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Revisiting guidelines for integration of flow cytometry results in the WHO classification of myelodysplastic syndromes-proposal from the International/European LeukemiaNet Working Group for Flow Cytometry in MDS.

Identifieur interne : 001B12 ( Ncbi/Merge ); précédent : 001B11; suivant : 001B13

Revisiting guidelines for integration of flow cytometry results in the WHO classification of myelodysplastic syndromes-proposal from the International/European LeukemiaNet Working Group for Flow Cytometry in MDS.

Auteurs : A. Porwit [Canada] ; A A Van De Loosdrecht [Pays-Bas] ; P. Bettelheim [Autriche] ; L Eidenschink Brodersen [États-Unis] ; K. Burbury [Australie] ; E. Cremers [Pays-Bas] ; M G Della Porta [Italie] ; R. Ireland [Royaume-Uni] ; U. Johansson [Royaume-Uni] ; S. Matarraz [Espagne] ; K. Ogata [Japon] ; A. Orfao [Espagne] ; F. Preijers [Pays-Bas] ; K. Psarra [Grèce] ; D. Subirá [Espagne] ; P. Valent [Autriche] ; V H J. Van Der Velden [Pays-Bas] ; D. Wells [États-Unis] ; T M Westers [Pays-Bas] ; W. Kern [Allemagne] ; M C Béné [France]

Source :

RBID : pubmed:24919805

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English descriptors

Abstract

Definite progress has been made in the exploration of myelodysplastic syndromes (MDS) by flow cytometry (FCM) since the publication of the World Health Organization 2008 classification of myeloid neoplasms. An international working party initiated within the European LeukemiaNet and extended to include members from Australia, Canada, Japan, Taiwan and the United States has, through several workshops, developed and subsequently published consensus recommendations. The latter deal with preanalytical precautions, and propose small and large panels, which allow evaluating immunophenotypic anomalies and calculating myelodysplasia scores. The current paper provides guidelines that strongly recommend the integration of FCM data with other diagnostic tools in the diagnostic work-up of MDS.

DOI: 10.1038/leu.2014.191
PubMed: 24919805

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pubmed:24919805

Le document en format XML

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<name sortKey="Valent, P" sort="Valent, P" uniqKey="Valent P" first="P" last="Valent">P. Valent</name>
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<name sortKey="Van Der Velden, V H J" sort="Van Der Velden, V H J" uniqKey="Van Der Velden V" first="V H J" last="Van Der Velden">V H J. Van Der Velden</name>
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<name sortKey="Bene, M C" sort="Bene, M C" uniqKey="Bene M" first="M C" last="Béné">M C Béné</name>
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<name sortKey="Matarraz, S" sort="Matarraz, S" uniqKey="Matarraz S" first="S" last="Matarraz">S. Matarraz</name>
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<name sortKey="Ogata, K" sort="Ogata, K" uniqKey="Ogata K" first="K" last="Ogata">K. Ogata</name>
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<country xml:lang="fr">Espagne</country>
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<name sortKey="Bene, M C" sort="Bene, M C" uniqKey="Bene M" first="M C" last="Béné">M C Béné</name>
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<nlm:affiliation>Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
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<region type="region">Pays de la Loire</region>
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<title level="j">Leukemia</title>
<idno type="eISSN">1476-5551</idno>
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<term>Myelodysplastic Syndromes (classification)</term>
<term>Myelodysplastic Syndromes (diagnosis)</term>
<term>World Health Organization</term>
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<div type="abstract" xml:lang="en">Definite progress has been made in the exploration of myelodysplastic syndromes (MDS) by flow cytometry (FCM) since the publication of the World Health Organization 2008 classification of myeloid neoplasms. An international working party initiated within the European LeukemiaNet and extended to include members from Australia, Canada, Japan, Taiwan and the United States has, through several workshops, developed and subsequently published consensus recommendations. The latter deal with preanalytical precautions, and propose small and large panels, which allow evaluating immunophenotypic anomalies and calculating myelodysplasia scores. The current paper provides guidelines that strongly recommend the integration of FCM data with other diagnostic tools in the diagnostic work-up of MDS.</div>
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<Year>2014</Year>
<Month>09</Month>
<Day>03</Day>
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<Year>2014</Year>
<Month>10</Month>
<Day>31</Day>
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<Year>2017</Year>
<Month>02</Month>
<Day>20</Day>
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<Volume>28</Volume>
<Issue>9</Issue>
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<Year>2014</Year>
<Month>Sep</Month>
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<Title>Leukemia</Title>
<ISOAbbreviation>Leukemia</ISOAbbreviation>
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<ArticleTitle>Revisiting guidelines for integration of flow cytometry results in the WHO classification of myelodysplastic syndromes-proposal from the International/European LeukemiaNet Working Group for Flow Cytometry in MDS.</ArticleTitle>
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<MedlinePgn>1793-8</MedlinePgn>
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<AbstractText>Definite progress has been made in the exploration of myelodysplastic syndromes (MDS) by flow cytometry (FCM) since the publication of the World Health Organization 2008 classification of myeloid neoplasms. An international working party initiated within the European LeukemiaNet and extended to include members from Australia, Canada, Japan, Taiwan and the United States has, through several workshops, developed and subsequently published consensus recommendations. The latter deal with preanalytical precautions, and propose small and large panels, which allow evaluating immunophenotypic anomalies and calculating myelodysplasia scores. The current paper provides guidelines that strongly recommend the integration of FCM data with other diagnostic tools in the diagnostic work-up of MDS.</AbstractText>
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<LastName>Porwit</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
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<Affiliation>Department of Pathobiology and Laboratory Medicine, University of Toronto, University Health Network, Toronto General Hospital, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>van de Loosdrecht</LastName>
<ForeName>A A</ForeName>
<Initials>AA</Initials>
<AffiliationInfo>
<Affiliation>Department of Hematology, Cancer Center Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
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<ForeName>P</ForeName>
<Initials>P</Initials>
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<ForeName>E</ForeName>
<Initials>E</Initials>
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<Affiliation>Department of Hematology, Cancer Center Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
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<LastName>Della Porta</LastName>
<ForeName>M G</ForeName>
<Initials>MG</Initials>
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<LastName>Ireland</LastName>
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</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ogata</LastName>
<ForeName>K</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Metropolitan Research Center for Blood Disorders MRC JAPAN, Midorigaoka, Chofu, Tokyo, Japan.</Affiliation>
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<Initials>A</Initials>
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</Author>
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<LastName>Preijers</LastName>
<ForeName>F</ForeName>
<Initials>F</Initials>
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<Affiliation>Department of Hematology, St Radboud University Medical Center, Nijmegen, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Psarra</LastName>
<ForeName>K</ForeName>
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</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Subirá</LastName>
<ForeName>D</ForeName>
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</Author>
<Author ValidYN="Y">
<LastName>Valent</LastName>
<ForeName>P</ForeName>
<Initials>P</Initials>
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<Affiliation>Department of Internal Medicine I, Division of Hematology and Hemostaseology and Ludwig Boltzmann Cluster Oncology, Medical University of Vienna, Vienna, Austria.</Affiliation>
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<Author ValidYN="Y">
<LastName>van der Velden</LastName>
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<ForeName>D</ForeName>
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<LastName>Westers</LastName>
<ForeName>T M</ForeName>
<Initials>TM</Initials>
<AffiliationInfo>
<Affiliation>Department of Hematology, Cancer Center Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
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<Author ValidYN="Y">
<LastName>Kern</LastName>
<ForeName>W</ForeName>
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<Affiliation>MLL Munich Leukemia Laboratory, Munich, Germany.</Affiliation>
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<AffiliationInfo>
<Affiliation>Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.</Affiliation>
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