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Histology of Functional Density in Postmenopausal Breast

Pilot Study to Examine Histological Characteristics of Mammographic Density With Molecular Breast Imaging: Part 1 - Postmenopausal Women

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01240278
Enrollment
25
Registered
2010-11-15
Start date
2010-11-30
Completion date
2022-04-27
Last updated
2022-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Dense Breasts

Brief summary

Increased mammographic density is recognized as an important risk factor for developing breast cancer, however, the underlying mechanism explaining this relationship is unclear. The investigators hypothesize that Molecular Breast Imaging (MBI) can more accurately distinguish dense tissue on mammography which is at high risk from dense tissue at low risk by indicating cellular activity in dense tissue as radiotracer uptake (functional density) in the breast. In this pilot study, the investigators want to compare the histological characteristics of breast tissue in patients with who have similar density on mammography but different levels of functional density on MBI.

Interventions

None listed

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age 40 or older 2. Be postmenopausal as defined as having at least 12 consecutive months of amenorrhea 3. Screening mammogram performed at Mayo Clinic Rochester within one year prior to the current MBI study which demonstrates 1. Negative or benign assessment (BIRADs category 1-2) 2. No proliferative benign lesions (e.g. fibroadenomas) identified 3. Heterogeneously dense or extremely dense parenchyma (BIRADs density category 3 or 4) 4. MBI performed less than one month prior to biopsy demonstrating either significant FD or photopenic FD.

Exclusion criteria

1. Using any exogenous hormones (e.g., hormonal contraceptives, sex steroid hormones) or any estrogen receptor modulating drugs (e.g., tamoxifen, raloxifene) or any aromatase inhibitors within six months prior to study biopsy. 2. Personal history of any cancer, except non-melanomatous skin cancer 3. Current breast symptoms 4. Breast implants 5. Known allergy to local anesthetic. 6. History of bleeding complications from prior interventions 7. Current use of anticoagulants (e.g., Coumadin or other blood thinners) 8. Major medical condition

Design outcomes

Primary

MeasureTime frame
proportion of epithelium vs stromawithin 1 month of functional density assessment on MBI

Secondary

MeasureTime frameDescription
Degree of lobular involutionwithin 1 month of functional density assessment on MBIDegree of lobular involution as assessed through qualitative and quantitative measurements will be compared between dense tissue which appears photopenic on MBI and dense tissue which appears functionally active on MBI.
Ki-67 cellular proliferation indexwithin 1 month of functional density assessment on MBIDegree of cellular proliferation as assessed through Ki-67 index will be compared between dense tissue which appears photopenic on MBI and dense tissue which appears functionally active on MBI.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026