Department of Oncology, Odense University Hospital, 5000 Odense, Denmark.
Support Care Cancer. 2011 Mar;19 Suppl 1:S15-23. doi: 10.1007/s00520-010-0951-5. Epub 2010 Aug 2.
This paper is a review of the recommendations for the prophylaxis of acute emesis induced by moderately emetogenic chemotherapy as concluded at the third Perugia Consensus Conference, which took place in June 2009. The review will focus on new studies appearing since the Second consensus conference in April 2004. The following issues will be addressed: dose and schedule of antiemetics, different groups of antiemetics such as corticosteroids, serotonin(3) receptor antagonists, dopamine(2) receptor antagonists, and neurokinin(1) receptor antagonists. Furthermore, antiemetic prophylaxis in patients receiving multiple cycles of moderately emetogenic chemotherapy will be reviewed. Consensus statements are given, including optimal dose and schedule of serotonin(3) receptor antagonists, dexamethasone, and neurokinin(1) receptor antagonists. The most significant recommendations (and changes since the 2004 version of the guidelines) are as follows: the best prophylaxis in patients receiving moderately emetogenic chemotherapy (not including a combination of an anthracycline plus cyclophosphamide) is the combination of palonosetron and dexamethasone on the day of chemotherapy, followed by dexamethasone on days 2-3. In patients receiving a combination of an anthracycline plus cyclophosphamide, a combination of a serotonin(3) receptor antagonist plus dexamethasone, plus the neurokinin(1) receptor antagonist aprepitant on the day of chemotherapy, followed by aprepitant days 2-3, is recommended.
本文是对 2009 年 6 月举行的第三届佩鲁贾共识会议上关于中度致吐性化疗引起急性呕吐预防建议的综述。该综述将重点关注自 2004 年 4 月第二届共识会议以来出现的新研究。将讨论以下问题:止吐药的剂量和方案、不同类别的止吐药,如皮质类固醇、5-羟色胺(3)受体拮抗剂、多巴胺(2)受体拮抗剂和神经激肽(1)受体拮抗剂。此外,还将回顾接受多周期中度致吐性化疗的患者的止吐预防。给出了共识声明,包括 5-羟色胺(3)受体拮抗剂、地塞米松和神经激肽(1)受体拮抗剂的最佳剂量和方案。最重要的建议(以及自 2004 年指南版本以来的变化)如下:接受中度致吐性化疗(不包括阿霉素加环磷酰胺联合治疗)的患者的最佳预防方案是在化疗当天联合应用帕洛诺司琼和地塞米松,随后在第 2-3 天应用地塞米松。接受阿霉素加环磷酰胺联合治疗的患者,推荐在化疗当天联合应用 5-羟色胺(3)受体拮抗剂加地塞米松和神经激肽(1)受体拮抗剂阿瑞匹坦,随后在第 2-3 天应用阿瑞匹坦。