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Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus
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 naiv...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857274/ https://www.ncbi.nlm.nih.gov/pubmed/29380254 http://dx.doi.org/10.1007/s13760-018-0882-3 |
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author | Lambert, Catherine Dubois, Benedicte Dive, Dominique Lysandropoulos, Andreas Selleslag, Dominik Vanopdenbosch, Ludo Van Pesch, Vincent Vanwijmeersch, Bart Janssens, Ann |
author_facet | Lambert, Catherine Dubois, Benedicte Dive, Dominique Lysandropoulos, Andreas Selleslag, Dominik Vanopdenbosch, Ludo Van Pesch, Vincent Vanwijmeersch, Bart Janssens, Ann |
author_sort | Lambert, Catherine |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5857274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58572742018-03-21 Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus Lambert, Catherine Dubois, Benedicte Dive, Dominique Lysandropoulos, Andreas Selleslag, Dominik Vanopdenbosch, Ludo Van Pesch, Vincent Vanwijmeersch, Bart Janssens, Ann Acta Neurol Belg Consensus paper and Guideline 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. Springer International Publishing 2018-01-27 2018 /pmc/articles/PMC5857274/ /pubmed/29380254 http://dx.doi.org/10.1007/s13760-018-0882-3 Text en © The Author(s) 2018, corrected publication March 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Consensus paper and Guideline Lambert, Catherine Dubois, Benedicte Dive, Dominique Lysandropoulos, Andreas Selleslag, Dominik Vanopdenbosch, Ludo Van Pesch, Vincent Vanwijmeersch, Bart Janssens, Ann Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus |
title | Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus |
title_full | Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus |
title_fullStr | Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus |
title_full_unstemmed | Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus |
title_short | Management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a Belgian consensus |
title_sort | management of immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab: a belgian consensus |
topic | Consensus paper and Guideline |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857274/ https://www.ncbi.nlm.nih.gov/pubmed/29380254 http://dx.doi.org/10.1007/s13760-018-0882-3 |
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