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

Author:

Fokken Hendrik1ORCID,Waclawski Julian1,Kattre Nadine1,Kloos Arnold1,Müller Sebastian23,Ettinger Max4,Kacprowski Tim23,Heuser Michael1,Maetzig Tobias56,Schwarzer Adrian167ORCID

Affiliation:

1. Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation Hannover Medical School Hannover Germany

2. Division Data Science in Biomedicine Peter L. Reichertz Institute for Medical Informatics of TU Braunschweig and Hannover Medical School Braunschweig Germany

3. Braunschweig Integrated Centre for Systems Biology (BRICS) TU Braunschweig Braunschweig Germany

4. Department of Orthopedic Surgery Hannover Medical School Hannover Germany

5. Department of Pediatric Hematology Hannover Medical School Hannover Germany

6. Institute of Experimental Hematology Hannover Medical School Hannover Germany

7. CCC‐MV and Department of Internal Medicine C University Medicine Greifswald Greifswald Germany

Abstract

AbstractMultiparameter 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.

Funder

Deutsche Krebshilfe

Else Kröner-Fresenius-Stiftung

José Carreras Leukämie-Stiftung

Publisher

Wiley

Subject

Cell Biology,Histology,Pathology and Forensic Medicine

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