Breast Cancer Clinical Trial
Development Of A Blood Test To Improve The Performance Of Breast Cancer Screening
Summary
The purpose of this study is to collect blood and tissue to help develop tests that might be able to detect cancer earlier. The investigator will be collecting these samples and reviewing test results from participants who have had an area of concern found on breast imaging, as well as from participants who are scheduled to have a routine breast cancer screening mammogram.
Eligibility Criteria
Inclusion Criteria:
Females with one or more BI-RADS 4 radiographic lesions who are undergoing ultrasound, stereotactic or MRI-guided breast biopsy at MSKCC or at an MSK Alliance Member Site. If multiple imaging modalities were employed (mammogram, ultrasound, MRI) and no integrated score is provided, then the highest BI-RADS score will be used.
Age ≥ 18 years at the time of breast biopsy
Willing to provide blood samples for research purposes before biopsy.
Able to provide written informed consent
Exclusion Criteria:
Women with a BI-RADS 4 lesion who had the lesion previously biopsied
Females with a current active malignancy other than non-melanoma skin cancers. Females are considered not to have a "current active" malignancy if they have completed therapy and have no evidence of systemic disease for at least three years from the initial diagnosis
Currently pregnant women
History of bilateral mastectomy.
Participant has or is currently participating in another GRAIL-sponsored protocol
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There are 7 Locations for this study
Hartford Connecticut, 06102, United States
Miami Florida, 33143, United States
Basking Ridge New Jersey, 07920, United States
Middletown New Jersey, 07748, United States
Commack New York, 11725, United States
Harrison New York, 10604, United States
New York New York, 10065, United States
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