Dense Breast Tissue Clinical Trial
Official title:
Molecular Breast Imaging: A Novel Technology for Detection of Malignant Breast Lesions.
Detection of breast cancer as early as possible is an ongoing imaging challenge.The purpose of the current study is to assess the clinical performance of the new scintigraphic technology, a dedicated breast gamma camera composed by the new generation of CZT detectors,for assessment of breast pathology specifically in women where current imaging techniques, mainly mammography are suboptimal. These cohort are patients with dense breast tissue and patients who are at high risk for breast cancer by a combination of other metrics, including family history and genetic testing. BRCA (breast cancer susceptibility gene), is particularly a relevant health problem among Ashkenazi Jews in Israel.
Recently, a breast-dedicated gamma camera has been used for assessment of breast malignancy
in over 1000 women in Mayo Clinic, Rochester, USA. Molecular Breast Imaging (MBI), which
utilizes a Cadmium-Zinc-Telluride (CZT) gamma camera for scintimammography, has been shown
to have a high sensitivity (91%) for the detection of breast lesions > 5 mm in diameter and
69% for tumors smaller than 5mm.
In Israel , genetic high- risk for breast cancer is highly relevant. We will offer the new
imaging technology, to a wide patients population/group from all over Israel , in which the
referring physician and/or the breast-imaging physician will look for additional imaging
modality. Therefore this stage will include:
- Women with equivocal findings on Mammography, US and/or MRI
- Women with discrepancy between CBE(clinical breast examination)and breast imaging
- Women with dense breast
- Women in high risk for Breast Cancer
Before the imaging procedure each woman will need to fill detailed questionnaire, specific
for the study, that will include information on her medical history, family history,
gynecology information, menstrual phase, use of hormones etc.
The images will be correlated with other imaging tests including mammography, US and MRI. We
will follow up the women for at least 6 months, including biopsy findings and or other
clinical and imaging exams.
This phase will include 500 women.
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Observational Model: Cohort, Time Perspective: Prospective