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A Retrospective Study on Infusion-Related Reactions to Rituximab in a Heterogeneous Pediatric Population
Clément Legeay1, Henrique Bittencourt1, Elie Haddad1
1Department of Pharmacy (CL, RT), CHU Ste Justine, University of Montreal, Montréal, Quebec, Canada; Department of Oncology-Haematology (HB), CHU Ste Justine, University of Montreal, Montréal, Quebec, Canada; Department of Pediatrics, Department of Microbiology, Infectiology and Immunology (EH), University of Montreal, Montreal, Quebec, Canada; Department of Pharmacy (JSR), CHU d'Angers, University of Angers, Angers, France; Department of Medical Information (VTS), CHU d'Angers, University of Angers, Angers, France.
Insights
Infusion-related reactions to rituximab were common with the first dose in pediatric patients but rare thereafter. Elevated absolute lymphocyte count was identified as a key risk factor for these reactions.
Area of Science:
- Pediatric Hematology/Oncology
- Immunology
- Pharmacology
Background:
- Rituximab is an important therapeutic agent used for various conditions in pediatric patients.
- Understanding infusion-related reactions (IRRs) is crucial for safe rituximab administration.
- Pediatric populations may exhibit unique responses to immunotherapy.
Purpose of the Study:
- To evaluate the incidence, severity, and risk factors of infusion-related reactions to rituximab.
- To analyze outcomes of these reactions in a diverse group of pediatric patients.
- To identify predictors for rituximab-induced infusion-related reactions.
Main Methods:
- Retrospective analysis of pediatric patients receiving rituximab between July 2010 and July 2012.
- Data collection included demographics, infusion details, reaction grading, and biological markers (absolute lymphocyte count, lactate dehydrogenase).
- Multivariate analysis was employed to identify significant risk factors for infusion-related reactions.
Main Results:
- Sixty-seven pediatric patients received 282 rituximab infusions for 17 different indications.
- Infusion-related reactions occurred in 30 patients (44.8%), predominantly grade 1 or 2.
- Reactions were significantly more frequent during the first infusion (39.2%) compared to subsequent infusions (2.7%).
- Elevated absolute lymphocyte count was the sole identified risk factor for infusion-related reactions (OR = 1.03; 95% CI: 1.01-1.06; p = 0.014).
Conclusions:
- Rituximab infusion-related reactions are frequent during the initial dose in pediatric patients but uncommon in later infusions.
- These reactions are generally mild and effectively managed with pharmacological interventions.
- Pre-infusion absolute lymphocyte count is a significant predictor of infusion-related reactions in pediatric rituximab recipients.
Objectives:
To assess risks and outcomes of infusion-related reactions to rituximab in a heterogeneous pediatric population.
Methods:
All patients who received rituximab between July 2010 and July 2012 were retrieved from the pharmacy software and included for analysis. Data were collected according to 4 categories: demographic data, infusion data, infusion-related reactions, and biological data considered as risk factors (i.e., absolute lymphocyte count, lactate dehydrogenase levels).
Results:
Sixty-seven patients treated for a total of 17 different indications were included. A total of 282 rituximab infusions were administered. Forty-three, mostly grade 1 or 2, infusion-related reactions occurred in 30 patients. Reactions occurred in 39.2% "first-dose" infusions, but this rate dropped drastically to 2.7% in subsequent doses. In multivariate analysis, high absolute lymphocyte count was the only risk factor for infusion-related reaction (OR = 1.03; 95% CI: 1.01-1.06; p = 0.014).
Conclusions:
Rituximab infusion-related reactions in a heterogeneous pediatric population were frequent on first infusion, but rare in subsequent ones. Overall, these reactions were mild and manageable through pharmacological treatment. Patients with an elevated absolute lymphocyte count before infusion were at greater risk for an infusion-related reaction.
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