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Published on: June 11, 2012
Hyperglycemia during induction therapy for acute lymphoblastic leukemia is temporally linked to pegaspargase
Netanya I Pollock1,2, Yael Flamand3, Jia Zhu1,2
1Division of Endocrinology, Boston Children's Hospital, Boston, Massachusetts, USA.
Insights
Hyperglycemia is common in children with acute lymphoblastic leukemia (ALL) treated with chemotherapy. Older age, female sex, and family history of diabetes increase risk, necessitating frequent glucose monitoring during induction therapy.
Area of Science:
- Pediatric Oncology
- Endocrinology
- Pharmacology
Background:
- Chemotherapy regimens including glucocorticoids and pegaspargase are known to cause hyperglycemia in children with acute lymphoblastic leukemia (ALL).
- The specific patterns and risk factors for this hyperglycemia during induction chemotherapy are not well understood.
- This study aimed to characterize hyperglycemia and its associated factors in pediatric ALL patients receiving these agents.
Purpose of the Study:
- To determine the pattern of hyperglycemia in children with ALL undergoing induction chemotherapy.
- To identify demographic and clinical factors associated with hyperglycemia during this treatment phase.
- To understand factors linked to the need for insulin treatment in these patients.
Main Methods:
- Retrospective analysis of 213 pediatric patients treated between 2010 and 2020.
- Data on demographics, glucose levels, and insulin regimens were collected.
- Hyperglycemia was defined as ≥200 mg/dl on at least two occasions; logistic regression identified predictive factors.
Main Results:
- The prevalence of hyperglycemia was 23%, with glucose levels peaking 3 days after pegaspargase administration.
- Predictors of hyperglycemia included older age (≥10 years), female sex, and a family history of diabetes.
- Older age, family history of diabetes, and higher BMI were associated with requiring insulin treatment.
Conclusions:
- Hyperglycemia onset is temporally linked to pegaspargase administration in pediatric ALL induction chemotherapy.
- Key risk factors for hyperglycemia include older age, female sex, and family history of diabetes.
- Frequent glucose monitoring is crucial during induction therapy for ALL to manage hyperglycemia effectively.
Background:
Chemotherapy regimens containing glucocorticoids and pegaspargase are associated with hyperglycemia; however, the pattern and underlying risk factors are not well characterized. We determined the pattern of hyperglycemia and associated factors in children with acute lymphoblastic leukemia (ALL) receiving glucocorticoids and pegaspargase during induction.
Methods:
Retrospective analysis of patients treated between 2010 and 2020 at a single institution. Pretreatment data, glucose values, and insulin regimens were abstracted from the record. Hyperglycemia was defined as two or more random glucose measurements ≥200 mg/dl. Analyses of demographic and clinical factors were conducted with logistic regression.
Results:
Two hundred thirteen patients, median age 6 years (range 1.0-18.9 years), 47% female, were included. The prevalence of hyperglycemia was 23% (n = 48). Mean glucose levels peaked 3 days following administration of pegaspargase. In multivariable analysis, age ≥10 years (odds ratio [OR] 6.2, 95% confidence interval [CI]: 2.9-13.4), female sex (OR 2.7, 95% CI: 1.2-6.2), and family history of diabetes (OR 3.2, 95% CI: 1.4-7.3) were predictive of hyperglycemia. Age ≥10 years (OR 19.4, 95% CI: 5.5-68.4), family history of diabetes (OR 8.2, 95% CI: 2.7-25.3), and higher body mass index (BMI) (OR 1.8, 95% CI: 1.1-2.9) were associated with insulin treatment.
Conclusions:
Onset of hyperglycemia in children receiving induction chemotherapy for ALL is temporally linked to administration of pegaspargase. Older age, female sex, and family history of diabetes are predictive of hyperglycemia during induction; older age, family history of diabetes, and higher BMI are associated with insulin treatment. Frequent glucose monitoring is indicated during induction therapy for ALL.
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