Suppr超能文献

急性髓系白血病患者基因突变的特征及其对预后的影响。

Features and impacts on the prognosis of gene mutations in patients with acute myeloid leukemia.

机构信息

Zhongshan People's Hospital, Zhongshan, China.

出版信息

Neoplasma. 2021 Sep;68(5):1072-1078. doi: 10.4149/neo_2021_201230N1426. Epub 2021 May 17.

Abstract

To explore features and impacts on the prognosis of common gene mutations in acute myeloid leukemia (AML), we assessed mutation status as well as variant allele frequency (VAF) of 24 genes in 81 AML patients by next-generation sequencing (NGS) technology. Eighty-six percentages of patients showed at least one mutation. Mutation in BCOR was associated with lower complete remission (CR) rate, whereas double mutation in CEBPA was associated with a favorable odds ratio for CR achievement. TP53 mutation was associated with inferior overall survival (OS) in univariate analysis. Multivariate analysis confirmed the negative effect of adverse cytogenetic abnormalities on survival. Mutation in RUNX1 and ZRSR2 had negative impacts on OS in patients with wild-type TP53. VAF of SRSF2 mutation was observed negatively correlated with OS. In conclusion, our study suggested that mutations in BCOR and spliceosomes might predict worse outcomes, and VAF of gene mutations may play a crucial role in outcomes of AML patients.

摘要

为了探究急性髓系白血病(AML)中常见基因突变的特征及其对预后的影响,我们采用下一代测序(NGS)技术评估了 81 例 AML 患者 24 个基因的突变状态和变异等位基因频率(VAF)。86%的患者至少存在一种突变。BCOR 突变与较低的完全缓解(CR)率相关,而 CEBPA 双突变与 CR 获得的有利优势比相关。TP53 突变在单因素分析中与总生存(OS)不良相关。多因素分析证实不良细胞遗传学异常对生存有负面影响。RUNX1 和 ZRSR2 突变对野生型 TP53 患者的 OS 有不良影响。SRSF2 突变的 VAF 与 OS 呈负相关。总之,我们的研究表明,BCOR 和剪接体中的突变可能预示着更差的预后,基因突变的 VAF 可能在 AML 患者的预后中起关键作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验