Sato Y, Une Y, Nagabuchi E, Matsuoka S, Kagaya H, Miyata S, Yakura Y, Uchino J
Gan To Kagaku Ryoho. 1986 Feb;13(2):337-41.
UFT, a combination antitumor drug consisting of 1 part Futraful and 4 parts Uracil, was administered preoperatively to 10 patients with gastric cancer, 9 patients with colo-rectal cancer and 1 patient with hepatocellular carcinoma. A pharmacokinetic study was then carried out after oral administration of 600 mg per day of UFT, measuring Uracil, Futraful and 5-FU levels in serum and tumor tissue. Preoperative total doses of UFT for gastric cancer were 3.0-11.4 g, for colo-rectal cancer 3.6-16.8 g and for hepatocellular carcinoma 8.4 g. Side effects, mainly gastrointestinal symptoms, were observed in 3 cases. Abnormalities of liver function test, depression of serum protein and bone marrow damage were observed in 4 cases. 5-FU concentration in the tumor tissue was higher than 0.05 mu/g in 15 of 19 patients (79%). This suggested that 5-FU was maintained in the tumor tissue for a longer period. However, it also suggested that the concentration of Uracil in the tumor tissue corresponded to the total dose of UFT as did the degree of side effects.
优福定(UFT)是一种由1份喃氟啶(Futraful)和4份尿嘧啶组成的联合抗肿瘤药物,术前给予10例胃癌患者、9例结直肠癌患者和1例肝细胞癌患者使用。随后在每天口服600毫克优福定后进行药代动力学研究,测定血清和肿瘤组织中尿嘧啶、喃氟啶和5-氟尿嘧啶(5-FU)的水平。胃癌术前优福定的总剂量为3.0 - 11.4克,结直肠癌为3.6 - 16.8克,肝细胞癌为8.4克。3例出现副作用,主要为胃肠道症状。4例出现肝功能检查异常、血清蛋白降低和骨髓损伤。19例患者中有15例(79%)肿瘤组织中5-FU浓度高于0.05微克/克。这表明5-FU在肿瘤组织中维持的时间更长。然而,这也表明肿瘤组织中尿嘧啶的浓度与优福定的总剂量以及副作用程度相对应。