Benoit Y, Hulstaert F, Vermylen C, Sariban E, Hoyoux C, Uyttebroeck A, Otten J, Laureys G, De Kerpel I, Nortier D
Ghent University Hospital, Belgium.
Med Pediatr Oncol. 1995 Dec;25(6):457-62. doi: 10.1002/mpo.2950250607.
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.
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。