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评价一种新的封闭系统自动化 RT-qPCR 检测方法,用于快速检测和监测急性髓系白血病患者常见核仁磷酸蛋白突变。

Evaluation of a New Closed-System Automated RT-qPCR Assay for the Rapid Detection and Monitoring of Common Nucleophosmin Mutations in Patients with Acute Myeloid Leukemia.

机构信息

Department of Pathology, Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA.

International Health Management Associates (IHMA), Schaumburg, IL 60173, USA.

出版信息

Int J Mol Sci. 2024 Jul 19;25(14):7912. doi: 10.3390/ijms25147912.

Abstract

Quantitative assessment of nucleophosmin 1 () mutation status is integral to evaluating measurable residual disease (MRD) in -mutated acute myeloid leukemia (AML) patients. In a retrospective study, leftover peripheral blood (PB) specimens (n = 40) which were collected for routine clinical diagnostic evaluations of AML disease burden were tested by both a novel automated RT-qPCR quantitative NPM1 assay (Xpert NPM1 mutation assay) and the NPM1 mutA, mutB&D MutaQuant kit. Based on a Deming regression analysis, there was a high correlation (slope = 0.92; intercept = 0.12; Pearson's r = 0.982) between the quantitative results of the Xpert NPM1 mutation assay and the NPM1 mutA, mutB&D MutaQuant kit. The Xpert test quantitative results are thus highly correlated with the comparator method and the former has potential as a useful alternative for the monitoring of AML patients with a known mutation.

摘要

定量评估核磷蛋白 1 (NPM1) 突变状态是评估 NPM1 突变型急性髓系白血病 (AML) 患者可测量残留疾病 (MRD) 的重要组成部分。在一项回顾性研究中,为常规临床诊断 AML 疾病负担而收集的剩余外周血 (PB) 标本(n=40),通过新型自动化 RT-qPCR 定量 NPM1 检测(Xpert NPM1 突变检测)和 NPM1 mutA、mutB&D MutaQuant 试剂盒进行了检测。基于 Deming 回归分析,Xpert NPM1 突变检测的定量结果与 NPM1 mutA、mutB&D MutaQuant 试剂盒高度相关(斜率=0.92;截距=0.12;Pearson's r=0.982)。因此,Xpert 检测的定量结果与比较方法高度相关,前者有可能成为监测已知 NPM1 突变的 AML 患者的有用替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88a0/11277538/8804d6c0b2e4/ijms-25-07912-g001.jpg

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