Autoimmunity and long-term safety and efficacy of alemtuzumab for multiple sclerosis: Benefit/risk following review of trial and post-marketing data.
Multiple sclerosis
alemtuzumab
autoimmunity
post-marketing
product surveillance
risk assessment
treatment outcome
Journal
Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185
Informations de publication
Date de publication:
04 2022
04 2022
Historique:
pubmed:
10
12
2021
medline:
6
4
2022
entrez:
9
12
2021
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 34882037
doi: 10.1177/13524585211061335
pmc: PMC8978465
doi:
Substances chimiques
Alemtuzumab
3A189DH42V
Banques de données
ClinicalTrials.gov
['NCT00050778', 'NCT00530348', 'NCT00548405', 'NCT00930553', 'NCT02255656']
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
842-846Références
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