Ondansetron. Therapeutic use as an antiemetic
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Abstract:
Ondansetron (GR 38032F) is a highly selective 5-HT3 receptor antagonist, one of a new class of compounds which may have several therapeutic applications. Animal and clinical studies show that ondansetron reduces the 24-hour incidence and severity of nausea and vomiting induced by cytotoxic drugs, including cisplatin, and by single exposure, high dose radiation. Ondansetron is more effective than high dose metoclopramide in the 24 hours following chemotherapy, and preliminary clinical evidence suggests that it is equally effective in the following 4 days. It is also more effective than the 'moderate' doses of metoclopramide used to suppress emesis following radiotherapy. The antiemetic efficacy of ondansetron is enhanced by dexamethasone in cisplatin-treated patients. Importantly, extrapyramidal effects have not been reported with ondansetron. Further comparisons are required with standard combination antiemetic therapy to complement the data presently available. Thus, ondansetron is a promising new agent for prophylaxis against nausea and vomiting in chemotherapy and radiotherapy. It may be particularly useful in young and elderly patients who are more susceptible to extrapyramidal symptoms induced by high dose metoclopramide. With its improved tolerability and clinical response profiles, ondansetron represents an important advance in a difficult area of therapeutics.
Insights
Ondansetron, a selective 5-HT3 antagonist, effectively reduces chemotherapy-induced nausea and vomiting. It offers improved tolerability and efficacy compared to metoclopramide, with no reported extrapyramidal effects.
Area of Science:
- Pharmacology
- Medical Therapeutics
Background:
- Ondansetron (GR 38032F) is a novel, selective 5-HT3 receptor antagonist.
- Nausea and vomiting are significant side effects of cytotoxic chemotherapy and radiotherapy.
Purpose of the Study:
- To evaluate the efficacy and tolerability of ondansetron in preventing chemotherapy- and radiotherapy-induced nausea and vomiting (CINV/RINV).
Main Methods:
- Clinical studies assessing ondansetron's antiemetic effects against cytotoxic drugs (e.g., cisplatin) and high-dose radiation.
- Comparative analysis against metoclopramide and assessment of dexamethasone's synergistic effect.
Main Results:
- Ondansetron significantly reduces the incidence and severity of nausea and vomiting within 24 hours and up to 4 days post-chemotherapy.
- It demonstrates superior efficacy to high-dose metoclopramide for CINV and moderate-dose metoclopramide for RINV.
- No extrapyramidal side effects were reported with ondansetron, unlike metoclopramide.
Conclusions:
- Ondansetron is a highly effective and well-tolerated agent for prophylaxis against CINV and RINV.
- It represents a significant therapeutic advance, particularly for vulnerable patient groups susceptible to metoclopramide's side effects.