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临床试验/NCT02030678
NCT02030678Unknown2 期

To Evaluate the Clinical Effect of Irinotecan Monotherapy in Treatment of Local Recurrence or Metastatic Breast Cancer Patients Who Accepted at Least 2 Kinds of Chemotherapy Regimens Including Antharcycline or Taxanes.

Liaoning Tumor Hospital & Institute1 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2014年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
124
试验地点
1
主要终点
Disease Control Rate

研究概览

简要总结

A phase II study of irinotecan in 3 line or more therapy in local recurrence or metastatic breast cancer. Evaluate the effect and safety of irinotecan in local recurrence or Metastatic breast cancer patients who recieved anthracycline or taxane drugs. The primary endpoint is Disease Control Rate and Progression free survival. The second endpoint is 3 or 4 grade Adverse Events 、overall survival.All the patients will recieve this therapy till disease progress or other occurrence of withdrawal standards.

详细描述

A phase II study of irinotecan in 3 line or more therapy in local recurrence or metastatic breast cancer. Evaluate the effect and safety of irinotecan in local recurrence or Metastatic breast cancer patients who recieved anthracycline or taxane drugs. The primary endpoint is Disease Control Rate and Progression free survival. The second endpoint is 3 or 4 grade Adverse Events 、overall survival. irinotecan 100mg/m2,iv,day1,day8,every 3cycles.If no AE happens, increase irinotecan dose to125mg/m2 at the second cycle.All the patients will recieve this therapy till disease progress or other occurrence of withdrawal standards.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Mestatic breast cancer patients whose disease recurrent after using anthracycline or taxane drugs

排除标准

  • Heart Disease.etc

研究组 & 干预措施

irinotecan Hydrochloride

Experimental

Irinotecan monotherapy (trade name: Aili; batches 180103AG [40 mg] and 171231AG [100 mg]) will be administered intravenously at a dose of 100 mg/m2 on days 1 and 8 of each 3-week cycle.

干预措施: irinotecan (Drug)

结局指标

主要结局

Disease Control Rate

时间窗: 3cycles (21days/cycle)

Disease Control Rate:Completely Response+Partial Response+Stable Disease

次要结局

未报告次要终点

研究者

发起方
Liaoning Tumor Hospital & Institute
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sun Tao

Director of Oncology

Liaoning Tumor Hospital & Institute

研究点 (1)

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