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Completed

NCT Number: NCT00500383

Breast Cancer Risk Assessment Using Optical Breast Spectroscopy (OBS)

This study aims to evaluate if a light based technique, called Optical Breast Spectroscopy (OBS) formerly known as Transillumination Breast Spectroscopy (TiBS), can be used to detect differences in breast tissue between high- and low-risk populations and within the high-risk population between BrCa1 or 2 carriers and non-carriers. These differences may include differences in breast tissue composition and metabolism at time of enrollment into the study (possibly reflecting changes occurring in adolescence) and in the rate of breast tissue change over time (possibly reflecting rate of tissue transformation from normal to ultimately malignant state).

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Key information

Age range

25 year–60 year

Sex eligibility

Female

Study type

Observational

Primary location

Juravinski Cancer Center, Hamilton Health Sciences, Hamilton, Ontario, Canada

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About this study

Preliminary data show Optical Breast Spectroscopy (OBS)has the ability to detect tissue differences with various pathologies and age-related changes in breast tissue over a two year period. In the present study, we want to determine whether OBS has the ability to detect optical differences between women who harbor a mutation in the breast cancer susceptibility gene, BrCa1 or BrCa2, and their age-matched controls (non-carriers). More specifically, possible differences in the breast tissue at time of enrollment into the study (reflecting changes potentially occurring in adolescence) and in the rate of breast tissue change over time (reflecting rate of tissue transformation from normal to ultimately malignant state). The overall goal is to develop a pre-screening technique to survey or monitor the risk of breast tissue and to advise the earliest point when imaging techniques (e.g. MRI) should be initiated or when more drastic primary prevention measures are recommended.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

BrCa carriers (cases)

  • Attending one of the three participating high-risk screening centres
  • Confirmed BrCa1 or BrCa2 mutation status through genetic testing

High-Risk (cases)

  • Attending one of the three participating high-risk screening centres
  • Confirmed negative BrCa1/2 status through genetic testing

BrCa non-carriers (controls)

  • Attain a GAIL model score of <1.1 and have <10% risk of carrying the BRCa mutation Determined by the Penn II model)
  • Controls from high-risk screening centre with confirmed BrCa1/2 negative status through genetic testing
  • Preference will be given to sisters or first degree cousins of BrCa carriers

Exclusion criteria

Cases and Controls

  • Prior diagnosis or Breast or Ovarian Cancer
  • Bilateral biopsy or fine needle aspiration within 1 year of study start
  • Bilateral mastectomy, lumpectomy or cosmetic alteration (reduction/augmentation)
  • Previous or current chemotherapy or prevention therapy (Tamoxifen)
  • Less than 3 years post pregnancy at study start
  • inability to provide informed consent due to language or cognitive difficulties

*For controls only

  • Family history of breast cancer where family member had an early diagnosis (before age 45 years)
  • Family history or ovarian cancer

Treatment and study plan

Primary outcomes

  1. Difference in rate of change between the high risk groups and the respective controls

    Time frame: over the 4 year duration of the study

    the primary optical measurements are utilized to determine principal component scores in the analysis which in turn will be used as time dependent variable in a linear regression analysis to determine the rate of change.

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Collaborators

  • Hamilton Health Sciences Corporation
  • Mount Sinai Hospital, Canada

Registry information

Important dates

Study start
2009
Primary completion
2015
Study completion
2015
First posted
Jul 12, 2007
Registry last updated
Mar 23, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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