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Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia

BACKGROUND: The epigenetic regulator additional sex combs-like 1 (ASXL1) is an adverse prognostic factor in acute myeloid leukemia (AML). However, the mutational spectrum and prognostic factors of ASXL1-mutated (ASXL1+) AML are largely unknown. We aim to evaluate the risk factors influencing the pro...

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Autores principales: Fan, Yi, Liao, Linxiao, Liu, Yajun, Wu, Zhenzhen, Wang, Chong, Jiang, Zhongxing, Wang, Shujuan, Liu, Yanfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502294/
https://www.ncbi.nlm.nih.gov/pubmed/34627254
http://dx.doi.org/10.1186/s12935-021-02233-y
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author Fan, Yi
Liao, Linxiao
Liu, Yajun
Wu, Zhenzhen
Wang, Chong
Jiang, Zhongxing
Wang, Shujuan
Liu, Yanfang
author_facet Fan, Yi
Liao, Linxiao
Liu, Yajun
Wu, Zhenzhen
Wang, Chong
Jiang, Zhongxing
Wang, Shujuan
Liu, Yanfang
author_sort Fan, Yi
collection PubMed
description BACKGROUND: The epigenetic regulator additional sex combs-like 1 (ASXL1) is an adverse prognostic factor in acute myeloid leukemia (AML). However, the mutational spectrum and prognostic factors of ASXL1-mutated (ASXL1+) AML are largely unknown. We aim to evaluate the risk factors influencing the prognosis of ASXL1+ AML. METHODS: We performed next-generation sequencing (NGS) in 1047 cases of de novo AML and discovered 91 ASXL1+ AML (8.7%). The Log-Rank test and Kaplan-Meier were used to evaluate survival rate, and the Cox regression model was used to analyze multivariate analysis. RESULTS: In a total of 91 ASXL1+ AML, 86% had one or more co-mutations. The factors that had adverse impact on overall survival (OS) and event-free survival (EFS) are defined as high risk factors, including age ≥ 60 years, WBC count ≥ 50 × 10(9)/L, FLT3-ITD mutations, RUNX1 mutations, and absence of AML1-ETO fusion gene. ASXL1 mutations without any risk factor were classified as single-hit ASXL1+ AML; ASXL1 mutations accompanied with one of the risk factors was referred to as double-hit ASXL1+ AML; ASXL1 mutations with two or more of the risk factors were designated as triple-hit ASXL1+ AML. The combination of these risk factors had a negative influence on the prognosis of ASXL1+ AML. The median OS was not attained in single-hit ASXL1+ AML, 29.53 months in double-hit ASXL1+ AML, and 6.67 months in triple-hit ASXL1+ AML (P = 0.003). The median EFS was not attained in single-hit ASXL1+ AML, 29.53 months in double-hit ASXL1+ AML, and 5.47 months in triple-hit ASXL1+ AML (P = 0.002). Allogenic hematopoietic stem cell transplantation (allo-HSCT) improved the prognosis of double/triple-hit ASXL1+ AML patients. CONCLUSIONS: Our study provided new insights into the mutational spectrum and prognostic factors of ASXL1+ AML patients. Our primary data suggest that the risk factors in ASXL1+ AML contribute to the poor outcome of these patients. The management of ASXL1+ AML patients should be based on the risk factors and allo-HSCT is highly recommended for consolidation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02233-y.
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spelling pubmed-85022942021-10-20 Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia Fan, Yi Liao, Linxiao Liu, Yajun Wu, Zhenzhen Wang, Chong Jiang, Zhongxing Wang, Shujuan Liu, Yanfang Cancer Cell Int Primary Research BACKGROUND: The epigenetic regulator additional sex combs-like 1 (ASXL1) is an adverse prognostic factor in acute myeloid leukemia (AML). However, the mutational spectrum and prognostic factors of ASXL1-mutated (ASXL1+) AML are largely unknown. We aim to evaluate the risk factors influencing the prognosis of ASXL1+ AML. METHODS: We performed next-generation sequencing (NGS) in 1047 cases of de novo AML and discovered 91 ASXL1+ AML (8.7%). The Log-Rank test and Kaplan-Meier were used to evaluate survival rate, and the Cox regression model was used to analyze multivariate analysis. RESULTS: In a total of 91 ASXL1+ AML, 86% had one or more co-mutations. The factors that had adverse impact on overall survival (OS) and event-free survival (EFS) are defined as high risk factors, including age ≥ 60 years, WBC count ≥ 50 × 10(9)/L, FLT3-ITD mutations, RUNX1 mutations, and absence of AML1-ETO fusion gene. ASXL1 mutations without any risk factor were classified as single-hit ASXL1+ AML; ASXL1 mutations accompanied with one of the risk factors was referred to as double-hit ASXL1+ AML; ASXL1 mutations with two or more of the risk factors were designated as triple-hit ASXL1+ AML. The combination of these risk factors had a negative influence on the prognosis of ASXL1+ AML. The median OS was not attained in single-hit ASXL1+ AML, 29.53 months in double-hit ASXL1+ AML, and 6.67 months in triple-hit ASXL1+ AML (P = 0.003). The median EFS was not attained in single-hit ASXL1+ AML, 29.53 months in double-hit ASXL1+ AML, and 5.47 months in triple-hit ASXL1+ AML (P = 0.002). Allogenic hematopoietic stem cell transplantation (allo-HSCT) improved the prognosis of double/triple-hit ASXL1+ AML patients. CONCLUSIONS: Our study provided new insights into the mutational spectrum and prognostic factors of ASXL1+ AML patients. Our primary data suggest that the risk factors in ASXL1+ AML contribute to the poor outcome of these patients. The management of ASXL1+ AML patients should be based on the risk factors and allo-HSCT is highly recommended for consolidation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02233-y. BioMed Central 2021-10-09 /pmc/articles/PMC8502294/ /pubmed/34627254 http://dx.doi.org/10.1186/s12935-021-02233-y Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Primary Research
Fan, Yi
Liao, Linxiao
Liu, Yajun
Wu, Zhenzhen
Wang, Chong
Jiang, Zhongxing
Wang, Shujuan
Liu, Yanfang
Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia
title Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia
title_full Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia
title_fullStr Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia
title_full_unstemmed Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia
title_short Risk factors affect accurate prognosis in ASXL1-mutated acute myeloid leukemia
title_sort risk factors affect accurate prognosis in asxl1-mutated acute myeloid leukemia
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502294/
https://www.ncbi.nlm.nih.gov/pubmed/34627254
http://dx.doi.org/10.1186/s12935-021-02233-y
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