Multiparameter flow cytometric remission is the most relevant prognostic factor for multiple myeloma patients who undergo autologous stem cell transplantation

Bruno Paiva(Complejo Hospitalario de Salamanca), María‐Belén Vídriales(Complejo Hospitalario de Salamanca), Jorge Cerveró(Complejo Hospitalario de Salamanca), Gema Mateo(Complejo Hospitalario de Salamanca), José J. Pérez(Complejo Hospitalario de Salamanca), María Ángeles Montalbán(Research Institute Hospital 12 de Octubre), Anna Sureda, Laura Montejano(Research Institute Hospital 12 de Octubre), Norma C. Gutiérrez(Complejo Hospitalario de Salamanca), Alfonso García de Coca(Hospital Clínico Universitario de Valladolid), Natalia de las Heras(Hospital de León), María‐Victoria Mateos(Complejo Hospitalario de Salamanca), M C López-Berges(Complejo Hospitalario de Salamanca), Raimundo García‐Boyero(Hospital General Universitari de Castelló), Josefina Galende(Hospital El Bierzo), José‐Ángel Hernández‐Rivas(Hospital General De Segovia), Luis Palomera(Hospital Clínico Universitario Lozano Blesa), Dolores Carrera(Hospital Universitario Central de Asturias), Rafael Martínez(Hospital Clínico San Carlos), Javier de la Rubia, Alejandro Martı́n(Hospital Virgen de la Concha), Joan Bladé(Consorci Institut D'Investigacions Biomediques August Pi I Sunyer), Juan José Lahuerta(Research Institute Hospital 12 de Octubre), Alberto Órfão(Universidad de Salamanca), Jesús F. San Miguel(Complejo Hospitalario de Salamanca)
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Abstract

Minimal residual disease (MRD) assessment is standard in many hematologic malignancies but is considered investigational in multiple myeloma (MM). We report a prospective analysis of the prognostic importance of MRD detection by multiparameter flow cytometry (MFC) in 295 newly diagnosed MM patients uniformly treated in the GEM2000 protocol VBMCP/VBAD induction plus autologous stem cell transplantation [ASCT]). MRD status by MFC was determined at day 100 after ASCT. Progression-free survival (PFS; median 71 vs 37 months, P < .001) and overall survival (OS; median not reached vs 89 months, P = .002) were longer in patients who were MRD negative versus MRD positive at day 100 after ASCT. Similar prognostic differentiation was seen in 147 patients who achieved immunofixation-negative complete response after ASCT. Moreover, MRD(-) immunofixation-negative (IFx(-)) patients and MRD(-) IFx(+) patients had significantly longer PFS than MRD(+) IFx(-) patients. Multivariate analysis identified MRD status by MFC at day 100 after ASCT as the most important independent prognostic factor for PFS (HR = 3.64, P = .002) and OS (HR = 2.02, P = .02). Our findings demonstrate the clinical importance of MRD evaluation by MFC, and illustrate the need for further refinement of MM re-sponse criteria. This trial is registered at http://clinicaltrials.gov under identifier NCT00560053.


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