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口服昂丹司琼控制顺铂引起的迟发性呕吐:昂丹司琼与安慰剂的一项大型、多中心、双盲、随机对照试验。

Oral ondansetron for the control of cisplatin-induced delayed emesis: a large, multicenter, double-blind, randomized comparative trial of ondansetron versus placebo.

作者信息

Navari R M, Madajewicz S, Anderson N, Tchekmedyian N S, Whaley W, Garewal H, Beck T M, Chang A Y, Greenberg B, Caldwell K C

机构信息

Simon-Williamson Clinic, Birmingham, AL 35211, USA.

出版信息

J Clin Oncol. 1995 Sep;13(9):2408-16. doi: 10.1200/JCO.1995.13.9.2408.

Abstract

PURPOSE

To investigate the efficacy and safety of oral ondansetron in the control of cisplatin-induced delayed emesis in patients who do not require rescue antiemetic therapy for acute emesis.

PATIENTS AND METHODS

Five hundred thirty-eight chemotherapy-naive patients who received cisplatin chemotherapy (> or = 70 mg/m2), and who were not rescued for acute emesis, were eligible to be randomized to receive one of the three oral regimens to control delayed emesis. Group I received placebo on days 2 to 6; group II received ondansetron 8 mg twice daily on days 2 and 3 and placebo on days 4 to 6; group III received ondansetron 8 mg twice daily on days 2 to 6. All patients received intravenous ondansetron (0.15 mg/kg every 4 hours for three doses) for the control of acute emesis on day 1. The number of emetic episodes on days 2 and 3 combined (days 2/3, when incidence and severity of delayed emesis were expected to be greatest) was considered the primary measure of efficacy.

RESULTS

Patients who received odansetron had significantly fewer emetic episodes on days 2/3, 4, and 5 than those who received placebo (P < or = .002 on each day). Additionally, significantly more patients who received ondansetron had a complete plus major response (C+MR; < or = two two emetic episodes) than those who received placebo on days 2/3 (56% v 37%, P = .001), 4 (94% v 85%, P = .005), and 5 (98% v 88%, P = .006). Patients who received ondansetron had significantly less nausea on day 2/3 when day-1 nausea was used as the baseline score (P = .025). Patients who received ondansetron also had significantly less nausea on day 4 (P = .042) and the results approached significance on day 5 (P = .066).

CONCLUSION

Oral ondansetron had a significant effect in the control of cisplatin-induced delayed emesis and nausea in patients who had not required rescue antiemetics during the acute emesis period. The control of delayed nausea and vomiting was most notable in the immediate 2 days following cisplatin administration, with the clinical difference narrowing between the two treatment arms on subsequent days.

摘要

目的

研究口服昂丹司琼对顺铂所致延迟性呕吐的疗效及安全性,这些患者急性呕吐时无需使用抢救性止吐治疗。

患者与方法

538例初治化疗患者接受顺铂化疗(≥70mg/m²),且急性呕吐时未接受抢救治疗, eligible随机分为三组口服方案之一以控制延迟性呕吐。第一组在第2至6天接受安慰剂;第二组在第2和3天每日两次口服8mg昂丹司琼,第4至6天接受安慰剂;第三组在第2至6天每日两次口服8mg昂丹司琼。所有患者在第1天接受静脉注射昂丹司琼(每4小时0.15mg/kg,共三剂)以控制急性呕吐。第2和3天合并的呕吐发作次数(第2/3天,此时延迟性呕吐的发生率和严重程度预计最高)被视为疗效的主要衡量指标。

结果

接受昂丹司琼治疗的患者在第2/3天、第4天和第5天的呕吐发作次数明显少于接受安慰剂的患者(每天P≤0.002)。此外,在第2/3天(56%对37%,P = 0.001)、第4天(94%对85%,P = 0.005)和第5天(98%对88%,P = 0.006),接受昂丹司琼治疗的患者中完全加主要缓解(C+MR;≤两次呕吐发作)的患者明显多于接受安慰剂的患者。以第1天的恶心作为基线评分时,接受昂丹司琼治疗的患者在第2/3天恶心明显减轻(P = 0.025)。接受昂丹司琼治疗的患者在第4天恶心也明显减轻(P = 0.042),第5天结果接近显著水平(P = 0.066)。

结论

口服昂丹司琼对急性呕吐期无需抢救性止吐药的患者顺铂所致延迟性呕吐及恶心有显著疗效。延迟性恶心和呕吐的控制在顺铂给药后的头两天最为显著,随后两天两组之间的临床差异缩小。

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