A randomized controlled Phase III trial comparing 2-weekly docetaxel combined with cisplatin plus fluorouracil (2-weekly DCF) with cisplatin plus fluorouracil (CF) in patients with metastatic or recurrent esophageal cancer: rationale, design and methods of Japan Clinical Oncology Group study JCOG1314 (MIRACLE study)

被引:21
|
作者
Kataoka, Kozo [1 ]
Tsushima, Takahiro [2 ]
Mizusawa, Junki [1 ]
Hironaka, Shuichi [3 ]
Tsubosa, Yasuhiro [4 ]
Kii, Takayuki [5 ]
Shibuya, Yuichi [6 ]
Chin, Keisho [7 ]
Katayama, Hiroshi [1 ]
Kato, Ken [8 ]
Fukuda, Haruhiko [1 ]
Kitagawa, Yuko [9 ]
机构
[1] Natl Canc Ctr, Ctr Res Adm & Support, JCOG Data Ctr, Operat Off, Tokyo 104, Japan
[2] Shizuoka Canc Ctr, Div Gastrointestinal Oncol, Shizuoka, Japan
[3] Chiba Canc Ctr, Clin Trial Promot Dept, Chiba 2608717, Japan
[4] Shizuoka Canc Ctr, Div Esophageal Surg, Shizuoka, Japan
[5] Osaka Med Coll, Canc Chemotherapy Ctr, Osaka, Japan
[6] Kochi Hlth Sci Ctr, Dept Gastroenterol Surg, Kochi, Japan
[7] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Gastroenterol, Tokyo, Japan
[8] Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, Japan
[9] Keio Univ, Sch Med, Dept Surg, Tokyo 160, Japan
关键词
metastatic or recurrent esophageal cancer; 2-weekly DCF; Phase III; SQUAMOUS-CELL CARCINOMA; COMBINATION CHEMOTHERAPY; 5-FLUOROURACIL; I/II; 5-FU; HEAD;
D O I
10.1093/jjco/hyv012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy with cisplatin plus fluorouracil is the current standard treatment for metastatic or recurrent esophageal cancer. We have developed a 2-weekly docetaxel combined with CF regimen and conducted a Phase I/II trial for metastatic or recurrent esophageal cancer (JCOG0807). Promising efficacy and safety were shown in JCOG0807, and we have commenced a Phase III trial in September 2014 to confirm the superiority of 2-weekly DCF to CF for patients with metastatic or recurrent esophageal cancer. A total of 240 patients will be accrued from 41 Japanese institutions over a period of 4 years. The primary end point is overall survival. The secondary end points are progression-free survival, response rate and proportion of adverse events. This trial has been registered in the UMIN Clinical Trials Registry as UMIN000015107 (http://www.umin.ac.jp/ctr/index.htm).
引用
收藏
页码:494 / 498
页数:5
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