Cassidy J, Raina V, Lewis C, Adams L, Soukop M, Rapeport W G, Zussman B D, Rankin E M, Kaye S B
CRC Department of Medical Oncology, Glasgow.
Br J Cancer. 1988 Nov;58(5):651-3. doi: 10.1038/bjc.1988.278.
Twenty patients receiving a variety of emetogenic cytotoxics (including cisplatin in 5) were given a single i.v. infusion of 40 micrograms kg-1 of BRL43694 (as the hydrochloride salt) in successive groups of 3-4 patients between 0-6 hours after chemotherapy. Eleven patients were completely protected from vomiting; 9 had mild to moderate nausea and vomiting, but none severe enough to require alternative anti-emetic 'rescue'. In 4 of the patients in whom BRL43694 was delayed until 4-6 h after chemotherapy, vomiting had already begun; in each case immediate termination of vomiting occurred when BRL43694 was infused. No adverse effects attributable to the anti-emetic were observed. Mean pharmacokinetic parameters in 14 patients in whom plasma assay data are available were: Maximum observed concentration = 30.7 ng ml-1; terminal phase half-life = 8.96 h; total body clearance = 0.376 (1 h-1) kg-1; apparent volume of distribution = 2.85 l kg-1. This study shows BRL43694 to be an effective and well tolerated anti-emetic. Further studies aimed at defining an optimal dose and schedule for use against the most emetogenic cytotoxics are in progress.
20名接受各种致吐性细胞毒性药物治疗的患者(其中5名接受顺铂治疗),在化疗后0至6小时内,以3至4名患者为一组,依次接受40微克/千克体重的BRL43694(盐酸盐形式)静脉输注。11名患者完全避免了呕吐;9名患者有轻度至中度恶心和呕吐,但均未严重到需要使用其他止吐“解救”药物的程度。在4名BRL43694延迟至化疗后4至6小时给药的患者中,呕吐已经开始;在每例患者中,输注BRL43694后呕吐立即停止。未观察到与该止吐药相关的不良反应。14名有血浆检测数据的患者的平均药代动力学参数为:最大观察浓度 = 30.7纳克/毫升;终末相半衰期 = 8.96小时;全身清除率 = 0.376(1/小时)千克-1;表观分布容积 = 2.85升/千克。本研究表明BRL43694是一种有效且耐受性良好的止吐药。旨在确定针对最强致吐性细胞毒性药物的最佳剂量和给药方案的进一步研究正在进行中。