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急性髓系白血病患儿WT1基因表达的实时定量PCR检测:预后意义、与疾病状态的相关性及流式细胞术检测残留病

Real-time quantitative PCR detection of WT1 gene expression in children with AML: prognostic significance, correlation with disease status and residual disease detection by flow cytometry.

作者信息

Trka J, Kalinová M, Hrusák O, Zuna J, Krejcí O, Madzo J, Sedlácek P, Vávra V, Michalová K, Jarosová M, Starý J

机构信息

CLIP - Childhood Leukaemia Investigation Prague, 2nd Medical School, Charles University, Prague, Czech Republic.

出版信息

Leukemia. 2002 Jul;16(7):1381-9. doi: 10.1038/sj.leu.2402512.

Abstract

The clinical significance of WT1 gene expression at diagnosis and during therapy of AML has not yet been resolved. We analysed WT1 expression at presentation in an unselected group of 47 childhood AML patients using real-time quantitative reverse-transcription PCR. We also showed that within the first 30 h following aspiration RQ-RT-PCR results were not influenced by transportation time. We observed lower levels of WT1 transcript in AML M5 (P = 0.0015); no association was found between expression levels and sex, initial leukocyte count and karyotype-based prognostic groups. There was significant correlation between very low WT1 expression at presentation and excellent outcome (EFS P = 0.0014). Combined analysis of WT1 levels, three-colour flow cytometry residual disease detection and the course of the disease in 222 samples from 28 children with AML showed remarkable correlation. Fourteen patients expressed high WT1 levels at presentation. In eight of them, who suffered relapse or did not reach complete remission, dynamics of WT1 levels clearly correlated with the disease status and residual disease by flow cytometry. We conclude that very low WT1 levels at presentation represent a good prognostic factor and that RQ-RT-PCR-based analysis of WT1 expression is a promising and rapid approach for monitoring of MRD in approximately half of paediatric AML patients.

摘要

WT1基因表达在急性髓系白血病(AML)诊断及治疗期间的临床意义尚未明确。我们采用实时定量逆转录聚合酶链反应(RQ-RT-PCR)分析了47例未经选择的儿童AML患者初诊时的WT1表达情况。我们还发现,在抽取样本后的最初30小时内,RQ-RT-PCR结果不受运输时间的影响。我们观察到AML M5中WT1转录水平较低(P = 0.0015);未发现表达水平与性别、初始白细胞计数及基于核型的预后分组之间存在关联。初诊时WT1表达极低与良好预后显著相关(无事件生存期,EFS,P = 0.0014)。对28例AML儿童患者的222份样本进行WT1水平、三色流式细胞术残留病检测及疾病进程的联合分析,结果显示显著相关性。14例患者初诊时WT1表达水平较高。其中8例复发或未达到完全缓解的患者,WT1水平变化与疾病状态及流式细胞术检测的残留病明显相关。我们得出结论,初诊时WT1水平极低代表良好的预后因素,基于RQ-RT-PCR的WT1表达分析是监测约半数儿童AML患者微小残留病(MRD)的一种有前景且快速的方法。

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