RT Journal Article T1 Measurable Residual Disease by Next-Generation Flow Cytometry in Multiple Myeloma. A1 Paiva, Bruno A1 Puig, Noemi A1 Cedena, Maria-Teresa A1 Rosiñol, Laura A1 Cordón, Lourdes A1 Vidriales, María-Belén A1 Burgos, Leire A1 Flores-Montero, Juan A1 Sanoja-Flores, Luzalba A1 Lopez-Anglada, Lucia A1 Maldonado, Roberto A1 de la Cruz, Javier A1 Gutierrez, Norma C A1 Calasanz, Maria-Jose A1 Martin-Ramos, Maria-Luisa A1 Garcia-Sanz, Ramón A1 Martinez-Lopez, Joaquin A1 Oriol, Albert A1 Blanchard, María-Jesús A1 Rios, Rafael A1 Martin, Jesus A1 Martinez-Martinez, Rafael A1 Sureda, Anna A1 Hernandez, Miguel-Teodoro A1 de la Rubia, Javier A1 Krsnik, Isabel A1 Moraleda, Jose-Maria A1 Palomera, Luis A1 Bargay, Joan A1 Van Dongen, Jacques J M A1 Orfao, Alberto A1 Mateos, Maria-Victoria A1 Blade, Joan A1 San-Miguel, Jesús F A1 Lahuerta, Juan-José A1 GEM (Grupo Español de Mieloma)/PETHEMA (Programa Para el Estudio de la Terapéutica en Hemopatías Malignas) Cooperative Study Group, AB Assessing measurable residual disease (MRD) has become standard with many tumors, but the clinical meaning of MRD in multiple myeloma (MM) remains uncertain, particularly when assessed by next-generation flow (NGF) cytometry. Thus, we aimed to determine the applicability and sensitivity of the flow MRD-negative criterion defined by the International Myeloma Working Group (IMWG). In the PETHEMA/GEM2012MENOS65 trial, 458 patients with newly diagnosed MM had longitudinal assessment of MRD after six induction cycles with bortezomib, lenalidomide, and dexamethasone (VRD), autologous transplantation, and two consolidation courses with VRD. MRD was assessed in 1,100 bone marrow samples from 397 patients; the 61 patients without MRD data discontinued treatment during induction and were considered MRD positive for intent-to-treat analysis. The median limit of detection achieved by NGF was 2.9 × 10-6. Patients received maintenance (lenalidomide ± ixazomib) according to the companion PETHEMA/GEM2014MAIN trial. Overall, 205 (45%) of 458 patients had undetectable MRD after consolidation, and only 14 of them (7%) have experienced progression thus far; seven of these 14 displayed extraosseous plasmacytomas at diagnosis and/or relapse. Using time-dependent analysis, patients with undetectable MRD had an 82% reduction in the risk of progression or death (hazard ratio, 0.18; 95% CI, 0.11 to 0.30; P The IMWG flow MRD-negative response criterion is highly applicable and sensitive to evaluate treatment efficacy in MM. YR 2019 FD 2019-11-26 LK http://hdl.handle.net/10668/14743 UL http://hdl.handle.net/10668/14743 LA en DS RISalud RD Apr 8, 2025