Department of Pathology, Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA.
International Health Management Associates (IHMA), Schaumburg, IL 60173, USA.
Int J Mol Sci. 2024 Jul 19;25(14):7912. doi: 10.3390/ijms25147912.
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.
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。