Department of Hematology and Oncology, University Hospital Mannheim, Heidelberg University, Mannheim, Germany.
PLoS One. 2018 Apr 24;13(4):e0196326. doi: 10.1371/journal.pone.0196326. eCollection 2018.
Quantitative real-time polymerase chain reaction (qRT-PCR) is state of the art in molecular monitoring of minimal residual disease in chronic myeloid leukemia (CML). In this context, maintenance of assay fidelity and detection of technical inaccuracy are crucial. Beside multiple common negative controls for the clinical sample preparations, quality control charts (QCC) are a common validation tool to sustain high process quality by continuously recording of qRT-PCR control parameters. Here, we report on establishment and benefit of QCC in qRT-PCR-based CML diagnostics. The absolute quantification of BCR-ABL1 fusion transcripts in patient samples is based on coamplification of a serially diluted reference plasmid (pME-2). For QCC establishment the measured Ct values of each pME-2 standard dilution (4-400,000) of a test set resembling 21 sequential qRT-PCR experiments were recorded and statistically evaluated. Test set data were used for determination of warning limits (mean +/- 2-fold standard deviation) and control (intervention) limits (mean +/- 3-fold standard deviation) to allow rapid detection of defined out-of-control situations which may require intervention. We have retrospectively analyzed QCC data of 282 sequential qRT-PCR experiments (564 reactions). Data evaluation using QCCs revealed three out-of-control situations that required intervention like experiment repeats, renewal of pME-2 standards, replacement of reagents or personnel re-training. In conclusion, with minimal more effort and hands-on time QCC rank among the best tools to grant high quality and reproducibility in CML routine molecular diagnosis.
实时荧光定量聚合酶链反应(qRT-PCR)是慢性髓细胞白血病(CML)微小残留病分子监测的最新技术。在这种情况下,保持检测的准确性和检测技术的不准确性至关重要。除了对临床样本制备的多种常见阴性对照外,质量控制图(QCC)也是一种常见的验证工具,通过连续记录 qRT-PCR 控制参数来维持高质量的过程。在这里,我们报告了 QCC 在基于 qRT-PCR 的 CML 诊断中的建立和益处。患者样本中 BCR-ABL1 融合转录本的绝对定量是基于对一系列稀释的参考质粒(pME-2)的共扩增。为了建立 QCC,记录并统计了测试集(类似于 21 个连续 qRT-PCR 实验)中每个 pME-2 标准稀释液(4-400,000)的测量 Ct 值。测试集数据用于确定警告限制(平均值 +/- 2 倍标准差)和控制(干预)限制(平均值 +/- 3 倍标准差),以快速检测可能需要干预的定义失控情况。我们回顾性分析了 282 个连续 qRT-PCR 实验(564 个反应)的 QCC 数据。使用 QCC 进行的数据评估显示了三种需要干预的失控情况,如实验重复、pME-2 标准更新、试剂更换或人员再培训。总之,只需付出最小的努力和操作时间,QCC 就可以成为保证 CML 常规分子诊断质量和可重复性的最佳工具之一。