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.

Oncology Reports
|April 11, 2001
PubMed

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.

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