Table 2.

Patient characteristics (immunotherapy cohort)

All patients (N = 45)Patients with TP53 mutations and/or 17p abnormalities (n = 15*)
Age, median (range), y 61 (27-81) 61 (27-81) 
Males/females, n 24/21 8/7 
AML risk stratification (2017 ELN), n (%)   
 Favorable 3 (6.7) 0 (0) 
 Intermediate 8 (17.8) 0 (0) 
 Adverse 34 (75.6) 15 (100) 
Secondary AML, n (%) 15 (33.3) 7 (46.7) 
No. of prior lines of therapy, median (range) 2 (1-9) 2 (1-4) 
All patients (N = 45)Patients with TP53 mutations and/or 17p abnormalities (n = 15*)
Age, median (range), y 61 (27-81) 61 (27-81) 
Males/females, n 24/21 8/7 
AML risk stratification (2017 ELN), n (%)   
 Favorable 3 (6.7) 0 (0) 
 Intermediate 8 (17.8) 0 (0) 
 Adverse 34 (75.6) 15 (100) 
Secondary AML, n (%) 15 (33.3) 7 (46.7) 
No. of prior lines of therapy, median (range) 2 (1-9) 2 (1-4) 
*

BM samples from 13 out of 15 patients were available for immune gene expression profiling. All 15 patients with TP53 mutations/17p abnormalities were included in clinical analyses.

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