Impact of Allogeneic Stem Cell Transplantation in First Complete Remission in Acute Myeloid Leukemia: a National Population-Based Cohort Study. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation Østgård, L. S., Lund, J. L., Nørgaard, J. M., Nørgaard, M. n., Medeiros, B. C., Nielsen, B. n., Nielsen, O. J., Overgaard, U. M., Kallenbach, M. n., Marcher, C. W., Riis, A. H., Sengeløv, H. n. 2017

Abstract

To examine the outcome of allogeneic stem cell transplantation (HSCT) in first complete remission (CR1) compared to chemotherapy alone in a population-based setting, we identified a cohort of acute myeloid leukemia (AML) patients aged 15-70 years diagnosed between 2000-2014 in Denmark. Using the Danish National Acute Leukemia Registry, we compared relapse risk, relapse-free survival (RFS), and overall survival between patients with non-favorable cytogenetic features receiving post-remission therapy with conventional chemotherapy-only versus those undergoing HSCT in CR1. To minimize immortal time bias, we performed Cox proportional hazards regression, included date of alloHSCT as a time-dependent covariate, and stratified results by age, (<60, =60 years) and cytogenetic risk group. Overall, 1031 patients achieved a CR1. Of these, 196 patients (19%) underwent HSCT. HSCT was associated with decreased relapse-rates (24% versus 49%), despite similar median-time to relapse (287 days versus 265 days). In all subgroups, the risk of relapse was lower, and both relapse-free and overall survival was superior among patients receiving HSCT (overall survival, adjusted mortality ratios (MRs): all patients: 0.54 (CI=0.42-0.71), patients<60 years, 0.58 (CI=0.42-0.81), patients=60 years, 0.42 (CI=0.26-0.69), intermediate risk cytogenetics, 0.63 (CI=0.43-0.87), and adverse risk cytogenetics, 0.40 (CI=0.24-0.67)). In conclusion, in this population-based nation-wide cohort study, HSCT was associated with improved survival both in younger and older patients with intermediate and adverse cytogenetic risk.

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