奥曲肽联合经动脉插管化疗栓塞治疗伴肝硬化肝细胞癌_临床医学论文.docVIP

奥曲肽联合经动脉插管化疗栓塞治疗伴肝硬化肝细胞癌_临床医学论文.doc

  1. 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
  2. 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  3. 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  4. 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  5. 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  6. 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  7. 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
奥曲肽联合经动脉插管化疗栓塞治疗伴肝硬化肝细胞癌_临床医学论文.doc

奥曲肽联合经动脉插管化疗栓塞治疗伴肝硬化肝细胞癌_临床医学论文 奥曲肽联合经动脉插管化疗栓塞治疗伴肝硬化肝细胞癌_临床医学论文 【摘要】   目的 评价奥曲肽联合经动脉插管化疗栓塞(TACE)治疗伴肝硬化肝细胞癌的临床效果。方法 选择Child-Pugh评分A或B级伴肝硬化肝细胞癌患者共55例。实验组24例,行TACE术后第1天开始使用奥曲肽0.2mg皮下注射,每天2次。对照组31例,接受TACE治疗。每3个月进行1次评价。对两组6个月及1、2、3年的生存率进行比较。结果 两组均无CR,实验组中16例PR,有效率为66.67%。对照组中11例PR,有效率为35.48%。两组有效率差异有显著性(0.05)。实验组3年生存率为45.83%,而对照组3年生存率为19.35%。两组3年生存率差异有显著性(0.05)。实验组中位生存期为31个月,对照组中位生存期为20个月。实验组中位TTP为9个月,对照组为6个月。奥曲肽副作用主要为轻度腹泻。结论 奥曲肽联合TACE治疗伴肝硬化肝细胞癌有明确的效果。 【关键词】 奥曲肽;肝硬化;肝细胞癌;化学栓塞,治疗性 Abstract: Objective This article is to evaluate the effects of octreotide in combination with transcatheter arterial chemoembolization (TACE) for hepatocellular carcinoma complicated with liver cirrhosis. Methods Fifty-five consecutive patients in Child-Pugh classification A and B were admitted into the 3-year trial. Twenty-four patients in the octreotide group received octreotide 0.2mg IH twice a day following the treatment of TACE on day 1. Thirty-one patients received TACE alone were enrolled into the control group. The efficacy were assessed once every 3 months. A comparison of the 6-month、1-year、2-year and 3-year survival rate between the two groups were performed. Results No complete response was got in both groups. In the octreotide group, partial response (PR) was got in 16 (66.67%) of the 24 patients, whereas in the control group, PR was achieved in 11 (35.48%) of the 31 patients. There was statistical significant difference in response rate between the two groups (0.05). The 3-year overall survival rate of the octreotide group and the control group were 45.83% and 19.35%, respectively. There was statistical significant difference in 3-year overall survival rate between the two groups (0.05). The overall survival rate of the octreotide group was significantly higher than that of the control group (p lt; 0.05). The median survival of the octreotide group and the control group were 31 months and 20 months, respectively. The aliment development in the octreotide group was 9 months vs 6 m

文档评论(0)

619731806 + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档