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Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus

Authors :
Andreas Lysandropoulos
Vincent Van Pesch
Catherine Lambert
Ludo Vanopdenbosch
Dominique Dive
Ann Janssens
Bart Vanwijmeersch
Bénédicte Dubois
Dominik Selleslag
UCL - SSS/IONS/CEMO - Pôle Cellulaire et moléculaire
UCL - SSS/IREC/SLUC - Pôle St.-Luc
UCL - (SLuc) Service d'hématologie
UCL - (SLuc) Service de neurologie
Source :
Acta neurologica Belgica, Vol. 118, no. 1, p. 7-11 (2018), Acta Neurologica Belgica
Publication Year :
2018
Publisher :
Springer Science and Business Media LLC, 2018.

Abstract

Alemtuzumab (Lemtrada) is a humanized monoclonal antibody indicated for the treatment of adult patients with relapsing-remitting multiple sclerosis with active disease defined by clinical or imaging features. Alemtuzumab demonstrated superior efficacy over active comparator in both treatment naive patients and those with inadequate response to prior therapy. Alemtuzumab is associated with a consistent and manageable safety and tolerability profile. Treatment with alemtuzumab for multiple sclerosis increases the risk for autoimmune adverse events including immune thrombocytopenia (ITP). Complete blood counts with differential should be obtained prior to initiation of treatment and at monthly intervals thereafter for 48 months after the last infusion. After this period of time, testing should be performed based on clinical findings suggestive of ITP. If ITP onset is confirmed, appropriate medical intervention should be promptly initiated, including immediate referral to a specialist. This paper presents the consensus of Belgian multiple sclerosis specialists and hematologists to guide the treating physician with practical recommendations. ispartof: Acta Neurologica Belgica vol:118 issue:1 pages:7-11 ispartof: location:Italy status: published

Details

ISSN :
22402993 and 03009009
Volume :
118
Database :
OpenAIRE
Journal :
Acta Neurologica Belgica
Accession number :
edsair.doi.dedup.....121faa467530e4cedc942a736979cc98
Full Text :
https://doi.org/10.1007/s13760-018-0882-3