Related Experiment Videos
Antiemetics in children receiving chemotherapy
Fausto Roila1, Petra Feyer, Ernesto Maranzano
1Medical Oncology Division, Policlinico Hospital, 06122 Perugia, Italy. roila.fausto@libero.it
Summary
Pediatric chemotherapy patients should receive a combination of 5-HT3 antagonists and dexamethasone to prevent acute emesis. Optimal dosing and scheduling for these antiemetic drugs in children require further investigation.
Area of Science:
- Pediatric Oncology
- Pharmacology
Background:
- Limited research exists on preventing chemotherapy-induced acute emesis in children.
- 5-HT3 antagonists demonstrate superior efficacy and safety compared to older antiemetics like metoclopramide, phenothiazines, and cannabinoids.
Purpose of the Study:
- To review the current evidence on antiemetic drug efficacy in pediatric patients undergoing chemotherapy.
- To establish optimal dosing and scheduling for 5-HT3 antagonists in children.
- To evaluate combination therapies for preventing chemotherapy-induced nausea and vomiting.
Main Methods:
- Review of existing pediatric studies on antiemetic drug prevention of acute emesis.
- Comparison of 5-HT3 antagonists with metoclopramide, phenothiazines, and cannabinoids.
- Analysis of combination therapy efficacy, specifically 5-HT3 antagonists with dexamethasone.
Main Results:
- 5-HT3 antagonists are more effective and safer than older antiemetic agents for pediatric acute emesis.
- Combination therapy with a 5-HT3 antagonist and dexamethasone enhances antiemetic efficacy compared to 5-HT3 antagonists alone.
- Optimal dose and scheduling of 5-HT3 antagonists in children remain undetermined.
Conclusions:
- A combination of a 5-HT3 antagonist and dexamethasone is recommended for all pediatric patients receiving chemotherapy with high or moderate emetogenic potential to prevent acute emesis.
- Further research is needed to determine optimal dosing and scheduling of 5-HT3 antagonists in pediatric populations.
- Current evidence does not address the prevention of chemotherapy-induced delayed and anticipatory emesis in children.