| Literature DB >> 25434303 |
J Schetelig1, M Schaich2, K Schäfer-Eckart3, M Hänel4, W E Aulitzky5, H Einsele6, N Schmitz7, W Rösler8, M Stelljes9, C D Baldus10, A D Ho11, A Neubauer12, H Serve13, J Mayer14, W E Berdel9, B Mohr2, U Oelschlägel2, S Parmentier2, C Röllig2, M Kramer2, U Platzbecker2, T Illmer2, C Thiede2, M Bornhäuser2, G Ehninger2.
Abstract
The optimal timing of allogeneic hematopoietic stem cell transplantation (HCT) in acute myeloid leukemia (AML) is controversial. We report on 1179 patients with a median age of 48 years who were randomized upfront. In the control arm, sibling HCT was scheduled in the first complete remission for intermediate-risk or high-risk AML and matched unrelated HCT in complex karyotype AML. In the experimental arm, matched unrelated HCT in first remission was offered also to patients with an FLT3-ITD (FMS-like tyrosine kinase 3-internal tandem duplication) allelic ratio >0.8, poor day +15 marrow blast clearance and adverse karyotypes. Further, allogeneic HCT was recommended in high-risk AML to be performed in aplasia after induction chemotherapy. In the intent-to-treat (ITT) analysis, superiority of the experimental transplant strategy could not be shown with respect to overall survival (OS) or event-free survival. As-treated analyses suggest a profound effect of allogeneic HCT on OS (HR 0.73; P=0.002) and event-free survival (HR 0.67; P<0.001). In high-risk patients, OS was significantly improved after allogeneic HCT in aplasia (HR 0.64; P=0.046) and after HCT in remission (HR 0.74; P=0.03). Although superiority of one study arm could not be demonstrated in the ITT analysis, secondary analyses suggest that early allogeneic HCT is a promising strategy for patients with high-risk AML.Entities:
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Year: 2014 PMID: 25434303 DOI: 10.1038/leu.2014.335
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528