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临床试验/EUCTR2012-003981-42-NL
EUCTR2012-003981-42-NL进行中(未招募)1 期

Estrogen receptor and androgen receptor imaging in metastatic breast cancer patients

niversity Medical Center Groningen0 个研究点开始时间: 2013年11月22日最近更新:

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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