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Lower‐risk myelodysplastic syndromes: Current treatment options for anemia

Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematological disorders. Treatment options are classified and defined by prognostic risk based on the International Prognostic Scoring System (IPSS) and, more recently, the revised IPSS (IPSS‐R). The treatment goal for lower‐risk MD...

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Autores principales: Meunier, Mathieu, Park, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713208/
https://www.ncbi.nlm.nih.gov/pubmed/36467818
http://dx.doi.org/10.1002/jha2.523
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author Meunier, Mathieu
Park, Sophie
author_facet Meunier, Mathieu
Park, Sophie
author_sort Meunier, Mathieu
collection PubMed
description Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematological disorders. Treatment options are classified and defined by prognostic risk based on the International Prognostic Scoring System (IPSS) and, more recently, the revised IPSS (IPSS‐R). The treatment goal for lower‐risk MDS is to correct cytopenias or their consequences, with the goal of maintaining or improving quality of life. Erythropoiesis‐stimulating agents (ESAs) play an important role in treating anemia. Individuals with MDS who have a 5q deletion are particularly sensitive to treatment with lenalidomide; however, this comprises the minority of patients with MDS. Luspatercept was recently approved in the United States and the European Union for the treatment of ESA‐refractory MDS with ring sideroblasts. Research into new treatment options, especially after ESA failure, is needed. In this review, we will focus on the current therapeutic options for MDS‐related anemia.
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spelling pubmed-97132082022-12-02 Lower‐risk myelodysplastic syndromes: Current treatment options for anemia Meunier, Mathieu Park, Sophie EJHaem Reviews Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematological disorders. Treatment options are classified and defined by prognostic risk based on the International Prognostic Scoring System (IPSS) and, more recently, the revised IPSS (IPSS‐R). The treatment goal for lower‐risk MDS is to correct cytopenias or their consequences, with the goal of maintaining or improving quality of life. Erythropoiesis‐stimulating agents (ESAs) play an important role in treating anemia. Individuals with MDS who have a 5q deletion are particularly sensitive to treatment with lenalidomide; however, this comprises the minority of patients with MDS. Luspatercept was recently approved in the United States and the European Union for the treatment of ESA‐refractory MDS with ring sideroblasts. Research into new treatment options, especially after ESA failure, is needed. In this review, we will focus on the current therapeutic options for MDS‐related anemia. John Wiley and Sons Inc. 2022-08-12 /pmc/articles/PMC9713208/ /pubmed/36467818 http://dx.doi.org/10.1002/jha2.523 Text en © 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Meunier, Mathieu
Park, Sophie
Lower‐risk myelodysplastic syndromes: Current treatment options for anemia
title Lower‐risk myelodysplastic syndromes: Current treatment options for anemia
title_full Lower‐risk myelodysplastic syndromes: Current treatment options for anemia
title_fullStr Lower‐risk myelodysplastic syndromes: Current treatment options for anemia
title_full_unstemmed Lower‐risk myelodysplastic syndromes: Current treatment options for anemia
title_short Lower‐risk myelodysplastic syndromes: Current treatment options for anemia
title_sort lower‐risk myelodysplastic syndromes: current treatment options for anemia
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713208/
https://www.ncbi.nlm.nih.gov/pubmed/36467818
http://dx.doi.org/10.1002/jha2.523
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