Breast Carcinoma Estrogen receptor negative TNM Breast tumor staging | Breast Carcinoma Progesterone receptor negative TNM Breast tumor staging | Operative Surgical Procedures Completion | Therapeutic radiology procedure Completion | Chemotherapy Completion
Item
prior diagnosis of stage 0 to iii breast cancer that is estrogen receptor negative, progesterone receptor negative with completion of definitive surgery, radiation therapy and/or chemotherapy.
boolean
C0678222 (UMLS CUI [1,1])
C0279756 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
C0678222 (UMLS CUI [2,1])
C0279766 (UMLS CUI [2,2])
C0474926 (UMLS CUI [2,3])
C0543467 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C1522449 (UMLS CUI [4,1])
C0205197 (UMLS CUI [4,2])
C0392920 (UMLS CUI [5,1])
C0205197 (UMLS CUI [5,2])
Chemotherapy Completion | Trastuzumab Completion | Therapeutic radiology procedure Completion | Standard of Care Completion
Item
completion of chemotherapy or trastuzumab for > six months and of radiation therapy for > 2 months, as applicable and 2 years or less from completion of standard therapy.
boolean
C0392920 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0728747 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C1522449 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C2936643 (UMLS CUI [4,1])
C0205197 (UMLS CUI [4,2])
Pregnancy Absent | Breast Feeding Absent
Item
greater than 1 year from pregnancy, lactation.
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Mammography | Absence Suspicion Breast Carcinoma
Item
mammogram within the six months prior to study enrollment that is not suspicious for breast cancer (acr class i-iii).
boolean
C0024671 (UMLS CUI [1])
C0332197 (UMLS CUI [2,1])
C0242114 (UMLS CUI [2,2])
C0678222 (UMLS CUI [2,3])
Cancer Other | Neoplasm Metastasis
Item
other current malignancy or metastatic malignancy of any kind.
boolean
C1707251 (UMLS CUI [1])
C0027627 (UMLS CUI [2])
Chemotherapy | Therapeutic radiology procedure | Cancer treatment
Item
ongoing chemotherapy, radiation therapy, or other cancer-related treatment.
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C0920425 (UMLS CUI [3])
Coumadin | Anticoagulants
Item
subjects on coumadin or other anticoagulants.
boolean
C0699129 (UMLS CUI [1])
C0003280 (UMLS CUI [2])
Breast implants
Item
subjects with breast implants.
boolean
C0179412 (UMLS CUI [1])
Therapeutic radiology procedure Both breasts | Bilateral mastectomy
Item
subjects who have had radiation to both breasts or who have undergone bilateral mastectomies.
boolean
C1522449 (UMLS CUI [1,1])
C0222605 (UMLS CUI [1,2])
C0191877 (UMLS CUI [2])
BARRIER Fine needle aspiration Sampling Fatty tissue of breast | BARRIER Fine needle aspiration Sampling Parenchymal Tissue Breast | Breast implants | Therapeutic radiology procedure Both breasts | Bilateral mastectomy | Fatty tissue of breast Insufficient Fine needle aspiration Sampling | Parenchymal Tissue Breast Insufficient Fine needle aspiration Sampling
Item
barriers to fine needle aspiration sampling of breast adipose tissue and/or parenchymal breast tissue, including breast implants, history of radiation to both breasts, bilateral mastectomies, and/or insufficient breast adipose/parenchymal tissue for adequate fine needle aspiration (fna) sampling.
boolean
C1706912 (UMLS CUI [1,1])
C1510483 (UMLS CUI [1,2])
C0441621 (UMLS CUI [1,3])
C1305788 (UMLS CUI [1,4])
C1706912 (UMLS CUI [2,1])
C1510483 (UMLS CUI [2,2])
C0441621 (UMLS CUI [2,3])
C4277702 (UMLS CUI [2,4])
C0006141 (UMLS CUI [2,5])
C0179412 (UMLS CUI [3])
C1522449 (UMLS CUI [4,1])
C0222605 (UMLS CUI [4,2])
C0191877 (UMLS CUI [5])
C1305788 (UMLS CUI [6,1])
C0231180 (UMLS CUI [6,2])
C1510483 (UMLS CUI [6,3])
C0441621 (UMLS CUI [6,4])
C4277702 (UMLS CUI [7,1])
C0006141 (UMLS CUI [7,2])
C0231180 (UMLS CUI [7,3])
C1510483 (UMLS CUI [7,4])
C0441621 (UMLS CUI [7,5])
Comorbidity Uncontrolled | Communicable Disease | Symptomatic congestive heart failure | Angina, Unstable | Cardiac Arrhythmia | Hypertensive disease | Mental disorders Limiting Protocol Compliance | Social situation Limiting Protocol Compliance
Item
uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, hypertension, or psychiatric illness/social situation that would limit compliance with study requirements.
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2])
C0742758 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C0003811 (UMLS CUI [5])
C0020538 (UMLS CUI [6])
C0004936 (UMLS CUI [7,1])
C0439801 (UMLS CUI [7,2])
C0525058 (UMLS CUI [7,3])
C0748872 (UMLS CUI [8,1])
C0439801 (UMLS CUI [8,2])
C0525058 (UMLS CUI [8,3])
Omega-3 Fatty Acids chronic | Supplements Interaction Omega-3 Fatty Acid Supplements
Item
chronic use of omega 3 fatty acid concentrates or capsules within the 3 months prior to entry on the study or any other supplements that might interact with omega 3 fatty acid supplements.
boolean
C0015689 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0242295 (UMLS CUI [2,1])
C0687133 (UMLS CUI [2,2])
C0015689 (UMLS CUI [2,3])
C0242295 (UMLS CUI [2,4])
Pregnancy | Breast Feeding
Item
pregnant or nursing women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Allergy to fish
Item
known sensitivity or allergy to fish.
boolean
C0856904 (UMLS CUI [1])
Aspirin Dose Full U/day | Anti-Inflammatory Agents, Non-Steroidal | Product Containing NSAIDs
Item
subjects on a standing regimen of full dose aspirin (greater than 325 mg/day), nsaids or nsaid-containing products.
boolean
C0004057 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0443225 (UMLS CUI [1,3])
C0456683 (UMLS CUI [1,4])
C0003211 (UMLS CUI [2])
C1514468 (UMLS CUI [3,1])
C0332256 (UMLS CUI [3,2])
C0003211 (UMLS CUI [3,3])