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An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype
Although clinical features, cytogenetics, and mutations are widely used to predict prognosis in patients with acute myeloid leukemia (AML), further refinement of risk stratification is necessary for optimal treatment, especially in cytogenetically normal (CN) patients. We sought to generate a simple...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770759/ https://www.ncbi.nlm.nih.gov/pubmed/26517675 |
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author | Chuang, Ming-Kai Chiu, Yu-Chiao Chou, Wen-Chien Hou, Hsin-An Tseng, Mei-Hsuan Kuo, Yi-Yi Chen, Yidong Chuang, Eric Y. Tien, Hwei-Fang |
author_facet | Chuang, Ming-Kai Chiu, Yu-Chiao Chou, Wen-Chien Hou, Hsin-An Tseng, Mei-Hsuan Kuo, Yi-Yi Chen, Yidong Chuang, Eric Y. Tien, Hwei-Fang |
author_sort | Chuang, Ming-Kai |
collection | PubMed |
description | Although clinical features, cytogenetics, and mutations are widely used to predict prognosis in patients with acute myeloid leukemia (AML), further refinement of risk stratification is necessary for optimal treatment, especially in cytogenetically normal (CN) patients. We sought to generate a simple gene expression signature as a predictor of clinical outcome through analyzing the mRNA arrays of 158 de novo CN AML patients. We compared the gene expression profiles of patients with poor response to induction chemotherapy with those who responded well. Forty-six genes expressed differentially between the two groups. Among them, expression of 11 genes was significantly associated with overall survival (OS) in univariate Cox regression analysis in 104 patients who received standard intensive chemotherapy. We integrated the z-transformed expression levels of these 11 genes to generate a risk scoring system. Higher risk scores were significantly associated with shorter OS (median 17.0 months vs. not reached, P < 0.001) in ours and another 3 validation cohorts. In addition, it was an independent unfavorable prognostic factor by multivariate analysis (HR 1.116, 95% CI 1.035~1.204, P = 0.004). In conclusion, we developed a simple mRNA expression signature for prognostication in CN-AML patients. This prognostic biomarker will help refine the treatment strategies for this group of patients. |
format | Online Article Text |
id | pubmed-4770759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-47707592016-03-21 An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype Chuang, Ming-Kai Chiu, Yu-Chiao Chou, Wen-Chien Hou, Hsin-An Tseng, Mei-Hsuan Kuo, Yi-Yi Chen, Yidong Chuang, Eric Y. Tien, Hwei-Fang Oncotarget Research Paper Although clinical features, cytogenetics, and mutations are widely used to predict prognosis in patients with acute myeloid leukemia (AML), further refinement of risk stratification is necessary for optimal treatment, especially in cytogenetically normal (CN) patients. We sought to generate a simple gene expression signature as a predictor of clinical outcome through analyzing the mRNA arrays of 158 de novo CN AML patients. We compared the gene expression profiles of patients with poor response to induction chemotherapy with those who responded well. Forty-six genes expressed differentially between the two groups. Among them, expression of 11 genes was significantly associated with overall survival (OS) in univariate Cox regression analysis in 104 patients who received standard intensive chemotherapy. We integrated the z-transformed expression levels of these 11 genes to generate a risk scoring system. Higher risk scores were significantly associated with shorter OS (median 17.0 months vs. not reached, P < 0.001) in ours and another 3 validation cohorts. In addition, it was an independent unfavorable prognostic factor by multivariate analysis (HR 1.116, 95% CI 1.035~1.204, P = 0.004). In conclusion, we developed a simple mRNA expression signature for prognostication in CN-AML patients. This prognostic biomarker will help refine the treatment strategies for this group of patients. Impact Journals LLC 2015-10-23 /pmc/articles/PMC4770759/ /pubmed/26517675 Text en Copyright: © 2015 Chuang et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Chuang, Ming-Kai Chiu, Yu-Chiao Chou, Wen-Chien Hou, Hsin-An Tseng, Mei-Hsuan Kuo, Yi-Yi Chen, Yidong Chuang, Eric Y. Tien, Hwei-Fang An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype |
title | An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype |
title_full | An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype |
title_fullStr | An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype |
title_full_unstemmed | An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype |
title_short | An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype |
title_sort | mrna expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770759/ https://www.ncbi.nlm.nih.gov/pubmed/26517675 |
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