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中国临床药理学与治疗学 ›› 2009, Vol. 14 ›› Issue (5): 541-545.

• 临床药理学 • 上一篇    下一篇

进展期胃癌术前顺铂腹腔内、静脉化疗药代动力学的比较研究

李豪侠1, 陈晓亮1, 马志敏2   

  1. 1杭州师范大学附属医院中西医结合科, 杭州310015, 浙江;
    2浙江大学医学院附属第一医院肿瘤外科, 杭州310003, 浙江
  • 收稿日期:2009-02-24 修回日期:2009-05-22 发布日期:2020-11-09
  • 作者简介:李豪侠, 男, 硕士, 副主任医师, 研究方向:肿瘤内科。Tel:0571-88303688 E-mail:hzlihaoxia @yahoo.com. cn

Study on cisplatin pharmacokinetics:preoperative intraperitoneal administration versus intravenous chemotherapy with cisplatin for advanced gastric carcinoma

LI Hao-xia1, CHEN Xiao-liang1, MA Zhi-min2   

  1. 1Department of Combination of TCM with Western Medicine, Affiliated Hospital of Hangzhou Normal University, Hangzhou 310015, Zhejiang, China;
    2Department of Oncological Surgery, First Affiliated Hospital of Medical College, Zhejiang University, Hangzhou 310003, Zhejiang, China
  • Received:2009-02-24 Revised:2009-05-22 Published:2020-11-09

摘要: 目的:比较研究进展期胃癌术前顺铂静脉与腹腔内给药的药代动力学特点。方法:50 例可切除进展期胃癌患者随机分成两组:腹腔给药组26 例, 静脉给药组24 例。顺铂60 mg/m2 分别于术前腹腔及静脉给药, 给药后180 min, 取腹腔液、胃左静脉血、外周血标本;270 min 取手术中肿瘤组织、癌旁正常组织标本。另取8 例分两组分别作顺铂腹腔内给药与静脉给药的药代动力学研究。测定各组织的铂含量作为顺铂的浓度指标, 铂浓度采用石墨炉原子分光光谱分析法测定。结果:顺铂腹腔给药时, 在腹腔内可维持较长时间的高浓度, 而血浆内的药物浓度与静脉给药时相近; 腹腔给药时AUC 为静脉给药时的近5 倍;顺铂术前给药后, 腹腔给药组腹腔液、胃左静脉的总铂浓度明显高于静脉给药组(P <0. 01), 分别高于静脉给药组的23. 4 倍、2. 53 倍;肿瘤组织内的浓度也比静脉给药组高, 差异有统计学意义(P <0. 05)。结论:顺铂腹腔内给药具有明显的药代动力学优势, 可作为进展期胃癌有效的辅助治疗手段。

关键词: 进展期胃癌, 顺铂, 药代动力学

Abstract: AIM:To compare the characteristics of cisplatin pharmacokinetics: preoperative intraperitoneal administration versus intravenous chemotherapy with cisplatin for advanced gastric carcinoma. METHODS: 50 patients with resectable advanced gastric cancer were randomly divided into 2 groups: 26 cases with preoperative intraperitoneal administration of cisplatin (i. p. group)and 24 cases with preoperative intravenous administration of cisplatin (i. v. group).Each patient was given 60 mg/m2 cisplatin intraperitoneally or intravenously. The peritoneal fluid, blood from gastric sinistral vein and peripheral blood were taken on the 180th minutes after the drug was administrated. Cancer tissues and normal tissues beside the cancer tissue were collected at the 270th minutes during operation. Another 8 cases were used to study the pharmacokinetics of intraperitoneal administration and intravenous chemotherapy with cisplatin. The concentrations of cisplatin in different samples were measured by the flameless type of atomic absorption spectrometry. RESULTS: The high cisplatin concentration in abdominal cavity could maintain for fairly longer time by intraperitoneal administration more than by intravenous administration. And the plasma concentrations of cisplatin in peritoneal cavity were similar by the two injection styles. The AUC with intraperitoneal administration was about five times than that with intravenous administration. The cisplatin concentrations of peritoneal fluid and vena gastrica sinistra blood in the i. p. group were 23. 4 and 2. 53 times higher than those in the i. v. group respectively (P <0. 01).The cisplatin of the cancer tissue in the i. p. group was higher than that in the i. v. group(P <0. 05).CONCLUSION:The intraperitioneal cisplatin chemotherapy has better pharmacokinetics parameters and could be a useful accessory treatment for the advanced gastric carcinoma cancer.

Key words: advanced gastric carcinoma, cisplatin, pharmacokinetics

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