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Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

In patients with chronic myelomonocytic leukemia (CMML), age>65 years is an adverse prognostic factor. Our objective in the current study was to examine risk factors for survival and treatment outcome in 261 ‘young' adults with CMML, as defined by age ⩽65 years. In multivariable analysis, lo...

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Autores principales: Patnaik, M M, Wassie, E A, Padron, E, Onida, F, Itzykson, R, Lasho, T L, Kosmider, O, Finke, C M, Hanson, C A, Ketterling, R P, Komrokji, R, Tefferi, A, Solary, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404217/
https://www.ncbi.nlm.nih.gov/pubmed/25555161
http://dx.doi.org/10.1038/bcj.2014.90
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author Patnaik, M M
Wassie, E A
Padron, E
Onida, F
Itzykson, R
Lasho, T L
Kosmider, O
Finke, C M
Hanson, C A
Ketterling, R P
Komrokji, R
Tefferi, A
Solary, E
author_facet Patnaik, M M
Wassie, E A
Padron, E
Onida, F
Itzykson, R
Lasho, T L
Kosmider, O
Finke, C M
Hanson, C A
Ketterling, R P
Komrokji, R
Tefferi, A
Solary, E
author_sort Patnaik, M M
collection PubMed
description In patients with chronic myelomonocytic leukemia (CMML), age>65 years is an adverse prognostic factor. Our objective in the current study was to examine risk factors for survival and treatment outcome in 261 ‘young' adults with CMML, as defined by age ⩽65 years. In multivariable analysis, lower HB (P=0.01), higher circulating blast % (P=0.002), ASXL1 (P=0.0007) and SRSF2 mutations (P=0.008) and Mayo-French cytogenetic stratification (P=0.04) negatively impacted survival. Similarly, leukemia-free survival was independently affected by higher circulating blast % (P<0.0001), higher bone marrow blast % (P=0.0007) and the presence of circulating immature myeloid cells (P=0.0002). Seventy-five (29%) patients received hypomethylating agents (HMA), with the median number of cycles being 5, and the median duration of therapy being 5 months. The over-all response rate was 40% for azacitidine and 30% for decitabine. Fifty-three (24%) patients underwent an allogeneic hematopoietic stem cell transplant (AHSCT), with a response rate of 56% and a non-relapse mortality of 19%. Survival in young adults with CMML, although higher than in older patients, is poor and even worse in the presence of ASXL1 and SRSF2 mutations. Treatment outcome was more impressive with AHSCT than with HMA and neither was influenced by ASXL1/SRSF2 mutations or karyotype.
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spelling pubmed-54042172017-05-19 Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome Patnaik, M M Wassie, E A Padron, E Onida, F Itzykson, R Lasho, T L Kosmider, O Finke, C M Hanson, C A Ketterling, R P Komrokji, R Tefferi, A Solary, E Blood Cancer J Original Article In patients with chronic myelomonocytic leukemia (CMML), age>65 years is an adverse prognostic factor. Our objective in the current study was to examine risk factors for survival and treatment outcome in 261 ‘young' adults with CMML, as defined by age ⩽65 years. In multivariable analysis, lower HB (P=0.01), higher circulating blast % (P=0.002), ASXL1 (P=0.0007) and SRSF2 mutations (P=0.008) and Mayo-French cytogenetic stratification (P=0.04) negatively impacted survival. Similarly, leukemia-free survival was independently affected by higher circulating blast % (P<0.0001), higher bone marrow blast % (P=0.0007) and the presence of circulating immature myeloid cells (P=0.0002). Seventy-five (29%) patients received hypomethylating agents (HMA), with the median number of cycles being 5, and the median duration of therapy being 5 months. The over-all response rate was 40% for azacitidine and 30% for decitabine. Fifty-three (24%) patients underwent an allogeneic hematopoietic stem cell transplant (AHSCT), with a response rate of 56% and a non-relapse mortality of 19%. Survival in young adults with CMML, although higher than in older patients, is poor and even worse in the presence of ASXL1 and SRSF2 mutations. Treatment outcome was more impressive with AHSCT than with HMA and neither was influenced by ASXL1/SRSF2 mutations or karyotype. Nature Publishing Group 2015-01 2015-01-02 /pmc/articles/PMC5404217/ /pubmed/25555161 http://dx.doi.org/10.1038/bcj.2014.90 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Patnaik, M M
Wassie, E A
Padron, E
Onida, F
Itzykson, R
Lasho, T L
Kosmider, O
Finke, C M
Hanson, C A
Ketterling, R P
Komrokji, R
Tefferi, A
Solary, E
Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome
title Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome
title_full Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome
title_fullStr Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome
title_full_unstemmed Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome
title_short Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome
title_sort chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404217/
https://www.ncbi.nlm.nih.gov/pubmed/25555161
http://dx.doi.org/10.1038/bcj.2014.90
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