Phase II Trial of Neoadjuvant Chemotherapy with XELOX plus Bevacizumab for Locally Advanced Rectal Cancer

被引:12
|
作者
Uehara, Keisuke [1 ]
Ishiguro, Seiji [1 ]
Sakamoto, Eiji [2 ]
Maeda, Atsuyuki [3 ]
Inoue, Masaya [4 ]
Tojima, Yuichiro [5 ]
Kobayashi, Satoshi [6 ]
Omiya, Naoki [7 ]
Ishizuka, Naoki [8 ]
Nakao, Akimasa [9 ]
Goto, Hidemi [7 ]
Nagino, Masato [1 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Surg, Div Surg Oncol, Nagoya, Aichi 4648601, Japan
[2] Nagoya Daini Red Cross Hosp, Dept Surg, Nagoya, Aichi, Japan
[3] Ogaki Municipal Hosp, Dept Surg, Gifu, Japan
[4] Handa City Hosp, Dept Surg, Aichi, Japan
[5] Chukyo Hosp, Dept Surg, Nagoya, Aichi, Japan
[6] Toyota Kosei Hosp, Dept Surg, Nagoya, Aichi, Japan
[7] Nagoya Univ, Grad Sch Med, Dept Gastroenterol, Nagoya, Aichi 4648601, Japan
[8] Int Med Ctr Japan, Res Inst, Dept Community Hlth & Med, Div Prevent Med, Tokyo, Japan
[9] Nagoya Univ, Dept Surg 2, Grad Sch Med, Nagoya, Aichi 4648601, Japan
关键词
rectal cancer; neoadjuvant chemotherapy; XELOX; bevacizumab; TOTAL MESORECTAL EXCISION; PREOPERATIVE RADIOTHERAPY; IRRADIATED PATIENTS; COLORECTAL-CANCER; SURVIVAL; BENEFIT;
D O I
10.1093/jjco/hyr084
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In Western countries, the standard treatment for locally advanced rectal cancer is preoperative chemoradiotherapy followed by total mesorectal excision. On the other hand, in Japan, treatment results without radiotherapy are by no means inferior; therefore, extrapolation of results of preoperative treatment in Western countries to Japan is controversial. We consider that survival may be improved by preoperative treatment with new anticancer agents as they are expected not only to decrease the local recurrence rate but also to prevent distant metastases. We are conducting a multicentre Phase II study to evaluate the safety and efficacy of neoadjuvant chemotherapy using XELOX plus bevacizumab without radiotherapy in patients with locally advanced rectal cancer. The primary endpoint of the study is treatment compliance. Secondary endpoints are overall survival, disease-free survival, local recurrence-free survival, objective response rate, R0 resection rate and adverse events. Thirty patients are required for this study.
引用
收藏
页码:1041 / 1044
页数:4
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