Authors
Daniele Avenoso, Vera Radici, Alessandro Leoni, Cristina Skert, Massimo Martino, Nicola Mordini, Francesco Saraceni, Attilio Olivieri, Fabio Ciceri, Cristina Tecchio, Alessandra Picardi, Giorgia Saporiti, Francesca Patriarca, Paola Bresciani, Chiara Nozzoli, Denise Maravalle, Nicola Polverelli, Gabriele Magliano, Enrico Morello, Mirko Farina, Simona Bernardi, Federica Re, Luca Garuffo, Simone Maifredi, Silvia Zanon, Rachele De Domenico, Michele Malagola, Domenico Russo
Published in
Bone marrow transplantation. Jun 24, 2026. Epub Jun 24, 2026.
Abstract
Evidences supporting the use of myeloablative-dose Treosulfan combined with Fludarabine remain largely retrospective, with outdated prospective studies available. In this phase II multicenter prospective trial, we evaluated the safety and efficacy of FT14 conditioning regimen in patients with acute myeloid leukemia undergoing allogeneic stem cell transplantation in first complete remission.(EudraCT Number:2021-006515-28; Clinical trial number NCT07232953). The study was designed to provide a non-inferior alternative to standard busulfan-containing regimens, which would enable effective transplantation while minimizing toxicity. The primary objective was 1-year Leukemia-free survival (LFS). In total, 82 patients were enrolled in the study with a median follow up of 19.7 months; donor used were matched sibling in 22, matched unrelated 52 and mismatched unrelated in 8 cases, respectively. LFS at 180-day and 365-day were 87.8% and 81.7%, respectively. Cumulative incidence of relapse at 1 year after allo-HSCT was 14.9% with mean time to relapse of 5.6 months. Also, FT14 regimen provided an excellent safety with nearly absent NRM, no cases of septic death, and no cases of primary graft failure. Our study supports the use of FT14 as effective myeloablative conditioning regimen for AML patients aged 40-65 y in first complete remission, especially in patients for whom busulfan based conditioning regimens poses excessive toxic risks.
PMID:
42342968
Bibliographic data and abstract were imported from PubMed on 25 Jun 2026.
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