Cheirsilpa A, Ratanatharathorn V, Sinlarat P, Chindavijak K, Lousoontornsiri W, Chakrapee-Sirisuk S, Srimuninimit V
National Cancer Institute, Bangkok, Thailand.
J Med Assoc Thai. 1994 Apr;77(4):201-6.
Ondansetron in the prophylaxis of Cisplatin-induced emesis and nausea. The 5-HT3 antagonist ondansetron clearly offers a new approach to the control of Cisplatin-induced emesis and has been evaluated in Thailand. To evaluate anti-emetic efficacy of ondansetron in the prevention of nausea and vomiting induced by Cisplatin containing cancer chemotherapy regimen, we carried out an open multicentre study from January 1991 to December 1992. In this study, patients receiving Cisplatin based chemotherapy received ondansetron 32 mg as a single intravenous dose over 15 minutes prior to the administration of Cisplatin. This was followed by oral ondansetron 8 mg three times a day, preferably one hour before each meal for 5 days. All patients were chemotherapy naive in-patients and were at least 18 years or older with Karnofsky performance status of at least 60 per cent. The number of emetic episodes, nausea and food intake were recorded during the 24 hours following Cisplatin administration. A total of 103 patients were recruited with 84 (81.6%) evaluable patients (48 men and 36 women) scheduled to receive cisplatin chemotherapy at dose 60 mg/m2 or more (60-100 mg/m2), either as single agent or combination therapy. Complete response (complete control of emesis) was achieved in 60 per cent; major response (1-2 emetic episodes) was 13 per cent; minor response (3-5 emetic episodes) was 13 per cent; and failure (5+ emetic episodes) was 10 per cent. Side effects were very mild and not significant. We conclude that ondansetron is efficacious in protecting patients from Cisplatin induced emesis and nausea.
昂丹司琼预防顺铂所致呕吐和恶心。5-羟色胺3拮抗剂昂丹司琼显然为控制顺铂所致呕吐提供了一种新方法,且已在泰国进行了评估。为评价昂丹司琼预防含顺铂的癌症化疗方案所致恶心和呕吐的抗呕吐疗效,我们于1991年1月至1992年12月开展了一项开放性多中心研究。在本研究中,接受基于顺铂化疗的患者在给予顺铂前15分钟静脉注射单次剂量32毫克昂丹司琼。随后口服昂丹司琼8毫克,每日三次,最好在每餐饭前一小时服用,共5天。所有患者均为初治化疗住院患者,年龄至少18岁,卡氏评分至少60%。在给予顺铂后的24小时内记录呕吐发作次数、恶心情况和食物摄入量。共招募了103例患者,其中84例(81.6%)为可评估患者(48例男性和36例女性),计划接受剂量为60毫克/平方米或更高(60 - 100毫克/平方米)的顺铂化疗,可为单药治疗或联合治疗。完全缓解(呕吐完全得到控制)率为60%;主要缓解(1 - 2次呕吐发作)率为13%;轻度缓解(3 - 5次呕吐发作)率为13%;无效(5次以上呕吐发作)率为10%。副作用非常轻微且不显著。我们得出结论,昂丹司琼在保护患者免受顺铂所致呕吐和恶心方面有效。