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Using Infrared Spectroscopy to Analyze Volatile Organic Compounds in the Breath of Patients to Detect Breast Cancer

Status: Recruiting
Location: See all (4) locations...
Study Type: Observational
SUMMARY

Researchers will compare the breath profiles of women with breast cancer and those without to determine whether there are disease-specific patterns that can be leveraged to facilitate breast cancer detection. Women with mammogram-confirmed breast tissue density undergoing standard-of-care breast cancer screening will be invited to participate. Those who provide informed consent will provide one breath sample and fill out a questionnaire about their medical history with help from the research coordinators. Breath samples will be collected prior to standard of care biopsy or MRI, and patients will be stratified into the case or control group based on their test results. The primary goal of this project is to use exhaled alveolar breath and the subsequent spectral data produced by Breathe BioMedical's cavity ring-down spectrometer to further develop Breathe BioMedical's technology and machine learning algorithms to determine the feasibility of detecting breast cancer in women aged 40 to 74. Secondarily, this project aims to identify patterns of VOCs that are either over- or under-represented in participants with breast cancer when compared to the breath profiles of participants without breast cancer. This project will also assess performance characteristics of the technology (e.g. sensitivity, specificity, false negative rate, and false positive rate) including subgroup analyses. This project aims to understand intra-subject variability by exploring differences in breath signatures before and after definitive management of breast cancer, including surgical resection.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 40
Maximum Age: 74
Healthy Volunteers: t
View:

• Female (sex as assigned at birth);

• Aged 40 - 74 years;

• Mammography confirmed breast tissue density (BI-RADS density score of A, B, C or D);

• Scheduled for standard of care biopsy or MRI;

• Fluent in language of consent (English, Spanish, or French);

• Ability to give informed consent;

• Able to provide a breath sample.

Locations
United States
Washington, D.c.
GW Comprehensive Breast Center
RECRUITING
Washington D.c.
Florida
Mayo Clinic Breast Clinic
RECRUITING
Jacksonville
North Carolina
Duke University Medical Cente
RECRUITING
Durham
Pennsylvania
Weinstein Imaging Associates
NOT_YET_RECRUITING
Pittsburgh
Contact Information
Primary
Sandra Veenstra
sandra.veenstra@breathebiomedical.com
(506) 855-2400
Time Frame
Start Date: 2025-02-25
Estimated Completion Date: 2027-12
Participants
Target number of participants: 5175
Treatments
Breast Cancer Cohort
Subjects with biopsy-proven primary breast cancer.
Control Cohort
Subjects with a negative MRI (for surveillance or diagnostic purposes with BI-RADS 1 or 2) that confirms the absence of breast cancer.
Breast Cancer Cohort - Surgery
Subjects with biopsy-proven primary breast cancer, who have undergone surgery at Mayo Clinic Florida or Duke University will be screened to provide a second breath sample. The second breath sample will be collected at least six months following the completion of all standard of care treatment (excluding adjuvant endocrine therapy and adjuvant HER2 directed monoclonal antibody such as trastuzumab).
Related Therapeutic Areas
Sponsors
Collaborators: Mayo Clinic, Weinstein Imaging Associates, Duke University, George Washington University
Leads: Breathe BioMedical Inc

This content was sourced from clinicaltrials.gov