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临床试验/NCT01439490
NCT01439490已完成2 期

Feasibility Study: FES-PET to Determine ER-expression in Epithelial Ovarian Cancer

University Medical Center Groningen1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2011年8月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
15
试验地点
1
主要终点
The feasibility of FES-PET to visualize and quantify ER-positive lesions in epithelial ovarian cancer.

研究概览

简要总结

Estrogens are implicated in the development of ovarian cancer and estrogen receptors (ER) alpha and beta are present in 20-100% of ovarian cancer patients. For this reason, antihormonal therapy with anti-estrogens or ER-antagonists is potentially an attractive treatment option. However, only a small proportion of patients (5-19%) will respond to antihormonal therapy. ER-expression in ER-positive breast cancer can be assessed by positron emission tomography (PET) with [18F]fluoroestradiol (FES). In this study the investigators will evaluate whether FES-PET can be used to visualize and quantify ER-expression in ovarian cancer. If these results are positive, this would warrant further exploration of FES-PET imaging in ovarian cancer.

详细描述

Investigators will evaluate whether FES-PET can be used to visualize and quantify ER-expression in ovarian cancer. If these results are positive, this would warrant further exploration of FES-PET imaging in ovarian cancer.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
Single (Investigator)

入排标准

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

入选标准

  • •Histological evidence or high clinical suspicion of epithelial ovarian cancer
  • •The presence of at least one measurable lesion (RECIST version 1.1).
  • •Histology or cytology can be obtained (may be ascites)
  • •Eastern Cooperative Oncology Group performance status 0-
  • •Postmenopausal status (defined as either >45 years with amenorrhea >12 months, or prior bilateral ovariectomy)
  • •No history of other ER-positive malignancies
  • •Signed written informed consent
  • •Able to comply with the protocol

排除标准

  • •Use of estrogen receptor ligands, including tamoxifen, fulvestrant or estrogens, during the 5 weeks before entry into the study
  • •Life-expectancy ≤ 3 months

研究组 & 干预措施

FES-PET

Experimental

Patients undergo FES-PET prior to obtaining histology

干预措施: FES-PET (Other)

结局指标

主要结局

The feasibility of FES-PET to visualize and quantify ER-positive lesions in epithelial ovarian cancer.

时间窗: approximately 1 month

Ovarian cancer patients planned for surgery or in which histology/cytology will be obtained, will undergo FES-PET/CT. FES-PET/CT will be qualitatively analyzed to determine whether ovarian cancer lesions can be visualized. FES-uptake will be quantified for all known lesions. Patient material will be stained for ER-expression to determine whether ER-positive metastases show FES-uptake.

次要结局

  • Correlation between FES-PET and immunohistochemistry (IHC)(approximately 1 month)
  • Concordance between CT-scan and FES-PET(approximately 1 month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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