Gender | Age
Item
the subject must be female and 18 years of age or older.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Breast Carcinoma Preoperative TNM Breast tumor staging
Item
the subject must be a preoperative clinical tis, t1, t2, t3, t4, as well as clinical n0 and clinical m0 breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
Breast Carcinoma Primary
Item
the subject must have a diagnosis of primary breast cancer.
boolean
C0678222 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Patient Appropriate Surgical intervention | Segmental Mastectomy | Sentinel Lymph Node Biopsy | Mastectomy
Item
the subject must be a candidate for surgical intervention, either with lumpectomy and slnb or with mastectomy and slnb, as the treatment of her breast cancer.
boolean
C0030705 (UMLS CUI [1,1])
C1548787 (UMLS CUI [1,2])
C0549433 (UMLS CUI [1,3])
C0024885 (UMLS CUI [2])
C0796693 (UMLS CUI [3])
C0024881 (UMLS CUI [4])
ECOG performance status
Item
the subject must have an eastern cooperative oncology group (ecog) performance status of grade 0 - 2
boolean
C1520224 (UMLS CUI [1])
Informed Consent
Item
the subject must provide written informed consent with health insurance portability and accountability act (hipaa) authorization before participating in the study
boolean
C0021430 (UMLS CUI [1])
Neoplasm Metastasis | Abnormality of the lymph nodes | Lymphadenopathy Palpable | Malignant cells Lymph nodes Core needle biopsy | Malignant cells Lymph nodes Surgical biopsy | Malignant cells Lymph nodes Fine needle aspiration
Item
the subject has clinical or radiological or pathologic evidence of metastatic cancer, including any abnormal or enlarged clinical palpable lymph nodes or core biopsy/surgical biopsy/fine-needle-aspiration evidence of malignant cell within any lymph nodes.
boolean
C0027627 (UMLS CUI [1])
C0149727 (UMLS CUI [2])
C0497156 (UMLS CUI [3,1])
C0522499 (UMLS CUI [3,2])
C0334227 (UMLS CUI [4,1])
C0024204 (UMLS CUI [4,2])
C1318309 (UMLS CUI [4,3])
C0334227 (UMLS CUI [5,1])
C0024204 (UMLS CUI [5,2])
C0565118 (UMLS CUI [5,3])
C0334227 (UMLS CUI [6,1])
C0024204 (UMLS CUI [6,2])
C1510483 (UMLS CUI [6,3])
Other Coding
Item
the subject has a known hypersensitivity to vital blue dye (vbd) in a case where vital blue dye was planned for use during slnb.
boolean
C3846158 (UMLS CUI [1])
Pregnancy test positive | Breast Feeding
Item
the subject has a positive pregnancy test or is lactating.
boolean
C0240802 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Operative Surgical Procedure Previous Breast Indicated | Operative Surgical Procedure Previous Axilla Indicated
Item
the subject has had prior surgery to the indicated breast or axilla.
boolean
C0543467 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0006141 (UMLS CUI [1,3])
C1444656 (UMLS CUI [1,4])
C0543467 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0004454 (UMLS CUI [2,3])
C1444656 (UMLS CUI [2,4])