调肝理脾方联合替吉奥胶囊治疗晚期原发性肝癌患者的临床观察

杜卫星, 叶青, 李金科, 等. 调肝理脾方联合替吉奥胶囊治疗晚期原发性肝癌患者的临床观察[J]. 中国中西医结合消化杂志, 2017, 25(5): 340-343. doi: 10.3969/j.issn.1671-038X.2017.05.05
引用本文: 杜卫星, 叶青, 李金科, 等. 调肝理脾方联合替吉奥胶囊治疗晚期原发性肝癌患者的临床观察[J]. 中国中西医结合消化杂志, 2017, 25(5): 340-343. doi: 10.3969/j.issn.1671-038X.2017.05.05
DU Wei-xing, YE Qing, LI Jin-ke, et al. Clinical observation of Tiaoganlipi decoction combined with S-1 capsule in the treatment of advanced primary liver cancer patients[J]. Chin J Integr Tradit West Med Dig, 2017, 25(5): 340-343. doi: 10.3969/j.issn.1671-038X.2017.05.05
Citation: DU Wei-xing, YE Qing, LI Jin-ke, et al. Clinical observation of Tiaoganlipi decoction combined with S-1 capsule in the treatment of advanced primary liver cancer patients[J]. Chin J Integr Tradit West Med Dig, 2017, 25(5): 340-343. doi: 10.3969/j.issn.1671-038X.2017.05.05

调肝理脾方联合替吉奥胶囊治疗晚期原发性肝癌患者的临床观察

  • 基金项目:

    湖北省重大科学技术成果(No:十科鉴字[2013]第65号)

详细信息
    作者简介:

    杜卫星,男,硕士,副主任医师,从事中医临床基础方面工作

    通讯作者: 叶青,E-mail:yeqing064@163.com
  • 中图分类号: R735.7

Clinical observation of Tiaoganlipi decoction combined with S-1 capsule in the treatment of advanced primary liver cancer patients

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  • [目的]探讨调肝理脾方联合替吉奥胶囊治疗晚期原发性肝癌患者的临床效果。[方法]采用回顾性研究方法,2011年2月~2014年8月选择在我院诊治的晚期原发性肝癌患者98例作为研究对象,根据治疗方法的不同分为中药组60例与常规组38例,常规组给予基于替吉奥胶囊的化疗方案治疗,中药组在常规组治疗的基础上给予调肝理脾方治疗,记录与随访2组近远期预后情况。[结果]中药组与常规组的治疗总有效率分别为66.7%和42.1%,中药组的治疗总有效率明显高于常规组(P<0.05)。2组毒副反应主要为血液毒性反应、肝肾功能异常、消化道反应、神经系统反应等,2组毒副反应情况比较差异无统计学意义(P>0.05)。治疗后中药组与常规组的KPS评分分别为(78.13±4.24)分和(69.14±5.10)分,都明显高于治疗前的(57.24±6.19)分和(58.14±7.30)分(P<0.05),且治疗后中药组的KPS评分明显高于常规组(P<0.05)。中药组的6个月与1年生存率分别为91.7%和66.7%,都明显高于常规组的71.1%和50.0%(P<0.05)。[结论]调肝理脾方联合替吉奥胶囊治疗晚期原发性肝癌患者能提高治疗疗效,不增加毒副反应的发生,改善临床功能症状,延长远期生存时间,有很好的应用价值。
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出版历程
收稿日期:  2016-12-09

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