Table 2.

ALL subtypes and risk groups by treatment arm and in the combined cohort

n (%)InO n = 43SC n = 48Combined n = 91Leukemic subtype–based classification of risk group 
BCR::ABL1+ 6 (14.0) 7 (14.6) 13 (14.3)  High-risk BCR::ABL1+ 
BCR::ABL1 like 7 (16.3) 5 (10.2) 12 (13.2) High-risk BCR::ABL1 
Low hypodiploidy 3 (7.0) 8 (16.7) 11 (12.1) High-risk BCR::ABL1 
KMT2A 2 (4.7) 6 (12.5) 8 (8.8) High-risk BCR::ABL1 
DUX4 3 (7.0) 2 (4.2) 5 (5.5) Standard to intermediate risk 
Hyperdiploid  3 (7.0) 3 (3.3) Standard to intermediate risk 
CDX2/UBTF 2 (4.7) 1 (2.1) 3 (3.3) Undetermined risk 
B-other 1 (2.3) 1 (2.1) 2 (2.2) Undetermined risk 
MEF2D 1 (2.3) 1 (2.1) 2 (2.2) Standard to intermediate risk 
PAX5alt 2 (4.2) 2 (2.2) Standard to intermediate risk 
TCF3::PBX1 1 (2.3) 1 (2.1) 2 (2.2) Standard to intermediate risk 
ZEB2/CEBP 2 (4.2) 2 (2.2) Undetermined risk 
ZNF384 1 (2.3) 1 (1.1) Standard to intermediate risk 
Low-blast§  13 (30.2) 12 (24.5) 25 (27.5) Low blast 
n (%)InO n = 43SC n = 48Combined n = 91Leukemic subtype–based classification of risk group 
BCR::ABL1+ 6 (14.0) 7 (14.6) 13 (14.3)  High-risk BCR::ABL1+ 
BCR::ABL1 like 7 (16.3) 5 (10.2) 12 (13.2) High-risk BCR::ABL1 
Low hypodiploidy 3 (7.0) 8 (16.7) 11 (12.1) High-risk BCR::ABL1 
KMT2A 2 (4.7) 6 (12.5) 8 (8.8) High-risk BCR::ABL1 
DUX4 3 (7.0) 2 (4.2) 5 (5.5) Standard to intermediate risk 
Hyperdiploid  3 (7.0) 3 (3.3) Standard to intermediate risk 
CDX2/UBTF 2 (4.7) 1 (2.1) 3 (3.3) Undetermined risk 
B-other 1 (2.3) 1 (2.1) 2 (2.2) Undetermined risk 
MEF2D 1 (2.3) 1 (2.1) 2 (2.2) Standard to intermediate risk 
PAX5alt 2 (4.2) 2 (2.2) Standard to intermediate risk 
TCF3::PBX1 1 (2.3) 1 (2.1) 2 (2.2) Standard to intermediate risk 
ZEB2/CEBP 2 (4.2) 2 (2.2) Undetermined risk 
ZNF384 1 (2.3) 1 (1.1) Standard to intermediate risk 
Low-blast§  13 (30.2) 12 (24.5) 25 (27.5) Low blast 

B-other, cases without an identified subtype-defining driver genetic alteration.

Paietta et al2.

ABL1 T315I mutations were reported in 9 patients (InO, n = 3; SC, n = 6).

Confirmed by RNA-sequencing copy number variation (analysis) for absence of fusions and absence of CREBBP mutations.

§

Low-blast: blasts of <30%; subtype undetermined.