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[WT1基因表达定量在急性髓系白血病微小残留病监测中的临床意义]

[Clinical significance of quantitation of WT1 gene expression for minimal residual disease monitoring of acute myelogenous leukemia].

作者信息

Kim Hye Ran, Shin Jeong Hwan, Lee Jeong Nyeo, Lee Eun Yup

机构信息

Department of Laboratory Medicine, Busan Paik Hospital, College of Medicine, Inje University, Busan, Korea.

出版信息

Korean J Lab Med. 2007 Oct;27(5):305-12. doi: 10.3343/kjlm.2007.27.5.305.

Abstract

BACKGROUND

Following induction chemotherapy for AML, a sensitive determination of minimal residual disease (MRD) in patients achieving complete remission (CR) should enable the detection of early relapse. This study was designed to verify if quantitative assessment of the Wilms' tumor (WT1) gene by real time polymerase chain reaction (RQ-PCR) can be used as a marker for MRD detection during the monitoring of AML.

METHODS

WT1 gene expression was quantified by RQ-PCR in 31 patients with AML at diagnosis (27 patients) and during follow-up (29 patients) relative to ABL control gene. In four patients, the WT1 gene expression was analyzed in comparison to a second PCR marker, PML-RARA fusion transcript. Prognostic significance of WT1 gene expression was analyzed at diagnosis and at the primary CR evaluation. Longitudinal WT1 gene analysis was performed in 17 AML patients.

RESULTS

At diagnosis, WT1 gene expression exceeded the control level in all of the patients. Higher levels of WT1 gene expression were not associated with shorter event free survival or overall survival at diagnosis. Higher levels of WT1 gene expression were associated with shorter event free survival after induction chemotherapy. Relapse was observed in eight of 17 patients analysed longitudinally, and an increase of WT1 gene expression preceded morphologic relapse in four patients with the fusion transcript negative. Concomitant monitoring of PML-RARA fusion transcript reveals the lack of a significant correlation withWT1 gene expression.

CONCLUSIONS

Quantitation of WT1 gene expression could be used for MRD monitoring of AML and for the early detection of relapse, especially in patients lacking specific molecular markers.

摘要

背景

急性髓系白血病(AML)诱导化疗后,对达到完全缓解(CR)的患者进行微小残留病(MRD)的灵敏检测应能实现早期复发的检测。本研究旨在验证通过实时聚合酶链反应(RQ-PCR)对威尔姆斯瘤(WT1)基因进行定量评估是否可作为AML监测期间MRD检测的标志物。

方法

采用RQ-PCR对31例AML患者诊断时(27例)及随访期间(29例)的WT1基因表达进行定量,并以ABL对照基因作为参照。在4例患者中,将WT1基因表达与另一种PCR标志物PML-RARA融合转录本进行比较分析。分析诊断时及初次CR评估时WT1基因表达的预后意义。对17例AML患者进行WT1基因的纵向分析。

结果

诊断时,所有患者的WT1基因表达均超过对照水平。诊断时较高水平的WT1基因表达与较短的无事件生存期或总生存期无关。诱导化疗后较高水平的WT1基因表达与较短的无事件生存期相关。在纵向分析的17例患者中,有8例出现复发,在4例融合转录本阴性的患者中,WT1基因表达增加先于形态学复发。同时监测PML-RARA融合转录本发现其与WT1基因表达无显著相关性。

结论

WT1基因表达定量可用于AML的MRD监测及复发的早期检测,尤其是在缺乏特异性分子标志物的患者中。

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