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Alemtuzumab in refractory Sézary syndrome

Sézary syndrome is a primary cutaneous T-cell lymphoma characterized by the triad of erythroderma, lymphadenopathy and circulating atypical cells. The emergence of new molecular targets has enabled the development of drugs such as alemtuzumab, an anti-CD52 monoclonal antibody, which has shown promis...

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Autores principales: Reifs, Carmen María Alcántara, Salido-Vallejo, Rafael, Garnacho-Saucedo, Gloria María, la Corte-Sánchez, Sofía De, González-Menchen, Alberto, García-Nieto, Antonio Vélez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087225/
https://www.ncbi.nlm.nih.gov/pubmed/27828640
http://dx.doi.org/10.1590/abd1806-4841.20164322
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author Reifs, Carmen María Alcántara
Salido-Vallejo, Rafael
Garnacho-Saucedo, Gloria María
la Corte-Sánchez, Sofía De
González-Menchen, Alberto
García-Nieto, Antonio Vélez
author_facet Reifs, Carmen María Alcántara
Salido-Vallejo, Rafael
Garnacho-Saucedo, Gloria María
la Corte-Sánchez, Sofía De
González-Menchen, Alberto
García-Nieto, Antonio Vélez
author_sort Reifs, Carmen María Alcántara
collection PubMed
description Sézary syndrome is a primary cutaneous T-cell lymphoma characterized by the triad of erythroderma, lymphadenopathy and circulating atypical cells. The emergence of new molecular targets has enabled the development of drugs such as alemtuzumab, an anti-CD52 monoclonal antibody, which has shown promising results in the treatment of this entity. We report the case of a 70-year-old male with refractory Sézary syndrome in whom treatment with alemtuzumab achieved an 80% skin lesion clearance with complete haematologic and radiologic response. The treatment was discontinued after 4 months due to adverse effects, with the patient showing a sustained response without disease progression after 13 months of follow-up.
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spelling pubmed-50872252016-11-01 Alemtuzumab in refractory Sézary syndrome Reifs, Carmen María Alcántara Salido-Vallejo, Rafael Garnacho-Saucedo, Gloria María la Corte-Sánchez, Sofía De González-Menchen, Alberto García-Nieto, Antonio Vélez An Bras Dermatol Case Report Sézary syndrome is a primary cutaneous T-cell lymphoma characterized by the triad of erythroderma, lymphadenopathy and circulating atypical cells. The emergence of new molecular targets has enabled the development of drugs such as alemtuzumab, an anti-CD52 monoclonal antibody, which has shown promising results in the treatment of this entity. We report the case of a 70-year-old male with refractory Sézary syndrome in whom treatment with alemtuzumab achieved an 80% skin lesion clearance with complete haematologic and radiologic response. The treatment was discontinued after 4 months due to adverse effects, with the patient showing a sustained response without disease progression after 13 months of follow-up. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC5087225/ /pubmed/27828640 http://dx.doi.org/10.1590/abd1806-4841.20164322 Text en ©2016 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Case Report
Reifs, Carmen María Alcántara
Salido-Vallejo, Rafael
Garnacho-Saucedo, Gloria María
la Corte-Sánchez, Sofía De
González-Menchen, Alberto
García-Nieto, Antonio Vélez
Alemtuzumab in refractory Sézary syndrome
title Alemtuzumab in refractory Sézary syndrome
title_full Alemtuzumab in refractory Sézary syndrome
title_fullStr Alemtuzumab in refractory Sézary syndrome
title_full_unstemmed Alemtuzumab in refractory Sézary syndrome
title_short Alemtuzumab in refractory Sézary syndrome
title_sort alemtuzumab in refractory sézary syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087225/
https://www.ncbi.nlm.nih.gov/pubmed/27828640
http://dx.doi.org/10.1590/abd1806-4841.20164322
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