PATTERN OF CARBOPLATIN-INDUCED EMESIS

Citation
A. Dubois et al., PATTERN OF CARBOPLATIN-INDUCED EMESIS, Anti-cancer drugs, 6(5), 1995, pp. 645-651
Citations number
28
Categorie Soggetti
Oncology,"Pharmacology & Pharmacy
Journal title
ISSN journal
09594973
Volume
6
Issue
5
Year of publication
1995
Pages
645 - 651
Database
ISI
SICI code
0959-4973(1995)6:5<645:POCE>2.0.ZU;2-H
Abstract
In contrast to the broad experience concerning the therapeutic use of carboplatin, only limited data are available regarding the patterns of carboplatin-induced emesis, one of its most distressing side effects. This study reports frequency, severity and time course of carboplatin -induced vomiting and nausea refractory to 5-HT3 antagonism. A total o f 216 patients receiving single-day carboplatin-based chemotherapy reg imen were enrolled into an open multicenter study focusing on the safe ty and efficacy of ondansetron 8 mg t.d.s. Emesis on day 1 occurred in 22% and nausea in 75% of the patients; 44% of patients reported some degree of vomiting within the 5 days observation period. The risk for emesis and nausea over 2-5 days was increased in patients suffering fr om emesis on day 1 (relative risk 2.25 for vomiting and 2.84 for nause a, respectively). The median cumulative number of emetic episodes was 0 for ail patients and 4 for the patients who did vomit at least on 1 day. Vomiting began on average 1.77 days following chemotherapy admini stration. The mean duration of vomiting was 2 days and 3.1 days for na usea. Carboplatin showed a monophasic prolonged pattern of emesis. The combination with cyclophosphamide led to an earlier onset and a highe r frequency of vomiting. The analysis of the pattern of emesis refract ory to 5-HT3 receptor blockade should help to describe the course of e mesis, which is probably triggered through a 5-HT3 receptor-independen t mechanisms.