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How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms
Myelodysplastic neoplasms, formerly known as myelodysplastic syndromes (MDS), represent a group of clonal disorders characterized by a high degree of clinical and molecular heterogeneity, and an invariable tendency to progress to acute myeloid leukemia. MDS typically present in the elderly with cyto...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063738/ https://www.ncbi.nlm.nih.gov/pubmed/36574201 http://dx.doi.org/10.1007/s44228-022-00024-4 |
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author | Gurnari, Carmelo Xie, Zhuoer Zeidan, Amer M. |
author_facet | Gurnari, Carmelo Xie, Zhuoer Zeidan, Amer M. |
author_sort | Gurnari, Carmelo |
collection | PubMed |
description | Myelodysplastic neoplasms, formerly known as myelodysplastic syndromes (MDS), represent a group of clonal disorders characterized by a high degree of clinical and molecular heterogeneity, and an invariable tendency to progress to acute myeloid leukemia. MDS typically present in the elderly with cytopenias of different degrees and bone marrow dysplasia, the hallmarks of the disease. Allogeneic hematopoietic stem cell transplant is the sole curative approach to date. Nonetheless, given the disease’s demographics, only a minority of patients can benefit from this procedure. Currently used prognostic schemes such as the Revised International Prognostic Scoring System (R-IPSS), and most recently the molecular IPSS (IPSS-M), guide clinical management by dividing MDS into two big categories: lower- and higher-risk cases, based on a cut-off score of 3.5. The main clinical problem of the lower-risk group is represented by the management of cytopenias, whereas the prevention of secondary leukemia progression is the goal for the latter. Herein, we discuss the non-transplant treatment of MDS, focusing on current practice and available therapeutic options, while also presenting new investigational agents potentially entering the MDS therapeutic arsenal in the near future. |
format | Online Article Text |
id | pubmed-10063738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-100637382023-04-01 How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms Gurnari, Carmelo Xie, Zhuoer Zeidan, Amer M. Clin Hematol Int Review Article Myelodysplastic neoplasms, formerly known as myelodysplastic syndromes (MDS), represent a group of clonal disorders characterized by a high degree of clinical and molecular heterogeneity, and an invariable tendency to progress to acute myeloid leukemia. MDS typically present in the elderly with cytopenias of different degrees and bone marrow dysplasia, the hallmarks of the disease. Allogeneic hematopoietic stem cell transplant is the sole curative approach to date. Nonetheless, given the disease’s demographics, only a minority of patients can benefit from this procedure. Currently used prognostic schemes such as the Revised International Prognostic Scoring System (R-IPSS), and most recently the molecular IPSS (IPSS-M), guide clinical management by dividing MDS into two big categories: lower- and higher-risk cases, based on a cut-off score of 3.5. The main clinical problem of the lower-risk group is represented by the management of cytopenias, whereas the prevention of secondary leukemia progression is the goal for the latter. Herein, we discuss the non-transplant treatment of MDS, focusing on current practice and available therapeutic options, while also presenting new investigational agents potentially entering the MDS therapeutic arsenal in the near future. Springer Netherlands 2022-12-27 /pmc/articles/PMC10063738/ /pubmed/36574201 http://dx.doi.org/10.1007/s44228-022-00024-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Gurnari, Carmelo Xie, Zhuoer Zeidan, Amer M. How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms |
title | How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms |
title_full | How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms |
title_fullStr | How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms |
title_full_unstemmed | How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms |
title_short | How I Manage Transplant Ineligible Patients with Myelodysplastic Neoplasms |
title_sort | how i manage transplant ineligible patients with myelodysplastic neoplasms |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063738/ https://www.ncbi.nlm.nih.gov/pubmed/36574201 http://dx.doi.org/10.1007/s44228-022-00024-4 |
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