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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.
Afiliação
  • Fan Y; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Liao L; Department of Intensive Care Unit, Zhongshan People's Hospital, Zhongshan, China.
  • Liu Y; Department of Orthopaedics, Brown University, Warren Alpert Medical School/Rhode Island Hospital, Providence, RI, USA.
  • Wu Z; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Wang C; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Jiang Z; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Wang S; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. fccwangsj1@zzu.edu.cn.
  • Liu Y; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. fccliuyf1@zzu.edu.cn.
Cancer Cell Int ; 21(1): 526, 2021 Oct 09.
Article em En | MEDLINE | ID: mdl-34627254
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 × 109/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.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancer Cell Int Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancer Cell Int Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China