Table 2.

Reason for truncation of asparaginase in the main and subcohort

Main cohort, n = 1401, n (% of the cohort)Subcohort, n = 1115, n (% of the cohort)No AEA,* n
Clinical hypersensitivity 208 (14.8) 157 (14.1) 139 
Pancreatitis 88 (6.3) 53 (4.8) 
Thrombosis 24 (1.7) 14 (1.3) — 
Hyperlipidemia 10 (0.7) 8 (0.7) — 
Liver toxicity 7 (0.5) 7 (0.6) — 
Other 21 (1.5) 16 (1.4) — 
Total no. of truncated patients 358 (25.5) 255 (22.9) 140 
 Including patients with silent inactivation (truncatedorAEA-— 301 186 
Main cohort, n = 1401, n (% of the cohort)Subcohort, n = 1115, n (% of the cohort)No AEA,* n
Clinical hypersensitivity 208 (14.8) 157 (14.1) 139 
Pancreatitis 88 (6.3) 53 (4.8) 
Thrombosis 24 (1.7) 14 (1.3) — 
Hyperlipidemia 10 (0.7) 8 (0.7) — 
Liver toxicity 7 (0.5) 7 (0.6) — 
Other 21 (1.5) 16 (1.4) — 
Total no. of truncated patients 358 (25.5) 255 (22.9) 140 
 Including patients with silent inactivation (truncatedorAEA-— 301 186 
*

The “No AEA” column only applies to patients in the subcohort.

Other: for example, sepsis, seizure, parental refusal, and abdominal pain.

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