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临床试验/NCT01777945
NCT01777945已完成不适用

Program for Assessment of Capecitabine (Xeloda) Plus Docetaxel First-line Therapies in HER2-negative Metastatic Breast Cancer (XEBRA Study)

Hoffmann-La Roche0 个研究点目标入组 46 人开始时间: 2012年12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
状态
已完成
入组人数
46
主要终点
Progression-free Survival (PFS)

研究概览

简要总结

This multicenter observational study will evaluate the efficacy and safety of Xeloda (capecitabine) in combination with docetaxel in first-line therapy in participants with HER2-negative metastatic breast cancer. Participants will be followed for approximately 6 months of treatment.

研究设计

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

入排标准

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

入选标准

  • Adult participants, >/= 18 years of age
  • HER2-negative metastatic breast cancer
  • Participants initiated on first-line therapy with Xeloda and docetaxel in accordance with the Summary of Product Characteristics; participants who started treatment with Xeloda and docetaxel no more than 3 months before enrollment in this study are also eligible

排除标准

  • Contraindications to Xeloda treatment according to the Summary of Product Characteristics

研究组 & 干预措施

Participants Receiving Capecitabine/Docetaxel

Participants received capecitabine and docetaxel according to individualized physician-prescribed regimens.

干预措施: capecitabine (Drug)

Participants Receiving Capecitabine/Docetaxel

Participants received capecitabine and docetaxel according to individualized physician-prescribed regimens.

干预措施: docetaxel (Drug)

结局指标

主要结局

Progression-free Survival (PFS)

时间窗: approximately 2 years

The time from enrollment until disease progression, assessed as the time to tumor progression, as evaluated by regular examinations per routine clinical practice, or death from any cause.

次要结局

  • Time to Treatment Failure(approximately 2 years)
  • Overall Response Rate(approximately 2 years)
  • Clinical Benefit Rate(approximately 2 years)
  • Duration of Treatment With Xeloda(approximately 2 years)
  • Number of Participants With Adverse Events(approximately 2 years)
  • Percentage of Capecitabine Dose Modifications(approximately 2 years)

研究者

申办方类型
Industry
责任方
Sponsor

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