Gerrard Gareth, Foong Hui En, Mudge Katherine, Alikian Mary, Apperley Jane F, Foroni Letizia
Centre for Haematology, Imperial College London, Du Cane Road, London W12 ONN, UK; Research Department of Pathology, UCL Cancer Institute, London WC1E 6DE, UK.
Centre for Haematology, Imperial College London, Du Cane Road, London W12 ONN, UK; Imperial Molecular Pathology, Imperial Healthcare NHS Trust, Hammersmith Hospital, Du Cane Road, London W12 OHS, UK.
Leuk Res. 2016 Oct;49:47-50. doi: 10.1016/j.leukres.2016.08.007. Epub 2016 Aug 13.
Molecular monitoring of BCR-ABL1 expression in chronic myeloid leukaemia (CML) is well established. As the International Scale (IS) normalised BCR-ABL1/ABL1 ratio at 3 months post-treatment is now an important milestone in patients' treatment schedule, the reliable and reproducible measurement of BCR-ABL1 levels is therefore paramount. IS conversion factors (CF) are established via sample exchange and yearly ratification with an external reference laboratory. Since any change to an established IS CF could lead to discontinuity in longitudinal results, we wished to add an internal verification step as an additional safeguard. We used the Cepheid GeneXpert qPCR and IS calibrated Xpert BCR-ABL Monitor cartridge system, parallel to our in-house pipeline on 50 CML samples, over the period of one week to verify the CF for those samples and compare it to the externally provided CF. The median non-IS in-house BCR-ABL1/ABL1 values were significantly different than that from the IS GeneXpert, but they became non-significant when adjusted to CF provided by the CXM and by the current external CF, validating it. These metrics can help decide to accept or reject an updated CF value, especially where a significant change in CF might lead to a discontinuity in ongoing patient monitoring.
慢性髓性白血病(CML)中BCR-ABL1表达的分子监测已得到广泛应用。由于治疗后3个月时国际标准(IS)归一化的BCR-ABL1/ABL1比值现已成为患者治疗计划中的一个重要里程碑,因此可靠且可重复地测量BCR-ABL1水平至关重要。IS转换因子(CF)是通过样本交换并每年与外部参考实验室核准来确定的。由于对既定的IS CF的任何更改都可能导致纵向结果的不连续性,我们希望增加一个内部验证步骤作为额外保障。我们在一周的时间内,使用赛沛GeneXpert定量聚合酶链反应(qPCR)和经IS校准的Xpert BCR-ABL监测试剂盒系统,与我们内部的检测流程并行检测50份CML样本,以验证这些样本的CF,并将其与外部提供的CF进行比较。内部非IS的BCR-ABL1/ABL1值中位数与IS GeneXpert的结果有显著差异,但在根据CXM和当前外部CF提供的CF进行调整后,差异不再显著,从而验证了该CF。这些指标有助于决定接受或拒绝更新后的CF值,特别是在CF的显著变化可能导致正在进行的患者监测出现不连续性的情况下。