We report the long-term results of a randomized trial (GITMO, AML-R2), comparing 1:1 the combination of busulfan and cyclophosphamide (BuCy2, n = 125) and the combination of busulfan and fludarabine (BuFlu, n = 127) as conditioning regimen in acute myeloid leukemia patients (median age 51 years, range 40–65) undergoing allogeneic hematopoietic stem cell transplantation. With a median follow-up of 6 years, significantly better non-relapse mortality (NRM) was confirmed in BuFlu recipients, which is sustained up to 4 years after transplant (10% vs. 20%, p = 0.0388). This difference was higher in patients older than 51 years (11% in BuFlu vs. 27% in BuCy2, p = 0.0262). The cumulative incidence of relapse, which was the first cause of death in the entire study population, did not differ between the two randomized arms. Similarly, the leukemia-free survival (LFS) and overall survival (OS) were not different in the two cohorts, even when stratifying patients per median age. Graft-and relapse-free survival (GRFS) in BuFlu arm vs. the BuCy2 arm was 25% vs. 20% at 4 years and 20% vs. 17% at 10 years. Hence, the benefit gained by NRM reduction is not offsets by an increased relapse. Leukemia relapse remains a major concern, urging the development of new therapeutic approaches.

Busulfan-fludarabine versus busulfan-cyclophosphamide for allogeneic transplant in acute myeloid leukemia: long term analysis of GITMO AML-R2 trial / Cavallaro, G.; Grassi, A.; Pavoni, C.; Mico, M. C.; Busca, A.; Cavattoni, I. M.; Santarone, S.; Borghero, C.; Olivieri, A.; Milone, G.; Chiusolo, P.; Musto, P.; Saccardi, R.; Patriarca, F.; Pane, F.; Saporiti, G.; Rivela, P.; Terruzzi, E.; Cerretti, R.; Marotta, G.; Carella, A. M.; Nagler, A.; Russo, D.; Corradini, P.; Bernasconi, P.; Iori, A. P.; Castagna, L.; Mordini, N.; Oldani, E.; Di Grazia, C.; Bacigalupo, A.; Rambaldi, A.. - In: BLOOD CANCER JOURNAL. - ISSN 2044-5385. - 14:1(2024). [10.1038/s41408-024-01116-5]

Busulfan-fludarabine versus busulfan-cyclophosphamide for allogeneic transplant in acute myeloid leukemia: long term analysis of GITMO AML-R2 trial

Cavallaro G.;Borghero C.;Olivieri A.;Patriarca F.;Pane F.;
2024

Abstract

We report the long-term results of a randomized trial (GITMO, AML-R2), comparing 1:1 the combination of busulfan and cyclophosphamide (BuCy2, n = 125) and the combination of busulfan and fludarabine (BuFlu, n = 127) as conditioning regimen in acute myeloid leukemia patients (median age 51 years, range 40–65) undergoing allogeneic hematopoietic stem cell transplantation. With a median follow-up of 6 years, significantly better non-relapse mortality (NRM) was confirmed in BuFlu recipients, which is sustained up to 4 years after transplant (10% vs. 20%, p = 0.0388). This difference was higher in patients older than 51 years (11% in BuFlu vs. 27% in BuCy2, p = 0.0262). The cumulative incidence of relapse, which was the first cause of death in the entire study population, did not differ between the two randomized arms. Similarly, the leukemia-free survival (LFS) and overall survival (OS) were not different in the two cohorts, even when stratifying patients per median age. Graft-and relapse-free survival (GRFS) in BuFlu arm vs. the BuCy2 arm was 25% vs. 20% at 4 years and 20% vs. 17% at 10 years. Hence, the benefit gained by NRM reduction is not offsets by an increased relapse. Leukemia relapse remains a major concern, urging the development of new therapeutic approaches.
2024
Busulfan-fludarabine versus busulfan-cyclophosphamide for allogeneic transplant in acute myeloid leukemia: long term analysis of GITMO AML-R2 trial / Cavallaro, G.; Grassi, A.; Pavoni, C.; Mico, M. C.; Busca, A.; Cavattoni, I. M.; Santarone, S.; Borghero, C.; Olivieri, A.; Milone, G.; Chiusolo, P.; Musto, P.; Saccardi, R.; Patriarca, F.; Pane, F.; Saporiti, G.; Rivela, P.; Terruzzi, E.; Cerretti, R.; Marotta, G.; Carella, A. M.; Nagler, A.; Russo, D.; Corradini, P.; Bernasconi, P.; Iori, A. P.; Castagna, L.; Mordini, N.; Oldani, E.; Di Grazia, C.; Bacigalupo, A.; Rambaldi, A.. - In: BLOOD CANCER JOURNAL. - ISSN 2044-5385. - 14:1(2024). [10.1038/s41408-024-01116-5]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/994275
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