Furuse Junji, Okusaka Takuji, Ohkawa Shinichi, Nagase Michitaka, Funakoshi Akihiro, Boku Narikazu, Yamao Kenji, Yamaguchi Taketo, Sato Toshiya
Division of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Cancer Chemother Pharmacol. 2009 Dec;65(1):113-20. doi: 10.1007/s00280-009-1011-z. Epub 2009 Apr 29.
The purpose of this study was to clarify the safety and efficacy of combination chemotherapy of uracil-tegafur (UFT) and doxorubicin (UFD regimen), and to identify the prognostic factors in patients with unresectable advanced biliary tract cancer who received systemic chemotherapy.
Patients with histologically or cytologically confirmed, measurable biliary tract cancer, including intrahepatic or extrahepatic cholangiocarcinoma, gallbladder cancer, and ampullary cancer, who were not suitable candidates for surgery, were eligible for the study. Patients received oral UFT at 300 mg/m(2) per day divided into two doses on days 1-14 and intravenous doxorubicin at 30 mg/m(2) on day 1. This cycle was repeated every 21 days. The relationship between the patient characteristics and the prognosis was examined. Univariate and multivariate analyses were conducted to identify the prognostic factors associated with survival.
Sixty-one patients from 12 institutions were enrolled in the late phase II study between April 2005 and March 2006. Of the 61 patients, 4 patients had partial responses, for an objective response rate of 6.6% (95% CI: 1.8-15.9%); 28 patients had stable disease, 27 had progressive diseases, and 2 patients were not evaluated. The median progression-free survival was 1.6 months, and the overall median survival time was 6.5 months. In the 85 patients who received this UFD chemotherapy in previous and late phase II studies, multivariate analysis revealed the ECOG performance status 1 (P = 0.001), gallbladder as the primary cancer site (P = 0.014), T-factor 4 of the TNM classification (P = 0.035), and elevated serum lactate dehydrogenase levels (P = 0.043) as being associated with a significantly shorter survival.
Combination chemotherapy of UFT and doxorubicin had minimum activity against advanced biliary tract cancer. Performance status was identified as the most important prognostic factor in patients who received systemic chemotherapy.
本研究旨在阐明尿嘧啶替加氟(UFT)与多柔比星联合化疗(UFD方案)的安全性和有效性,并确定接受全身化疗的不可切除晚期胆管癌患者的预后因素。
组织学或细胞学确诊、可测量的胆管癌患者,包括肝内或肝外胆管癌、胆囊癌和壶腹癌,若不适合手术则符合本研究条件。患者在第1 - 14天每天口服UFT 300 mg/m²,分两次给药,第1天静脉注射多柔比星30 mg/m²。每21天重复此周期。检查患者特征与预后的关系。进行单因素和多因素分析以确定与生存相关的预后因素。
2005年4月至2006年3月期间,来自12个机构的61例患者参加了晚期II期研究。61例患者中,4例部分缓解,客观缓解率为6.6%(95%CI:1.8 - 15.9%);28例病情稳定,27例病情进展,2例未评估。无进展生存期的中位数为1.6个月,总生存期的中位数为6.5个月。在之前和晚期II期研究中接受此UFD化疗的85例患者中,多因素分析显示东部肿瘤协作组(ECOG)体能状态评分为1(P = 0.001)、胆囊为原发癌部位(P = 0.014)、TNM分类的T因子为4(P = 0.035)以及血清乳酸脱氢酶水平升高(P = 0.043)与生存期显著缩短相关。
UFT与多柔比星联合化疗对晚期胆管癌的活性最低。体能状态被确定为接受全身化疗患者最重要的预后因素。