Stage II Breast Cancer Clinical Trial
Official title:
Sonography Compared With MRI in Pre-Operative Evaluation of Patients With Breast Cancer to Determine Extent of Breast Disease
This clinical trial studies mammography and targeted ultrasound with or without whole-breast ultrasound or contrast-enhanced magnetic resonance imaging (MRI) in finding out the extent of disease before surgery in patients with newly diagnosed breast cancer. New diagnostic imaging procedures, such as whole-breast ultrasound or contrast-enhanced MRI, may help find out how far breast cancer has spread. It is not yet known whether mammography and targeted ultrasound are more effective with or without whole-breast ultrasound or contrast-enhanced MRI in finding out how far breast cancer has spread.
PRIMARY OBJECTIVES:
I. To determine how surgical treatment is influenced by the three imaging arms.
II. To compare three imaging arms in terms of accurately measuring the size of the index
lesion and the number and location of tumor foci (using surgical pathology as gold standard).
SECONDARY OBJECTIVES:
I. In women with dense breasts: To retrospectively compare the accuracy of three imaging arms
in measuring the size of the index lesion and the number and location of tumor foci (using
surgical pathology as the gold standard).
II. To report the incidence of synchronous contralateral breast cancers detected by the three
imaging arms.
OUTLINE: Patients are assigned to 1 of 3 treatment groups.
GROUP 1: Patients undergo standard of care diagnostic imaging comprising bilateral
mammography and targeted breast ultrasound.
GROUP 2: Patients undergo standard of care diagnostic imaging as in Group 1. Patients also
undergo bilateral whole-breast ultrasound.
GROUP 3: Patients undergo standard of care diagnostic imaging as in Group 1. Patients also
undergo bilateral breast contrast-enhanced MRI.
All patients undergo standard of care breast conserving surgery, or mastectomy if the tests
indicate a change in the surgical plan.
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