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Published on: June 21, 2024
Efficacy and Safety of Different 5-HT3 Receptor Antagonists as Monotherapy for Preventing Nausea and Vomiting in
Hong Sun1, Xiuwen Zhang1, Xiu Xin1
1Department of Pharmacy, Eye & ENT Hospital , Fudan University, Shanghai, China.
Abstract:
This study aims to compare the efficacy and safety of different 5-HT3 receptor antagonists as monotherapy for nausea and vomiting in patients undergoing surgery or chemotherapy. A thorough search of various electronic databases was conducted to determine the randomized controlled trials comparing the efficacy and safety of different 5-HT3 receptor antagonists as monotherapy for preventing nausea and vomiting in patients undergoing surgery or chemotherapy. Primary outcomes included nausea, vomiting, and adverse events. A network meta-analysis was performed to compare each outcome. Seventeen trials were included in this study. For the control of nausea, palonosetron was the optimal choice among 5-HT3 receptor antagonists (surface under the cumulative ranking curve, SUCRA = 86.95%), regardless of whether the patients were undergoing surgery (SUCRA = 82.04%) or chemotherapy (SUCRA = 71.63%). As for controlling vomiting, palonosetron was still the optimal choice among different 5-HT3 receptor antagonists (SUCRA = 80.87%). In surgical patients, granisetron was the most effective in controlling vomiting (SUCRA = 88.04%). When considering the drug doses, palonosetron 0.25 mg was the optimal regimen for controlling both nausea and vomiting. In terms of safety, palonosetron 0.25 mg and granisetron 3 mg were the safest regimens among different 5-HT3 receptor antagonists. Among the various 5-HT3 receptor antagonists, palonosetron at a dosage of 0.25 mg emerged as the optimal choice for chemotherapy patients, while granisetron at a dosage of 3 mg proved to be the best option for surgical patients, taking into account both efficacy and safety. The study protocol was registered with PROSPERO (CRD42024552117).
Insights
Palonosetron is the best 5-HT3 receptor antagonist for controlling nausea and vomiting in patients undergoing surgery or chemotherapy. Palonosetron 0.25 mg and granisetron 3 mg are the safest and most effective regimens.
Area of Science:
- Pharmacology
- Oncology
- Anesthesiology
Background:
- Nausea and vomiting are common side effects of chemotherapy and surgery.
- 5-HT3 receptor antagonists are frequently used to prevent these symptoms.
Purpose of the Study:
- To compare the efficacy and safety of different 5-HT3 receptor antagonists as monotherapy for managing chemotherapy-induced and post-operative nausea and vomiting.
- To identify optimal drug choices and dosages for specific patient populations.
Main Methods:
- A systematic literature search was conducted to identify relevant randomized controlled trials.
- A network meta-analysis was performed to compare the efficacy and safety outcomes of various 5-HT3 receptor antagonists.
- Surface Under the Cumulative Ranking Curve (SUCRA) was used to rank treatment effectiveness.
Main Results:
- Palonosetron demonstrated superior efficacy in controlling nausea across both surgical and chemotherapy patient groups.
- Palonosetron was also the optimal choice for controlling vomiting overall.
- For surgical patients, granisetron was most effective for vomiting control.
- Palonosetron 0.25 mg and granisetron 3 mg were identified as the safest and most effective regimens for nausea and vomiting control, respectively.
Conclusions:
- Palonosetron 0.25 mg is recommended as the optimal monotherapy for chemotherapy-induced nausea and vomiting.
- Granisetron 3 mg is recommended as the optimal monotherapy for surgical nausea and vomiting.
- These findings provide evidence-based guidance for selecting 5-HT3 receptor antagonists to improve patient outcomes.
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