Skip to main content
. 2023 Dec 2;8(1):164–171. doi: 10.1182/bloodadvances.2023011862

Table 1.

Demographic characteristics of the University of Chicago ALL cohort (n = 221)

N (%)
Age, median (range), y 43 (18-88)
Female sex, n (%) 105 (48)
BMI, n (%)
 <30 150 (68)
 30-40 54 (24)
 >40 17 (8)
Race/ethnicity, n (%)
 NHW 131 (59)
 Hispanic 48 (22)
 NHB 33 (15)
 Asian 7 (3)
 >1 race 2 (1)
Median income, n (%)
 High 129 (59)
 Middle 73 (33)
 Low 17 (8)
Immunophenotype, n (%)
 B-ALL 185 (84)
 Pre–T-ALL 25 (11)
 ETP-ALL 11 (5)
ALL subtype, n (%)
 B-ALL
 Ph+ 50 (23)
 Ph-like 26 (12)
 Low hypodiploid 17 (8)
 KMT2A-rearranged 13 (6)
 High hyperdiploid 8 (4)
 T-ALL
 HOXA-dysregulated 10 (5)
 TAL1-rearranged 5 (3)
Firstline therapy
 CALGB 10403 based 104 (47)
 HyperCVAD based 41 (19)
 CALGB 10701 25 (11)
 Lower-intensity chemotherapy 12 (5)
 TKI + antibody 11 (5)
 A41703 7 (3)
 Mini-hyperCVD + venetoclax 7 (3)
 Inotuzumab 5 (2)
 TKI 4 (2)
 Asciminib + dasatinib 3 (1)
 Blinatumomab 2 (1)
Allogeneic HCT, n (%) 49 (22)

CVAD, cyclophosphamide, vincristine, adriamycin, dexamethasone; ETP, early T precursor; HCT, hematopoietic cell transplant; Ph, Philadelphia chromosome; T-ALL, T-cell ALL; TKI, tyrosine kinase inhibitor.