Age
Item
individuals aged 25 years or older
boolean
C0001779 (UMLS CUI [1])
Breast Imaging finding Quantity | Biopsy Patient need for
Item
individuals who have at least one breast imaging finding requiring biopsy, specifically:
boolean
C0006141 (UMLS CUI [1,1])
C1287399 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0005558 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
Abnormality of the breast Suspicious for Malignancy Imaging | Abnormality of the breast Suggestive of Malignant Neoplasm Imaging | Mammography | Ultrasonography | MRI | BIRADS | Biopsy Patient need for | Breast Carcinoma | FDG-PET Scan
Item
individuals who have a breast abnormality(ies) moderately suspicious for or highly suggestive of malignancy on imaging with mammography, ultrasound, or mri (as per acr birads™ 4c or 5) and requiring biopsy confirmation or o individuals with known breast cancer who have additional imaging abnormality(ies) suspicious for malignancy detected on a high-resolution fdg pet scan
boolean
C4025829 (UMLS CUI [1,1])
C4050405 (UMLS CUI [1,2])
C0011923 (UMLS CUI [1,3])
C4025829 (UMLS CUI [2,1])
C0332299 (UMLS CUI [2,2])
C0006826 (UMLS CUI [2,3])
C0011923 (UMLS CUI [2,4])
C0024671 (UMLS CUI [3])
C0041618 (UMLS CUI [4])
C0024485 (UMLS CUI [5])
C1511314 (UMLS CUI [6])
C0005558 (UMLS CUI [7,1])
C0686904 (UMLS CUI [7,2])
C0678222 (UMLS CUI [8])
C3641247 (UMLS CUI [9])
Imaging Work up | Abnormality of the breast Mammography
Item
individuals who had recent conventional imaging work-up including x-ray mammography of the breast containing the abnormality of interest.
boolean
C0011923 (UMLS CUI [1,1])
C0750430 (UMLS CUI [1,2])
C4025829 (UMLS CUI [2,1])
C0024671 (UMLS CUI [2,2])
Tumor size Suspected | Lesion Mammography | Lesion Ultrasonography | Lesion MRI | Biopsy | CT
Item
individuals with suspected tumor size measuring one cm or less on mammography and/or ultrasound and/or mri if the lesion is visible on any of these modalities, except that each site may enroll up to three patients each where the lesion of interest as measured on mammography (or ultrasound and/or mri if not detectable on mammography) is more than 1 cm. (note: the study will target patient enrollment such that at least 50% of the lesions to undergo biopsy across all sites will be less than 1 cm in diameter as measured on mammography, or as measured by other modalities, such as ultrasound, ct, or mri, if the lesion is not detectable or measurable on mammography.)
boolean
C0475440 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C0221198 (UMLS CUI [2,1])
C0024671 (UMLS CUI [2,2])
C0221198 (UMLS CUI [3,1])
C0041618 (UMLS CUI [3,2])
C0221198 (UMLS CUI [4,1])
C0024485 (UMLS CUI [4,2])
C0005558 (UMLS CUI [5])
C0040405 (UMLS CUI [6])
Study Subject Participation Status Agreement | Informed Consent
Item
individuals who have agreed to participate in the study and who have signed study-specific informed consent
boolean
C2348568 (UMLS CUI [1,1])
C0680240 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Pregnancy | Possible pregnancy
Item
women who are or may be pregnant
boolean
C0032961 (UMLS CUI [1])
C0425965 (UMLS CUI [2])
Breast Feeding | Breast Feeding Discontinued Recently
Item
women who are currently lactating or discontinued breastfeeding < 2 months prior to the study
boolean
C0006147 (UMLS CUI [1])
C0006147 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C0332185 (UMLS CUI [2,3])
Age
Item
age less than 25 years
boolean
C0001779 (UMLS CUI [1])
Breast implant | Breast Containing Lesion
Item
individuals with breast implant(s) in the breast containing the lesion of interest
boolean
C0179412 (UMLS CUI [1])
C0006141 (UMLS CUI [2,1])
C0332256 (UMLS CUI [2,2])
C0221198 (UMLS CUI [2,3])
Sentinel Lymph Node Biopsy Tc-99m Scheduled | PET Biopsy
Item
individuals who are scheduled for a sentinel node procedure using radioactive tc-99m within 24 hours of pet-guided biopsy
boolean
C0796693 (UMLS CUI [1,1])
C0303611 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C0032743 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
Medical contraindication Core biopsy | Medical contraindication Invasive procedure | Blood Coagulation Disorders | Communicable Disease | Anticoagulants Discontinue Unwilling
Item
patients with contraindications for core biopsy and other invasive procedures such as blood coagulation disorders, infection, or who are unwilling to discontinue use of anticoagulant medication prior to the procedure
boolean
C1301624 (UMLS CUI [1,1])
C1318309 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C4048276 (UMLS CUI [2,2])
C0005779 (UMLS CUI [3])
C0009450 (UMLS CUI [4])
C0003280 (UMLS CUI [5,1])
C1444662 (UMLS CUI [5,2])
C0558080 (UMLS CUI [5,3])
Diabetes Mellitus, Insulin-Dependent | Non-Insulin-Dependent Diabetes Mellitus Poorly controlled
Item
individuals with type i or poorly controlled type ii diabetes mellitus
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2,1])
C3853134 (UMLS CUI [2,2])
Blood glucose measurement | Positron Emission Mammography
Item
individuals with a blood glucose level that is above 140 mg/dl at the time of pem imaging
boolean
C0392201 (UMLS CUI [1])
C3897879 (UMLS CUI [2])
Informed Consent Unable
Item
inability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Operative Surgical Procedure Breast Involved
Item
individuals who have had surgery on the study breast(s) within the past 12 months
boolean
C0543467 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
C1314939 (UMLS CUI [1,3])