Fig. 4: Additional transcriptional biomarkers for pediatric AML.

a Isolating AMLs that did not have one of the five core fusion alterations, additional cytomolecular subtypes clustered with one another based on LSC47: NPM1, CEBPA, and FLT3 internal tandem duplication (ITD) mutation. b Kaplan–Meier estimates for the probability of EFS within the training cohort for CEBPA, FLT3-ITD, and Other Subtype AMLs. Survival differences were determined using the log-rank test (two-sided and without multiple-testing adjustments). c Notable genes included in LSC47 but not LSC17. Genes are connected to the cytomolecular classes based on whether they contribute to the associated LSC signature and score.