Literature DB >> 1829954

Reduction of carboplatin induced emesis by ondansetron.

V J Harvey1, B D Evans, P L Mitchell, D Mak, L M Neave, G B Langley, D S Dickson.   

Abstract

Ondansetron is a selective 5-HT3 antagonist with significant antiemetic properties in patients receiving cytotoxic chemotherapy. Patients who had suffered severe vomiting on carboplatin alone (23 patients with ovarian carcinoma) or in combination (two patients with testicular cancer) despite intensive antiemetic regimens were treated with ondansetron, given as 8 mg immediately prior to carboplatin followed by 8 mg orally, 8 hourly for 5 days. Twenty-five patients received 58 courses of ondansetron. In the first 24 h after the first course of chemotherapy with ondansetron, 17 patients (68%) experienced no vomiting, five patients (20%) had almost complete control and the other three patients had partial control. During the subsequent 4 days slightly lesser control was achieved. Nausea was similarly controlled in most patients. Twenty-two patients stated a preference for ondansetron with future chemotherapy. Fourteen patients received additional chemotherapy with ondansetron and in only three patients did the efficacy of therapy lessen. Toxicity was mild and transient with headache and constipation predominant. No extrapyramidal reaction was seen. Sedation was absent. Ondansetron is highly effective in refractory vomiting associated with carboplatin chemotherapy. It may be particularly beneficial when an extrapyramidal reaction has occurred on previous antiemetics and when sedation is unacceptable.

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Year:  1991        PMID: 1829954      PMCID: PMC1972533          DOI: 10.1038/bjc.1991.206

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  9 in total

1.  Dose-ranging evaluation of the serotonin antagonist GR-C507/75 (GR38032F) when used as an antiemetic in patients receiving anticancer chemotherapy.

Authors:  M G Kris; R J Gralla; R A Clark; L B Tyson
Journal:  J Clin Oncol       Date:  1988-04       Impact factor: 44.544

2.  Efficacy of ondansetron (GR 38032F) and the role of serotonin in cisplatin-induced nausea and vomiting.

Authors:  L X Cubeddu; I S Hoffmann; N T Fuenmayor; A L Finn
Journal:  N Engl J Med       Date:  1990-03-22       Impact factor: 91.245

3.  Comparison of the 5-hydroxytryptamine3 (serotonin) antagonist ondansetron (GR 38032F) with high-dose metoclopramide in the control of cisplatin-induced emesis.

Authors:  M Marty; P Pouillart; S Scholl; J P Droz; M Azab; N Brion; E Pujade-Lauraine; B Paule; D Paes; J Bons
Journal:  N Engl J Med       Date:  1990-03-22       Impact factor: 91.245

4.  Ondansetron: a new antiemetic for patients receiving cisplatin chemotherapy.

Authors:  L H Einhorn; C Nagy; K Werner; A L Finn
Journal:  J Clin Oncol       Date:  1990-04       Impact factor: 44.544

5.  A comparison of ondansetron with metoclopramide in the prophylaxis of chemotherapy-induced nausea and vomiting: a randomized, double-blind study. International Emesis Study Group.

Authors:  S Kaasa; S Kvaløy; M A Dicato; F Ries; J V Huys; E Royer; L Carruthers
Journal:  Eur J Cancer       Date:  1990-03       Impact factor: 9.162

6.  Prevention of emesis in patients receiving cytotoxic drugs by GR38032F, a selective 5-HT3 receptor antagonist.

Authors:  D Cunningham; J Hawthorn; A Pople; J C Gazet; H T Ford; T Challoner; R C Coombes
Journal:  Lancet       Date:  1987-06-27       Impact factor: 79.321

7.  Early clinical studies with cis-diammine-1,1-cyclobutane dicarboxylate platinum II.

Authors:  A H Calvert; S J Harland; D R Newell; Z H Siddik; A C Jones; T J McElwain; S Raju; E Wiltshaw; I E Smith; J M Baker; M J Peckham; K R Harrap
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

8.  Protection from nausea and vomiting in cisplatin-treated patients: high-dose metoclopramide combined with methylprednisolone versus metoclopramide combined with dexamethasone and diphenhydramine: a study of the Italian Oncology Group for Clinical Research.

Authors:  F Roila; M Tonato; C Basurto; M Picciafuoco; S Bracarda; D Donati; P Malacarne; L Monici; F Di Costanzo; L Patoia
Journal:  J Clin Oncol       Date:  1989-11       Impact factor: 44.544

9.  GR 38032F (GR-C507/75): a novel compound effective in the prevention of acute cisplatin-induced emesis.

Authors:  P J Hesketh; W K Murphy; E P Lester; D R Gandara; A Khojasteh; E Tapazoglou; G P Sartiano; D R White; K Werner; J M Chubb
Journal:  J Clin Oncol       Date:  1989-06       Impact factor: 44.544

  9 in total
  5 in total

Review 1.  Ondansetron: a pharmacoeconomic and quality-of-life evaluation of its antiemetic activity in patients receiving cancer chemotherapy.

Authors:  G L Plosker; R J Milne
Journal:  Pharmacoeconomics       Date:  1992-10       Impact factor: 4.981

2.  Low-dose intravenous ondansetron (8 mg) plus dexamethasone: an effective regimen for the control of carboplatin-induced emesis.

Authors:  M Markman; A Kennedy; K Webster; G Peterson; B Kulp; J Belinson
Journal:  J Cancer Res Clin Oncol       Date:  1997       Impact factor: 4.553

Review 3.  Ondansetron. An update of its therapeutic use in chemotherapy-induced and postoperative nausea and vomiting.

Authors:  Anthony Markham; Eugene M Sorkin
Journal:  Drugs       Date:  1993-06       Impact factor: 9.546

Review 4.  Comparative adverse effect profiles of platinum drugs.

Authors:  M J McKeage
Journal:  Drug Saf       Date:  1995-10       Impact factor: 5.606

Review 5.  [Management of chemotherapy-induced emesis: what is the standard after 20 years of clinical research].

Authors:  A Du Bois
Journal:  Med Klin (Munich)       Date:  1998-01
  5 in total

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