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Risks and mitigation strategies to prevent etoposide infusion-related reactions in children
Emma M Tillman1, Sarah L Suppes2, Nicholas Miles1
1Division of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Insights
Etoposide infusion reactions in pediatric cancer patients are uncommon but can occur. Strategies like pre-treatment and extended infusions help manage these adverse drug reactions (ADRs).
Area of Science:
- Pediatric Oncology
- Clinical Pharmacology
- Patient Safety
Background:
- Etoposide is a critical antineoplastic agent for pediatric cancers.
- Infusion-related reactions are a known complication of etoposide therapy.
- Understanding the incidence and management of these reactions is crucial for patient care.
Purpose of the Study:
- To compare etoposide infusion-related reactions over a decade at two pediatric hospitals.
- To analyze the impact of interventions on reaction rates.
- To evaluate the safety of rechallenging patients after adverse drug reactions (ADRs).
Main Methods:
- Retrospective analysis of etoposide infusion-related reactions over 10 years.
- Comparison of reaction rates between two freestanding pediatric hospitals.
- Evaluation of outcomes for patients rechallenged after experiencing ADRs.
Main Results:
- Overall infusion reaction rate was 1% across both institutions.
- Specific rates at Children's Mercy Hospital increased post-2017 (4.8% in 2018, 3.4% in 2019, 7.9% in 2020) following in-line filter implementation.
- 41% of 32 patients with reactions were rechallenged and tolerated future doses with modifications.
Conclusions:
- Multicenter collaboration is vital for investigating adverse drug reactions (ADRs).
- Variations in clinical practice can reveal important information about ADRs and risk factors.
- Management strategies, including pre-treatment and extended infusions, enable safe rechallenge of patients.
Abstract:
Etoposide is an antineoplastic agent widely used for treatment of many pediatric cancers. Etoposide has been associated with infusion-related reactions. In this brief report, we compare etoposide infusion-related reactions that occurred over a 10-year period at two freestanding pediatric hospitals. Infusion reactions occurred in 1% of patients at two hospitals across the study period. Rates of 4.8%, 3.4%, and 7.9% were observed at Children's Mercy Hospital during 2018, 2019, and 2020, respectively, after the implementation of in-line filters during etoposide infusions in late 2017. Of the 32 patients who experienced adverse reactions, 41% were rechallenged after the reaction and all were able to tolerate at least one future dose with either pre-treatment or extending infusion duration. This work highlights the importance of a multicenter approach to investigating adverse drug reactions (ADRs) as variation in practice can provide key information about ADRs and potential risk factors.
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