Efficacy of alemtuzumab over 6 years in relapsing-remitting multiple sclerosis patients who relapsed between courses 1 and 2: Post hoc analysis of the CARE-MS studies.
Mult Scler. 2020 11; 26(13):1719-1728.MS

Abstract

BACKGROUND

Alemtuzumab is administered as two annual courses for relapsing-remitting multiple sclerosis (MS). Patients may relapse before completing the two-course regimen.

OBJECTIVE

The objective was to evaluate 6-year outcomes in patients who relapsed between alemtuzumab Courses 1 and 2 (early relapsers).

METHODS

Post hoc analysis of patients from the Comparison of Alemtuzumab and Rebif® Efficacy in Multiple Sclerosis (CARE-MS) studies who enrolled in the extension.

RESULTS

Early relapsers (CARE-MS I: 15%; CARE-MS II: 24%) had more relapses in 1-2 years pre-alemtuzumab and higher mean baseline Expanded Disability Status Scale score than patients without relapse. Their annualized relapse rate declined from Year 1 (CARE-MS I: 1.3; CARE-MS II: 1.2) to Year 2 following Course 2 (0.3; 0.5) and remained low thereafter. Over 6 years, 60% remained free of 6-month confirmed disability worsening; 24% (CARE-MS I) and 34% (CARE-MS II) achieved 6-month confirmed disability improvement. During Year 6, 69% (CARE-MS I) and 68% (CARE-MS II) were free of magnetic resonance imaging (MRI) disease activity. Median percent yearly brain volume loss (Year 1: -0.67% (CARE-MS I); -0.47% (CARE-MS II)) declined after Course 2 (Year 6: -0.24%; -0.13%).

CONCLUSION

Early relapsers' outcomes improved after completing the second alemtuzumab course. These findings support administering the approved two-course regimen to maximize clinical benefit.

CLINICALTRIALS.GOV REGISTRATION NUMBERS

CARE-MS I, II, extension: NCT00530348, NCT00548405, NCT00930553.

Links

Publisher Full Text
ncbi.nlm.nih.gov
journals.sagepub.com
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Authors+Show Affiliations

Van Wijmeersch B
Rehabilitation and MS Center Overpelt; BIOMED, Hasselt University, Hasselt, Belgium.
Singer BA
The MS Center for Innovations in Care, Missouri Baptist Medical Center, St Louis, MO, USA.
Boster A
OhioHealth Neurological Physicians, Columbus, OH, USA.
Broadley S
School of Medicine, Griffith University, Southport, QLD, Australia.
Fernández Ó
Fundación IMABIS, Hospital Universitario Carlos Haya, Málaga, Spain.
Freedman MS
University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Izquierdo G
Virgen Macarena University Hospital, Seville, Spain.
Lycke J
Institution of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Pozzilli C
Sapienza University of Rome, Rome, Italy.
Sharrack B
NIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals, University of Sheffield, Sheffield, UK.
Steingo B
Fort Lauderdale Multiple Sclerosis Center, Fort Lauderdale, FL, USA.
Wiendl H
University of Münster, Münster, Germany.
Wray S
Hope Neurology PLLC, Knoxville, TN, USA.
Ziemssen T
Center of Clinical Neuroscience, Carl Gustav Carus University Hospital, Dresden, Germany.
Chung L
Sanofi, Cambridge, MA, USA.
Margolin DH
Sanofi, Cambridge, MA, USA; Cerevance, Boston, MA, USA.
Thangavelu K
Sanofi, Cambridge, MA, USA; EMD Serono, Billerica, MA, USA.
Vermersch P
University of Lille, INSERM U995, CHU Lille, FHU Imminent, Lille, France.

Pub Type(s)

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

Language

eng

PubMed ID

31675266