TY - JOUR
T1 - Phase II trial of neoadjuvant chemotherapy with XELOX plus bevacizumab for locally advanced rectal cancer
AU - Uehara, Keisuke
AU - Ishiguro, Seiji
AU - Sakamoto, Eiji
AU - Maeda, Atsuyuki
AU - Inoue, Masaya
AU - Tojima, Yuichiro
AU - Kobayashi, Satoshi
AU - Omiya, Naoki
AU - Ishizuka, Naoki
AU - Nakao, Akimasa
AU - Goto, Hidemi
AU - Nagino, Masato
PY - 2011/8
Y1 - 2011/8
N2 - 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.
AB - 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.
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U2 - 10.1093/jjco/hyr084
DO - 10.1093/jjco/hyr084
M3 - Article
C2 - 21803876
AN - SCOPUS:79961044483
SN - 0368-2811
VL - 41
SP - 1041
EP - 1044
JO - Japanese journal of clinical oncology
JF - Japanese journal of clinical oncology
IS - 8
M1 - hyr084
ER -