EUCTR2012-003981-42-NL进行中(未招募)1 期
Estrogen receptor and androgen receptor imaging in metastatic breast cancer patients
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Metastatic breast cancer, with at least one known metastasis outside of the liver
- •2. Presence of a lesion that is safely accessible for tumor biopsy (may be liver lesion)
- •3. Postmenopausal status defined as one of the following:
- •a. age =60 years
- •b. previous bilateral oophorectomy
- •c. age <60 years and amenorrhea for >12 months in the absence of interfering hormonal therapies (such as LH-RH agonists and ER-antagonists)
- •d. patients age <60 years using an ER-antagonist should have amenorrhea for > 12 months and FSH >24 U/L and LH >14 U/L
- •e. patient age <60 years using LH-RH agonists should continue LH-RH-agonists until after the PET procedures
- •4. Initially ER-positive tumor histology.
- •5. ECOG performance status 0-2.
- •6. Signed written informed consent
- •7. Able to comply with the protocol
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 10
排除标准
- •1. Use of estrogen receptor ligands, including tamoxifen, fulvestrant or estrogens, or androgen receptor ligands, during the 6 weeks before entry into the study
- •2. Life-expectancy = 3 months
研究者
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