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    CITATIONS
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    Título
    New criteria to identify risk of progression in monoclonal gammopathy of uncertain significance and smoldering multiple myeloma based on multiparameter flow cytometry analysis of bone marrow plasma cells
    Autor(es)
    Pérez Persona, Ernesto
    Vidriales Vicente, María BelénAutoridad USAL
    Mateo, Gemma
    García Sanz, RamónAutoridad USAL
    Mateos Manteca, María VictoriaAutoridad USAL
    de Coca, Alfonso García
    Galende, Josefina
    Martín-Núñez, Guillermo
    Alonso, José M.
    de las Heras, Natalia
    Hernández, José M.
    Martin, Alejandro
    López-Berges, Consuelo
    Orfao de Matos Correia e Vale, José AlbertoAutoridad USAL
    San Miguel Izquierdo, Jesús Fernando
    Palabras clave
    Mieloma múltiple
    Fecha de publicación
    2007-10-01
    Editor
    American Society of Hematology
    Citación
    Pérez-Persona, E., Vidriales, M. B., Mateo, G., García-Sanz, R., Mateos, M. V., de Coca, A. G., ... & San Miguel, J. F. (2007). New criteria to identify risk of progression in monoclonal gammopathy of uncertain significance and smoldering multiple myeloma based on multiparameter flow cytometry analysis of bone marrow plasma cells. Blood, The Journal of the American Society of Hematology, 110(7), 2586-2592. https://doi.org/10.1182/blood-2007-05-088443. Epub 2007 Jun 18. PMID: 17576818.
    Resumen
    [EN] Monoclonal gammopathy of uncertain significance (MGUS) and smoldering multiple myeloma (SMM) are plasma cell disorders with a risk of progression of approximately 1% and 10% per year, respectively. We have previously shown that the proportion of bone marrow (BM) aberrant plasma cells (aPCs) within the BMPC compartment (aPC/BMPC) as assessed by flow cytometry (FC) contributes to differential diagnosis between MGUS and multiple myloma (MM). The goal of the present study was to investigate this parameter as a marker for risk of progression in MGUS (n = 407) and SMM (n = 93). Patients with a marked predominance of aPCs/BMPC (> or = 95%) at diagnosis displayed a significantly higher risk of progression both in MGUS and SMM (P< .001). Multivariate analysis for progression-free survival (PFS) selected the percentage aPC/BMPC (> or = 95%) as the most important independent variable, together with DNA aneuploidy and immunoparesis, for MGUS and SMM, respectively. Using these independent variables, we have identified 3 risk categories in MGUS (PFS at 5 years of 2%, 10%, and 46%, respectively; P< .001) and SMM patients (PFS at 5 years of 4%, 46%, and 72%, respectively; P < .001). Our results show that multiparameter FC evaluation of BMPC at diagnosis is a valuable tool that could help to individualize the follow-up strategy for MGUS and SMM patients.
    URI
    http://hdl.handle.net/10366/154361
    ISSN
    0006-4971
    DOI
    10.1182/blood-2007-05-088443
    Versión del editor
    https://doi.org/10.1182/blood-2007-05-088443
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