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托烷司琼预防131例接受细胞毒性化疗儿童恶心和呕吐的疗效观察

Tropisetron in the prevention of nausea and vomiting in 131 children receiving cytotoxic chemotherapy.

作者信息

Benoit Y, Hulstaert F, Vermylen C, Sariban E, Hoyoux C, Uyttebroeck A, Otten J, Laureys G, De Kerpel I, Nortier D

机构信息

Ghent University Hospital, Belgium.

出版信息

Med Pediatr Oncol. 1995 Dec;25(6):457-62. doi: 10.1002/mpo.2950250607.

Abstract

Tropisetron (Navoban, Sandoz Pharma Ltd., Basel, Switzerland), a selective antagonist of the serotonin receptor (5-HT3) dosed once-daily at 0.2 mg/kg (with a maximum of 5 mg daily), was evaluated in the prevention of chemotherapy-induced nausea and vomiting in 131 children with a median age of 5 years (age 10 weeks to 21 years). Acute lymphocytic leukemia was the most common malignancy (49%). Most children (82%) had received cytotoxic chemotherapy before enrollment. Patients received tropisetron during one or more courses of chemotherapy (455 courses in total). Tropisetron was administered slowly intravenously as a single dose before the start of chemotherapy on day 1 and intravenously or by mouth the subsequent days as a single daily dose (median treatment duration: 5 days). Response to tropisetron per 24 hour period on the first 5 days of each chemotherapy course was graded as complete (absence of both nausea and vomiting), partial (one to four vomits and/or less than 5 hours of nausea), or failure. Overall complete response on day 1 was observed in 305 out of 455 chemotherapy courses (67%). The patients receiving intravenous chemotherapy (N = 92) had a 70% complete response rate and a 26% partial response rate on day 1, both for course 1 and course 2. The percentage of complete responders increased the subsequent days of the course. Emesis after day 1 was observed primarily during courses with the most emetogenic chemotherapy. No side-effects of tropisetron other than a single case of diarrhoea were documented in this study.

摘要

托烷司琼(商品名:呕必停,山德士制药有限公司,瑞士巴塞尔)是一种5-羟色胺受体(5-HT3)的选择性拮抗剂,每日剂量为0.2毫克/千克(最大剂量为每日5毫克)。对131名年龄中位数为5岁(年龄范围为10周至21岁)的儿童进行了该药预防化疗引起的恶心和呕吐的评估。急性淋巴细胞白血病是最常见的恶性肿瘤(占49%)。大多数儿童(82%)在入组前已接受过细胞毒性化疗。患者在一个或多个化疗疗程中接受托烷司琼治疗(总共455个疗程)。托烷司琼在第1天化疗开始前缓慢静脉注射单剂量,随后几天通过静脉注射或口服给予单剂量(治疗持续时间中位数:5天)。每个化疗疗程的前5天中,托烷司琼每24小时的反应分为完全缓解(无恶心和呕吐)、部分缓解(1至4次呕吐和/或恶心时间少于5小时)或未缓解。在455个化疗疗程中,有305个疗程在第1天观察到总体完全缓解(67%)。接受静脉化疗的患者(N = 92)在第1天的第1疗程和第2疗程中,完全缓解率为70%,部分缓解率为26%。完全缓解者的百分比在疗程的后续几天有所增加。第1天后的呕吐主要发生在具有最强致吐性化疗的疗程中。本研究中除1例腹泻外,未记录到托烷司琼的其他副作用。

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