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Randomized double-blind comparison of three dose levels of intravenous ondansetron in the prevention of cisplatin-induced emesis
Authors:Steven M Grunberg  Montague Lane  Eric P Lester  Kasi S Sridhar  Joanne Mortimer  William Murphy  Polly E Sanderson
Institution:(1) Baylor College of Medicine, 77030 Houston, TX, USA;(2) University of Tennessee, 38613 Memphis, TN, USA;(3) University of Miami, 33101 Miami, FL, USA;(4) Washington University School of Medicine, 63110 St Louis, MO, USA;(5) M. D. Anderson Cancer Center, 77030 Houston, TX, USA;(6) Glaxo Inc., 27709 Research Triangle Park, NC, USA;(7) LAC/USC Medical Center, 2025 Zonal Avenue, Unit 1, Room 10-436, 90033 Los Angeles, CA, USA
Abstract:The selective 5-hydroxytryptamine3 (5HT3) antagonist ondansetron has been shown to be an effective antiemetic in patients receiving cisplatin chemotherapy. This double-blind study compared the efficacy and safety of three doses of intravenous ondansetron in the prevention of nausea and vomiting associated with high-dose (ge100 mg/m2) cisplatin chemotherapy. A total of 125 patients were randomized (1ratio1ratio1) to receive 0.015, 0.15, or 0.30 mg/kg every 4 h for a total of 3 doses. All patients were monitored for emetic episodes, adverse events, and laboratory safety parameters for 24 h following cisplatin administration. The 0.15-mg/kg dose was superior to the 0.015-mg/kg dose with respect to the median number of emetic episodes (P=0.033) and complete response (no emetic episodes,P=0.005). No statistically significant difference was found between the 0.15 and the 0.30-mg/kg groups. The most common adverse event was headache. Three 0.15-mg/kg doses of intravenous ondansetron are safe, effective, and adequate for the control of cisplatin-induced emesis.This study was supported by a grant from Glaxo Inc.
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