Consensus proposal for 5HT3 antagonists in the prevention of acute emesis related to highly emetogenic chemotherapy -: Dose, schedule, and route of administration

被引:36
作者
Gandara, DR
Roila, F
Warr, D
Edelman, MJ
Perez, EA
Gralla, RJ
机构
[1] Univ Calif Davis, Ctr Canc, Sacramento, CA 95817 USA
[2] Monteluce Policlin, Div Med Oncol, I-06122 Perugia, Italy
[3] Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON M5G 2M9, Canada
[4] VA No Calif Hlth Care Syst, Martinez, CA 94553 USA
[5] Mayo Clin, Jacksonville, FL 32224 USA
[6] Alton Ochsner Med Fdn & Ochsner Clin, New Orleans, LA 70121 USA
关键词
chemotherapy induced emesis; serotonin receptors; ondansetron; granisetron; dolesetron; tropisetron;
D O I
10.1007/s005200050160
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Selective antagonists to the Type 3 serotonin receptor (5HT(3)) in combination with corticosteroids are now considered the standard of care for the prevention of emesis from moderately to highly emetogenic chemotherapy. Here we address issues of optimal dose, schedule and route of administration of four currently available selectable 5HT(3) antagonists. This paper utilizes an evidence based medicine approach to the literature regarding this class of drugs, emphasizing the results large, randomized, controlled trials to make formal recommendations concerning optimal use of this important new class of anti-emetic agents. We conclude that for each drug there is a plateau in therapeutic efficacy at a definable dose level above which further dose escalation does not improve outcome. Furthermore, a single dose is as effective as multiple doses or continuous infusion, and finally, emerging data demonstrate that the oral route is equally efficacious as the intravenous route of administration, even with highly emetogenic chemotherapy.
引用
收藏
页码:237 / 243
页数:7
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