Gender | Age
Item
women ≥ 20 years in age;
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Gender | Breast-Conserving Surgery Invasive carcinoma of breast | Negative Surgical Margin | Therapeutic radiology procedure Completed
Item
women who underwent breast-conserving surgery for invasive breast cancer, whose final margins were negative and who finished radiation therapy at least 6 months prior to this study;
boolean
C0079399 (UMLS CUI [1])
C0917927 (UMLS CUI [2,1])
C0853879 (UMLS CUI [2,2])
C1709157 (UMLS CUI [3])
C1522449 (UMLS CUI [4,1])
C0205197 (UMLS CUI [4,2])
Biopsy of breast Absent
Item
no history of breast biopsy of the breast within 6 months prior to this study;
boolean
C0405352 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
signed study-specific informed consent prior to registration;
boolean
C0021430 (UMLS CUI [1])
Mastectomy Contralateral Absent
Item
has not had contralateral mastectomy;
boolean
C0024881 (UMLS CUI [1,1])
C0441988 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Neoplasm Metastasis Absent
Item
no known metastatic disease;
boolean
C0027627 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Pregnancy Absent | Breast Feeding Absent
Item
not pregnant or lactating;
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Sign or Symptom Absent Breast Carcinoma | Breast Palpable mass Absent | No nipple discharge | Bleeding from nipple Absent | Mass of axilla Absent | Absence Breast skin change Abnormal | Absence Nipples skin change Abnormal
Item
no present signs or symptoms of breast cancer [no palpable mass(es), bloody or spontaneous clear nipple discharge, axillary mass, or abnormal skin changes in the breast(s) or nipple(s)].
boolean
C3540840 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C1403543 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0425813 (UMLS CUI [3])
C0281789 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C0238729 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C0332197 (UMLS CUI [6,1])
C0006141 (UMLS CUI [6,2])
C1399787 (UMLS CUI [6,3])
C0205161 (UMLS CUI [6,4])
C0332197 (UMLS CUI [7,1])
C0028109 (UMLS CUI [7,2])
C1399787 (UMLS CUI [7,3])
C0205161 (UMLS CUI [7,4])
Medical contraindication Absent MRI
Item
no contraindications to mri examination.
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
MRI Absent | Ultrasonography Absent | Mammography Absent
Item
no prior mri, us or mammography within the 6 months prior to the study.
boolean
C0024485 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0041618 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0024671 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Contrast-enhanced MRI Breast
Item
had a screening contrast-enhanced breast mri within the past 24 months or diagnostic contrast-enhanced mri on any study breasts within the past 12 months;
boolean
C1707501 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
Operation on breast | Core biopsy of breast
Item
had breast surgery and/or a core biopsy on the study breast(s) performed within the prior 6 months on the study
boolean
C3714726 (UMLS CUI [1])
C0842740 (UMLS CUI [2])
Chemotherapy | Exception Individual Cancer History | Exception Chemoprevention Tamoxifen | Exception Evista | Exception Raloxifene | Exception Arimidex | Exception Anastrozole | Exception Aromasin | Exception Exemestane | Exception Aromatase Inhibitors
Item
currently receiving chemotherapy [with exception to participant with personal history of cancer, and on chemoprevention with tamoxifen, evista (raloxifene), arimidex (anastrozole), aromasin (exemestane) or other aromatase inhibitor];
boolean
C0392920 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C1512706 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0282515 (UMLS CUI [3,2])
C0039286 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0720318 (UMLS CUI [4,2])
C1705847 (UMLS CUI [5,1])
C0244404 (UMLS CUI [5,2])
C1705847 (UMLS CUI [6,1])
C0878174 (UMLS CUI [6,2])
C1705847 (UMLS CUI [7,1])
C0290883 (UMLS CUI [7,2])
C1705847 (UMLS CUI [8,1])
C0876723 (UMLS CUI [8,2])
C1705847 (UMLS CUI [9,1])
C0851344 (UMLS CUI [9,2])
C1705847 (UMLS CUI [10,1])
C0593802 (UMLS CUI [10,2])
Renal Insufficiency Severe | Estimated Glomerular Filtration Rate | Dialysis
Item
participant with severely impaired renal function with estimated glomerular filtration rate (gfr) < 30 ml/min/1.73m2 and/or on dialysis.
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3811844 (UMLS CUI [2])
C0011946 (UMLS CUI [3])