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

Author:

Pérez-Persona Ernesto1,Vidriales María-Belén12,Mateo Gema1,García-Sanz Ramón12,Mateos Maria-Victoria1,de Coca Alfonso García3,Galende Josefina4,Martín-Nuñez Guillermo5,Alonso José M.6,de las Heras Natalia7,Hernández José M.8,Martín Alejandro9,López-Berges Consuelo1,Orfao Alberto210,San Miguel Jesús F.12

Affiliation:

1. Department of Hematology, University Hospital, Salamanca;

2. Centro de Investigación del Cancer, Universidad de Salamanca/Consejo Superior de Investigaciones Cientificas (CSIC), Salamanca;

3. Department of Hematology, University Hospital, Valladolid;

4. Department of Hematology, Hospital Comarcal del Bierzo, Ponferrada, León;

5. Department of Hematology, Hospital Nuestra Señora del Puerto de Plasencia, Cáceres;

6. Department of Hematology, Hospital Río Carrión, Palencia, Caceres;

7. Department of Hematology, Complejo Hospitalario, León;

8. Department of Hematology, General Hospital, Segovia;

9. Department of Hematology, Hospital Virgen de la Concha, Zamora; and

10. Department of Cytometry, University of Salamanca, Salamanca, Spain

Abstract

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 (≥ 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 (≥ 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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