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    Haematologica. 2014 Oct 24. pii: haematol.2014.110452. doi: 10.3324/haematol.2014.110452
    Validation of cytogenetic risk groups according to International Prognostic Scoring Systems by peripheral blood CD34+FISH: results from a German diagnostic study in comparison with an international control group.
    Braulke F1,  Platzbecker U2,  Müller-Thomas C3,  Götze K4,  Germing U5,  Brümmendorf TH6,  Nolte F7,  Hofmann WK8,  Giagounidis AA9,  Lübbert M10,  Greenberg PL11,  Bennett JM12,  Solé F13,  Mallo M14,  Slovak ML15,  Ohyashiki K16,  Le Beau MM17,  Tüchler H18,  Pfeilstöcker M19,  Nösslinger T20,  Hildebrandt B21,  Shirneshan K22,  Aul C23,  Stauder R24,  Sperr WR25,  Valent P26,  Fonatsch C27,  Trümper L28,  Haase D29,  Schanz J30
    Author information
    1Department of Hematology and Medical Oncology, University Medicine of Goettingen, Germany friederike.braulke@med.uni-goettingen.de.
    2Department of Hematology and Oncology, University of Dresden, Germany.
    3Department of Hematology and Oncology, Technical University of Munich, Germany.
    4Department of Hematology and Oncology, Technical University of Munich, Germany.
    5Department of Hematology and Oncology, University of Duesseldorf, Germany.
    6Department of Hematology and Oncology, Uniklinik, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen, Germany.
    7Department of Hematology and Oncology, University Hospital of Mannheim, Germany.
    8Department of Hematology and Oncology, University Hospital of Mannheim, Germany.
    9Department of Hematology and Oncology, Marienhospital, Duesseldorf, Germany.
    10Department of Hematology and Oncology, University of Freiburg Medical Center, Germany.
    11Department of Hematology, Stanford University Cancer Center, CA, USA.
    12University of Rochester Medical Center, NY, USA.
    13Institut de Recerca Contra la Leucemia Josep Carreras, Badalona, Spain.
    14Institut de Recerca Contra la Leucemia Josep Carreras, Badalona, Spain.
    15Sonora Quest Laboratories, Phoenix, AZ, USA.
    16Tokyo Medical University, Tokyo, Japan.
    17University of Chicago, IL, USA.
    18Hanusch Hospital, Boltzmann Institute for Leukemia Research, Vienna, Austria.
    19Third Medical Department for Hematology and Oncology and L. Boltzmann Institute for Leukemia Research and Hematology, Hanusch Hospital, Vienna, Austria.
    20Third Medical Department for Hematology and Oncology and L. Boltzmann Institute for Leukemia Research and Hematology, Hanusch Hospital, Vienna, Austria.
    21Department of Human Genetics, University of Düsseldorf, Germany.
    22Department of Hematology and Medical Oncology, University Medicine of Goettingen, Germany.
    23Department of Hematology, Oncology, and Clinical Immunology, St. Johannes Hospital, Duisburg, Germany.
    24Department of Internal Medicine, Innsbruck Medical University, Austria.
    25Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Austria.
    26Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Austria.
    27Department of Medical Genetics, Medical University of Vienna, Vienna, Austria.
    28Department of Hematology and Medical Oncology, University Medicine of Goettingen, Germany.
    29Department of Hematology and Medical Oncology, University Medicine of Goettingen, Germany.
    30Department of Hematology and Medical Oncology, University Medicine of Goettingen, Germany.
    Abstract

    International Prognostic Scoring Systems are used to determine the individual risk profile of myelodysplastic syndrome patients. For the assessment of International Prognostic Scoring Systems, an adequate chromosome banding analysis of the bone marrow is essential. Cytogenetic information is not available for a substantial number of patients (5%-20%) with dry marrow or an insufficient number of metaphase cells. For these patients, a valid risk classification is impossible. In the study presented here, the International Prognostic Scoring Systems were validated based on fluorescence in situ hybridization analyses using extended probe panels applied to cluster of differentiation 34 positive (CD34(+)) peripheral blood cells of 328 MDS patients of our prospective multicenter German diagnostic study and compared to chromosome banding results of 2902 previously published patients with myelodysplastic syndromes. For cytogenetic risk classification by fluorescence in situ hybridization analyses of CD34(+) peripheral blood cells, the groups differed significantly for overall and leukemia-free survival by uni- and multivariate analyses without discrepancies between treated and untreated patients. Including cytogenetic data of fluorescence in situ hybridization analyses of peripheral CD34(+) blood cells (instead of bone marrow banding analysis) into the complete International Prognostic Scoring System assessment, the prognostic risk groups separated significantly for overall and leukemia-free survival. Our data show that a reliable stratification to the risk groups of the International Prognostic Scoring Systems is possible from peripheral blood in patients with missing chromosome banding analysis by using a comprehensive probe panel (clinicaltrials.gov identifier:01355913).


    Copyright© Ferrata Storti Foundation.

    Publikations ID: 25344522
    Quelle: öffnen
     
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