Table 3.

Proportion of patients with high-risk acute lymphoblastic leukemia with adverse events in induction on pediatric protocols by age25 

Cohort, No. (%)*P value
Overall (N = 235)<15 years (n = 176)≥15 years (n = 59)
Any adverse event 190 (80.9) 139 (78.9) 51 (86.4) .21 
Infection 83 (35.3) 62 (35.2) 21 (35.6) .96 
Hypertension 72 (30.6) 52 (29.6) 20 (33.9) .53 
Hepatotoxicity 72 (30.6) 45 (25.6) 27 (45.8) <.01 
Fever 58 (24.7) 44 (25.0) 14 (23.7) .84 
Hypoxia 46 (19.6) 35 (19.9) 11 (18.6) .84 
Hyperglycemia 42 (17.9) 26 (14.8) 16 (27.1) .03 
Sepsis 28 (11.9) 21 (11.9) 7 (11.9) .98 
Hypotension 27 (11.5) 18 (10.2) 9 (15.3) .29 
Thromboembolism 21 (8.9) 12 (6.8) 9 (15.3) .04 
Neuropathy 11 (4.7) 6 (3.4) 5 (8.5) .11 
Hyponatremia 8 (3.4) 6 (3.4) 2 (3.4) 
Pancreatitis 8 (3.4) 6 (3.4) 2 (3.4) 
Seizure 6 (2.6) 4 (2.3) 2 (3.4) .64 
Ileus 5 (2.1) 4 (2.3) 1 (1.7) 
Constipation 3 (1.3) 3 (1.7) 0 (0.0) .6 
ARDS 3 (1.3) 1 (1.7) 2 (1.1) 
Stroke 2 (0.9) 1 (0.6) 1 (1.7) .44 
Anaphylaxis 2 (0.9) 1 (0.6) 1 (1.7) .44 
Cohort, No. (%)*P value
Overall (N = 235)<15 years (n = 176)≥15 years (n = 59)
Any adverse event 190 (80.9) 139 (78.9) 51 (86.4) .21 
Infection 83 (35.3) 62 (35.2) 21 (35.6) .96 
Hypertension 72 (30.6) 52 (29.6) 20 (33.9) .53 
Hepatotoxicity 72 (30.6) 45 (25.6) 27 (45.8) <.01 
Fever 58 (24.7) 44 (25.0) 14 (23.7) .84 
Hypoxia 46 (19.6) 35 (19.9) 11 (18.6) .84 
Hyperglycemia 42 (17.9) 26 (14.8) 16 (27.1) .03 
Sepsis 28 (11.9) 21 (11.9) 7 (11.9) .98 
Hypotension 27 (11.5) 18 (10.2) 9 (15.3) .29 
Thromboembolism 21 (8.9) 12 (6.8) 9 (15.3) .04 
Neuropathy 11 (4.7) 6 (3.4) 5 (8.5) .11 
Hyponatremia 8 (3.4) 6 (3.4) 2 (3.4) 
Pancreatitis 8 (3.4) 6 (3.4) 2 (3.4) 
Seizure 6 (2.6) 4 (2.3) 2 (3.4) .64 
Ileus 5 (2.1) 4 (2.3) 1 (1.7) 
Constipation 3 (1.3) 3 (1.7) 0 (0.0) .6 
ARDS 3 (1.3) 1 (1.7) 2 (1.1) 
Stroke 2 (0.9) 1 (0.6) 1 (1.7) .44 
Anaphylaxis 2 (0.9) 1 (0.6) 1 (1.7) .44 

Bold values indicate statistically significant results.

Permission to use data was obtained from the authors of the primary manuscript. All patients in the cohort were treated on pediatric protocols for high-risk acute lymphoblastic leukemia. Patients ranged from age 1.0 to 19.8 years. Adverse events are grade ≥3 unless otherwise specified.

ARDS, acute respiratory distress syndrome.

*

Percentages represent column percentages.

Clinically significant grade 2 to 5 adverse event.

or Create an Account

Close Modal
Close Modal