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临床试验/NCT04541420
NCT04541420已完成不适用

An Observational, Retrospective Study of Eribulin in Advanced Breast Cancer

Fudan University1 个研究点 分布在 1 个国家目标入组 208 人开始时间: 2019年12月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
208
试验地点
1
主要终点
PFS

研究概览

简要总结

To evaluate the efficacy and safety of Eribulin in patients with advanced breast cancer.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Advanced breast cancer included unresectable locally advanced breast cancer, de novo stage IV breast cancer, and recurrent metastatic breast cancer.
  • Eribulin treatment of advanced breast cancer for at least one cycle, between Dec 2019 and Aug
  • Available medical history.

排除标准

  • Incomplete medical history.

结局指标

主要结局

PFS

时间窗: 6 weeks

Progression free survival

Adverse events

时间窗: 6 weeks

Number of participants with treatment-related adverse events as assessed by Common Terminology Criteria for Adverse Events version 4.0 (CTCAE v4.0)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Biyun Wang, MD

Professor

Fudan University

研究点 (1)

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