A 19-color single-tube full spectrum flow cytometry assay for the detection of measurable residual disease in acute myeloid leukemia

被引:2
作者
Fokken, Hendrik [1 ]
Waclawski, Julian [1 ]
Kattre, Nadine [1 ]
Kloos, Arnold [1 ]
Mueller, Sebastian [2 ,3 ,4 ]
Ettinger, Max [5 ]
Kacprowski, Tim [2 ,3 ,4 ]
Heuser, Michael [1 ]
Maetzig, Tobias [6 ,7 ]
Schwarzer, Adrian [1 ,7 ,8 ,9 ,10 ]
机构
[1] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpla, Hannover, Germany
[2] TU Braunschweig, Peter L Reichertz Inst Med Informat, Div Data Sci Biomed, Braunschweig, Germany
[3] Hannover Med Sch, Braunschweig, Germany
[4] TU Braunschweig, Braunschweig Integrated Ctr Syst Biol BRICS, Braunschweig, Germany
[5] Hannover Med Sch, Dept Orthoped Surg, Hannover, Germany
[6] Hannover Med Sch, Dept Pediat Hematol, Hannover, Germany
[7] Hannover Med Sch, Inst Expt Hematol, Hannover, Germany
[8] Univ Med Greifswald, CCC MV, Greifswald, Germany
[9] Univ Med Greifswald, Dept Internal Med C, Greifswald, Germany
[10] Univ Med Greifswald, Dept Internal Med C, Sauerbruchstr 1, D-17475 Greifswald, Germany
关键词
acute myeloid leukemia; full spectrum flow cytometry; measurable residual disease; Flow-MRD; PROGNOSTIC IMPACT; AML; MRD;
D O I
10.1002/cyto.a.24811
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multiparameter flow cytometry (MFC) has emerged as a standard method for quantifying measurable residual disease (MRD) in acute myeloid leukemia. However, the limited number of available channels on conventional flow cytometers requires the division of a diagnostic sample into several tubes, restricting the number of cells and the complexity of immunophenotypes that can be analyzed. Full spectrum flow cytometers overcome this limitation by enabling the simultaneous use of up to 40 fluorescent markers. Here, we used this approach to develop a good laboratory practice-conform single-tube 19-color MRD detection assay that complies with recommendations of the European LeukemiaNet Flow-MRD Working Party. We based our assay on clinically-validated antibody clones and evaluated its performance on an IVD-certified full spectrum flow cytometer. We measured MRD and normal bone marrow samples and compared the MRD data to a widely used reference MRD-MFC panel generating highly concordant results. Using our newly developed single-tube panel, we established reference values in healthy bone marrow for 28 consensus leukemia-associated immunophenotypes and introduced a semi-automated dimensionality-reduction, clustering and cell type identification approach that aids the unbiased detection of aberrant cells. In summary, we provide a comprehensive full spectrum MRD-MFC workflow with the potential for rapid implementation for routine diagnostics due to reduced cell requirements and ease of data analysis with increased reproducibility in comparison to conventional FlowMRD routines.
引用
收藏
页码:181 / 195
页数:15
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