Literature DB >> 8459987

Role of ondansetron plus dexamethasone in fractionated chemotherapy.

U Räth1, B K Upadhyaya, E Arechavala, H Böckmann, D Dearnaley, J P Droz, S D Fosså, R Henriksson, W E Aulitzky, W G Jones.   

Abstract

This randomised, double-blind, parallel-group study was carried out to compare the efficacy and safety profile of ondansetron plus dexamethasone and metoclopramide plus dexamethasone in patients receiving fractionated cisplatin (20-25 mg/m2/day) chemotherapy for the treatment of testicular cancer. An interim analysis of 95 patients showed that the ondansetron regimen was significantly superior compared to the metoclopramide regimen (p < 0.001). According to the study protocol the study was terminated at this stage. At the time the decision to stop the study was taken, a total of 113 patients had been enrolled and were evaluable on an 'intention to treat' basis. Fifty-six of these had received ondansetron (32 mg i.v. single dose/day) plus dexamethasone (20 mg i.v. single dose/day) and 57 were given metoclopramide (2 mg/kg or 1 mg/kg i.v. twice a day) plus dexamethasone (20 mg i.v. single dose/day). The ondansetron regimen was significantly superior in the control of emesis and nausea. Seventy-one percent of patients experienced 2 or fewer emetic episodes over the entire 5-day study period compared with 26% of patients given metoclopramide (p < 0.001). Seventy-nine percent of patients in the ondansetron group experienced 'none' or only 'mild' nausea compared with 39% of patients in the metoclopramide group (p < 0.001). The dose of metoclopramide had to be reduced during the study from 2 mg/kg i.v. twice daily to 1 mg/kg i.v. twice daily because 4 of the first 8 patients randomised to this treatment experienced extrapyramidal reactions. Ondansetron was well tolerated and it did not induce any extrapyramidal reactions. The results of this study show that ondansetron plus dexamethasone represents a very effective treatment option for patients receiving fractionated cisplatin chemotherapy for testicular cancer.

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Year:  1993        PMID: 8459987     DOI: 10.1159/000227172

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


  5 in total

1.  The action of the NK1 tachykinin receptor antagonist, CP 99,994, in antagonizing the acute and delayed emesis induced by cisplatin in the ferret.

Authors:  J A Rudd; C C Jordan; R J Naylor
Journal:  Br J Pharmacol       Date:  1996-11       Impact factor: 8.739

2.  A phase II study of ondansetron as antiemetic prophylaxis in patients receiving high-dose polychemotherapy and stem cell transplantation.

Authors:  V Barbounis; G Koumakis; M Vassilomanolakis; H Hatzichristou; S Tsousis; A P Efremidis
Journal:  Support Care Cancer       Date:  1995-09       Impact factor: 3.603

3.  An interaction of ondansetron and dexamethasone antagonizing cisplatin-induced acute and delayed emesis in the ferret.

Authors:  J A Rudd; R J Naylor
Journal:  Br J Pharmacol       Date:  1996-05       Impact factor: 8.739

4.  Randomized, double-blind trial comparing the antiemetic effect of tropisetron plus metopimazine with tropisetron plus placebo in patients receiving multiple cycles of multiple-day cisplatin-based chemotherapy.

Authors:  J Herrstedt; T C Sigsgaard; H A Nielsen; J Handberg; S W Langer; S Ottesen; P Dombernowsky
Journal:  Support Care Cancer       Date:  2006-11-09       Impact factor: 3.359

Review 5.  Palonosetron in the management of chemotherapy-induced nausea and vomiting in patients receiving multiple-day chemotherapy.

Authors:  Mary Lou Affronti; Joseph Bubalo
Journal:  Cancer Manag Res       Date:  2014-09-05       Impact factor: 3.989

  5 in total

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