Sato Yozo, Inaba Yoshitaka, Yamaura Hidekazu, Shimamoto Hiroshi, Nishiofuku Hideyuki, Oyama Takashi, Kanemitsu Yukihide, Sawaki Akira, Arai Yasuaki, Muro Kei
Dept. of Diagnostic and Interventional Radiology, Aichi Cancer Center, National Cancer Center Hospital.
Gan To Kagaku Ryoho. 2006 Jul;33(7):887-90.
The clinical efficacy and safety of tegafur/uracil (UFT) plus oral Leucovorin (LV) regimen for advanced or metastatic colorectal cancer were studied retrospectively. From September 2003 to March 2005, 82 patients were treated with UFT (300 mg/m(2)/day)/LV (75 mg/day) at our institute. The objective overall response rate was 14. 8% (95% confidence interval, 5.3 to 24.3%) in 54 evaluable patients. The response rate was 33.3% for previously untreated patients and 5.5% for previously treated patients, respectively. Grade 3 or more severe adverse reactions such as diarrhea or liver function abnormalities were only 7.3%. In 28 previously untreated patients,the median survival was 25.8 months with 1-and 2-year survival rates of 88.0% and 60.5%, respectively. This retrospective study demonstrated the reproducible activity and safety of UFT/LV for advanced or metastatic colorectal cancer in clinical practice.