Department of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama 241-0815, Japan.
Jpn J Clin Oncol. 2012 Jan;42(1):74-7. doi: 10.1093/jjco/hyr166. Epub 2011 Nov 17.
This randomized Phase II trial will compare the outcome of neoadjuvant chemotherapy using two and four courses of S-1 plus cisplatin or S-1 plus cisplatin plus docetaxel by a two-by-two factorial design for patients with macroscopically resectable serosa-positive gastric cancer. After neoadjuvant chemotherapy, patients will receive D2 gastrectomy followed by S-1 chemotherapy for 1 year postoperatively. The primary endpoint is the 3-year overall survival. The sample size is 120 for the two hypotheses: the superiority of four courses compared with two courses and the superiority of S-1 plus cisplatin plus docetaxel compared with S-1 plus cisplatin. This trial will be able to define the more suitable number of cycles and better regimen of neoadjuvant chemotherapy for gastric cancer.
这项随机的 II 期临床试验将比较两种和四种 S-1 联合顺铂或 S-1 联合顺铂加多西他赛新辅助化疗方案治疗浆膜阳性可切除胃癌患者的疗效,采用两因素两水平析因设计。新辅助化疗后,患者将接受 D2 胃切除术,术后 1 年接受 S-1 化疗。主要终点是 3 年总生存率。对于两个假设,样本量为 120:与两周期相比,四周期的优越性和 S-1 联合顺铂加多西他赛优于 S-1 联合顺铂。本试验将能够确定更适合的化疗周期数和更好的新辅助化疗方案。