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Lookup NU author(s): Professor Alan Calvert
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In this double-blind study, the efficacy and safety of a single intravenous dose of a novel antiemetic, granisetron, was assessed at two dose levels (40 g/kg and 160 g/kg). A group of 355 patients were given prophylactic granisetron prior to receiving highdose cisplatin chemotherapy. In the first 24 h, 57% and 59% of patients, respectively, experienced no vomiting and no more than mild nausea. Two further doses of granisetron (40 g/kg) were permitted in the first 24 h to treat any emergent symptoms of nausea and vomiting; 66 patients (39%) in the 40-g/kg treatment group and 56 patients (34%) in the 160-g/kg group received at least one additional dose. Additional treatment with granisetron resulted in resolution or improvement of symptoms in at least 73% of these patients. Over the 7-day study period, 52% of patients in the lower-dose group and 48% in the higher required no further conventional antiemetic therapy. The two different dose levels were equal both in terms in efficacy and safety. Granisetron was well tolerated throughout the dose range of the study [40–240 g kg-1 (24 h)-1]. The commonest adverse event was headache, seen in 14%–16% of patients. In all but one case this resolved spontaneously or responded to simple treatment
Author(s): Goedhals L, Jordaan JP, Kaye SB, Armand JP, Veenhof CHN, Falkson G, Soukop M, Schneider M, Oberling F, Bui BN, Roche H, Adenis L, Caty A, Blijham GH, Deweweire A, Coiffier B, Sotto JJ, Vanheukelom LS, Tagnon A, Slee PHTJ, Kroeks MVAM, Ravez P, Cupissol D, Keizer HJ, Brunner K, Calvert AH, Yernault JC, Libert P, Brohee D
Publication type: Article
Publication status: Published
Journal: Supportive Care in Cancer
Year: 1994
Volume: 2
Issue: 3
Pages: 177-183
Print publication date: 01/05/1994
ISSN (print): 0941-4355
ISSN (electronic): 1433-7339
URL: http://dx.doi.org/10.1007/BF00417477
DOI: 10.1007/BF00417477
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