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pubmed-article:7833098pubmed:abstractTextIn a double-blind, placebo-controlled, escalating dose study, 44 children receiving cancer chemotherapy of various degrees of emetogenicity were randomly allocated to once-daily treatment with tropisetron 0.05 mg/kg (6 patients), 0.10 mg/kg (5 patients), 0.20 mg/kg (6 patients), 0.33 mg/kg (6 patients), 0.50 mg/kg (6 patients) or placebo (15 patients). All doses of tropisetron were well tolerated; no tropisetron recipient discontinued treatment because of intolerance and no adverse effect could be plausibly correlated to tropisetron administration. Therapeutic plasma concentrations of tropisetron (> 3 ng/ml) were present for 9 h after administration of doses of 0.10 mg/kg or more. Tropisetron at doses of at least 0.20 mg/kg was significantly more effective in preventing vomiting than lower tropisetron doses or placebo, both in terms of treatment failure (> four vomits) (P = 0.015) and patient and investigator efficacy ratings (P = 0.04 for investigator rating; P = 0.035 for patient rating). Further comparative studies of the efficacy of tropisetron in chemotherapy-induced emesis in children are warranted.lld:pubmed
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pubmed-article:7833098pubmed:pagination1436-41lld:pubmed
pubmed-article:7833098pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:7833098pubmed:articleTitleSafety, tolerability, efficacy and plasma concentrations of tropisetron after administration at five dose levels to children receiving cancer chemotherapy.lld:pubmed
pubmed-article:7833098pubmed:affiliationDivision of Pediatric Oncology, Institute Gustave Roussy, Villejuif, France.lld:pubmed
pubmed-article:7833098pubmed:publicationTypeJournal Articlelld:pubmed
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pubmed-article:7833098pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed