Gender | Age
Item
female patients between 18 and 80 years of age at the time of enrollment
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Breast Carcinoma
Item
histopathologically or cytologically confirmed diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
Segmental Mastectomy Completed | Sentinel Lymph Node Biopsy Completed | Excision of axillary lymph nodes Completed
Item
completed lumpectomy and sentinel lymph node biopsy or axillary lymph node dissection
boolean
C0024885 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0796693 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0193867 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
Informed Consent
Item
signed and dated ethics-approved informed consent form prior to any study procedures
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
ability to comply with the requirements of the study
boolean
C0525058 (UMLS CUI [1])
Adjuvant Radiation Therapy Scheduled
Item
scheduled adjuvant radiation therapy treatment
boolean
C1706721 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Recurrent disease Locally | Neoplasm Metastasis
Item
clinical or radiological evidence of local recurrence or metastatic disease
boolean
C0277556 (UMLS CUI [1,1])
C1517927 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2])
Prior radiation therapy Axilla Ipsilateral | Prior radiation therapy Breast Ipsilateral
Item
previous history of radiation therapy to ipsilateral axilla and/or breast area
boolean
C0279134 (UMLS CUI [1,1])
C0004454 (UMLS CUI [1,2])
C0441989 (UMLS CUI [1,3])
C0279134 (UMLS CUI [2,1])
C0006141 (UMLS CUI [2,2])
C0441989 (UMLS CUI [2,3])
Boost radiation therapy Planned | Dementia | Psychotic Disorders | Mental state Impairment Preventing Informed Consent | Mental state Impairment Preventing Self-care | Mental state Preventing Toxicity Reporting
Item
planned boost of radiation dementia, psychoses, or other significant impairment of mental status that would prohibit the understanding and giving of informed consent or the participation in self-care or toxicity reporting
boolean
C2919491 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0497327 (UMLS CUI [2])
C0033975 (UMLS CUI [3])
C0278060 (UMLS CUI [4,1])
C0221099 (UMLS CUI [4,2])
C1292733 (UMLS CUI [4,3])
C0021430 (UMLS CUI [4,4])
C0278060 (UMLS CUI [5,1])
C0221099 (UMLS CUI [5,2])
C1292733 (UMLS CUI [5,3])
C3872897 (UMLS CUI [5,4])
C0278060 (UMLS CUI [6,1])
C1292733 (UMLS CUI [6,2])
C0600688 (UMLS CUI [6,3])
C0700287 (UMLS CUI [6,4])
Medical History Study Subject Participation Status Inappropriate | Comorbidity Study Subject Participation Status Inappropriate
Item
any significant history or concurrent disease which, in the judgment of the investigator would make the patient inappropriate for entry to this study
boolean
C0262926 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C0009488 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C1548788 (UMLS CUI [2,3])
Medical contraindication Therapeutic radiology procedure | Scleroderma
Item
history of contraindications of radiation such as scleroderma
boolean
C1301624 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C0011644 (UMLS CUI [2])