Randomized phase II study comparing mitomycin, cisplatin plus doxifluridine with cisplatin plus doxifluridine in advanced unresectable gastric cancer

被引:0
作者
Koizumi, W
Fukuyama, Y
Fukuda, T
Akiya, T
Hasegawa, K
Kojima, Y
Ohn, N
Kurihara, M
机构
[1] Kitasato Univ, Sch Med, Dept Internal Med, Tokyo Cooperat Oncol Grp, Sagamihara, Kanagawa 2288520, Japan
[2] Kimitsu Chuo Hosp, Dept Internal Med, Kisarazu City, Chiba 2920822, Japan
[3] Gunma Canc Ctr Hosp, Dept Surg, Ohta, Gunma 3730828, Japan
[4] Gunma Canc Ctr Hosp, Dept Internal Med, Ohta, Gunma 3730828, Japan
[5] Tsuboi Hosp, Dept Internal Med, Kouiyama City, Fukushima 9638002, Japan
[6] Toho Univ, Sch Med, Ohmori Hosp, Dept Internal Med,Ohta Ku, Tokyo 1438541, Japan
[7] Chugai Pharmaceut Co Ltd, Chuou Ku, Tokyo 1048301, Japan
[8] Showa Univ, Sch Med, Toyosu Hosp, Dept Internal Med,Koto Ku, Tokyo 1358577, Japan
关键词
mitomycin; cisplatin; doxifluridine; gastric cancer; inoperable; combination therapy;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Various chemotherapies have been used to treat inoperable gastric cancer. Most combination therapies include cisplatin (CDDP) and fluoropyrimidine (5-FUs), which are thought of as key drugs. In the present study, we randomly compared mitomycin (MMC) and CDDP plus doxifluridine (5'-DFUR), which is an oral 5-FU and an intermediate metabolite of capecitabine (Xeloda), with CDDP plus 5'-DFUR in advanced unresectable gastric cancer. Regimen A was CDDP (70 mg/m(2), by 2-hour intravenous drip infusion on day 1), MMC (7 mg/m(2), injected intravenous on day 2), and oral 5'-DFUR (1200 mg/m(2), on days 4 to 7, 11 to 14, 18 to 21 and 25 to 28; 3 days rest and 4 days administration). Regimen B was identical to regimen A without MMC. Results: The response rate was 25.0% (8/32 patients) in Regimen A, 17.2% (5/29) in Regimen B (p=0.541). The median survival time was 241 days in Regimen A and 179 days in Regimen B (p=0.498). In Regimen A, although no significant difference was observed, end points such as response rate and survival improved Thus, we concluded that a randomized controlled phase III study with more subjects should be conducted.
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页码:2465 / 2470
页数:6
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