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RecruitingNCT05369546Updated Feb 2, 2023

Lesion Composition and Quantitative Imaging Analysis on Breast Cancer Diagnosis

An observational study in Breast Cancer, sponsored by University of Hawaii. Recruiting at 3 sites in United States. Open to female participants aged 20 Years to 85 Years. Per ClinicalTrials.gov, last updated 2023-02-02.

Sponsored by University of Hawaii · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2025, 1 year 3 months ago, but the record still lists the study as recruiting.
  • Started Aug 2022; still recruiting 4 years 2 months later.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
600
Ages
20 Years to 85 Years
Sex
Female
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Study summary

The objective is to better identify suspicious breast lesions that need to be biopsied for malignancy in women currently recommended for biopsy. The long-term goal is to reduce unnecessary biopsies and increase biopsy yield. To do this, the investigators have developed an innovative way to use FDA-approved breast imaging protocols to acquire multispectral images to measure the composition of suspicious breast lesions. The central hypothesis is that breast tissue composition in combination with analysis of morphological and textural tissue characteristics on digital breast tomosynthesis (DBT) imaging will yield significantly higher breast cancer specificity than conventional interpretation of DBT alone.

Read the detailed description

Women with dense breast have not been shown to benefit by increased cancer detection of volumetric digital breast tomosynthesis (DBT) but may benefit by lower recall rates. DBT screening biopsy rates are similar to 2D digital mammography; higher for first screening exams, lower thereafter with adjustment for age and breast density. In the U.S., 71% of biopsies do not result in a breast cancer diagnosis among women ages 40-79 who undergo breast cancer screening. To address the high rate of unnecessary biopsies, an innovative way to use FDA-approved breast imaging protocols has been developed to acquire multispectral images to measure the lipid/water/protein (L/W/P) composition of suspicious breast lesions. Malignant breast tissue has unique L/W/P composition fractions when compared to normal or benign breast tissue. This proposal aims to increase biopsy yield (BI-RADS-PPV3) through combining L/W/P biological biomarkers with quantitative morphological and textural image analysis. This combination of composition and physical descriptions of suspicious breast lesions is called q3CB. The benefits of adding q3CB to the current DBT screening/diagnostic imaging paradigm, that may already include computer aided detection, is not known. This study is designed to compare the expected biopsy yield with and without q3CB in a clinical reader study and explore how q3CB may be combine with existing technologies. The central hypothesis is that biological L/W/P fractions in breast tissue in combination with analysis of morphological and textural tissue characteristics will yield significantly higher breast cancer specificity than conventional interpretation of DBT alone. The objective is to better identify suspicious breast lesions that need to be biopsied for malignancy in women currently recommended for biopsy. The long-term goal is to reduce unnecessary biopsies and increase biopsy yield. The investigators rationale for the proposed research is that biological L/W/P descriptions of breast lesions will lead to more specific biopsy decisions and a better understanding of cancer types. Specifically, the project aims are 1) develop q3CB lesion signatures for distinguishing breast cancer lesions from benign lesions, using 600 prospectively-acquired DBT exams of women recommended to undergo biopsy; 2) conduct a clinical reader study to compare radiologists' performance on standard-of-care FFDM or DBT without and with the inclusion of q3CB signatures; 3) Investigate the utility of q3CB lesion signatures in a screening paradigm to improve sensitivity and specificity on CADe-identified suspicious lesions in the tasks of assessing malignancy as well as in associating with their association with cancer subtypes; Exploratory) explore the added sensitivity and specificity of dual-energy DBT in phantom studies that explore lesion size, composition, and breast density. The innovation of this study is the full characterization of lipid/water/protein lesion composition with DBT and how it complements existing computer aided diagnostic programs paired with clinical radiologists providing evidence ready for clinical translation of this unique and emerging technology.

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Conditions studied

  • Breast Cancer

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03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's planned enrollment of 600 is above the median of 184 across 2,642 observational studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

University of Hawaii is the lead sponsor of 96 studies on the registry; 21 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 3 (43%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years to 85 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All 600 women will be recruited and enrolled from one of three sites: Queen's Medical Center (Honolulu, HI), East Hawaii Women's Imaging Center (Hilo, HI), and H. Lee Moffitt Cancer Center \& Research Institute (Tampa, FL).

Inclusion criteria

  • Had a recent diagnostic mammogram with a BI-RADS diagnostic score 4 or 5 assigned by a radiologist (BIRADS are standardized mammography assessment categories: 4 is for "Suspicious abnormality", 5 is for "Highly suggestive of malignancy".
  • Have not had biopsy

Exclusion criteria

Exclusion Criteria:

  • Pregnant or breast feeding
  • History of breast cancer or a mastectomy (removal of the breast) with Systemic Therapy (ex. Chemotherapy, hormones and hormone inhibitors, etc.).
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Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
600 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testq3CB

    The q3CB/ncCEM/DBT acquisition protocol consists of a combination of DBT volume reconstructions and projection dual-energy mammograms acquired with a clinical contrast enhanced mammography (CEM) protocol, without contrast administration agent.

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What researchers measure

Primary outcomes

  1. Quantify biological composition of lesions

    Quantify the biological composition (lipid/water/protein) of suspicious lesions.

    Time frame: Baseline

  2. Quantify morphology of lesions

    Quantify morphology/texture (radiomics) of suspicious lesions.

    Time frame: Baseline

Secondary outcomes

  1. Comparison of radiologists' image interpretations with and without q3CB signatures

    Difference in AUC between the "1st read" and "2nd read" image interpretations. In the "1st read," they will be provided with the FFDM/DBT images and in the "2nd read," they will also be provided with the ncCEM q3CB composition and radiomics signature (likelihood of malignancy).

    Time frame: Baseline

  2. Sensitivity and Specificity of readers' responses for the BI-RADs assessment categories

    Sensitivity and specificity values will be calculated: a BI-RADS assessment of 4a or higher (i.e., 4a, 4b, 4c, and 5) defined a positive call for cancer diagnosis and, conversely, a BI-RADS assessment of 3 or lower (i.e., 3, 2, and 1) defined a negative call for cancer diagnosis.

    Time frame: Baseline

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Study locations

3 of 3 sites recruiting
  • H. Lee Moffitt Cancer Center & Research Institute, Inc.
    Tampa, Florida 33612, United States
    • Emily Research Services Project Coordinator · Contact · emily.amato@moffitt.org · 813-745-5501
    • Bethany L Niell, MD · Principal investigator
    • Dana K Ataya, MD · Principal investigator
    Recruiting
  • Hawaii Radiology Associates, LTD (East Hawaii Women's Imaging Center)
    Hilo, Hawaii 96720, United States
    • Scott Grosskreutz, MD · Contact · 808-935-1825
    • Scott Grosskreutz, MD · Principal investigator
    Recruiting
  • The Queen's Medical Center
    Honolulu, Hawaii 96822, United States
    • Richmond Clinical Research Associate · Contact · riwong@queens.org · 808-691-7609
    • Todd Seto, MD · Principal investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 2, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05369546
Lead sponsor
University of Hawaii
Collaborators
H. Lee Moffitt Cancer Center and Research Institute, Queen's Medical Center, Hawaii Radiologic Associates, Ltd.
Responsible party
Sponsor
First posted
May 11, 2022
Start date
Aug 1, 2022
Primary completion
Jul 2025 (estimated)
Completion
Jul 2026 (estimated)
Last update
Feb 2, 2023

Study contacts

John A Shepherd, PhD
Contact
johnshep@hawaii.edu
808-440-5234
Leila Kazemi
Contact
lkazemi@hawaii.edu
808-440-5231
John A Shepherd, PhD
principal investigator · University of Hawaii Cancer Research Center

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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