Repositori URV

Identificador: imarina:9280994

Handle: https://hdl.handle.net/20.500.11797/imarina9280994

Autores:
Palazon-Carrion, NataliaMartin Garcia-Sancho, AlejandroNogales-Fernandez, EstebanJimenez-Cortegana, CarlosCarnicero-Gonzalez, FernandoRios-Herranz, Eduardode la Cruz-Vicente, FatimaRodriguez-Garcia, GuillermoFernandez-Alvarez, RubenMartinez-Banaclocha, NatividadGuma-Padro, JosepGomez-Codina, JoseSalar-Silvestre, AntonioRodriguez-Abreu, DelvysGalvez-Carvajal, LauraLabrador, JorgeGuirado-Risueno, MariaGarcia-Dominguez, Daniel JHontecillas-Prieto, LourdesEspejo-Garcia, PabloFernandez-Roman, IsabelProvencio-Pulla, MarianoSanchez-Beato, MargaritaNavarro, MartaMarylene, LejeuneAlvaro-Naranjo, TomasCasanova-Espinosa, MariaSanchez-Margalet, VictorRueda-Dominguez, Antoniode la Cruz-Merino, Luis

Resumen:
New therapeutic options are needed in relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). Lenalidomide-based schedules can reverse rituximab refractoriness in lymphoma.In the phase II R2-GDP trial, 78 patients unsuitable for autologous stem cell transplant received treatment with the following schedule: lenalidomide 10 mg Days (D)1-14, rituximab 375 mg/m2 D1, cisplatin 60 mg/m2 D1, gemcitabine 750 mg/m2 D1 and D8, and dexamethasone 20 mg D1-3, up to 6 cycles (induction phase), followed by lenalidomide 10 mg (or last lenalidomide dose received) D1-21 every 28 days (maintenance phase). Primary endpoint was overall response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), safety, and monitorization of key circulating immune biomarkers (EU Clinical Trials Register number: EudraCT 2014-001620-29).After a median follow-up of 37 months, ORR was 60.2% [37.1% complete responses (CR) and 23.1% partial responses (PR)]. Median OS was 12 months (47 vs. 6 months in CR vs. no CR); median PFS was 9 months (34 vs. 5 months in CR vs. no CR). In the primary refractory population, ORR was 45.5% (21.2% CR and 24.3% PR). Most common grade 3-4 adverse events were thrombocytopenia (60.2%), neutropenia (60.2%), anemia (26.9%), infections (15.3%), and febrile neutropenia (14.1%). Complete responses were associated with a sharp decrease in circulating myeloid-derived suppressor cells and regulatory T cells.R2-GDP schedule is feasible and highly active in R/R DLBCL, including the primary refractory population. Immune biomarkers showed differences in responders versus progressors.©2022 The Authors; Published by the American Association for Cancer Research.