Institute of Hematology Oncology, 08036 Bacelona, Spain.
Anticancer Res. 2010 Jul;30(7):2977-84.
This study investigated the effect of seizure prophylaxis on busulfan (Bu) plasma exposure. Twenty-four adult patients received an intravenous Bu-cyclophoshamide conditioning regimen prior to bone marrow transplantation. Busilvex (0.8 mg/kg) was administered every six hours during four consecutive days. Clonazepam (0.025 to 0.03 mg/kg/day as a continuous 12-h i.v. infusion) was administered at least 12 hours prior to i.v. Bu dosing and continued until 24 hours after the last dose. Pharmacokinetic (PK) data were compared with those previously collected in patients (n=127) treated with phenytoin for seizure prophylaxis. Through population PK analysis, a 10% average increase (coefficient of variation, RSE=5.35%) in total clearance of Bu was quantified when Bu was associated with clonazepam as compared to phenytoin, which was considered as not being clinically relevant. The suspected induction on Bu metabolism by phenytoin should have resulted in the opposite effect. The patient efficacy and safety profiles were comparable between the two cohorts.
本研究旨在探讨癫痫预防对白消安(Bu)血浆暴露的影响。24 名成年患者在骨髓移植前接受静脉注射 Bu-环磷酰胺预处理方案。在连续四天内,每六小时给予 Busilvex(0.8mg/kg)。在静脉注射 Bu 给药前至少 12 小时开始给予氯硝西泮(0.025 至 0.03mg/kg/天,作为连续 12 小时静脉输注),并持续至最后一次给药后 24 小时。比较了与先前接受苯妥英钠预防癫痫发作的患者(n=127)的药代动力学(PK)数据。通过群体 PK 分析,与苯妥英钠相比,当 Bu 与氯硝西泮联合使用时,Bu 的总清除率平均增加了 10%(变异系数,RSE=5.35%),这被认为无临床意义。苯妥英钠对 Bu 代谢的诱导作用本应产生相反的效果。两组患者的疗效和安全性相似。