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Multicenter prospective evaluation of diagnostic potential of flow cytometric aberrancies in myelodysplastic syndromes by the ELN iMDS flow working group.
Kern, Wolfgang; Westers, Theresia M; Bellos, Frauke; Bene, Marie Christine; Bettelheim, Peter; Brodersen, Lisa Eidenschink; Burbury, Kate; Chu, Sung-Chao; Cullen, Matthew; Porta, Matteo Della; Dunlop, Alan Stewart; Johansson, Ulrika; Matarraz, Sergio; Oelschlaegel, Uta; Ogata, Kiyoyuki; Porwit, Anna; Preijers, Frank; Psarra, Katherina; Saft, Leonie; Subirá, Dolores; Weiß, Elisabeth; van der Velden, Vincent H J; van de Loosdrecht, Arjan.
Afiliação
  • Kern W; MLL Munich Leukemia Laboratory, Munich, Germany.
  • Westers TM; Department of Hematology, Amsterdam University Medical Centers, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Bellos F; MLL Munich Leukemia Laboratory, Munich, Germany.
  • Bene MC; Hematology Biology, Nantes University Hospital, Nantes, France.
  • Bettelheim P; Department of Hematology, Elisabethinen Hospital, Linz, Upper Austria, Austria.
  • Brodersen LE; Hematologics, Inc., Seattle, Washington, USA.
  • Burbury K; Peter MacCallum Cancer Centre, Melbourne, Australia.
  • Chu SC; Department of Hematology and Oncology, Buddhist Tzu Chi General Hospital, Hualien, Taiwan.
  • Cullen M; Haematological Malignancy Diagnostic Service, St James's University Hospital, Leeds, UK.
  • Porta MD; Department of Biomedical Sciences, IRCCS Humanitas Research Hospital, Humanitas University, Milan, Italy.
  • Dunlop AS; Department of Haematology, College Hospital London, London, England.
  • Johansson U; Laboratory Medicine, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.
  • Matarraz S; Cytometry Service (NUCLEUS), Department of Medicine and IBSAL, Cancer Research Center (IBMCC, University of Salamanca-CSIC), Salamanca, Spain and Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Salamanca, Spain.
  • Oelschlaegel U; Department of Internal Medicine, University Hospital of Technical University Dresden, Dresden, Germany.
  • Ogata K; Metropolitan Research and Treatment Centre for Blood Disorders (MRTC Japan), Tokyo, Japan.
  • Porwit A; Division of Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.
  • Preijers F; Department of Laboratory Medicine, Laboratory of Hematology, Radboudumc, Nijmegen, The Netherlands.
  • Psarra K; Immunology Histocompatibility Department, Evangelismos Hospital, Athens, Greece.
  • Saft L; Clinical Pathology and Cancer Diagnostics, Karolinska University Hospital and Institute, Stockholm, Sweden.
  • Subirá D; Department of Medical Immunology, Hospital Universitario de Guadalajara, Guadalajara, Spain.
  • Weiß E; MLL Munich Leukemia Laboratory, Munich, Germany.
  • van der Velden VHJ; Laboratory Medical Immunology, Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • van de Loosdrecht A; Department of Hematology, Amsterdam University Medical Centers, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Cytometry B Clin Cytom ; 104(1): 51-65, 2023 01.
Article em En | MEDLINE | ID: mdl-36416672
ABSTRACT

BACKGROUND:

Myelodysplastic syndromes (MDS) represent a diagnostic challenge. This prospective multicenter study was conducted to evaluate pre-defined flow cytometric markers in the diagnostic work-up of MDS and chronic myelomonocytic leukemia (CMML).

METHODS:

Thousand six hundred and eighty-two patients with suspected MDS/CMML were analyzed by both cytomorphology according to WHO 2016 criteria and flow cytometry according to ELN recommendations. Flow cytometric readout was categorized 'non-MDS' (i.e. no signs of MDS/CMML and limited signs of MDS/CMML) and 'in agreement with MDS' (i.e., in agreement with MDS/CMML).

RESULTS:

Flow cytometric readout categorized 60% of patients in agreement with MDS, 28% showed limited signs of MDS and 12% had no signs of MDS. In 81% of cases flow cytometric readouts and cytomorphologic diagnosis correlated. For high-risk MDS, the level of concordance was 92%. A total of 17 immunophenotypic aberrancies were found independently related to MDS/CMML in ≥1 of the subgroups of low-risk MDS, high-risk MDS, CMML. A cut-off of ≥3 of these aberrancies resulted in 80% agreement with cytomorphology (20% cases concordantly negative, 60% positive). Moreover, >3% myeloid progenitor cells were significantly associated with MDS (286/293 such cases, 98%).

CONCLUSION:

Data from this prospective multicenter study led to recognition of 17 immunophenotypic markers allowing to identify cases 'in agreement with MDS'. Moreover, data emphasizes the clinical utility of immunophenotyping in MDS diagnostics, given the high concordance between cytomorphology and the flow cytometric readout. Results from the current study challenge the application of the cytomorphologically defined cut-off of 5% blasts for flow cytometry and rather suggest a 3% cut-off for the latter.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Leucemia Mielomonocítica Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Cytometry B Clin Cytom Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Leucemia Mielomonocítica Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Cytometry B Clin Cytom Ano de publicação: 2023 Tipo de documento: Article