Gandara D R, Roila F, Warr D, Edelman M J, Perez E A, Gralla R J
U.C. Davis Cancer Center, Sacramento, CA 95817, USA.
Support Care Cancer. 1998 May;6(3):237-43. doi: 10.1007/s005200050160.
Selective antagonists to the Type 3 serotonin receptor (5HT3) 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 5HT3 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.
5-羟色胺3型受体(5HT3)选择性拮抗剂与皮质类固醇联合使用,现被视为预防中度至高度致吐性化疗引起呕吐的标准治疗方法。在此,我们探讨四种目前可用的选择性5HT3拮抗剂的最佳剂量、给药方案和给药途径问题。本文采用循证医学方法研究此类药物的文献,强调大型随机对照试验的结果,以便就这类重要新型止吐药物的最佳使用提出正式建议。我们得出结论,对于每种药物,在可确定的剂量水平上存在治疗效果的平台期,高于该剂量进一步增加剂量并不能改善疗效。此外,单次给药与多次给药或持续输注一样有效,最后,新出现的数据表明,即使是高度致吐性化疗,口服给药途径与静脉给药途径同样有效。