Primary results of a randomized two-by-two factorial phase II trial comparing neoadjuvant chemotherapy with two and four courses of cisplatin/S-1 and docetaxel/cisplatin/S-1 as neoadjuvant chemotherapy for advanced gastric cancer

被引:10
|
作者
Hayashi, Tsutomu [1 ]
Yoshikawa, Takaki [1 ]
Sakamaki, Kentaro [2 ]
Nishikawa, Kazuhiro [3 ]
Fujitani, Kazumasa [4 ]
Tanabe, Kazuaki [5 ]
Misawa, Kazunari [6 ]
Matsui, Takanori [7 ]
Miki, Akira [8 ]
Nemoto, Hiroshi [9 ]
Fukunaga, Tetsu [10 ]
Kimura, Yutaka [11 ]
Hihara, Jun [12 ]
机构
[1] Natl Canc Ctr, Gastr Surg, Chuo Ku, Tokyo, Japan
[2] Yokohama City Univ, Ctr Data Sci, Yokohama, Kanagawa, Japan
[3] Natl Hosp Org Osaka Natl Hosp, Osaka, Japan
[4] Osaka Gen Med Ctr, Osaka, Japan
[5] Hiroshima Univ, Grad Sch, Hiroshima, Japan
[6] Aichi Canc Ctr Hosp, Nagoya, Aichi, Japan
[7] Aichi Hosp, Aichi Canc Ctr, Nagoya, Aichi, Japan
[8] Kobe City Med Ctr Gen Hosp, Kobe, Hyogo, Japan
[9] Showa Univ, Fujigaoka Hosp, Yokohama, Kanagawa, Japan
[10] St Marianna Univ, Univ Hosp, Sch Med, Kawasaki, Kanagawa, Japan
[11] Sakai City Med Ctr, Sakai, Osaka, Japan
[12] Hiroshima City Asa Hosp, Hiroshima, Japan
来源
ANNALS OF GASTROENTEROLOGICAL SURGERY | 2020年 / 4卷 / 05期
关键词
cisplatin/S-1; docetaxel/cisplatin/S-1; gastric cancer; neoadjuvant therapy; D2; GASTRECTOMY; ADJUVANT CHEMOTHERAPY; PLUS CISPLATIN; OPEN-LABEL; S-1; SURGERY;
D O I
10.1002/ags3.12352
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: Neoadjuvant chemotherapy (NAC) is promising to improve the survival of resectable gastric cancer. However, suitable regimen and treatment duration for NAC have not yet been established. Methods: We conducted a randomized phase II trial to compare two and four courses of neoadjuvant S-1/cisplatin (SC) and S-1/cisplatin/docetaxel(DCS) using a two-by-two factorial design for locally resectable advanced gastric cancer. Patients with M0 and either T4 or T3 in case of junctional cancer or scirrhous-type cancer received two or four courses of SC or DCS. Then, patients underwent D2 gastrectomy and adjuvant S-1 chemotherapy for 1 year. The primary endpoint was 3-year overall survival. The planned sample size was 120 eligible patients. Results: Between October 2011 and September 2014, 132 patients were assigned to CS (n = 66; 33 in 2-courses and 33 in 4-courses) and DCS (n = 66; 33 in 2-courses and 33 in 4-courses). The 3-year OS was 58.1% in CS and 60.0% in DCS with hazard ratio of 0.80 (95% CI, 0.48-1.34), while it was 53.1% in the two courses and 65.0% in the four courses with hazard ratio of 0.72 (95% CI, 0.43-1.22). In the survival analysis by duration in each regimen, the 3-year OS was 58.1% for both two and four courses in CS, while it was 48.5% for two courses of DCS and 71.9% for four courses of DCS. Conclusions: Considering high 3-year OS, four courses DCS has a value to be tested in a future phase III study to confirm superiority of neoadjuvant chemotherapy for locally advanced gastric cancer.
引用
收藏
页码:540 / 548
页数:9
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