Di Jing, Sheng Tao, Arora Ranjana, Stocks-Candelaria Jennifer, Wei Sainan, Lutz Charles, Yalniz Fevzi F, Zhang Shulin
Department of Pathology and Laboratory Medicine, University of Kentucky HealthCare, University of Kentucky, Lexington, Kentucky.
Pathology and Cytology Laboratories Inc., Lexington, Kentucky.
J Mol Diagn. 2025 Feb;27(2):100-108. doi: 10.1016/j.jmoldx.2024.11.002. Epub 2024 Nov 29.
Accurate monitoring of minimal residual disease (MRD) is crucial for effective management of patients with acute myeloid leukemia (AML). This study aims to validate MRD detection of the seven most common IDH1 and IDH2 mutations in patients with AML using a QuantStudio 3D digital PCR platform. This assay demonstrated a high concordance for the variant allele frequencies between digital PCR and next-generation sequencing assays. Precision analysis revealed only small variation (<0.5 log10) for all mutations near or at the limit of detection level. This validation also showed a great reproducibility for interrun and intrarun comparisons (28 runs, variation ranges from 0 to 0.48 log10), ensuring comparable results for patient follow-ups. The limit of detection was determined to be 0.1% for all mutations, except the IDH2 R140Q mutation, which was 0.5%. Controls and acceptable ranges were also established for each mutation during validation. This study suggests that the QuantStudio 3D digital PCR assay is a quantitative, sensitive, and reproducible platform for monitoring MRD in patients with AML.
准确监测微小残留病(MRD)对于急性髓系白血病(AML)患者的有效管理至关重要。本研究旨在使用QuantStudio 3D数字PCR平台验证AML患者中7种最常见的IDH1和IDH2突变的MRD检测。该检测方法在数字PCR和下一代测序检测之间的变异等位基因频率上显示出高度一致性。精密度分析表明,在检测限水平附近或处于检测限水平的所有突变,其变异仅很小(<0.5 log10)。该验证还显示了批间和批内比较具有很高的重复性(28次运行,变异范围为0至0.48 log10),确保了患者随访结果的可比性。除IDH2 R140Q突变的检测限为0.5%外,所有突变的检测限均确定为0.1%。在验证过程中,还为每个突变建立了对照和可接受范围。本研究表明,QuantStudio 3D数字PCR检测是监测AML患者MRD的定量、灵敏且可重复的平台。