Multiparameter flow cytometry (MFC) is one of the essential ancillary methods in bone marrow (BM) investigation of patients with cytopenia and suspected myelodysplastic syndrome (MDS). MFC can also be applied in the follow-up of MDS patients undergoing treatment. This document summarizes recommendations from the International/European Leukemia Net Working Group for Flow Cytometry in Myelodysplastic Syndromes (ELN iMDS Flow) on the analytical issues in MFC for the diagnostic work-up of MDS. Recommendations for the analysis of several BM cell subsets such as myeloid precursors, maturing granulocytic and monocytic components and erythropoiesis are given. A core set of 17 markers identified as independently related to a cytomorphologic diagnosis of myelodysplasia is suggested as mandatory for MFC evaluation of BM in a patient with cytopenia. A myeloid precursor cell (CD34(+)CD19(-)) count >3% should be considered immunophenotypically indicative of myelodysplasia. However, MFC results should always be evaluated as part of an integrated hematopathology work-up. Looking forward, several machine-learning-based analytical tools of interest should be applied in parallel to conventional analytical methods to investigate their usefulness in integrated diagnostics, risk stratification, and potentially even in the evaluation of response to therapy, based on MFC data. In addition, compiling large uniform datasets is desirable, as most of the machine-learning-based methods tend to perform better with larger numbers of investigated samples, especially in such a heterogeneous disease as MDS.

Multiparameter flow cytometry in the evaluation of myelodysplasia: Analytical issues. Recommendations from the European LeukemiaNet/International Myelodysplastic Syndrome Flow Cytometry Working Group / Porwit, Anna; Béné, Marie C; Duetz, Carolien; Matarraz, Sergio; Oelschlaegel, Uta; Westers, Theresia M; Wagner-Ballon, Orianne; Kordasti, Shahram; Valent, Peter; Preijers, Frank; Alhan, Canan; Bellos, Frauke; Bettelheim, Peter; Burbury, Kate; Chapuis, Nicolas; Cremers, Eline; Della Porta, Matteo G; Dunlop, Alan; Eidenschink-Brodersen, Lisa; Font, Patricia; Fontenay, Michaela; Hobo, Willemijn; Ireland, Robin; Johansson, Ulrika; Loken, Michael R; Ogata, Kiyoyuki; Orfao, Alberto; Psarra, Katherina; Saft, Leonie; Subira, Dolores; Te Marvelde, Jeroen; Wells, Denise A; Van Der Velden, Vincent H J; Kern, Wolfgang; Van De Loosdrecht, Arjan A. - In: CYTOMETRY. PART B, CLINICAL CYTOMETRY. - ISSN 1552-4957. - 104:1(2023), pp. 27-50. [10.1002/cyto.b.22108]

Multiparameter flow cytometry in the evaluation of myelodysplasia: Analytical issues. Recommendations from the European LeukemiaNet/International Myelodysplastic Syndrome Flow Cytometry Working Group

Kordasti, Shahram
Membro del Collaboration Group
;
2023-01-01

Abstract

Multiparameter flow cytometry (MFC) is one of the essential ancillary methods in bone marrow (BM) investigation of patients with cytopenia and suspected myelodysplastic syndrome (MDS). MFC can also be applied in the follow-up of MDS patients undergoing treatment. This document summarizes recommendations from the International/European Leukemia Net Working Group for Flow Cytometry in Myelodysplastic Syndromes (ELN iMDS Flow) on the analytical issues in MFC for the diagnostic work-up of MDS. Recommendations for the analysis of several BM cell subsets such as myeloid precursors, maturing granulocytic and monocytic components and erythropoiesis are given. A core set of 17 markers identified as independently related to a cytomorphologic diagnosis of myelodysplasia is suggested as mandatory for MFC evaluation of BM in a patient with cytopenia. A myeloid precursor cell (CD34(+)CD19(-)) count >3% should be considered immunophenotypically indicative of myelodysplasia. However, MFC results should always be evaluated as part of an integrated hematopathology work-up. Looking forward, several machine-learning-based analytical tools of interest should be applied in parallel to conventional analytical methods to investigate their usefulness in integrated diagnostics, risk stratification, and potentially even in the evaluation of response to therapy, based on MFC data. In addition, compiling large uniform datasets is desirable, as most of the machine-learning-based methods tend to perform better with larger numbers of investigated samples, especially in such a heterogeneous disease as MDS.
2023
ELN; consensus; flow cytometry; myelodysplastic syndromes; standardization
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11566/316353
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