5-HT3 receptor antagonists: Differences and similarities

被引:39
作者
Roila, F
Ballatori, E
Tonato, M
DelFavero, A
机构
[1] UNIV AQUILA,DEPT INTERNAL MED,MED STAT UNIT,I-67100 LAQUILA,ITALY
[2] UNIV PERUGIA,DEPT INTERNAL MED & ONCOL SCI,I-06100 PERUGIA,ITALY
关键词
anti-emetics; ondansetron; granisetron; tropisetron; dolasetron;
D O I
10.1016/S0959-8049(97)00003-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Differences among 5-HT3 receptor antagonists have been reported in pharmacological studies with regard to selectivity of receptor binding, potency, duration of action and dose-response curves. However, whether these pharmacological differences can affect clinical efficacy and safety remains to be determined. A careful analysis of the literature revealed 22 comparative studies among the 5-HT, receptor antagonists available for review. Unfortunately, several of these trials have some important shortcomings especially in the study design, the size of population studied and the type of anti-emetic treatment selected, making their conclusions often difficult to interpret. However, among these studies, seven large, double-blind clinical trials have clearly shown that the antiemetic activity and tolerability of ondansetron, granisetron, tropisetron and dolasetron is almost identical at least in the prevention of cisplatin-induced emesis. Therefore, from the efficacy and safety point of view, there is no reason to prefer one with respect to the other compound. From the economic perspective, instead, differences may exist and they are strictly related to the dose and schedule of administration chosen for each compound. The information available on the use of 5-HT3 receptor antagonists in the prevention of emesis induced by moderately emetogenic chemotherapy is at best scant. Contrasting results have been reported and only one well-conducted study has been published in full. Therefore, the possible differences among the various compounds are difficult to evaluate. More studies should be carried out in this group of patients. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1364 / 1370
页数:7
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