Sg. Berrak et al., Doxorubicin cardiotoxicity in children: Reduced incidence of cardiac dysfunction associated with continuous-infusion schedules, ONCOL REP, 8(3), 2001, pp. 611-614
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 cont
inuous infusion of doxorubicin at a dosage of 60 mg/m(2) over 24 h (61 pati
ents) or at a dosage of 75 mg/m(2) over 72 h (36 patients). The drug was ad
ministered every 3 weeks. The cardiac status of patients was evaluated as a
baseline and every 6 months during, and following therapy (median, 30.5 mo
nths). 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 inci
dence of doxorubicin-induced cardiotoxicity was compared with that seen in
a control group of pediatric patients previously treated with doxorubicin a
t 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) i
n the control group. No changes in the levels of tumor response were noted
in children treated by continuous infusion when compared with historical co
ntrols. Continuous-infusion schedules of doxorubicin thus result in fewer i
ncidences of cardiotoxicity in children and should be considered for wider
application in pediatric cancer patients receiving doxorubicin.