety and efficacy of alemtuzumab for multiple sclerosis: Benefit/risk following review of trial and post-marketing data |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.1177/13524585211061335 |
dc.subject.decs | esclerosis múltiple |
dc.subject.decs | /farmacoterapia |
dc.subject.decs | autoinmunidad |
dc.subject.decs | resultado del tratamiento |
dc.relation.publishversion | https://doi.org/10.1177/13524585211061335 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [Coles AJ, Jones JL] Department of Clinical Neuroscience, School of Medicine, University of Cambridge, Cambridge, UK. [Vermersch P] Univ. Lille, INSERM UMR-S1172—Lille Neuroscience et Cognition, CHU Lille, FHU Precise, Lille, France. [Traboulsee A] The University of British Columbia, Vancouver, BC, Canada. [Bass AD] Neurology Center of San Antonio, San Antonio, TX, USA. [Boster A] Boster MS Center, Columbus, OH, USA. [Montalban X] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain |
dc.identifier.pmid | 34882037 |
dc.identifier.wos | 000729548200001 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |