Best Practices for Long-Term Monitoring and Follow-Up of Alemtuzumab-Treated MS Patients in Real-World Clinical Settings.

alemtuzumab anti-CD52 monoclonal antibody autoimmune events best practices disease-modifying therapy monitoring real-world settings relapsing-remitting multiple sclerosis

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2019
Historique:
received: 06 09 2018
accepted: 25 02 2019
entrez: 11 4 2019
pubmed: 11 4 2019
medline: 11 4 2019
Statut: epublish

Résumé

Multiple sclerosis (MS) is a chronic autoimmune neurological disease that typically affects young adults, causing irreversible physical disability and cognitive impairment. Alemtuzumab, administered intravenously as 2 initial courses of 12 mg/day (5 consecutive days at baseline, and 3 consecutive days 12 months later), resulted in significantly greater improvements in clinical and MRI outcomes vs. subcutaneous interferon beta-1a over 2 years in patients with active relapsing-remitting MS (RRMS) who were either treatment-naive (CARE-MS I; NCT00530348) or had an inadequate response to prior therapy (CARE-MS II; NCT00548405). Efficacy with alemtuzumab was maintained over 7 years in subsequent extension studies (NCT00930553; NCT02255656), in the absence of continuous treatment and with a consistent safety profile. There is an increased incidence of autoimmune events in patients treated with alemtuzumab (mainly thyroid events, but also immune thrombocytopenia and nephropathy), which imparts a need for mandatory safety monitoring for 4 years following the last treatment. The risk management strategy for alemtuzumab-treated patients includes laboratory monitoring and a comprehensive patient education and support program that enables early detection and effective management of autoimmune events, yielding optimal outcomes for MS patients. Here we provide an overview of tools and techniques that have been implemented in real-world clinical settings to reduce the burden of monitoring for both patients and healthcare providers, including customized educational materials, the use of social media, and interactive online databases for managing healthcare data. Many practices are also enhancing patient outreach efforts through coordination with specialized nursing services and ancillary caregivers. The best practice recommendations for safety monitoring described in this article, based on experiences in real-world clinical settings, may enable early detection and management of autoimmune events, and help with implementation of monitoring requirements while maximizing the benefits of alemtuzumab treatment for MS patients.

Identifiants

pubmed: 30967831
doi: 10.3389/fneur.2019.00253
pmc: PMC6439479
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

253

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Auteurs

Krista Barclay (K)

Vancouver Coastal Health, Vancouver, BC, Canada.

Robert Carruthers (R)

University of British Columbia, Vancouver, BC, Canada.

Anthony Traboulsee (A)

University of British Columbia, Vancouver, BC, Canada.

Ann D Bass (AD)

Neurology Center of San Antonio, San Antonio, TX, United States.

Christopher LaGanke (C)

North Central Neurology Associates, Cullman, AL, United States.

Antonio Bertolotto (A)

Azienda Ospedaliero Universitaria San Luigi, Orbassano, Italy.

Aaron Boster (A)

OhioHealth Neurological Physicians, Columbus, OH, United States.

Elisabeth G Celius (EG)

Oslo University Hospital Ullevål and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Jérôme de Seze (J)

Clinical Research Center (CIC), INSERM 1434, Strasbourg University, Strasbourg, France.

Dionisio Dela Cruz (DD)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Mario Habek (M)

University of Zagreb, School of Medicine and University Medical Center, Zagreb, Croatia.

Jong-Mi Lee (JM)

Stanford Healthcare, Palo Alto, CA, United States.

Volker Limmroth (V)

Klinik für Neurologie und Palliativmedizin, Cologne, Germany.

Sven G Meuth (SG)

Clinic of Neurology with Institute of Translational Neurology, University Hospital Müenster, Müenster, Germany.

Celia Oreja-Guevara (C)

El Instituto de Investigación Sanitaria del Hospital Clínico San Carlos, Hospital Clínico San Carlos, Madrid, Spain.

Patricia Pagnotta (P)

Neurology Associates, Maitland, FL, United States.

Cindy Vos (C)

Revalidatie & MS Centrum, Overpelt, Belgium.

Tjalf Ziemssen (T)

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

Darren P Baker (DP)

Sanofi, Cambridge, MA, United States.

Bart Van Wijmeersch (BV)

Rehabilitation & MS-Centre Overpelt, Hasselt University, Hasselt, Belgium.

Classifications MeSH