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. 2020 Oct 15;4(20):5011–5024. doi: 10.1182/bloodadvances.2020002512

Table 1.

Patient series

Wet laboratory In silico
SAL Bologna TCGA*
No. of patients 40 24 147
Males/females, n 26/14 17/7 81/66
Age, n
 0-14 y 0 0 0
 15-39 y 2 3 27
 40-59 y 13 12 45
 >60 y 25 9 75
WBC count at presentation, median (range), ×103/μL 10.55 (0.8-218.5) 45 (1.5-153) 20 (1-297)
Percentage of BM blasts, median (range) 63.7 (30-90) 16.5 (0.4-57) 72 (11-99)
Cytogenetic risk group, n (%)
 ELN favorable 0 (0) 6 (26.1) 17 (12)
 ELN intermediate 0 (0) 7 (30.4) 96 (65)
 ELN adverse 40 (100) 5 (21.7) 32 (22)
 NA 0 (0) 5 (21.7) 2 (1)
TP53 status
 Mutated 40 2 14
 WT 0 22
 Not tested/not available 133
Induction chemotherapy
 7 + 3 5 2 113
 Fludarabine based 8
 Daunorubicin + cytarabine 21 0
 MAV 12 5
 HMAs 3 14
 Lenalidomide 1 9
 Other 1 6 11
Cohort-wide OS (mo from diagnosis), median (range) 5.06 (0.03-158.3) 16.5 (0.3-57) 15.5 (0.1-118.1)

SAL, Studien-Allianz Leukämie; ELN, European Leukemia-Net; HMAs, hypomethylating agents; MAV, mitoxantrone, cytarabine, and etoposide; WBC, white blood cell.

*

Cases of newly diagnosed nonpromyelocytic AML with RNA-sequencing data and clinical annotation.