Prevention of emesis in patients receiving cytotoxic drugs by GR38032F, a selective 5-HT3 receptor antagonist
- PMID: 2885454
- DOI: 10.1016/s0140-6736(87)92208-2
Prevention of emesis in patients receiving cytotoxic drugs by GR38032F, a selective 5-HT3 receptor antagonist
Abstract
15 patients receiving cytotoxic drugs (other than cisplatin) that had previously produced nausea and vomiting refractory to first-line antiemetics were given a selective 5-HT3 receptor antagonist (GR38032F), 4 mg intravenously and 4 mg orally, immediately before chemotherapy, the oral dose being repeated 5 and 10 h later. Nausea, vomiting, and side-effects were recorded for the ensuing 24 h. The 15 patients received a total of thirty-one courses of chemotherapy. Only 1 patient vomited. The only adverse events were dryness of the mouth in 1 patient, mild sedation in 1, and diarrhoea in 1, and these were not clearly drug related.
Similar articles
-
Dose ranging phase I study of the serotonin antagonist GR38032F for prevention of cisplatin-induced nausea and vomiting.J Clin Oncol. 1989 Aug;7(8):1137-41. doi: 10.1200/JCO.1989.7.8.1137. J Clin Oncol. 1989. PMID: 2526864
-
Oral ondansetron for the control of delayed emesis after cisplatin. Report of a phase II study and a review of completed trials to manage delayed emesis.Cancer. 1992 Aug 15;70(4 Suppl):1012-6. Cancer. 1992. PMID: 1386282 Review.
-
Control of refractory, chemotherapy-induced emesis with the serotonin antagonist ondansetron (GR38032F).Oncology. 1991;48(5):403-5. doi: 10.1159/000226969. Oncology. 1991. PMID: 1836058
-
5-HT3 receptor antagonists for the prevention of chemotherapy-induced nausea and vomiting. A comparison of their pharmacology and clinical efficacy.Drugs. 1998 Feb;55(2):173-89. doi: 10.2165/00003495-199855020-00002. Drugs. 1998. PMID: 9506240 Review.
-
A single-blind comparison of intravenous ondansetron, a selective serotonin antagonist, with intravenous metoclopramide in the prevention of nausea and vomiting associated with high-dose cisplatin chemotherapy.J Clin Oncol. 1991 May;9(5):721-8. doi: 10.1200/JCO.1991.9.5.721. J Clin Oncol. 1991. PMID: 1826739 Clinical Trial.
Cited by
-
Effect of selective 5HT3 antagonist (GR 38032F) on small intestinal transit and release of gastrointestinal peptides.Dig Dis Sci. 1989 Oct;34(10):1511-5. doi: 10.1007/BF01537102. Dig Dis Sci. 1989. PMID: 2529108 Clinical Trial.
-
Ondansetron--a new safe and effective antiemetic in patients receiving high-dose melphalan.Cancer Chemother Pharmacol. 1990;25(6):449-53. doi: 10.1007/BF00686058. Cancer Chemother Pharmacol. 1990. PMID: 2138064
-
5-HT3 receptor antagonists. An overview of their present status and future potential in cancer therapy-induced emesis.Drugs. 1991 Oct;42(4):551-68. doi: 10.2165/00003495-199142040-00002. Drugs. 1991. PMID: 1723361 Review.
-
Ondansetron (GR38032F) plus dexamethasone: effective anti-emetic prophylaxis for patients receiving cytotoxic chemotherapy.Br J Cancer. 1990 Feb;61(2):323-4. doi: 10.1038/bjc.1990.62. Br J Cancer. 1990. PMID: 2138031 Free PMC article. No abstract available.
-
Characteristics of 5-HT3 binding sites in NG108-15, NCB-20 neuroblastoma cells and rat cerebral cortex using [3H]-quipazine and [3H]-GR65630 binding.Br J Pharmacol. 1991 Apr;102(4):919-25. doi: 10.1111/j.1476-5381.1991.tb12277.x. Br J Pharmacol. 1991. PMID: 1830236 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical