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临床试验/NCT03629717
NCT03629717已完成早期 1 期

RANKL Inhibition and Breast Tissue Biomarkers in Premenopausal Women With Dense Breasts

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2018年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
10
试验地点
1
主要终点
Effect of denosumab on breast tissue gene pathway gene expression

研究概览

简要总结

A robust knowledge of how to reduce breast density could play a key role in breast cancer prevention in premenopausal women, but viable preventative targets to reduce breast density-associated breast cancer risk are yet to be developed. The investigators propose to investigate the effect of RANKL inhibition with denosumab on breast tissue markers in high-risk premenopausal women with dense breasts. Study findings could provide robust evidence to move forward with a clinical trial targeting RANKL inhibition in premenopausal breast cancer prevention.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Premenopausal.
  • At least 35 years of age.
  • Dense breasts on routine mammogram.
  • Willing to take calcium (1,200mg) and vitamin D (800 IU) daily.
  • At increased risk for breast cancer using any of the following:
  • Positive family history of breast cancer
  • Breast cancer risk prediction models
  • Able and willing to return for repeat biopsy.
  • Able to understand and willing to sign an IRB-approved written informed consent document.

排除标准

  • Current use of tamoxifen, aromatase inhibitors, or bisphosphonates.
  • Concurrently participating in another cancer chemoprevention trial (unless no longer receiving the intervention).
  • Pregnant or lactating.
  • Recent tooth extraction or dental procedure.
  • Unhealed and/or planned dental/oral surgery.
  • History of osteonecrosis/osteomyelitis of the jaw.
  • History of osteoporosis or severe osteopenia.
  • Unable/unwilling to return for repeat biopsy.

研究组 & 干预措施

Denosumab

Experimental

An ultrasound-guided core needle breast biopsy will be performed on day 1 prior to the intervention. A single dose of subcutaneous denosumab 60mg will be administered immediately after the core biopsy on day 1. This will take place on an outpatient basis. Repeat core-needle biopsy will take place on Day 60 (+/-10 days). Blood samples will also be collected at the time of core-needle biopsy to allow for biomarker assay. Gene expression analyses will be done using NanoString nCounter gene expression system.

干预措施: Ultrasound-guided core needle biopsy (Procedure)

Denosumab

Experimental

An ultrasound-guided core needle breast biopsy will be performed on day 1 prior to the intervention. A single dose of subcutaneous denosumab 60mg will be administered immediately after the core biopsy on day 1. This will take place on an outpatient basis. Repeat core-needle biopsy will take place on Day 60 (+/-10 days). Blood samples will also be collected at the time of core-needle biopsy to allow for biomarker assay. Gene expression analyses will be done using NanoString nCounter gene expression system.

干预措施: Denosumab (Drug)

Denosumab

Experimental

An ultrasound-guided core needle breast biopsy will be performed on day 1 prior to the intervention. A single dose of subcutaneous denosumab 60mg will be administered immediately after the core biopsy on day 1. This will take place on an outpatient basis. Repeat core-needle biopsy will take place on Day 60 (+/-10 days). Blood samples will also be collected at the time of core-needle biopsy to allow for biomarker assay. Gene expression analyses will be done using NanoString nCounter gene expression system.

干预措施: Blood draw (Procedure)

Denosumab

Experimental

An ultrasound-guided core needle breast biopsy will be performed on day 1 prior to the intervention. A single dose of subcutaneous denosumab 60mg will be administered immediately after the core biopsy on day 1. This will take place on an outpatient basis. Repeat core-needle biopsy will take place on Day 60 (+/-10 days). Blood samples will also be collected at the time of core-needle biopsy to allow for biomarker assay. Gene expression analyses will be done using NanoString nCounter gene expression system.

干预措施: Calcium (Drug)

Denosumab

Experimental

An ultrasound-guided core needle breast biopsy will be performed on day 1 prior to the intervention. A single dose of subcutaneous denosumab 60mg will be administered immediately after the core biopsy on day 1. This will take place on an outpatient basis. Repeat core-needle biopsy will take place on Day 60 (+/-10 days). Blood samples will also be collected at the time of core-needle biopsy to allow for biomarker assay. Gene expression analyses will be done using NanoString nCounter gene expression system.

干预措施: Vitamin D (Drug)

结局指标

主要结局

Effect of denosumab on breast tissue gene pathway gene expression

时间窗: Between baseline and day 60

The investigators will evaluate changes in pathway gene expression between baseline and day 60 using NanoString NCounter platform

Effect of denosumab on pathways that may influence breast cancer development as measured by spatial transcriptomic analysis

时间窗: Between baseline and day 60

The investigators will evaluate changes in breast tissue spatial transcriptomics.

Effect of denosumab on pathways that may influence breast cancer development as measured by metabolomic analysis

时间窗: Between baseline and day 60

The investigators will evaluate changes in metabolomics.

次要结局

  • Correlation of breast tissue gene expression with circulating biomarker levels(60 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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