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Updated: Jul 30, 2026

A Doxorubicin-induced Cardiomyopathy Model in Adult Zebrafish
Published on: June 7, 2018
Doxorubicin cardiotoxicity in children: reduced incidence of cardiac dysfunction associated with continuous-infusion
S G Berrak1, M S Ewer, N Jaffe
1Departments of Medical Specialties and Melanoma/Sarcoma and the Division of Pediatrics, The University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Insights
Continuous doxorubicin infusion significantly reduces cardiotoxicity in pediatric cancer patients. This method offers a safer alternative to rapid infusion, with comparable tumor response rates and lower cardiac complication risks.
Area of Science:
- Pediatric Oncology
- Cardiology
- Pharmacology
Background:
- Doxorubicin is a vital chemotherapy agent for pediatric cancers.
- Rapid infusion of doxorubicin is associated with significant cardiotoxicity.
- Continuous infusion may mitigate cardiac side effects.
Purpose of the Study:
- To evaluate the cardiotoxicity of continuous infusion doxorubicin in children.
- To compare cardiotoxicity rates between continuous and rapid infusion doxorubicin.
- To assess the impact of continuous infusion on tumor response.
Main Methods:
- Retrospective review of 97 pediatric patients treated with doxorubicin.
- Continuous infusion at 60 mg/m2 (24h) or 75 mg/m2 (72h) every 3 weeks.
- Cardiac status assessed via echocardiography; compared to historical rapid infusion controls.
Main Results:
- Only one case of congestive heart failure (1%) observed with continuous infusion.
- Significantly lower cardiotoxicity incidence (p=0.03) and mortality (p<0.01) compared to rapid infusion.
- Tumor response rates were comparable between continuous infusion and historical controls.
Conclusions:
- Continuous infusion doxorubicin is associated with a substantially lower incidence of cardiotoxicity in pediatric cancer patients.
- This administration method provides a favorable safety profile without compromising anti-tumor efficacy.
- Continuous infusion should be considered for broader use in pediatric doxorubicin therapy.
Abstract:
We retrospectively reviewed the medical records of 97 children (59 boys and 38 girls) with a median age of 13 +/- 4 years who had been treated with continuous infusion of doxorubicin at a dosage of 60 mg/m2 over 24 h (61 patients) or at a dosage of 75 mg/m2 over 72 h (36 patients). The drug was administered every 3 weeks. The cardiac status of patients was evaluated as a baseline and every 6 months during, and following therapy (median, 30.5 months). The evaluations included M-mode and two-dimensional echocardiography. Congestive heart failure developed in only one patient in this series, an 8-year-old girl who ultimately died of her cardiac complication. This incidence of doxorubicin-induced cardiotoxicity was compared with that seen in a control group of pediatric patients previously treated with doxorubicin at similar dosages but with a rapid infusion. The result compared favorably to the 13% incidence of cardiotoxicity (p = 0.03) and 7% mortality (p < 0.01) in the control group. No changes in the levels of tumor response were noted in children treated by continuous infusion when compared with historical controls. Continuous-infusion schedules of doxorubicin thus result in fewer incidences of cardiotoxicity in children and should be considered for wider application in pediatric cancer patients receiving doxorubicin.
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