Skip to main content
. 2021 Mar 29;12:634956. doi: 10.3389/fphar.2021.634956

TABLE 2.

Baseline characteristics of relapsed ALL patients with or without NR3C1 mutations.

Characteristic Without NR3C1 mutations With NR3C1 mutations p Value
Case number (N = ) 16 2
Age (%) > = 1, = <10 14 (87.5) 0 (0.0) 0.039
<1, >10 2 (12.5) 2 (100.0)
Gender (%) Female 7 (43.8) 1 (50.0) 1
Male 9 (56.2) 1 (50.0)
WBC (%) <50 × 109/L 16 (100.0) 2 (100.0) NA
Liver (%) <2 cm 10 (62.5) 1 (50.0) 1
> = 2, <5 cm 4 (25.0) 1 (50.0)
> = 5 cm 2 (12.5) 0 (0.0)
Spleen (%) <2 cm 10 (71.4) 1 (100.0) 1
> = 2, <5 cm 4 (28.6) 0 (0.0)
> = 5 cm 16 (100.0) 2 (100.0) NA
Immunophenotype (%) B-ALL 16 (100.0) 2 (100.0) NA
Fusion genes (%) Not identified 10 (62.5) 1 (50.0) 0.641
ETV6-RUNX1 3 (18.8) 1 (50.0)
E2A-fusion 1 (6.2) 0 (0.0)
BCR-ABL 1 (6.2) 0 (0.0)
Others 1 (6.2) 0 (0.0)
BM relapse (%) No 4 (25.0) 0 (0.0) 1
Yes 12 (75.0) 2 (100.0)
CNS relapse (%) No 13 (81.2) 2 (100.0) 1
Yes 3 (18.8) 0 (0.0)
Testis relapse (%) No 11 (68.8) 2 (100.0) 1
Yes 5 (31.2) 0 (0.0)
Combination relapse (%) No 13 (81.2) 2 (100.0) 1
Yes 3 (18.8) 0 (0.0)
Risk stratification (%) Standard risk 4 (25.0) 0 (0.0) 0.255
Intermediate risk 11 (68.8) 1 (50.0)
High risk 1 (6.2) 1 (50.0)

NA, not applicable.