Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus.
Catherine Marie LambertBenedicte DuboisDominique DiveAndreas LysandropoulosDominik SelleslagLudo VanopdenboschVincent Van PeschBart VanwijmeerschAnn JanssensPublished in: Acta neurologica Belgica (2018)
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.
Keyphrases
- multiple sclerosis
- monoclonal antibody
- white matter
- randomized controlled trial
- emergency department
- primary care
- healthcare
- end stage renal disease
- stem cells
- high resolution
- rheumatoid arthritis
- chronic kidney disease
- palliative care
- clinical practice
- ejection fraction
- photodynamic therapy
- study protocol
- peripheral blood
- open label
- fluorescence imaging
- smoking cessation
- peritoneal dialysis