Invasive carcinoma of breast | Endocrine receptor assay | Tumor grade | HER2 expression
Item
invasive breast carcinoma with histologically confirmed hormone receptor analysis, the grade of the tumor, the expression of her-2.
boolean
C0853879 (UMLS CUI [1])
C0523374 (UMLS CUI [2])
C0475753 (UMLS CUI [3])
C0069515 (UMLS CUI [4,1])
C0597360 (UMLS CUI [4,2])
Lesion Unifocal TNM clinical staging | Lesion Multifocal TNM clinical staging | Microcalcification Present | Microcalcification Absent
Item
lesion classified t1-t2-t3 unifocal or multifocal with or without associated microcalcifications
boolean
C0221198 (UMLS CUI [1,1])
C0443337 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0221198 (UMLS CUI [2,1])
C0205292 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C0521174 (UMLS CUI [3,1])
C0150312 (UMLS CUI [3,2])
C0521174 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Lesion Identified MRI
Item
lesion recognizable and identifiable in mri
boolean
C0221198 (UMLS CUI [1,1])
C0205396 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
Indication Mastectomy | Axillary lymph nodes Involved | Axillary lymph nodes Uninvolved
Item
indication of mastectomy with or without axillary
boolean
C3146298 (UMLS CUI [1,1])
C0024881 (UMLS CUI [1,2])
C0729594 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C0729594 (UMLS CUI [3,1])
C0205429 (UMLS CUI [3,2])
Location of lesion | Distance Skin | Distance Nipple | Distance Pectoralis major
Item
lesion located more than 10 mm from the skin, the nipple and pectoralis major
boolean
C2184261 (UMLS CUI [1])
C0012751 (UMLS CUI [2,1])
C1123023 (UMLS CUI [2,2])
C0012751 (UMLS CUI [3,1])
C0028109 (UMLS CUI [3,2])
C0012751 (UMLS CUI [4,1])
C0585574 (UMLS CUI [4,2])
Medical contraindication Absent MRI | Artificial cardiac pacemaker
Item
no cons-indication to mri (pacemaker)
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
C0030163 (UMLS CUI [2])
Gender | Age
Item
women whose age is ≥ 18 years
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Premenopausal state Contraceptive Agents
Item
if premenopausal patient: patient contraceptives
boolean
C0232969 (UMLS CUI [1,1])
C0009871 (UMLS CUI [1,2])
Informed Consent
Item
patient has signed informed consent
boolean
C0021430 (UMLS CUI [1])
Affiliation Social Security Program
Item
affiliation to a social security scheme
boolean
C1510825 (UMLS CUI [1,1])
C0037435 (UMLS CUI [1,2])
Neoplasm TNM clinical staging | Lesion Non-Palpable
Item
tumor-td t4b classified or non-palpable lesion
boolean
C0027651 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0221198 (UMLS CUI [2,1])
C4086626 (UMLS CUI [2,2])
Age | Indication Adjuvant Chemotherapy | Indication Neoadjuvant Chemotherapy
Item
if age <70 years: no indication of adjuvant chemotherapy and neoadjuvant
boolean
C0001779 (UMLS CUI [1])
C3146298 (UMLS CUI [2,1])
C0085533 (UMLS CUI [2,2])
C3146298 (UMLS CUI [3,1])
C0600558 (UMLS CUI [3,2])
C3665472 (UMLS CUI [3,3])
MRI Lesion Unidentified | Location Distance Skin | Location Distance Pectoralis major | Lesion Diameter
Item
mri lesions have not been identified, located within 10 mm of the skin and pectoral muscle, greater than 25 mm diameter
boolean
C0024485 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C0205427 (UMLS CUI [1,3])
C1515974 (UMLS CUI [2,1])
C0012751 (UMLS CUI [2,2])
C1123023 (UMLS CUI [2,3])
C1515974 (UMLS CUI [3,1])
C0012751 (UMLS CUI [3,2])
C0585574 (UMLS CUI [3,3])
C0221198 (UMLS CUI [4,1])
C1301886 (UMLS CUI [4,2])
Lacking Able to lie down Prone Position Quiet
Item
inability to hold still in the prone position, arms extended, for 30 minutes
boolean
C0332268 (UMLS CUI [1,1])
C0560841 (UMLS CUI [1,2])
C0033422 (UMLS CUI [1,3])
C0439654 (UMLS CUI [1,4])
Medical contraindication MRI
Item
contraindication to mri
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Patient Deprivation Freedom | Protection of patient Legal | Informed Consent Unable
Item
patient deprived of liberty and major subject of a measure of legal protection or unable to consent
boolean
C0030705 (UMLS CUI [1,1])
C0871712 (UMLS CUI [1,2])
C0016694 (UMLS CUI [1,3])
C0412786 (UMLS CUI [2,1])
C1301860 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
Study Subject Participation Status | Interventional Study
Item
patient participating in another interventional clinical trial within 30 days prior to baseline and during the trial.
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2])