The persistence of immunophenotypically normal residual bone marrow plasma cells at diagnosis identifies a good prognostic subgroup of symptomatic multiple myeloma patients

Author:

Paiva Bruno1,Vidriales Maria-Belén12,Mateo Gema12,Pérez Jose J.1,Montalbán Maria Angeles3,Sureda Anna4,Montejano Laura3,Gutiérrez Norma C.12,García de Coca Alfonso5,de las Heras Natalia6,Mateos Maria Victoria12,López-Berges Maria Consuelo1,García-Boyero Raimundo7,Galende Josefina8,Hernández Jose9,Palomera Luis10,Carrera Dolores11,Martínez Rafael12,de la Rubia Javier13,Martín Alejandro14,González Yolanda15,Bladé Joan16,Lahuerta Juan José3,Orfao Alberto217,San-Miguel Jesús F.12,

Affiliation:

1. Hospital Universitario de Salamanca, Salamanca;

2. Centro de Investigación del Cáncer, Salamanca;

3. Hospital 12 de Octubre, Madrid;

4. Hospital Santa Creu I Sant Pau, Barcelona;

5. Hospital Clínico Universitario de Valladolid, Valladolid;

6. Complejo Hospitalario de León, León;

7. Hospital General de Castellón, Castellón;

8. Hospital del Bierzo, Ponferrada;

9. Hospital General de Segovia, Segovia;

10. Hospital Lozano Blesa, Zaragoza;

11. Hospital Central de Asturias, Oviedo;

12. Clínico San Carlos, Madrid;

13. Hospital La Fe, Valencia;

14. Hospital Virgen de la Concha, Zamora;

15. Hospital Dr. Josep Trueta, Gerona;

16. Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer Barcelona, Barcelona; and

17. Servicio General de Citometría, Universidad de Salamanca, Salamanca, Spain

Abstract

Abstract Multiparameter flow cytometry immunophenotyping allows discrimination between normal (N-) and myelomatous (MM-) plasma cells (PCs) within the bone marrow plasma cell compartment (BMPCs). Here we report on the prognostic relevance of detecting more than 5% residual normal plasma cells from all bone marrow plasma cells (N-PCs/BMPCs) by multiparameter flow cytometry in a series of 594 newly diagnosed symptomatic MM patients, uniformly treated according to the Grupo Español de MM 2000 (GEM2000) protocol. Our results show that symptomatic MM patients with more than 5% N-PCs/BMPCs (n = 80 of 594; 14%) have a favorable baseline clinical prospect, together with a significantly lower frequency of high-risk cytogenetic abnormalities and higher response rates. Moreover, this group of patients had a significantly longer progression-free survival (median, 54 vs 42 months, P = .001) and overall survival (median, not reached vs 89 months, P = .04) than patients with less than or equal to 5% N-PCs/BMPCs. Our findings support the clinical value of detecting residual normal PCs in MM patients at diagnosis because this reveals a good prognostic category that could benefit from specific therapeutic approaches. This trial was registered at www.clinicaltrials.gov as NCT00560053.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference21 articles.

1. Prognostic value of immunophenotyping in multiple myeloma: a study by the PETHEMA/GEM cooperative study groups on patients uniformly treated with high-dose therapy.;Mateo;J Clin Oncol,2008

2. Immunophenotyping of plasma cells in multiple myeloma.;Mateo;Methods Mol Med,2005

3. Immunophenotypic characterization of plasma cells from monoclonal gammopathy of undetermined significance patients: implications for the differential diagnosis between MGUS and multiple myeloma.;Ocqueteau;Am J Pathol,1998

4. 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.;Perez-Persona;Blood,2007

5. Flow cytometric minimal residual disease monitoring in patients with multiple myeloma undergoing autologous stem cell transplantation: a retrospective study.;Liu;Leuk Lymphoma,2008

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