Milano G, Roman P, Khater R, Frenay M, Renee N, Namer M
Laboratory of Pharmacokinetics, Centre Antoine Lacassagne, Nice, France.
Int J Cancer. 1988 Apr 15;41(4):537-41. doi: 10.1002/ijc.2910410411.
This non-randomized study reports pharmaco-clinical data on 5-FU administered by the widely used 5-day continuous infusion schedule to 42 patients with metastatic colorectal cancer; 5-FU was given by hepatic intra-arterial route (h.i.a.) at doses ranging from 800 to 1,450 mg/m2, and by a systemic intravenous route (i.v.) at doses ranging from 650 to 1,300 mg/m2. 5-FU blood levels were available for a total of 179 cycles. Toxicity was dose-dependent during h.i.a. cycles but not during i.v. cycles. For h.i.a. cycles, 1,000 mg/m2/day represented the threshold dose for tolerance. The individual total cycle drug concentration-time product might predict toxicity for both i.v. and h.i.a. cycle when the threshold is set at 30,000 ng/ml.hr. These data may be of practical value for improving the therapeutic index of 5-day continuous treatment by 5-FU given by i.v. or h.i.a. routes.
这项非随机研究报告了42例转移性结直肠癌患者采用广泛使用的5天持续输注方案给予5-氟尿嘧啶(5-FU)的药物临床数据;5-FU通过肝动脉内途径(h.i.a.)给药,剂量范围为800至1450mg/m²,通过全身静脉途径(i.v.)给药,剂量范围为650至1300mg/m²。共获得179个周期的5-FU血药浓度数据。在肝动脉内给药周期中,毒性呈剂量依赖性,而在静脉给药周期中则不然。对于肝动脉内给药周期,1000mg/m²/天是耐受的阈值剂量。当阈值设定为30000ng/ml·小时时,个体总周期药物浓度-时间乘积可能预测静脉给药和肝动脉内给药周期的毒性。这些数据对于提高通过静脉或肝动脉内途径给予5-FU进行5天持续治疗的治疗指数可能具有实际价值。