Purpose: To determine the effect of standard antiemetic treatment in childr
en receiving various combination chemotherapy regimens.
Methods: A validated nausea/vomiting survey was administered to 78 patients
receiving 13 different emetogenic chemotherapy regimens. Patients received
antiemetic prophylaxis with ondansetron (0.3 mg/kg/day) alone for moderate
ly emetogenic chemotherapy regimens or ondansetron (0.45 mg/kg/day) and met
hylprednisolone (4 mg/kg/day) for severely emetogenic chemotherapy regimens
. A total of 324 different courses of chemotherapy were surveyed. Nausea an
d vomiting severity, duration, number of emetic episodes, appetite, daily a
ctivity interference, and rates of both complete and good antiemetic protec
tion were determined for each chemotherapy protocol. Differences between ge
nders and ages were analyzed.
Results: Chemotherapy combinations containing platinum compounds were found
to be highly emetogenic and nauseating despite antiemetic therapy with ond
ansetron plus a corticosteroid. In addition, complete antiemetic protection
for the combination of vincristine, cyclophosphamide, and dactinomycin was
poor. For most of the severely emetogenic chemotherapy protocols, patients
experienced good protection from nausea and vomiting less than 60% of the
time, despite the use of ondansetron plus methylprednisolone. Significant d
ifferences were found in rates of residual nausea and vomiting and failure
of antiemetic protection among the severely emetogenic chemotherapy protoco
ls despite identical antiemetic therapy. Good protection fates were higher
for moderately emetogenic chemotherapy treated with ondansetron alone.
Conclusions: The currently recommended prophylactic therapy for pediatric p
atients receiving severely emetogenic chemotherapy:fails to provide protect
ion for many patients receiving commonly administered chemotherapy regimens
and for most pediatric patients receiving platinum-containing chemotherapy
combinations. New and refined antiemetic strategies are needed to improve
efficacy in the pediatric population.