Fluorouracil versus combination of irinotecan plus cisplatin versus S-1 in metastatic gastric cancer: a randomised phase 3 study

被引:527
作者
Boku, Narikazu [1 ]
Yamamoto, Seiichiro [2 ]
Fukuda, Haruhiko [2 ]
Shirao, Kuniaki [3 ]
Doi, Toshihiko [4 ]
Sawaki, Akira [5 ]
Koizumi, Wasaburo [6 ]
Saito, Hiroshi [7 ]
Yamaguchi, Kensei [8 ]
Takiuchi, Hiroya [9 ]
Nasu, Junichiro
Ohtsu, Atsushi [4 ]
机构
[1] Shizuoka Canc Ctr, Div Gastrointestinal Oncol, Nagaizumi, Shizuoka 4118777, Japan
[2] Natl Canc Ctr, Japan Clin Oncol Grp, Ctr Data, Ctr Canc Control & Informat Serv, Tokyo 104, Japan
[3] Natl Canc Ctr, Tokyo, Japan
[4] Natl Canc Ctr Hosp E, Chiba, Japan
[5] Aichi Canc Ctr Hosp, Aichi, Japan
[6] Kitasato Univ E Hosp, Kanagawa, Japan
[7] Yamagata Prefectural Cent Hosp, Yamagata, Japan
[8] Saitama Canc Ctr, Saitama, Japan
[9] Osaka Med Coll, Osaka, Japan
关键词
HIGH-DOSE METHOTREXATE; III TRIAL; EUROPEAN-ORGANIZATION; 1ST-LINE THERAPY; SUPPORTIVE CARE; DOXORUBICIN; 5-FLUOROURACIL; CHEMOTHERAPY; LEUCOVORIN; MITOMYCIN;
D O I
10.1016/S1470-2045(09)70259-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The best chemotherapy regimen for metastatic gastric cancer is uncertain, but promising findings have been reported with irinotecan plus cisplatin and S-1 (tegafur, 5-chloro-2,4-dihydropyrimidine, and potassium oxonate)We aimed to investigate the superiority of irinotecan plus cisplatin and non-inferiority of S-1 compared with fluorouracil, with respect to overall survival, in patients with metastatic gastric cancer. Methods We undertook a phase 3 open label randomised trial in 34 institutions in Japan. We enrolled patients aged 20-75 years or younger, who had histologically proven gastric adenocarcinoma, and randomly assigned them by minimisation to receive either: a continuous infusion of fluorouracil (800 mg/m(2) per day, on days 1-5) every 4 weeks (n=234); intravenous irinotecan (70 mg/m(2), on days 1 and 15) and cisplatin (80 mg/m(2), on day 1) every 4 weeks (n=236); or oral S-1 (40 mg/m(2), twice a day, on days 1-28) every 6 weeks (n=234). The primary endpoint was overall survival. Analyses were done by intention to treat. This study is registered with Clinicaltrials.gov, number NCT00142350, and with UMIN-CTR, number C000000062. Findings All randomised patients were included in the primary analysis. Median overall survival was 10.8 months (IQR 5.7-17.8) for individuals assigned fluorouracil, 12.3 months (8.1-19.5) for those allocated irinotecan plus cisplatin (hazard ratio 0.85 [95% Cl 0.70-1.04]; p=0.0552), and 11.4 months (6.4-21.3) for those assigned S-1 (0.83 [0.68-1.01]; p=0.0005 for non-inferiority). Three treatment-related deaths occurred in the irinotecan plus cisplatin group and one was recorded in the S-1 group. Interpretation S-1 is non-inferior to fluorouracil and, in view of the convenience of an oral administration, could replace intravenous fluorouracil for treatment of unresectable or recurrent gastric cancer, at least in Asia. Irinotecan plus cisplatin is not superior to fluorouracil in this setting.
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收藏
页码:1063 / 1069
页数:7
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