• T R Spitzer, J C Bryson, E Cirenza, R Foelber, M Wallerstadt, C Stout, R L Kunka, P B Plagge, and A Dubois.
• Glaxo Inc, Research Triangle Park, NC.
• J. Clin. Oncol. 1994 Nov 1; 12 (11): 2432-8.

PurposeTo evaluate oral ondansetron in the prevention of total-body irradiation (TBI)-induced nausea and vomiting.MethodsTwenty patients who received 4 days of TBI as part of their preparative regimen before bone marrow transplantation were randomized to receive either 8-mg oral doses of ondansetron or placebo. Administration of drug was double-blinded. Initial rescue therapy consisted of intravenous (i.v.) ondansetron 0.15 mg/kg following two or more emetic episodes between successive fractions of TBI or five total emetic episodes during the 4 days of therapy. If, after receipt of i.v. ondansetron, patients had two or more emetic episodes between fractions of TBI or five total emetic episodes, additional antiemetics were administered.ResultsPatients who received oral ondansetron had significantly fewer emetic episodes compared with those who received placebo (P = .005) over the entire 4-day study period. Oral ondansetron was also significantly superior to placebo with respect to the time of onset of emesis or rescue (P = .003). Six of 10 patients treated with oral ondansetron completed the study without additional antiemetic therapy, while none of 10 patients who received placebo completed the study without rescue antiemetic therapy. Six placebo patients who received initial rescue therapy with i.v. ondansetron required no additional antiemetics. No relationships were apparent between peak ondansetron concentration (Cmax) or area under the concentration versus time curve (AUC) and number of emetic episodes.ConclusionOral ondansetron is an effective therapy for the prevention of emesis induced by TBI.

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