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高致吐风险化疗后预防呕吐和恶心的共识建议。

Consensus recommendations for the prevention of vomiting and nausea following high-emetic-risk chemotherapy.

机构信息

Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.

出版信息

Support Care Cancer. 2011 Mar;19 Suppl 1:S25-32. doi: 10.1007/s00520-010-0976-9. Epub 2010 Aug 28.

Abstract

In this update of our 2005 document, we used an evidence-based approach whenever possible to formulate recommendations, emphasizing the results of controlled trials concerning the best use of antiemetic agents for the prevention of emesis and nausea following anticancer chemotherapies of high emetic risk. A three-drug combination of a 5-hydroxytryptamine type 3 receptor (5-HT(3)) receptor antagonist, dexamethasone, and aprepitant beginning before chemotherapy and continuing for up to 4 days remains the standard of care. We address issues of dose, schedule, and route of administration of five selective 5-HT(3) receptor antagonists. We conclude that, for each of these five drugs, there is a plateau in therapeutic efficacy above which further dose escalation does not improve outcome. In trials designed to prove the equivalence of palonosetron to ondansetron and granisetron, palonosetron proved superior in emesis prevention, while adverse effects were comparable. Furthermore, for all classes of antiemetic agents, a single dose is as effective as multiple doses or a continuous infusion. The oral route is as efficacious as the intravenous route of administration.

摘要

在对我们 2005 年文件的这次更新中,我们尽可能采用循证方法来制定建议,强调高致吐风险的抗癌化疗后预防呕吐和恶心的止吐药物最佳使用的对照试验结果。化疗前开始并持续 4 天的一种 5-羟色胺 3 型(5-HT3)受体拮抗剂、地塞米松和阿瑞匹坦的三联药物组合仍然是标准治疗方法。我们讨论了五种选择性 5-HT3 受体拮抗剂的剂量、方案和给药途径问题。我们得出结论,对于这五种药物中的每一种,在治疗效果达到平台期后,进一步增加剂量并不能改善结果。在旨在证明帕洛诺司琼与昂丹司琼和格拉司琼等效的试验中,帕洛诺司琼在预防呕吐方面表现出优越性,而不良反应则相当。此外,对于所有类别的止吐药物,单剂量与多剂量或持续输注一样有效。口服途径与静脉给药途径一样有效。

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