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Depth of response in multiple myeloma: A pooled analysis of three PETHEMA/GEM clinical trials

Authors :
European Research Council
International Myeloma Foundation
Federación Española de Enfermedades Raras
Asociación Española Contra el Cáncer
Red Temática de Investigación Cooperativa en Cáncer (España)
Instituto de Salud Carlos III
European Commission
Lahuerta, Juan José
Paiva, Bruno
Vidriales, Maria Belén
Cordón, Lourdes
Cedena, Maria-Teresa
Puig, Noemi
Martínez-López, Joaquín
Rosiñol, Laura
Gutiérrez, Norma Carmen
Martín-Ramos, María-Luisa
Oriol, Albert
Teruel, Ana-Isabel
Echeveste, María-Asunción
Paz, Raquel de
Arriba, Felipe de
Hernandez, Miguel T.
Palomera, Luis
Martínez, Rafael
Martín, Alejandro
Alegre, Adrián
Rubia, Javier de la
Orfao, Alberto
Mateos, Maria Victoria
Bladé, Joan
San Miguel, Jesús F.
European Research Council
International Myeloma Foundation
Federación Española de Enfermedades Raras
Asociación Española Contra el Cáncer
Red Temática de Investigación Cooperativa en Cáncer (España)
Instituto de Salud Carlos III
European Commission
Lahuerta, Juan José
Paiva, Bruno
Vidriales, Maria Belén
Cordón, Lourdes
Cedena, Maria-Teresa
Puig, Noemi
Martínez-López, Joaquín
Rosiñol, Laura
Gutiérrez, Norma Carmen
Martín-Ramos, María-Luisa
Oriol, Albert
Teruel, Ana-Isabel
Echeveste, María-Asunción
Paz, Raquel de
Arriba, Felipe de
Hernandez, Miguel T.
Palomera, Luis
Martínez, Rafael
Martín, Alejandro
Alegre, Adrián
Rubia, Javier de la
Orfao, Alberto
Mateos, Maria Victoria
Bladé, Joan
San Miguel, Jesús F.
Publication Year :
2017

Abstract

[Purpose]: To perform a critical analysis on the impact of depth of response in newly diagnosed multiple myeloma (MM). [Patients and Methods]: Data were analyzed from 609 patients who were enrolled in the GEM (Grupo Español de Mieloma) 2000 and GEM2005MENOS65 studies for transplant-eligible MM and the GEM2010MAS65 clinical trial for elderly patients with MM who had minimal residual disease (MRD) assessments 9 months after study enrollment. Median follow-up of the series was 71 months. [Results]: Achievement of complete remission (CR) in the absence of MRD negativity was not associated with prolonged progression-free survival (PFS) and overall survival (OS) compared with near-CR or partial response (median PFS, 27, 27, and 29 months, respectively; median OS, 59, 64, and 65 months, respectively). MRD-negative status was strongly associated with prolonged PFS (median, 63 months; P < .001) and OS (median not reached; P < .001) overall and in subgroups defined by prior transplantation, disease stage, and cytogenetics, with prognostic superiority of MRD negativity versus CR particularly evident in patients with high-risk cytogenetics. Accordingly, Harrell C statistics showed higher discrimination for both PFS and OS in Cox models that included MRD (as opposed to CR) for response assessment. Superior MRD-negative rates after different induction regimens anticipated prolonged PFS. Among 34 MRD-negative patients with MM and a phenotypic pattern of bone marrow involvement similar to monoclonal gammopathy of undetermined significance at diagnosis, the probability of >operational cure> was high; median PFS was 12 years, and the 10-year OS rate was 94%. [Conclusion]: Our results demonstrate that MRD-negative status surpasses the prognostic value of CR achievement for PFS and OS across the disease spectrum, regardless of the type of treatment or patient risk group. MRD negativity should be considered as one of the most relevant end points for transplant-eligible and elderly fit p

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1103439404
Document Type :
Electronic Resource