ACTRN12617001109392已完成未知
An observational study to assess the ability of the thymine loading test to prospectively categorise patients with gastrointestinal or breast cancer who cannot tolerate fluoropyrimidine treatment.
niversity of Auckland0 个研究点目标入组 166 人开始时间: 2017年7月28日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 166
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Age >18 years.
- •- To receive 5-FU or capecitabine (GI) or capecitabine (mBC) as part of standard care for histologically or cytologically confirmed gastrointestinal (GI) cancer or metastatic breast cancer (mBC); OR
- •- To receive capecitabine as part of standard care for residual disease present at surgery following neoadjuvant chemotherapy for breast cancer
- •- Able to provide written informed consent
排除标准
- •- Pregnant or breast feeding
- •- Concurrent abdomino-pelvic radiation therapy
- •- Irinotecan containing schedules
- •- Prior history of infusional 5-FU or capecitabine
研究者
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