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昂丹司琼联合地塞米松与甲氧氯普胺联合地塞米松及苯海拉明用于顺铂治疗的卵巢癌患者。意大利止吐研究组。

Ondansetron plus dexamethasone versus metoclopramide plus dexamethasone plus diphenhydramine in cisplatin-treated patients with ovarian cancer. Italian Group for Antiemetic Research.

出版信息

Support Care Cancer. 1994 May;2(3):167-70.

PMID:8032702
Abstract

Female patients with ovarian cancer are at high risk for emesis. A study evaluating the antiemetic activity and tolerability of ondansetron plus dexamethasone compared to metoclopramide plus dexamethasone plus diphenhydramine in this group of patients has been performed. A group of 63 patients with ovarian cancer undergoing cisplatin treatment were enrolled in the study. Vomiting, nausea and other side-effects were evaluated by the investigators during the first 24 h and recorded by the patients on a diary card on days 2-4. Ondansetron plus dexamethasone showed a higher antiemetic activity during the first 24 h after cisplatin administration in all three cycles of cisplatin treatment, giving over 90% complete protection from vomiting at the first cycle. The efficacy of ondansetron plus dexamethasone decreased at the second cycle, but the percentage of complete protection from vomiting always remained better than 70%; there was poorer protection in the metoclopramide group, and its effect was similar during all three cycles. Ondansetron plus dexamethasone was also found to be more efficacious than the metoclopramide regimen on the second day after cisplatin administration, while on days 3-4 a high rate of complete protection from emesis was achieved by both antiemetic therapies (> 80%). About 40%-55% of patients receiving ondansetron plus dexamethasone and about 65%-85% of patients treated with metoclopramide plus dexamethasone plus diphenhydramine reported nausea or vomiting during days 1-4. Ondansetron plus dexamethasone is more efficacious than metoclopramide plus dexamethasone plus diphenhydramine but new strategies to improve antiemetic efficacy in ovarian cancer patients must be outlined.

摘要

卵巢癌女性患者发生呕吐的风险很高。一项针对该组患者评估昂丹司琼加地塞米松与甲氧氯普胺加地塞米松加苯海拉明的止吐活性和耐受性的研究已经开展。一组63例接受顺铂治疗的卵巢癌患者被纳入该研究。研究人员在最初24小时内对呕吐、恶心及其他副作用进行评估,患者在第2 - 4天通过日记卡记录相关情况。在顺铂治疗的所有三个周期中,昂丹司琼加地塞米松在顺铂给药后的最初24小时内显示出更高的止吐活性,在第一个周期中能提供超过90%的完全防吐保护。昂丹司琼加地塞米松的疗效在第二个周期有所下降,但完全防吐保护的百分比始终保持在70%以上;甲氧氯普胺组的保护效果较差,且在所有三个周期中效果相似。还发现昂丹司琼加地塞米松在顺铂给药后第二天比甲氧氯普胺方案更有效,而在第3 - 4天,两种止吐疗法均实现了较高的完全防吐保护率(> 80%)。在第1 - 4天,约40% - 55%接受昂丹司琼加地塞米松治疗的患者和约65% - 85%接受甲氧氯普胺加地塞米松加苯海拉明治疗的患者报告有恶心或呕吐。昂丹司琼加地塞米松比甲氧氯普胺加地塞米松加苯海拉明更有效,但必须概述提高卵巢癌患者止吐疗效的新策略。

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