Long-term benefits of autologous stem cell transplantation versus intensive chemotherapy consolidation for acute myeloid leukemia patients: A propensity score matching analysis from the PETHEMA AML registry
Alfonso-Pierola, Ana; Martínez-Cuadrón, David; Rodríguez-Veiga, Rebeca; Gil, Cristina; Martínez-Sánchez, Pilar; Bernal, Teresa; Benavente, Celina; Romero-Riquelme, Mónica-A; Serrano-López, Josefina; Bergua, Juan-M; García-Boyero, Raimundo; Tormo, Mar; Herrera, Pilar; Sossa-Melo, Claudia-L; Pérez-Simon, José-A; Rodríguez-Medina, Carlos; Bass-Maturana, María-F; López-Lorenzo, José-L; Algarra-Algarra, Lorenzo; Vidriales-Vicente, Belén; Pérez-Encinas, Manuel; Barrios-García, Manuel; Vives, Susana; Sayas-Lloris, María-J; Capurro, Marisa; Hidalgo, Sebastian; Olave, Mayte; Cuervo-Lozada, Diana; Lavilla-Rubira, Esperanza; Casado, Felipe; Mena-Duran, Armando; Valero-Núñez, Marta; Casado-Calderón, Soledad; Balerdi, Amaia; Torres, Vivianne; Fernández, Rosa; Noriega, Victor; Stevenazzi, Mariana; Labrador, Jorge; León-Maldonado, Pilar; de-Rueda-Ciller, Beatriz; Arce-Fernández, Olga; Amigo, María-Luz; Raposo-Puglia, José-Ángel; Sole, María; Boluda, Blanca; Ayala, Rosa; Barragán, Eva; Montesinos, Pau
Fecha:
2025-11
Resumen:
While allogeneic stem cell transplantation (allo-SCT) is the preferred consolidation for high and most intermediate-risk acute myeloid leukemia (AML) patients in first remission, the role of autologous SCT (auto-SCT) vs. chemotherapy (CT) when allo-SCT is not feasible or indicated, remains controversial. We conducted a real-world, retrospective cohort study using the PETHEMA AML registry to compare auto-SCT and CT. Multivariate Cox regression and propensity score matching (PS-matching) were used to adjust for confounding factors. A total of 1272 patients in first remission and who received 2 consolidation courses were included (615 receiving additional CT cycles and 657 undergoing auto-SCT). Overall, 78.08% of auto-SCT patients were diagnosed before 2017, compared to 38.11% in the CT cohort (p < 0.001). In the overall cohort, auto-SCT was associated with significantly prolonged overall survival (OS) (HR: 0.73, p < 0.001) and relapse-free survival (RFS) (HR: 0.73, p < 0.001). This benefit was particularly evident in patients ?65 years, those with normal karyotype, and FLT3-ITD negativity. In the PS-matched cohort, the RFS advantage persisted (HR: 0.80, p = 0.092), but OS differences were not statistically significant (HR: 0.91, p = 0.563). The role of auto-SCT in the genomic and targeted agent era should not be discarded.
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