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联合化疗治疗晚期胰腺癌的疗效分析
引用本文:张蓓,刘志苏,孙权,黄汉涛.联合化疗治疗晚期胰腺癌的疗效分析[J].肝胆外科杂志,2005,13(1):26-28.
作者姓名:张蓓  刘志苏  孙权  黄汉涛
作者单位:1. 武汉大学附属中南医院,武汉,430071
2. 武警湖北总队医院
摘    要:目的探讨吉西他滨和5-氟尿嘧啶联合治疗晚期胰腺癌的疗效和可能的影响机制。方法实验组22例接受吉西他滨、5-氟尿嘧啶和四氢叶酸联合化疗,对照组21例接受5-氟尿嘧啶 四氢叶酸联合化疗,比较他们的近期疗效、疾病相关症状改善状况和不良反应。通过高效液相色谱技术检测第1、5天时2组病人5-氟尿嘧啶的血浆浓度和半衰期。结果实验组病人的近期疗效、疾病相关症状改善均好于对照组,但不良反应也增加。实验组病人血浆中5-氟尿嘧啶的血药浓度增高,半衰期延长,上述变化贯穿于5-氟尿嘧啶的整个治疗过程。结论吉西他滨可改善5-氟尿嘧啶治疗晚期胰腺癌的疗效,其机制与它能长时间的提高5-氟尿嘧啶在体内的有效浓度有关。

关 键 词:胰腺癌  吉西他滨  5-氟尿嘧啶  药物代谢动力学
文章编号:1006-4761(2005)01-0026-03
修稿时间:2004年2月9日

EFFECT OF GEMCITABINE PLUS 5-FLUOROURACIL AND FOLINIC ACID TO TREAT THE PATIENTS WITH ADVANCED PANCREATIC ADENOCARCINOMA
ZHANG Bei,LIU Zhi-su,SUN Quan,et al..EFFECT OF GEMCITABINE PLUS 5-FLUOROURACIL AND FOLINIC ACID TO TREAT THE PATIENTS WITH ADVANCED PANCREATIC ADENOCARCINOMA[J].Journal of Hepatobiliary Surgery,2005,13(1):26-28.
Authors:ZHANG Bei  LIU Zhi-su  SUN Quan  
Institution:ZHANG Bei,LIU Zhi-su,SUN Quan,et al.Department of General Surgery,The Zhongnan Hospital,Wuhan University,Wuhan 430071 Huang Han-tao,Department of General Surgery,The Hubei Armed Policemem Hospital,Wuhan 430061)
Abstract:Objective To investigate the effects and the mechanism of gemcitabine plus 5-fluorouracial and folinic acid for patients with advanced pancreatic adenocarcinoma.Methods 43 untreated patients were collected and divided into two groups:the experimental group who received chemotherapy with gemcitabine(1000mg/m 2 in a intravenous on days 1,8 and 16,plus folinic acid(100mg/m 2)and 5-FU(400mg/m 2)administered by a i.v.infusion on days1-5;the control group received FA and 5-FU in the same way.5-FU pharmacokinetics were compared in two groups.Result The objective response was 31.8% and DRSI was 68.2% in the experimental group,which was respectively 14.3% and 33.3% respectively in the control group.There was a significant increase in systemic(5-FU) exposure and toxicity in the experimental group.Conclusion It is certain for the combined application of gemcitabine and 5-FU to treat pancreatic adenocarcinoma.The enhanced 5-FU systemic exposure found in the presence of GEM may explain the higher level of toxicity and antitumour activity in this trial.
Keywords:Pancreatic adenocarcinoma  Gemcitabine  5-Fluorouracil  Pharmacokinetics
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