| Literature DB >> 30943060 |
Ofrat Beyar-Katz1, Noa Lavi1, Shimrit Ringelstein-Harlev1, Israel Henig1, Dana Yehudai-Ofir1, Nuhad Haddad1, Riva Fineman1, Yishai Ofran1,2, Yuval Nov3, Dvora Sahar1, Nivin Moustafa-Hawash4, Jacob M Rowe1,5,2, Tsila Zuckerman1,2.
Abstract
Autologous stem cell transplantation (ASCT), intensifying anti-leukemic effects without significant treatment-related mortality (TRM), is particularly appealing in AML with favorable genetic/molecular profile. This study retrospectively evaluated the outcomes of post-remission treatment in consecutive favorable-risk AML patients. Sixty-six patients were included: 32 had mutated NPM1/wild-type FLT-ITD, 16 had t(8:21) and 18 - inv(16). Forty patients received chemotherapy alone, 26 underwent ASCT upfront. In time-dependent analysis, the ASCT group demonstrated higher relapse-free (RFS) (p = .001) and overall survivals (OS) (p = .0007). The 1-year RFS and OS were 44.2% vs 88% and 71% vs 96% for chemotherapy and ASCT, respectively. The corresponding TRM was 4/40 (10.0%) and 0/26 (0%), with relapse rates of 70.0% and 19.2% (p = .0002). In multivariate analysis, ASCT was associated with superior OS and RFS. In conclusion, ASCT offers significantly superior RFS and OS in favorable-risk AML in first complete remission. These data support the recent resurgence of interest in ASCT for AML.Entities:
Keywords: Acute myeloid leukemia (AML); NPM1 mutation; autologous SCT (ASCT); core-binding factor (CBF) translocation
Year: 2019 PMID: 30943060 DOI: 10.1080/10428194.2019.1594214
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022