Literature DB >> 2965755

Dose-ranging evaluation of the serotonin antagonist GR-C507/75 (GR38032F) when used as an antiemetic in patients receiving anticancer chemotherapy.

M G Kris1, R J Gralla, R A Clark, L B Tyson.   

Abstract

GR-C507/75 (GR38032F) antagonizes the 5-HT3 (serotonin) receptor and prevents cisplatin-induced emesis in animals. In this dose-ranging trial, 44 patients with cancer receiving chemotherapy known to produce nausea and vomiting (including cisplatin, cyclophosphamide, and doxorubicin) received three intravenous (IV) infusions of GR-C507/75 every two hours beginning 30 minutes before chemotherapy. Ten dosage levels were explored, ranging from 0.04 mg/kg to 0.35 mg/kg in each of the three infusions. Toxicities were mild and included sedation, dizziness, headache, transient elevations of SGOT or alanine aminotransferase (ALT), and dry mouth. No akathisia or acute dystonic reactions were observed. Antiemetic effects were seen in patients receiving cisplatin at 120 mg/m2. GR-C507/75 can be safely administered on this schedule at IV dosages up to 0.35 mg/kg in patients receiving chemotherapy. Further studies of this agent at higher dosages and by different schedules are appropriate.

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Year:  1988        PMID: 2965755     DOI: 10.1200/JCO.1988.6.4.659

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  26 in total

Review 1.  Stratified administration of serotonin 5-HT3 receptor antagonists (setrons) for chemotherapy-induced emesis. Economic implications.

Authors:  L A Sanchez; M Holdsworth; S B Bartel
Journal:  Pharmacoeconomics       Date:  2000-12       Impact factor: 4.981

2.  Antiemetic study design: desirable objectives, stratifications and analyses.

Authors:  I N Olver
Journal:  Br J Cancer Suppl       Date:  1992-12

3.  GR38032F, a 5HT3 receptor antagonist, in the prophylaxis of acute cisplatin-induced nausea and vomiting.

Authors:  M Marty; J P Droz; P Pouillart; B Paule; N Brion; J Bons
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

4.  A phase I/II study of the 5-HT3 antagonist GR38032F in the anti-emetic prophylaxis of patients receiving high-dose cisplatin chemotherapy.

Authors:  D B Smith; E S Newlands; G J Rustin; R H Begent; S M Crawford; K D Bagshawe; L Carruthers
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

Review 5.  Physiology and pathophysiology of colonic motor activity (1).

Authors:  S K Sarna
Journal:  Dig Dis Sci       Date:  1991-06       Impact factor: 3.199

Review 6.  5-HT3 receptor antagonists. An overview of their present status and future potential in cancer therapy-induced emesis.

Authors:  M S Aapro
Journal:  Drugs       Date:  1991-10       Impact factor: 9.546

Review 7.  Antiemetics in cancer chemotherapy: historical perspective and current state of the art.

Authors:  M Tonato; F Roila; A Del Favero; E Ballatori
Journal:  Support Care Cancer       Date:  1994-05       Impact factor: 3.603

Review 8.  Delayed emesis: a dilemma in antiemetic control.

Authors:  R A Clark; R J Gralla
Journal:  Support Care Cancer       Date:  1993-07       Impact factor: 3.603

Review 9.  Progress in controlling emesis with cancer chemotherapy.

Authors:  R J Gralla; R A Clark
Journal:  Support Care Cancer       Date:  1993-07       Impact factor: 3.603

10.  Randomized double-blind comparison of three dose levels of intravenous ondansetron in the prevention of cisplatin-induced emesis.

Authors:  S M Grunberg; M Lane; E P Lester; K S Sridhar; J Mortimer; W Murphy; P E Sanderson
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

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