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Pharmacokinetics of 5-FU after S-1 oral administration for adjuvant chemotherapy in gastric cancer patients

机译:S-1口服后胃癌患者5-FU的药代动力学

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We studied the pharmacokinetics of 5-FU after S-1 oral administration at the usual dose (80 mg/m2) for adjuvant chemotherapy in 13 advanced gastric cancer patients (Stage II, III), and at a decreased dose (60 mg/m2) for adjuvant or combined chemotherapy in 13 advanced gastric cancer patients. Pharmacokinetic parameters of 5-FU in the serum were as follows: Cmax, 159 .9 2+/-45.2 ng/mL, Tmax, 2.17+/-0.58 h;T1/2, 3.13+/-2.88 h; and AUC(0-8), 768.0+/-260.8 ng h/mL in the patients with the usual dose, and Cmax, 117.3+/-55.1 ng/mL; Tmax, 2.62+/-0.9 6 h; T1/2, 3.09+/-1.9 5 h and AUC(0-8), 565.9+/-216.8 ng h/mL in the patients with the decreased dose. No difference in AUC was observed between operative methods. Adverse events of more than grade 3 were recognized in 7 patients, and AUC of 6 patients were more than 800 ng h/mL. The plasma concentration of 5-FU was quite different between patients. The difference of Cmax and AUC was 3-4 times. It was concluded that we must pay attention to individual differences in the plasma concentration of 5-FU in postoperative gastric cancer patients when S-1 would be administered.
机译:我们研究了13例晚期胃癌患者(II,III期)以常规剂量(80 mg / m2)以常规剂量(80 mg / m2)进行S-1口服给药后5-FU的药代动力学,并以降低的剂量(60 mg / m2)进行了研究)用于13例晚期胃癌患者的辅助或联合化疗。血清中5-FU的药代动力学参数如下:Cmax,159.9 2 +/- 45.2ng / mL,Tmax,2.17 +/- 0.58h; T1 / 2,3.13 +/- 2.88h;和。常规剂量的患者的AUC(0-8)为768.0 +/- 260.8 ng h / mL,Cmax为117.3 +/- 55.1 ng / mL;最高温度,2.62 +/- 0.9 6 h;剂量降低的患者的T1 / 2、3.09 +/- 1.9 5 h和AUC(0-8),565.9 +/- 216.8 ng h / mL。两种手术方法之间的AUC没有差异。在7例患者中发现了超过3级的不良事件,其中6例患者的AUC超过800 ng h / mL。患者之间的5-FU血浆浓度差异很大。 Cmax和AUC的差是3-4倍。结论是,当使用S-1时,我们必须注意术后胃癌患者5-FU血浆浓度的个体差异。

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