Miki Ikuya, Tamura Takao, Nakamura Tsutomu, Makimoto Hiroo, Hamana Noriko, Uchiyama Hitoshi, Shirasaka Daisuke, Morita Yoshinori, Yamada Hiroyuki, Aoyama Nobuo, Sakaeda Toshiyuki, Okumura Katsuhiko, Kasuga Masato
Division of Diabetes, Digestive, and Kidney Diseases, Department of Clinical Molecular Medicine, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
Ther Drug Monit. 2005 Jun;27(3):369-74. doi: 10.1097/01.ftd.0000162554.23501.e6.
The variations of plasma concentrations of 5-fluorouracil (5-FU) were investigated in 30 esophageal cancer patients treated with repetitive protracted venous infusion (PVI) of 5-FU-based chemoradiotherapy, and in an attempt to find a new possible candidate that explains their variations, CLOCK T3111C genetic polymorphism was examined. The patients have received 2 courses of chemoradiotherapy consisting of 2 cycles of 5-day PVI of 5-FU (400 mg/m/d) with cisplatin and concurrent radiation. The plasma concentrations of 5-FU were determined at 5 PM on day 3 and 5 AM on day 4 after the beginning of each 5-FU infusion. The CLOCK T3111C genotype was determined by polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP) and by direct sequencing. Plasma concentrations were measured in 239 samples. In the first course, the plasma concentrations of 5-FU at 5 AM were significantly lower than those at 5 PM in the first cycle, whereas a similar tendency was observed in the second cycle, although not significantly (Wilcoxon signed-rank test). The plasma concentrations of 5-FU at 5 PM and 5 AM in the second cycle were both significantly higher than those in the first cycle, and their coefficient of variation in the former was also significantly smaller than that in the latter. These phenomena in the first course were also observed in the second one. These results revealed the elevation of plasma drug concentration and its reduced circadian variation during repetitive PVI of 5-FU. In 5-FU-based chemotherapy, its administration schedule should be made in consideration of these phenomena. The CLOCK T3111C genotype did not have a significant impact on the variation of the plasma concentrations of 5-FU in this study population. Further studies are needed to clarify the mechanism of these phenomena and to identify an easy-to-assess marker of circadian rhythms for use in individualizing delivery of 5-FU.
对30例接受基于5-氟尿嘧啶(5-FU)的重复长时间静脉输注(PVI)化疗放疗的食管癌患者,研究其血浆5-氟尿嘧啶浓度的变化,并为找出解释这些变化的新潜在因素,检测了生物钟基因CLOCK T3111C的基因多态性。患者接受了2个疗程的化疗放疗,包括2个周期,每个周期5天的5-FU(400mg/m²/d)与顺铂的PVI及同步放疗。在每次5-FU输注开始后的第3天下午5点和第4天上午5点测定5-FU的血浆浓度。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和直接测序法确定CLOCK T3111C基因型。共检测了239个样本的血浆浓度。在第一个疗程中,第一个周期上午5点的5-FU血浆浓度显著低于下午5点的浓度,第二个周期也观察到类似趋势,但不显著(Wilcoxon符号秩检验)。第二个周期下午5点和上午5点的5-FU血浆浓度均显著高于第一个周期,且前者的变异系数也显著小于后者。第一个疗程中的这些现象在第二个疗程中也有观察到。这些结果揭示了在5-FU重复PVI过程中血浆药物浓度升高及其昼夜变化减小。在基于5-FU的化疗中,制定给药方案时应考虑这些现象。在本研究人群中,CLOCK T3111C基因型对5-FU血浆浓度的变化没有显著影响。需要进一步研究以阐明这些现象的机制,并确定一种易于评估的昼夜节律标志物,用于5-FU的个体化给药。