位置:成果数据库 > 期刊 > 期刊详情页
伊立替康联合雷替曲塞治疗晚期结直肠癌的临床观察
  • ISSN号:2095-0616
  • 期刊名称:《中国医药科学》
  • 时间:0
  • 分类:R735.3[医药卫生—肿瘤;医药卫生—临床医学]
  • 作者机构:[1]南京医科大学附属江苏省肿瘤医院肿瘤内科,江苏南京210009
  • 相关基金:吴阶平基金(320.6750.13115); 江苏省“六大人才高峰”高层次人才培养计划(2013-WSW-035)
中文摘要:

目的观察伊立替康联合雷替曲塞方案治疗晚期结直肠癌的有效性和安全性。方法收集28例一线化疗方案治疗失败或缓解后再进展的晚期结直肠腺癌患者,行伊立替康联合雷替曲塞化疗,方案:伊立替康150~180mg/m2,静脉滴注,第一天;雷替曲塞3mg/m2静脉滴注,第一天;21d为1个周期,21d后再重复给药,每2~3个周期后评价疗效,治疗期间评估不良反应。结果所有患者均可评价疗效,其中PR 2例,SD19例,PD 7例,无CR者,ORR为7.14%,DCR为75%。中位PFS 6个月,中位OS不小于11.5个月。最常见的毒副反应是中性粒细胞减少和腹泻。结论雷替曲塞联合伊立替康方案有效率高,毒副反应小,可以作为晚期结直肠癌的二线治疗方案。

英文摘要:

Objective To observe the efficacy and toxicity of irinotecan plus raltitrexed as second-line chemotherapy for advanced colorectal cancer. Methods Twenty-eight patients with advanced colorectal cancer who failed to first-line chemotherapy.The doses of drugs were as follows,CPT-11 150-180mg/m2 ivgtt on day 1 and raltitrexed 3mg/m2 on day 1.One cycle lasted 21 days.After every two or three cycles,therapeutic efficacy was evaluated.The efficacy,side effects,and safety of the treatment were observed. Results All patients successfully completed the the treatment plan. There was 0 case of complete recovery, 2 partial recovery, 19 stable disease,and 7 progressive disease.The overall response rate was 7.14%,the disease control rate was 75%.The mean progression free survival was 6 months,and the mean overall survival was no less than 11.5 months.The most common side effects were neutropenia and diarrhea. Conclusion Irinotecan plus raltitrexed as second-line chemotherapy for advanced colorectal cancer has a high efficacy with acceptable tolerability,and is a therapy worth considering for advanced colorectal cancer.

同期刊论文项目
同项目期刊论文
期刊信息
  • 《中国医药科学》
  • 主管单位:国家卫生和计划生育委员会
  • 主办单位:海峡两岸医药卫生交流协会
  • 主编:
  • 地址:北京市朝阳区东四环中路78号楼(大成国际中心B座)708-2室
  • 邮编:100124
  • 邮箱:zgyykx@vip.163.com
  • 电话:010-59625651
  • 国际标准刊号:ISSN:2095-0616
  • 国内统一刊号:ISSN:11-6006/R
  • 邮发代号:82-519
  • 获奖情况:
  • 国内外数据库收录:
  • 被引量:30571