期刊文献+

IF方案治疗晚期胃癌的临床观察

Clinical observation of IF regimen in advanced gastric cancer
下载PDF
导出
摘要 目的:评价IF方案在晚期胃癌治疗中的有效性及安全性。方法:21例晚期胃癌患者,以伊立替康80mg/m2静脉滴注半小时,随后亚叶酸500mg/m2静脉滴注2小时,接着开始持续静脉滴注氟脲嘧啶2000mg/m222个小时,每周1次,连用6周,休息1周后重复。结果:19例可评价患者中,没有CR病例,PR7例(36.8%),PR+SD78.9%。中位生存期10月。不良反应以血液学不良为主,多为I-Ⅱ度(87.0%)。结论:IF方案对晚期胃癌有一定疗效,不良反应可以耐受。 Objective: To evaluate the efficacy and toxicity of IF regimen (irinotecan combined with 5 - fluoroureil) in the treatmeant of advanced gastric cancer. Methods:Twenty -one patients with advanced gastric cancer, were treated with IF regimen ( CPT - 11 80 mg/m2 iv as 30 - min infusion, followed by CF 500 mg/m2 iv over 2h, followed by 5 -FU 2000 mg/m2 iv over 22h, weekly for 6 weeks). Results:Twenty -one patients were treated with IF regimen,nineteen of them was evaluated. The overall response rate was 78.9% ,no complete response was observed, and seven cases partieal response(63.8% ). Median survival was 10 months. Most of toxicities was grade Ⅰ-Ⅱ (87.0%). Conclusion:IF regimen is effective and well tolerable chemotherapy for advanced gastric cancer.
出处 《现代肿瘤医学》 CAS 2009年第6期1136-1137,共2页 Journal of Modern Oncology
关键词 胃癌 伊立替康 氟尿嘧啶 化学疗法 gastric cancer irinoteean 5 - fluorourcil chemotherapy
  • 相关文献

参考文献8

  • 1李连弟,饶克勤,张思维,鲁凤珠,邹小农.中国12市县1993年~1997年肿瘤发病和死亡登记资料统计分析[J].中国肿瘤,2002,11(9):497-507. 被引量:193
  • 2Pyrhonen S,Kuitunen T,Nyandoto P,et al.Randomised comparison of fluorouracil,epidoxorubicin and methotrexate(FEMTX) plus supportive care with supportive care alone in patients with non-resectable gastric cancer[J].Br J Cancer,1995,71:587-591. 被引量:1
  • 3Murad AM,Santiago FF,Petroianu A,et al.Modified therapy with 5-fluorouracil,doxorubicin,and methotrexate in advanced gastric cancer[J].Cancer,1993,72:37-41. 被引量:1
  • 4Schipper DL,Wagener DJ.Chemotherapy of gastric cancer[J].Anticancer Drugs,1996,7:137-149. 被引量:1
  • 5Glimelius B,Ekstrom K,Hoffman K,et al.Randomized comparison between chemotherapy plus best supportive care with best supportive care in advanced gastric cancer[J].Ann Oncol,1997,8:163-168. 被引量:1
  • 6Cutsem EV,Moiseyenko VM,Tjulandin S,et al.Phase Ⅲ study of docetaxel and cisplatin plus fluorouracil compared with cisplatin and fluorouracil as first-line therapy for advanced gastric cancer:A report of the V325 Study Group[J].J Clin Oncol,2006,24:4991-4997. 被引量:1
  • 7Dank M,Zaluski J,Barone C,et al.Randomized phase 3 trial of irinotecan(CPT-11) + 5FU/folinic acid(FA) vs CDDP + 5FU in 1st-line advanced gastric cancer patients[J].J Clin Oncol,2005,23:308s. 被引量:1
  • 8王丽焱,汤致强.抗肿瘤药伊立替康的研究进展[J].国外医学(药学分册),2004,31(1):7-11. 被引量:45

二级参考文献20

  • 1Cersosmio RJ. Irinotecan: a new antineoplastic agent for the management of colorectal cancer[J].Ann Pharmacother,1998, 32(12) :1324 - 1333. 被引量:1
  • 2Rivory LP, Chatelut E; Canal P ,et al. Kinetics of the in vivo inter-conversion of the carboxylatee and lactone forms of irinoteacan (CPT-11) and of its metabohte SN-38 in patients[J]. Cancer Res,1994, 54(24):6330-6333. 被引量:1
  • 3Ratain MJ. Insights into the phamacokinetics and pharmacodynamics of irinotecan[J]. Clin Cancer Res. 2000, 6(9) : 3393 - 3394. 被引量:1
  • 4De Bruijn P, Verweij J,Loos WJ,et al.Determination of irinotecan(CPT-11 )and its active metabolite SN-38 in human plasma by reversed-phase high-performance liquid chromatography with fluorescence detection[J]. Chromatogr B Biomed Sci Appl, 1997, 698 ( 1/2 ) : 277-228. 被引量:1
  • 5Escoriaza J, Aldaz A, Castellanos C,et al. Simple and rapid determination of irinotecan and its metabolite SN-38 in plasma by high-performance liquid Chromatography: application to clinical pharmacokinetic studies[J]. J Chromatogr B Biomed Sci Appl . 2000. 740(2) :159-168. 被引量:1
  • 6Ragot S, Marquet P, Lachatre F,et al.Sensitive determination of irinotecan (CVF-11) and its active metabolite SN-38 in human serum using liquid chromatography-electrospray mass spectrometry [ J]. J Chromatogr B Biomed Sci Appl,1999, 7.36(1/2) : 175 - 184. 被引量:1
  • 7Saita T, Fujito H, Mori M. Development of ELISAs for irinotecan and its active metabolite SN-38[J].Biol Pharm Bull, 2000, 23(8):911-916. 被引量:1
  • 8Chabot GG, Abrigerges D, Catimel G et al. Population pharmacokinetics and pharmacodynamics of irinotecan(CPT-11) and active metabolite SN-38 during phase Ⅰ trials[J]. Arm Oncol, 1995, 6(2) : 141 - 151. 被引量:1
  • 9Ma MK, McLeod HL.Lessons learned from the metabolic pathway[J]. Curr Med Chem, 2003, 10(1):41 - 49. 被引量:1
  • 10Ando Y, Saka H, Ando M, et al. Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis[J]. Cancer Res, 2000, 60(24):6921 -6926. 被引量:1

共引文献235

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部