Between December 2002 and November 2008, 657 patients between the ages of 17 and 60 years with de novo untreated AML were enrolled on ECOG-ACRIN Cancer Research Group study E1900 (#NCT00049517) as detailed in Fernandez et al.17 Cytogenetic risk assignment was according to Slovak et al.20 Patients were classified as indeterminate risk if they had unknown cytogenetic risk as per Slovak et al or lacked sufficient data for classification. Testing for presence of an FMS-like tyrosine kinase internal tandem duplication (FLT3-ITD) and mixed-lineage leukemia partial tandem duplication (MLL-PTD) was conducted centrally as previously described.17,21-23 Sequencing of NPM1, DNMT3A, IDH1/2, NRAS, CEBPA, TET2, WT1, KIT, RUNX1, ASXL1, PHF6, KRAS, PTEN, and TP53 was later conducted on banked samples as described by Patel et al.18 FLT3-ITD allelic ratio was not available. The median follow-up time from the patients still alive and included in the current analysis, calculated from the time of randomization for induction therapy, was 80.1 months (range, 0.8-120.4 months). In total, 25 (4%) patients were lost to follow-up.
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