Nakagami Y, Lin T T, Ito H, Hirasawa S, Tannawa K, Fujioka Y, Ogawa H, Tanaka K, Yamada N, Ishii Y
Department of Urology, First Hospital of Nippon Medical School.
Hinyokika Kiyo. 1987 Oct;33(10):1728-32.
The safety of prolonged administration of UFT in which tegafur and uracil were mixed in a ratio of 1:4 in molar fraction was studied in 44 cases of bladder cancer and 10 cases of renal cell carcinoma. Daily doses of UFT were 300-600 mg, and average total doses administered were 102.0 g for bladder cancer and 116.6 g for renal cell carcinoma cases. Incidence of adverse effects were 25.0% in bladder cancer and 18.5% in renal cell carcinoma cases. Anorexia, nausea, vomiting and decrease in WBC were observed, but rates of having discontinued the administration of UFT were very low, being 9.1% in bladder cancer and 10.0% in renal cell carcinoma. Thus, UFT was considered to be tolerable during prolonged use in bladder cancer and renal cell carcinoma and also a drug in which more usefulness is expected in multidisciplinary treatments in future.
对44例膀胱癌患者和10例肾细胞癌患者研究了以摩尔分数1:4的比例混合替加氟和尿嘧啶的优福定长期给药的安全性。优福定的日剂量为300 - 600毫克,膀胱癌患者的平均总给药剂量为102.0克,肾细胞癌患者为116.6克。膀胱癌患者的不良反应发生率为25.0%,肾细胞癌患者为18.5%。观察到有厌食、恶心、呕吐和白细胞减少的情况,但优福定停药率非常低,膀胱癌患者为9.1%,肾细胞癌患者为10.0%。因此,优福定在膀胱癌和肾细胞癌的长期使用中被认为是可耐受的,并且也是一种未来有望在多学科治疗中发挥更大作用的药物。