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培他滨在中晚期肝癌中的临床应用 被引量:1

Study on Capecitabine Combined For Advanced Liver Cancer
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摘要 目的探讨卡培他滨联合肝动脉插管化疗栓塞(TACE)在中晚期肝癌患者中的临床应用。方法中晚期肝癌患者随机分为两组,治疗组20例,对照组40例。治疗组采用TACE一周后,服用卡培他滨每日2.0 g/m2,分2次口服,服用2周,停用2周为1个疗程。对照组采用单纯TACE治疗,两组中TACE治疗每月1次。结果治疗组20例患者中完全缓解(CR)0例,部分缓解(PR)13例,无变化(SD)6例,恶化(PD)1例,总有效率为65.0%,甲胎蛋白(AFP)下降率为60.0%,肿瘤缩小率为70.0%,中位生存期为11.5个月。对照组40例患者中,CR0例,PR12例,SD16例,PD12例,总有效率为30.0%,AFP下降率为32.4%,肿瘤缩小率为32.4%,中位生存期为7.6个月。治疗组和对照组手足综合征发生率55.0%和10.0%,骨髓抑制25.0%和22.5%,腹泻15.0%和12.5%,肝脏毒性90.0%和82.5%,以上并发症多为Ⅰ~Ⅱ级,均可耐受,除手足综合征外,其他并发症经过治疗后均恢复正常。结论希罗达联合TACE治疗中晚期肝癌的安全性、疗效,均优于单纯TACE。 Objective To evaluate the clinical efficacy of capecitabine combined with chemoembolization (TACE) for advanced liver cancer. Methods Forty patients with liver cancer were retrospectively divided into two groups : Treatment group, on the basis of TACE, 20 patients received oral capeeitabine at 2000 mg/m2 , twice - daily for 14 days followed by 7 - day rest period and repeated in every three week intervals for more than two cycles. Control group, 20 patients received TACE only at 1 - month intervals for at least two cycles. Results In capecitabine and TACE group: there were 0 CR, 13 PR, 6 SD and 1 PD; the overall response rate was 65.0% ; the AFP and tumor reduction rates were 60. 0% and 70. 0% ; the median survival time was 11.5 months. In the TACE only group: there were 0 CR, 12 PR, 16 SD and 12 PD; the overall response rate was 30. 0 % ; the AFP and tumor reduction rates were 32. 4% and 32.4 % ; the median survival time was 7.6months. Comparison of complications: the incidence of hand- foot syndrome of the treatment group and the control group was 55.0% and 10. 0% respectively, the incidence of bone barrow suppression of the treatment group and the control group was 25.0% and 22. 5% respectively, the incidence of diarrhea of the treatment group and the control group was 15.0% and 12. 5% respectively, the incidence of liver toxicity of the treatment group and the control group was 90. 0% and 82. 5% respectively, Most of these toxicities were tolerable at grade 1 -2. Conclusion Capecitabine combined with TACE may be safe and effective for advanced liver cancer and superior to single TACE.
出处 《实用心脑肺血管病杂志》 2009年第10期855-857,共3页 Practical Journal of Cardiac Cerebral Pneumal and Vascular Disease
关键词 肝肿瘤 卡培他滨 肝动脉插管化疗栓塞 Liver neoplasms Capecitabine Chemoembolization
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参考文献12

  • 1管忠震,刘冬耕,郁宝铭,吴唯勤,时德,赵瑜,魏于全,邹立群,伍晓汀,庄文,冯奉仪,张频,于世英,熊慧华,付强,郑树,黄建瑾,伍钢,杨传永,孙圣荣,阮庆兰.希罗达一线治疗晚期或复发性结直肠癌[J].中华肿瘤杂志,2004,26(2):119-121. 被引量:72
  • 2Walko CM, Lindley C. Capecitabine: a review [ J]. Clin Ther, 2005, 27 : 23 - 44. 被引量:1
  • 3Tebbutt N. REAL - 2: p romising results for Xeloda vs 5 - FU at planned interim analysis [ J ]. Proc Am Soc Clin Oncol, 2002, 21: 131. 被引量:1
  • 4周俭,汤钊猷,樊嘉,吴志全,纪元,鲍卫华,王鲁,叶胜龙.血小板衍化内皮细胞生长因子在肝癌中的表达及干预治疗[J].中华医学杂志,2000,80(11):831-834. 被引量:8
  • 5原发性肝癌的临床诊断与分期标准[J].现代实用医学,2002,14(4):213-213. 被引量:73
  • 6潘宏铭,徐农,耿宝琴..肿瘤内科诊治策略[M],2002.
  • 7McKendrick J, Coutsouvelis J. Capecitabine: effective oral fluoropyrimidine chemotherapy [ J ]. ExpertOp in Pharmacother, 2005, 6: 1231 - 1239. 被引量:1
  • 8Miwa M, Ura M, Nishida M, et al. Design of a novel oral fluoropyrimidine carbamate, capecitabine, which generates 5 - fluorouracil selectively in tumours by enzymes concentrated in human liver and cancer tissue. Eur J Cancer, 1998, 34: 1274-1281. 被引量:1
  • 9Pickard M, Dive C, Kinsella AR. Differences in resistance to 5 - fluorouracil as a function of cell cycle delay and not apoptosis [ J ]. Br J Cancer, 1995, 72: 1389. 被引量:1
  • 10Olivier M, Eric S, Arlette H, et al. Sensitization of cancer cells treated with cytotoxic drugs to Fasmediated cytotoxicity [ J]. Journal of the National Cancer Institute, 1997, 89 : 784. 被引量:1

二级参考文献10

  • 1Sun F X,Int J Cancer,1996年,66卷,239页 被引量:1
  • 2Johannes Schüller,Jim Cassidy,Etienne Dumont,Brigitte Roos,Sarah Durston,Ludger Banken,Masahiro Utoh,Kazushige Mori,Erhard Weidekamm,Bruno Reigner. Preferential activation of capecitabine in tumor following oral administration to colorectal cancer patients[J] 2000,Cancer Chemotherapy and Pharmacology(4):291~297 被引量:1
  • 3Moiler P,Koretz,Leithauser F,et al.Expression of APO-1( CD95 ), a member of the NGF TNF receptor superfamily, in normal and neoplastic colon epithelium[].International Journal of Cancer.1994 被引量:1
  • 4Huang D C,Cory S,Strasser A.bcl -2, bcl -XL and adenovirus protein EIB 19KD are functionally equivalent in their ability to inhibit cell death[].Oncegene.1997 被引量:1
  • 5Marian B,Partik G,Hochegger K,et al.Inhibition of epidermal growth-factor-receptor-dependent signalling by tyrphostins A25 and AG1478 blocks growth and induces apoptosis in colorectal tumor cells in vitro[].Journal of Cancer Research and Clinical Oncology.1999 被引量:1
  • 6Sharma A,Adam E,Schumacher U.The action of 5-fluorouracil on human HT29 colon cancer cells grown in SCID mice: mitosis, apoptosis and cell differentiation[].British Journal of Cancer.1997 被引量:1
  • 7Raff M C.Social controls on cell survival and cell death[].Nature.1992 被引量:1
  • 8Olivier M,Eric S,Arlette H,et al.Sensitization of cancer cells treated with cytotoxic drugs to Fas-mediated cytotoxicity[].Journal of the National Cancer Institute.1997 被引量:1
  • 9Itoh N,Tsujimoto Y,Nagata S.Effect of bcl -2 on Fas antigenmediated cell death[].J Immunol.1993 被引量:1
  • 10Kishiji M,Adachi Y,Sogo S,et al.Apoptosis of colorectal adenocarcinoma ( COLO201 ) by tumor necrosis factor-alpha( TNF- ) and or interferon-gamma ( IFN- ), resulting from down-modulation of bcl -2 expression[].Clinical and Experimental Immunology.1998 被引量:1

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