Zhou Yi, Wood Brent L
Department of Laboratory Medicine, University of Washington, 825 Eastlake Ave E, Rm G7-800, Seattle, WA, 98109, USA.
Curr Hematol Malig Rep. 2017 Dec;12(6):557-567. doi: 10.1007/s11899-017-0419-5.
The presence of measurable ("minimal") residual disease (MRD) after induction and/or consolidation chemotherapy is a significant risk factor for relapse in patients with acute myeloid leukemia (AML). In recognition of the clinical significance of AML MRD, the European LeukemiaNet (ELN) recently recommended the establishment of CR-MRD as a separate category of treatment response. This recommendation represents a major milestone in the integration of AML MRD testing in standard clinical practice. This review article summarizes the methodologies employed in AML MRD detection and their application in clinical studies that provide evidence supporting the clinical utility of AML MRD testing. Future MRD evaluations in AML likely will require an integrated approach combining multi-parameter flow cytometry and high-sensitivity molecular techniques applied to time points during and after completion of therapy in order to provide the most accurate and comprehensive assessment of treatment response.
诱导化疗和/或巩固化疗后出现可测量的(“微小”)残留病(MRD)是急性髓系白血病(AML)患者复发的重要危险因素。认识到AML-MRD的临床意义,欧洲白血病网(ELN)最近建议将完全缓解伴MRD(CR-MRD)确立为一种单独的治疗反应类别。这一建议是AML-MRD检测纳入标准临床实践的一个重要里程碑。这篇综述文章总结了AML-MRD检测所采用的方法及其在临床研究中的应用,这些临床研究为AML-MRD检测的临床实用性提供了证据支持。未来AML的MRD评估可能需要一种综合方法,将多参数流式细胞术和高灵敏度分子技术应用于治疗期间及完成后的时间点,以便对治疗反应提供最准确和全面的评估。