Alikian Mary, Gale Robert Peter, Apperley Jane F, Foroni Letizia
Centre for Haematology, Department of Medicine, Imperial College London Hammersmith Hospital, London UK; Imperial Molecular Pathology, Imperial College Healthcare Trust, Hammersmith Hospital, London, UK.
Centre for Haematology, Department of Medicine, Imperial College London Hammersmith Hospital, London UK.
Biomol Detect Quantif. 2017 Feb 14;11:4-20. doi: 10.1016/j.bdq.2017.01.001. eCollection 2017 Mar.
Chronic myeloid leukemia (CML) is the paradigm for targeted cancer therapy. RT-qPCR is the gold standard for monitoring response to tyrosine kinase-inhibitor (TKI) therapy based on the reduction of blood or bone marrow . Some patients with CML and very low or undetectable levels of transcripts can stop TKI-therapy without CML recurrence. However, about 60 percent of patients discontinuing TKI-therapy have rapid leukaemia recurrence. This has increased the need for more sensitive and specific techniques to measure residual CML cells. The clinical challenge is to determine when it is safe to stop TKI-therapy. In this review we describe and critically evaluate the current state of CML clinical management, different technologies used to monitor measurable residual disease (MRD) focus on comparingRT-qPCR and new methods entering clinical practice. We discuss advantages and disadvantages of new methods.
慢性髓性白血病(CML)是靶向癌症治疗的典范。基于血液或骨髓中相关指标的降低,逆转录定量聚合酶链反应(RT-qPCR)是监测酪氨酸激酶抑制剂(TKI)治疗反应的金标准。一些慢性髓性白血病患者的转录本水平极低或检测不到,他们可以停止TKI治疗而不会出现慢性髓性白血病复发。然而,约60%停止TKI治疗的患者会出现白血病快速复发。这就增加了对更敏感、更特异的技术来检测残留慢性髓性白血病细胞的需求。临床面临的挑战是确定何时停止TKI治疗是安全的。在本综述中,我们描述并批判性地评估了慢性髓性白血病临床管理的现状,用于监测可测量残留疾病(MRD)的不同技术,重点比较了RT-qPCR和进入临床实践的新方法。我们还讨论了新方法的优缺点。