Trial Information

Infrared Imaging (Breast Scan IR) for Early Breast Cancer Detection

The research study will evaluate the sensitivity and specificity of a new non-invasive
digital infrared imaging system as an adjunctive test for breast cancer detection (as
approved by the FDA under 21 CFR 884.2980). The technology and device (BreastScan IRÔ) have
been developed by Infrared Sciences Corp. and has undergone more than 3 years of preliminary
testing. The device's utility will be investigated with regard to its sensitivity in
detecting breast cancer, and its ability to identify the size of the breast cancer.
Additionally, the negative predictive value of the device will be investigated. This device
does not diagnose breast cancer, however it records temperature data and other physiological
parameters of the breast, and compares them to a database of patients with known breast
health.

The examination process is simple and non-invasive. The patient sits disrobed from the
waist up, appropriately positioned in the ergonomic chair with her arms
supported at eye level. Temperature controlled air flow is then directed at the
breasts for a 4-minute interval while the infrared camera records skin surface
cool down at 250 frames per minute. The stored images are fed into proprietary
computer software designed to extract specific thermal parameters, including various
temperature differences and thermal symmetry measurements. Additionally, the software
will focus on areas of the breasts, when compared to its immediate surroundings,
that behave abnormally. The program produces a color coded post-processed image of the
breasts showing one or more these identified sites, as well as the result of all measured
parameters. The combination of these parameters are evaluated for risk in a weighted
"evaluation" algorithm, as determined by the information in the database. The results of
the digital infrared scan will be correlated with the results of the subsequent breast
biopsy.

Selected patients will be required to sign an informed consent form. These patients will
have been recommended to have a biopsy, based either on mammography or ultrasound. The
patients overall breast density will be noted. Each patient will be "imaged" with the
BreastScan IR system, and the raw data stored. The computer will analyze the raw data, and
will produce a report showing the results of the test. This report will be stored for use
once the results of the patient's biopsy is known.

For each patient, the report will provide an evaluation of "risk" as well as other data that
will help localize any suspicious sites. Comparison will be made with actual radiology and
pathology results.

If a patient is determined by biopsy to have any form or breast cancer, or atypical
hyperplasia, the investigator will examine the BreastScan IR report, and verify that this
patient was evaluated as "Risk" (one or more positive risk signs). If sufficient
information is provided in the pathology or radiology report to determine the site(s) in
the breast, the investigator will again verify that the BreastScan IR report correctly
localizes the breast and quadrant of the known cancer. The incidence of incorrect
evaluations will be recorded for determination of the system's sensitivity to breast cancer.

If a patient is determined by biopsy to have any non-malignant condition, such as a cyst or
fibroadenoma, the investigator will determine if the BreastScan IR report evaluated the
patient as "Normal" (zero positive signs) or as "Risk".

Methodology:

Two hundred (200) female patients will be selected from a normal screening process. Those
patients that have a finding that is suspicious for cancer (BIRADS 3) or highly suspicious
for cancer (BIRADS 4,5), and/or that have been scheduled for a biopsy, will be included in
this study. The patients will be asked to sign an informed consent form.

Data:

The data collected in this trial will be blinded to the patient as well as the radiologist.
The data for an individual patient will be stored locally, within the BreastScan IR system,
and will not be available to anyone except authorized research investigators. The data
will be stored for future use and analysis. Since this data must be compared to an actual
radiology/pathology report, the data cannot be anonymous, but will be confidential.

Patient Risk:

The test is completely non-invasive, and presents no risk whatsoever to the patient. The
infrared camera records infrared energy emitted from the patient's body. Cool air is not
excessively cold, and does not present any discomfort to most patients.

Benefits:

The main objective of the test is to develop a tool that will help diagnose breast cancer by
providing accurate adjunctive information to the patient's doctor. Preliminary studies
indicate that this test is 99% sensitive to breast cancer. A patient with a "normal"
(negative) result will have a very small chance that an occult cancer is still harbored in
the breast. Conversely, a patient that has an abnormal test will require further work-up.

We hope to benefit two groups of women that now account for largest proportion of "missed"
cancers. Namely, those women with dense breast tissue, and those women under 40 who are at
the pre-mammography age, and who generally have dense breast tissue. A non-invasive test
that can help with improved screening, is urgently needed to improve the detection
statistics in these groups, and hopefully lead to early intervention of those patients at
high risk.