Table 1.

Characteristics of patients with ALL, overall and by DI

VariableEntire cohort (n = 644)Normal DI (n = 455)High DI (n = 189)P value
Age at diagnosis, median (range), y 5 (1-18) 5 (1-18) 4 (1-18) .7 
Age at study enrollment, median (range), y 6 (2-19) 6 (2-19) 6 (2-19) .9 
Length of follow-up from study enrollment, median (range), y 7.9 (0.2-13.0) 7.9 (0.4-10.6) 7.9 (0.2-13.0) .7 
Male, n (%) 444 (68.9) 312 (68.6) 132 (69.8) .8 
Race/ethnicity, n (%)     
African American or Black 115 (17.9) 78 (17.1) 37 (19.6) .2 
Asian 98 (15.2) 76 (16.7) 22 (11.6) 
Hispanic 215 (33.4) 143 (31.4) 72 (38.1) 
Non-Hispanic White 216 (33.5) 158 (34.7) 58 (30.7) 
ALL subtype, n (%)     
B-lymphoblastic leukemia 569 (89.2) 399 (88.9) 170 (90.0) .5 
T-lymphoblastic leukemia 69 (10.8) 50 (11.1) 19 (10.1) .7 
NCI risk group, n (%)     
Standard risk 377 (59.0) 263 (58.2) 114 (60.7) .5 
Cytogenetics, n (%)     
Favorable 262 (43.3) 197 (45.7) 65 (37.4) .07 
Neutral 307 (50.7) 213 (49.4) 94 (54.0) 
Unfavorable 36 (6.0) 21 (4.9) 15 (8.6) 
Treatment interruptions during months 1-4     
Patients, n (%) 163 (25.3) 110 (24.2) 53 (28.0) .6 
Days, mean (±SD) 5.5 (9.0) 5.3 (9.2) 6.1 (8.5) .3 
Treatment interruptions during months 5-6     
Patients, n (%) 156 (24.4) 93 (20.5) 63 (34.1) <.001 
Days, mean (±SD) 2.7 (6.2) 2.3 (6.2) 3.6 (6.0) .02 
VariableEntire cohort (n = 644)Normal DI (n = 455)High DI (n = 189)P value
Age at diagnosis, median (range), y 5 (1-18) 5 (1-18) 4 (1-18) .7 
Age at study enrollment, median (range), y 6 (2-19) 6 (2-19) 6 (2-19) .9 
Length of follow-up from study enrollment, median (range), y 7.9 (0.2-13.0) 7.9 (0.4-10.6) 7.9 (0.2-13.0) .7 
Male, n (%) 444 (68.9) 312 (68.6) 132 (69.8) .8 
Race/ethnicity, n (%)     
African American or Black 115 (17.9) 78 (17.1) 37 (19.6) .2 
Asian 98 (15.2) 76 (16.7) 22 (11.6) 
Hispanic 215 (33.4) 143 (31.4) 72 (38.1) 
Non-Hispanic White 216 (33.5) 158 (34.7) 58 (30.7) 
ALL subtype, n (%)     
B-lymphoblastic leukemia 569 (89.2) 399 (88.9) 170 (90.0) .5 
T-lymphoblastic leukemia 69 (10.8) 50 (11.1) 19 (10.1) .7 
NCI risk group, n (%)     
Standard risk 377 (59.0) 263 (58.2) 114 (60.7) .5 
Cytogenetics, n (%)     
Favorable 262 (43.3) 197 (45.7) 65 (37.4) .07 
Neutral 307 (50.7) 213 (49.4) 94 (54.0) 
Unfavorable 36 (6.0) 21 (4.9) 15 (8.6) 
Treatment interruptions during months 1-4     
Patients, n (%) 163 (25.3) 110 (24.2) 53 (28.0) .6 
Days, mean (±SD) 5.5 (9.0) 5.3 (9.2) 6.1 (8.5) .3 
Treatment interruptions during months 5-6     
Patients, n (%) 156 (24.4) 93 (20.5) 63 (34.1) <.001 
Days, mean (±SD) 2.7 (6.2) 2.3 (6.2) 3.6 (6.0) .02 

NCI risk group includes both B-cell and T-cell ALL. Favorable cytogenetics included t(12;21); hyperdiploidy; trisomy 4 and 10; or trisomy 4, 10, and 17. Unfavorable cytogenetics included t(9;22), t(4;11), hypodiploidy, or extreme hypodiploidy. Neutral cytogenetics implied absence of favorable or unfavorable cytogenetics. Data were missing across ALL subtype (n = 6; all in normal DI group), NCI risk group (n = 5, 3 in normal DI group and 2 in high DI group), and cytogenetics (n = 39, 24 in normal DI group and 15 in high DI group). Proportions exclude missing data. P value compares characteristics between patients in normal DI and high DI groups.

SD, standard deviation.

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