Preliminary study on the optimal dosage schedule for oral tegafur/uracil (UFT) chemotherapy

被引:14
作者
Sadahiro S. [1 ,3 ]
Mukai M. [1 ]
Tokunaga N. [1 ]
Tajima T. [1 ]
Makuuchi H. [1 ]
Yoshida M. [2 ]
Okabe H. [2 ]
Uchida J. [2 ]
Takeda S. [2 ]
Unemi N. [2 ]
机构
[1] Department of Surgery, Tokai University School of Medicine, Isehara
[2] Anticancer Antimicrobials Res. Lab., Taiho Pharmaceutical Co. Ltd., Tokushima
[3] Department of Surgery, Tokai University School of Medicine, Bohseidai
关键词
Chemotherapy; Donryu rats; Dosage schedule; Dose intensity; UFT; Yoshida sarcoma;
D O I
10.1007/BF02490095
中图分类号
学科分类号
摘要
Background: We evaluated a new dose-intensive schedule for oral UFT (tegafur and uracil in a molar ratio of 1:4) administered for 5 consecutive days followed by 2 drug-free days (weekly-5 method), in comparison with conventional daily administration (weekly-7 method), in Yoshida-sarcoma- bearing rats. Methods: The single dose of 20 mg/kg of UFT for rats corresponds to the human single dose when converted to dose per unit of body- surface area. The drug was administered 3 times a day for the weekly-5 method and twice a day for the weekly-7 method. A 7-day period was considered 1 course. The total doses per course were almost the same in both methods. Antitumor efficacy and survival effect were evaluated after 3 courses. Body weight changes and food consumption were also measured as indices of toxicity. The plasma pharmacokinetics were analyzed by simulating dosage patterns. Results: Significant tumor-growth inhibition was seen with both the weekly-5 and the weekly-7 methods as compared to the control. Moreover, the weekly-5 method showed higher tumor-growth inhibition and a better survival effect than the weekly-7 method. These results appear to be related to the duration of plasma concentrations of 5-FU being maintained above a certain concentration for a longer time with the weekly-5 method. Food consumption with the weekly-5 method recovered to the control level after the drug-free period, and body weight gain was also favorable. Conclusion: The results of this study suggest that the dose-intensive method of administering UFT orally for the weekly-5 method is a useful dosage schedule. Thus, this dosage schedule is recommended for use in clinical trials.
引用
收藏
页码:7 / 12
页数:5
相关论文
共 13 条
[1]  
Fujii, S., Ikenaka, K., Fukushima, M., Shirasaka, T., Effect of uracil and its derivatives on antitumor activity of 5-fluorouracil and 1-(2-tetrahydro-furyl)-5-fluorouracil (1987) Gann, 69, pp. 763-772
[2]  
Ota, K., Taguchi, T., Kimura, K., Report on nationwide pooled data and cohort investigation in UFT phase II study (1987) Jpn J Cancer Chemother, 14, pp. 2749-2757
[3]  
Pazdur, R., Lassere, Y., Rhodes, V., Ajani, Ja., Sugarman, Sm., Patt, Yz., Jones, Dv., Levn, B., Phase II trial of uracil and tegafur plus oral leucovorin: An effective oral regimen in the treatment of metastatic colorectal carcinoma (1994) J Clin Oncol, 12, pp. 2296-2300
[4]  
Coppin, C.M.L., The description of chemotherapy delivery: Options and pitfalls (1987) Sem Oncol, 14, pp. 34-42
[5]  
Taguchi, T., Furue, S., Koyama, Y., Saito, T., Ito, K., Majima, S., Kimura, K., Inokuchi, K., Phase I study of UFT (1980) Jpn J Cancer Chemother, 7, pp. 966-972
[6]  
Maehara, Y., Sugimachi, K., Ogawa, M., Kakegawa, T., Shimazu, H., Tomita, M., Postoperative adjuvant chemotherapy based on the differentiation for gastric cancer (1994) J Jpn Soc Cancer Ther, 20, p. 248
[7]  
Aota, M., Nakayama, S., Yokomise, H., Jinno, K., Daitoh, N., Serum and tissue concentration of UFT in patients with lung cancer (1986) Jpn J Cancer Chemother, 13, pp. 3046-3055
[8]  
Maehara, Y., Sugimachi, K., Kikuchi, K., Inokuchi, K., Komi, N., Hattori, T., Taguchi, T., Ogawa, N., Cooperative study of surgical adjuvant chemotherapy for colorectal cancer, five-year results after surgery (1993) Jpn J Cancer Chemother, 20, pp. 109-115
[9]  
Kimura, K., Suga, S., Shimaji, T., Kitamura, M., Kubo, K., Suzuoki, Y., Isobe, K., Clinical basis of chemotherapy for gastric cancer with uracil and 1- (2′-tetrahydrofuryl)-5-fluorouracil (1980) Gastroenterol Jpn, 15, pp. 324-329
[10]  
Marunaka, T., Umeno, Y., Yoshida, K., Nagamachi, M., Minami, Y., Fujii, S., High pressure liquid chromatographic determination of ftorafur and GLC-mass spectrometric determination of 5-fluorouracil and uracil in biological materials after oral administration of uracil plus ftorafur (1980) J Pharm Sci, 69, pp. 1296-1300