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Evaluation of aprepitant and fosaprepitant in pediatric patients
Yoshimasa Saito1, Tadashi Kumamoto2, Takamichi Arima1
1Department of Pharmacy, National Cancer Center Hospital, Tokyo, Japan.
Insights
Aprepitant and fosaprepitant show similar efficacy and safety in preventing chemotherapy-induced nausea and vomiting (CINV) in pediatric patients. Complete response rates were comparable between the two neurokinin-1 receptor antagonists.
Area of Science:
- Oncology
- Pharmacology
- Pediatrics
Background:
- Chemotherapy-induced nausea and vomiting (CINV) is a significant challenge in pediatric cancer care.
- Neurokinin-1 receptor antagonists, such as aprepitant and fosaprepitant, are crucial in CINV management.
- While effective in adults, fosaprepitant's efficacy in pediatric patients compared to aprepitant required investigation.
Purpose of the Study:
- To compare the efficacy and safety of aprepitant versus fosaprepitant in pediatric patients undergoing chemotherapy.
- To evaluate complete response (CR) rates and identify potential risk factors for CINV in children.
Main Methods:
- A retrospective study included pediatric patients (<18 years) receiving aprepitant or fosaprepitant for CINV from 2015-2018.
- The primary endpoint was CR (no vomiting/rescue medication) within 120 hours post-chemotherapy.
- Safety was assessed by severe adverse events, and age and sex were analyzed as risk factors.
Main Results:
- A total of 125 chemotherapy cycles were analyzed.
- Complete response rates were similar: 45.0% for aprepitant and 42.2% for fosaprepitant (P=0.852).
- No severe adverse events were reported; age (6-14 years) was associated with lower CR rates.
Conclusions:
- Aprepitant and fosaprepitant are safe and equally effective for pediatric CINV prevention.
- Patient age may influence the effectiveness of these neurokinin-1 receptor antagonists.
- Further research into age-related efficacy is warranted.
Background:
Single-dose i.v. fosaprepitant has been approved as an alternative to 3 day oral aprepitant, a neurokinin-1 receptor antagonist, and improves prevention of chemotherapy-induced nausea and vomiting (CINV). Because fosaprepitant has shown similar efficacy to aprepitant in adult patients only, this study compared the efficacy and safety of aprepitant and fosaprepitant in pediatric patients.
Methods:
Children younger than 18 years who received aprepitant or fosaprepitant to manage CINV between January 2015 and March 2018 at the National Cancer Center Hospital (Tokyo) were recruited to this study. The primary endpoint was complete response (CR; no vomiting/rescue medication) between 0 and 120 h after the start of chemotherapy. Secondary endpoints were safety based on the frequency of severe adverse events, and evaluation of patient characteristics as risk factors (effect of age and sex).
Results:
A total of 125 chemotherapy cycles were evaluated. In the aprepitant group, CR was observed in 36 of 80 treatment cycles (45.0%), whereas in the fosaprepitant group, it was observed in 19 of 45 cycles (42.2%; P = 0.852). No treatment-related severe adverse events were observed in either group. The number of non-CR was greater than that of CR in patients aged 6-14 years. The difference in CR rate between male and female patients was not statistically significant (47.1% vs 40.0%, respectively; P = 0.471).
Conclusions:
Aprepitant and fosaprepitant were safely used and may be equally useful for pediatric patients receiving highly emetogenic chemotherapy. CR rate may be associated with patient age.
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