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临床试验/NCT01652560
NCT01652560Unknown不适用

Observational Studies of the Application of Bevacizumab in HER2-negative Breast Cancer Neoadjuvant Chemotherapy

LiNanlin,Ph.D, Chief Physician,Clinical Professor1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2012年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
50
试验地点
1
主要终点
Objective Response Rate

研究概览

简要总结

  • The purpose of this study is to evaluate the efficacy and safety of the application of bevacizumab combined neoadjuvant chemotherapy in HER2-negative breast cancer.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • HER2-negative breast cancer patients
  • Without surgery
  • Plans to neoadjuvant chemotherapy

排除标准

  • HER2-positive breast cancer patients
  • Post-operative patients

研究组 & 干预措施

bevacizumab combined neoadjuvant chemotherapy

干预措施: bevacizumab (Drug)

结局指标

主要结局

Objective Response Rate

时间窗: From enrollment to disease progression

From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 5 years.

次要结局

  • overall response(From enrollment to disease progression)

研究者

发起方
LiNanlin,Ph.D, Chief Physician,Clinical Professor
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

LiNanlin,Ph.D, Chief Physician,Clinical Professor

The department of Vascular endocrine surgery

Xijing Hospital

研究点 (1)

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