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临床试验/NCT03220893
NCT03220893已完成不适用

Density MATTERS [Molecular Breast Imaging (MBI) And Tomosynthesis To Eliminate the ReServoir]

Mayo Clinic5 个研究点 分布在 1 个国家目标入组 3,023 人开始时间: 2017年6月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
3,023
试验地点
5
主要终点
Rate of Detection of Invasive Cancers

研究概览

简要总结

This study compares molecular breast imaging (MBI) and digital breast tomosynthesis (DBT) in screening patients with dense breast tissue. Breast imaging may help doctors find breast cancer sooner, when it may be easier to treat. Molecular breast imaging (MBI) uses an injection of a small amount of radioactive material that is taken up in tissues of the body that are actively changing, such as breast cancer. A specialized camera, called a gamma camera, takes pictures of the gamma rays emitted by this material. MBI may detect cancers that are not visible on mammograms. This study may help researchers determine how MBI testing compares to DBT screening.

详细描述

This study includes women age 40-75 who are presenting for breast cancer screening and had mammographically dense breasts on their last mammogram. Participants undergo annual DBT and MBI screening for two years. The primary aim for this study is to compare the rate of detection of invasive cancers between DBT alone vs. the combination of DBT with supplemental MBI at the first year of screening.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
40 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patient is a consenting female age 40-75 years
  • Patient is scheduled for routine screening DBT
  • Patient is asymptomatic for breast disease
  • Patient had heterogeneously dense or extremely dense breasts on most recent prior mammography examination (Breast Imaging Reporting and Data System [BI-RADS] c or d) within 24 months of enrollment
  • Patient is able to participate fully in all aspects of the study (completing study visits and study data collection)
  • Patient understands and signs the study informed consent
  • Patient anticipates being able to return one year after study enrollment to complete the second round of screening

排除标准

  • Patient is currently pregnant or plans to become pregnant during the course of the study
  • Patient is currently lactating
  • Patient has had a prior MBI
  • Patient has had a prior whole breast ultrasound (WBUS) for screening, with either a hand-held ultrasound probe or automated system, within 12 months prior to study enrollment
  • Patient has had a prior breast MRI
  • Patient has had a prior contrast-enhanced mammogram (contrast enhanced spectral mammography [CESM] or contrast-enhanced digital mammography [CEDM])
  • Patient is concurrently participating in any other breast imaging research studies that involve undergoing additional breast imaging tests beyond routine screening with mammography, including but not limited to contrast-enhanced mammography, WBUS, MBI, or contrast-enhanced breast MRI
  • Patient has had a breast biopsy within 3 months prior to study enrollment
  • Patient has had breast surgery within 12 months prior to study enrollment
  • Patient is currently undergoing treatment for breast cancer or planning surgery for a high-risk breast lesion (atypical ductal hyperplasia [ADH], atypical lobular hyperplasia [ALH], lobular carcinoma in situ [LCIS], papilloma, radial scar)
  • Patient is currently taking a chemoprevention agent for breast cancer risk reduction or osteoporosis prevention (tamoxifen, raloxifene, anastrazole, letrozole, exemestane)
  • Patient has a known history of any condition or factor judged by the investigator to preclude participation in the study or which might hinder study adherence

研究组 & 干预措施

DBT alone

Experimental

All participants undergo DBT screening

干预措施: Digital Breast Tomosynthesis (DBT) (Procedure)

DBT + MBI

Experimental

All participants undergo DBT screening + supplemental MBI

干预措施: Digital Breast Tomosynthesis (DBT) (Procedure)

DBT + MBI

Experimental

All participants undergo DBT screening + supplemental MBI

干预措施: Scintimammography (Radiation)

结局指标

主要结局

Rate of Detection of Invasive Cancers

时间窗: At year 1 screening

Compare the rate of detection of invasive cancers between DBT alone versus (vs.) the combination of digital breast tomosynthesis (DBT) with supplemental molecular breast imaging (MBI) at initial (year 1) screening. For each modality, the detection rate of invasive cancers will be estimated as the proportion of participants in the analysis set who had an invasive cancer detected by the modality and verified by pathology.

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Sponsor
主要研究者

Carrie Hruska

Principal Investigator

Mayo Clinic

研究点 (5)

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