塔利卡平(NAC-68075)是一种新型结构的植物生物碱。

Cancer chemotherapy reports Pub Date : 1975-09-01
P J Creaven, M H Cohen, O S Selawry, F Tejada, L E Broder
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引用次数: 0

摘要

对36例患者进行了每日和每周x6静脉输注塔利卡平(一种新型结构的植物生物碱)的初步临床试验。28例患者接受单次给药33个疗程,剂量为200-1900 mg/m2。在最大耐受剂量为1400mg /m2时,毒性作用包括手臂疼痛(九或十)、中枢神经系统抑制(七)、恶心和呕吐(十之二)、低血压(十之二)、高血压(十之二)、心律失常(室性早搏)(十之一)和心电图改变(主要是t波变平)(十之五)。在每周给药的最大耐受剂量为1100mg /m2/周x6时,8例中有7例出现手臂疼痛,3例出现中枢神经系统抑制,1例出现低血压,8例中有3例出现心电图改变。II期试验的推荐剂量为1100mg /m2/周,静脉输注2小时。
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Phase I study of thalicarpine (NAC-68075), a plant alkaloid of noval structure.

An initial clinical trial of daily and weekly X 6 ihtravenous infusions of thalicarpine, a plant alkaloid of novel structure, was carried out in 36 patients. Twenty-eight patients received 33 courses of single-dose administration at doses of 200-1900 mg/m2. At the maximum tolerable dose of 1400 mg/m2, toxic effects included arm pain (nine or ten), central nervous system depression (seven of ten), nausea and vomiting (two of ten), hypotension (two of ten), hypertension (two of ten), arrhythmia (premature ventricular contractions) (one of ten), and electrocardiographic changes (mainly T-wave flattening) (five of ten). At the maximum tolerable dose for weekly administration, 1100 mg/m2/week X 6, arm pain was seen in seven of eight, central nervous system depression in three of eight, hypotension in one of eight, and electrocardiographic changes in three of eight. The recommended dose for phase II trials is 1100 mg/m2/week by a 2-hour intravenous infusion.

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