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骨髓增生异常综合征患者基因突变与临床特征相关性及预后

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目的:探索骨髓增生异常综合征(MDS)基因突变与临床特征的相关性及预后分析.方法:收集兰州大学第一医院2015年6月至2023年2月期间131例MDS患者的临床资料,随访期间其中19例进展为继发性急性髓系白血病(sAML).利用二代测序技术检测MDS疾病相关基因突变类型并绘制突变谱,结合患者临床资料分析其之间相关性及预后.结果:131例MDS患者中位年龄58(17-86)岁,男女比例约为1.3:1.131例中共检测出148个基因突变、25种突变类型,其中U2AF1、ASXL1常与其它基因发生共突变,且分别与20q-和正常核型伴随出现.SETBP1和SRSF2多见于60岁以上患者,NPM1和WT1常见于60岁以下患者,老年患者的基因突变数目多于年轻患者.,男性SF3B1和RUNX1基因突变发生率高于女性,女性DNMT3A基因突变发生率高于男性.MDS进展为sAML患者组的基因突变数目高于MDS组(1.8vs1.0个,P=0.006).单因素、多因素分析结果显示,IPSS-R预后评分≥3.5分和TP53是MDS患者预后不良的危险因素.单等位基因TP53突变和野生型TP53患者OS优于双等位基因突变型(P=0.003);未转白患者OS优于sAML患者(P=0.01);移植患者OS明显优于未移植患者(P=0.036).结论:基因突变与细胞遗传学指标和临床特征(外周血细胞数、性别、年龄)密切相关.IPSS-R预后评分、TP53是影响MDS患者OS的危险因素.
The Correlation of Gene Mutation and Clinical Characteristics in Patients with Myelodysplastic Syndrome and Prognostic Analysis
Objective:To explore the correlation between gene mutations and clinical characteristics,prognosis of myelodysplastic syndromes(MDS).Methods:Clinical data of 131 patients with MDS were collected from the First Hospital of Lanzhou University from June 2015 to February 2023,which 19 of them developed into secondary acute myeloid leukemia(sAML)during follow-up time.Second generation sequencing technology was used to detect the mutation types of MDS disease-related genes,drawn gene maps,and analyzed their correlation and prognosis based on the clinical data of patients.Results:The median age of 131 MDS patients was 58(17-86)years old.The ratio of male to female was 1.3:1.A total of 148 gene mutations and 25 types were found in the center.U2AF1 and ASXL1 were often co-mutations with other genes,which were accompanied by 20q-and normal karyotype(NK)respectively.SETBP1 and SRSF2 were more common in patients over 60 years old,while NPM1 and WT1 under 60 years.Older patients had a higher the number of genetic mutations than younger patients.The incidence of SF3B1 and RUNX1 in males was higher than females and DNMT3A in females was higher than males.The number of gene mutations in sAML was higher than MDS(1.8 vs 1.0,P=0.006).The univariate and multivariate analysis showed that IPSS-R prognostic score≥ 3.5,TP53 were adverse factors for poor prognosis in MDS patients.Patients with monoallelic mutation(ma-TP53)and wild-type(wt-TP53)TP53 had OS better than biallelic mutation(bi-TP53)(P=0.003).The OS of MDS patients was better than sAML(P=0.01)and transplant patients was significantly better than non-transplant patients(P=0.036).Conclusion:Gene mutation is closely related to cytogenetic indexes and clinical features(peripheral blood cell count,sex,age).IPSS-R prognostic score and TP53 were risk factors affecting OS in MDS patients.

myelodysplastic syndromecomutationcytogeneticsclinical phenotypeprognosis

张婉婉、张雅丽、任崇崇、吴庭恺、刘蓓

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甘肃省兰州大学第一临床医学院

兰州大学第一医院血液内科,甘肃兰州 730000

骨髓增生异常综合征 共突变 细胞遗传学 临床表型 预后

甘肃省自然科学基金

18JR3RA356

2024

中国实验血液学杂志
中国病理生理学会

中国实验血液学杂志

CSTPCD北大核心
影响因子:0.988
ISSN:1009-2137
年,卷(期):2024.32(1)
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