替吉奥胶囊联合伊立替康治疗晚期结直肠癌的临床观察

颜芳, 孟荣荣, 陈琳, 傅强

颜芳, 孟荣荣, 陈琳, 傅强. 替吉奥胶囊联合伊立替康治疗晚期结直肠癌的临床观察[J]. 实用临床医药杂志, 2013, (1): 70-72,75. DOI: 10.7619/jcmp.201301022
引用本文: 颜芳, 孟荣荣, 陈琳, 傅强. 替吉奥胶囊联合伊立替康治疗晚期结直肠癌的临床观察[J]. 实用临床医药杂志, 2013, (1): 70-72,75. DOI: 10.7619/jcmp.201301022
YAN Fang, MENG Rongrong, CHEN Lin, FU Qiang. Clinical observation on gimeracil and oteracil porassium capsules combined with irinotecan for advanced colorectal cancer[J]. Journal of Clinical Medicine in Practice, 2013, (1): 70-72,75. DOI: 10.7619/jcmp.201301022
Citation: YAN Fang, MENG Rongrong, CHEN Lin, FU Qiang. Clinical observation on gimeracil and oteracil porassium capsules combined with irinotecan for advanced colorectal cancer[J]. Journal of Clinical Medicine in Practice, 2013, (1): 70-72,75. DOI: 10.7619/jcmp.201301022

替吉奥胶囊联合伊立替康治疗晚期结直肠癌的临床观察

基金项目: 中国高校医学期刊临床专项资金
详细信息
  • 中图分类号: R735.3

Clinical observation on gimeracil and oteracil porassium capsules combined with irinotecan for advanced colorectal cancer

  • 摘要: 目的 评价替吉奥胶囊联合伊立替康治疗晚期结直肠癌的临床疗效及不良反应.方法 选择晚期结直肠癌一线治疗失败并有可评价病灶的患者54例,予以IRIS方案(伊立替康,替吉奥)化疗.评价客观疗效,并观察不良反应;观察治疗前后患者生存质量、外周血中自然杀伤(NK)细胞及T细胞亚群变化、外周血中血管内皮生长因子(VEGF)水平.结果 全部54例患者均可评价疗效,有效率(RR)20.1%,疾病控制率(DCR)59.3%,疾病进展时间(TTP)为4.8月.不良反应主要是中性粒细胞减少、腹泻及胆碱能综合征,无毒性相关死亡病例.54例患者治疗后生存质量改善率为87.0%;治疗后NK细胞活性提高、CD4+/CD8+提高、血清VEGF水平降低.结论 替吉奥胶囊联合伊立替康治疗晚期结直肠癌疗效较好,不良反应患者可耐受,可进一步研究推广.
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出版历程
  • 发布日期:  2013-05-01

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