Autologous stem cell transplantation for relapsed/refractory large B-cell lymphoma: a multicenter GETH-TC/GELTAMO study
Bento, Leyre; Gutiérrez, Antonio; Martínez, Carmen; Orti-Verdet, María-Consejo; Sorribes, Marina; Caballero, Ana-Carolina; Peña, Marta; Pérez, Ariadna; Jiménez-Ubieto, Ana; Medina, Lucía; Bastos-Oreiro, Mariana; Fernández-Caldas-González, Paula; Navarro, Belén; Salcedo, Isabel; Abrisqueta, Pau; Español-Morales, Ignacio; Cornago, Javier; Martín-Moro, Fernando; García, Lucía; Gómez, Pilar; Varela, María-Rosario; Puente, María; Zanabili, Joud; Zudaire, Teresa; Zeberio, Izaskun; del-Campo, Raquel; González, Leslie; González, Pedro; Blázquez, Cristina; Rovira, Jordina; Sitges, Marta; Franch-Sarto, Mireia; Cabero, Almudena; Mussetti, Alberto; Montoro, Juan; Sampol, Antonia; Sureda, Anna; Caballero, Dolores; Martín-García-Sancho, Alejandro
Fecha:
2025-07-08
Resumen:
We performed a retrospective multicenter study including 791 patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL) who underwent autologous stem cell transplantation (ASCT). After a median follow-up of 74 months from infusion, 65% were alive and 84% free of disease. Progression-free survival (PFS) and overall survival (OS) at 6 years were 51% and 63%, respectively. Non-relapse mortality at 1 year was 9%. Age >60 years at ASCT (hazard ratio [HR], 1.31; 95% CI, 1.06-1.62; P = .011), ASCT as ?3rd line (HR, 1.81; 95% CI, 1.42-2.31; P < .001), and partial response (PR) vs complete response (CR) at ASCT (HR, 1.46; 95% CI. 1.18-1.81; P < .001) were independent variables influencing PFS. Age >60 years at ASCT (HR, 1.62; 95% CI, 1.24-2.12; P < .001), time period before 1 November 2012 (HR, 1.40; 95% CI, 1.07-1.83; P = .014), ASCT as ?3rd line (HR, 1.77; 95% CI, 1.32-2.37; P < .001), PR vs CR (HR, 1.58; 95% CI, 1.22-2.05; P < .001), and stable disease vs CR pre-ASCT (HR, 3.41; 95% CI, 1.81-6.45; P < .001) were variables associated with worse OS. Refractory/early relapse did not significantly influence survival (6-year PFS and OS in patients with refractory, early, and late relapse were 54% and 64%, 46% and 62%, and 49% and 63%, respectively). To our knowledge, this is the largest series analyzing the efficacy of ASCT in patients with R/R LBCL after rituximab-containing frontline therapy. Our results indicate that ASCT is a curative option for patients with chemosensitive disease.
Mostrar el registro completo del ítem