Long-term results of the GIMEMA VEL-03-096 trial in MM patients receiving VTD consolidation after ASCT: MRD kinetics' impact on survival

S. Ferrero, M. Ladetto, D. Drandi, F. Cavallo, E. Genuardi, M. Urbano, S. Caltagirone, M. Grasso, F. Rossini, T. Guglielmelli, C. Cangialosi, A. M. Liberati, V. Callea, T. Carovita, C. Crippa, L. De Rosa, F. Pisani, A. P. Falcone, P. Pregno, S. OlivaC. Terragna, P. Musto, R. Passera, M. Boccadoro, A. Palumbo

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Polymerase chain reaction (PCR)-based minimal residual disease (MRD) analysis is a useful prognostic tool in multiple myeloma (MM), although its long-term impact still needs to be addressed. This report presents the updated results of the GIMEMA-VEL-03-096 trial. Thirty-nine MM patients receiving bortezomib-thalidomide-dexamethasone after autologous transplantation were monitored for MRD by both nested and real-time quantitative-PCR until relapse. Our data confirm the strong impact of MRD on survival: overall survival was 72% at 8 years median follow-up for patients in major MRD response versus 48% for those experiencing MRD persistence (P=0.041). In addition, MRD kinetics resulted predictive for relapse: indeed median remission duration was not reached for patients in major MRD response, 38 months for those experiencing MRD reappearance and 9 months for patients with MRD persistence (P<0.001). Moreover: (1) 26 patients achieving major MRD response (67%) benefit of excellent disease control (median TNT: 42 months); (2) MRD reappearance heralds relapse, with a TNT comparable to that of MRD persistence (9 versus 10 months, P=0.706); (3) the median lag between MRD reappearance and need for salvage treatment is 9 months. These results suggest the usefulness of a long-term MRD monitoring in MM patients and the need for maintenance or pre-emptive treatments ensuring durable responses.

Lingua originaleInglese
pagine (da-a)689-695
Numero di pagine7
RivistaLeukemia
Volume29
Numero di pubblicazione3
DOI
Stato di pubblicazionePubblicato - 9 mar 2015
Pubblicato esternamente

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