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.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 26 11 2019
medline: 25 9 2021
entrez: 26 11 2019
Statut: ppublish

Résumé

Alemtuzumab 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 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.

Sections du résumé

BACKGROUND
Alemtuzumab is given as two annual courses. Patients with continued disease activity may receive as-needed additional courses.
OBJECTIVE
To evaluate efficacy and safety of additional alemtuzumab courses in the CARE-MS (Comparison of Alemtuzumab and Rebif
METHODS
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.
RESULTS
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.
CONCLUSION
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.

Identifiants

pubmed: 31762387
doi: 10.1177/1352458519888610
pmc: PMC7720359
doi:

Substances chimiques

Alemtuzumab 3A189DH42V
Interferon beta-1a XRO4566Q4R

Banques de données

ClinicalTrials.gov
['NCT00530348', 'NCT00548405', 'NCT00930553', 'NCT02255656']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1866-1876

Investigateurs

Darren P Baker (DP)
Ericka M Bueno (EM)
Colin Mitchell (C)
Rebecca L Orndorff (RL)
Valerie P Zediak (VP)

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Auteurs

Giancarlo Comi (G)

Department of Neurology, University Vita-Salute San Raffaele, Milan, Italy.

Raed Alroughani (R)

Department of Medicine, Amiri Hospital, Sharq, Kuwait.

Aaron L Boster (AL)

OhioHealth Neurological Physicians, Columbus, OH, USA.

Ann D Bass (AD)

Neurology Center of San Antonio, San Antonio, TX, USA.

Regina Berkovich (R)

Keck School of Medicine, University of Southern California, Los Angeles, CA, USA/Regina Berkovich, MD, PhD, Inc., West Hollywood, CA, USA.

Óscar Fernández (Ó)

Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, Spain.

Ho Jin Kim (HJ)

Research Institute and Hospital, National Cancer Center, Goyang, South Korea.

Volker Limmroth (V)

Klinik für Neurologie und Palliativmedizin, Cologne, Germany.

Jan Lycke (J)

Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.

Richard Al Macdonell (RA)

Department of Neurology, Austin Health and Florey Institute of Neuroscience and Mental Health, Melbourne, VIC, Australia.

Basil Sharrack (B)

NIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals, University of Sheffield, Sheffield, UK.

Barry A Singer (BA)

MS Center for Innovations in Care, Missouri Baptist Medical Center, St Louis, MO, USA.

Patrick Vermersch (P)

Univ. Lille, INSERM U995, CHU Lille, FHU Imminent, F-59000 Lille, France.

Heinz Wiendl (H)

Department of Neurology, University of Münster, Münster, Germany.

Tjalf Ziemssen (T)

Center of Clinical Neuroscience, Carl Gustav Carus University Hospital, Dresden, Germany.

Alan Jacobs (A)

Sanofi, Cambridge, MA, USA.

Nadia Daizadeh (N)

Sanofi, Cambridge, MA, USA.

Claudio E Rodriguez (CE)

Sanofi, Cambridge, MA, USA.

Anthony Traboulsee (A)

Division of Neurology, Department of Medicine, The University of British Columbia, Vancouver, BC, Canada.

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Classifications MeSH