Egorin M J, Van Echo D A, Whitacre M Y, Forrest A, Sigman L M, Engisch K L, Aisner J
Cancer Res. 1986 Mar;46(3):1513-20.
In a Phase I study, menogaril (7-OMEN) was administered daily for 5 days/course, every 21-28 days. Dosages of 3.5, 7, 11.5, 17, and 31.5 mg/m2 were infused over 1 h, and dosages of 42, 50, and 56 mg/m2 were infused over 2 h. Pharmacokinetics was studied at all dosages. Plasma and urine samples were collected from 24 patients, and bile samples were also collected from 2 patients. 7-OMEN and metabolites were measured by high performance liquid chromatography. 7-OMEN was the major plasma fluorescent species at all times, with only trace amounts of N-demethyl menogaril observed. 7-OMEN disappeared from plasma biexponentially with t1/2 alpha 0.19 +/- 0.04 (mean +/- SE) h and t1/2 beta 13.22 +/- 1.54 h. Plasma pharmacokinetics of 7-OMEN was linear from 3.5-56 mg/m2; area under the curve increased proportionally with dosage. Total body clearance of 7-OMEN was 28.18 +/- 3.33 liter/m2/h, Vc was 224 +/- 30.8 liter/m2, and Vss was 370 +/- 25.7 liter/m2. Plasma pharmacokinetics of 7-OMEN studied on multiple days of a given course were similar. Urinary excretion of 7-OMEN and fluorescent metabolites accounted for 5.4 +/- 0.4% of the daily dose. Parent compound still represented greater than or equal to 80% of urinary drug fluorescence after 24 h. N-demethyl menogaril was the only other fluorescent drug species detected in urine. In two patients with biliary tract drains, biliary excretion of drug fluorescence accounted for 2.2-4.2% of the daily dose. Only 7-OMEN and N-demethyl menogaril were detected in bile by high performance liquid chromatography and thin layer chromatography. 7-OMEN was the major fluorescent biliary species, but, by 24 h, N-demethyl menogaril accounted for approximately 40% of biliary drug fluorescence. When considered in light of each patient's observed toxicities, excellent relationships were observed between the plasma area under the curve of 7-OMEN and the percentage of decreases in WBC and absolute neutrophil count. These latter findings should be useful in developing more precise and intelligent dosing schemes for 7-OMEN.
在一项I期研究中,美诺加(7-OMEN)每21 - 28天给药一次,每日给药5天/疗程。3.5、7、11.5、17和31.5 mg/m²的剂量在1小时内输注,42、50和56 mg/m²的剂量在2小时内输注。对所有剂量进行了药代动力学研究。从24名患者中采集血浆和尿液样本,还从2名患者中采集胆汁样本。7-OMEN及其代谢产物通过高效液相色谱法测定。7-OMEN始终是主要的血浆荧光物质,仅观察到痕量的N-去甲基美诺加。7-OMEN从血浆中呈双指数消失,t1/2α为0.19±0.04(均值±标准误)小时,t1/2β为13.22±1.54小时。7-OMEN的血浆药代动力学在3.5 - 56 mg/m²范围内呈线性;曲线下面积随剂量成比例增加。7-OMEN的总体清除率为28.18±3.33升/m²/小时,Vc为224±30.8升/m²,Vss为370±25.7升/m²。在给定疗程的多天内研究的7-OMEN血浆药代动力学相似。7-OMEN及其荧光代谢产物的尿排泄占每日剂量的5.4±0.4%。24小时后,母体化合物仍占尿药荧光的≥80%。N-去甲基美诺加是在尿液中检测到的唯一其他荧光药物物质。在两名有胆道引流管的患者中,药物荧光的胆汁排泄占每日剂量的2.2 - 4.2%。通过高效液相色谱法和薄层色谱法在胆汁中仅检测到7-OMEN和N-去甲基美诺加。7-OMEN是主要的胆汁荧光物质,但到24小时时,N-去甲基美诺加约占胆汁药物荧光的40%。结合每位患者观察到的毒性来看,7-OMEN的血浆曲线下面积与白细胞和绝对中性粒细胞计数下降百分比之间存在良好的相关性。后一项发现对于制定更精确和合理的7-OMEN给药方案应是有用的。