Breast Carcinoma Patients | Group experimental
Item
inclusion criteria for breast cancer patients for experimental group:
boolean
C0678222 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0441833 (UMLS CUI [2,1])
C1517586 (UMLS CUI [2,2])
Age
Item
1. patient is over the age of 40.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
2. patient is willing to participate as evidenced by signing the written informed consent form.
boolean
C0021430 (UMLS CUI [1])
Referral for Breast Carcinoma Surgery | Mammography | Tumor Markers Blood | Ultrasonography, Mammary | CT of breast | Biopsy of breast
Item
3. patient referred to the department of oncology/ surgery for operative treatment of breast cancer with previously detected disease. positive conventional tests finding can include (but not limited to) the record of screening or diagnostic mammography, blood oncomarkers, breast ultrasound, breast ct, biopsy.
boolean
C2585524 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,3])
C0024671 (UMLS CUI [2])
C0041365 (UMLS CUI [3,1])
C0005767 (UMLS CUI [3,2])
C0080264 (UMLS CUI [4])
C0412609 (UMLS CUI [5])
C0405352 (UMLS CUI [6])
Patients untreated | Chemotherapy Absent | Pharmaceutical Preparations Hormonal Absent | Therapeutic radiology procedure Absent
Item
4. non-treated patients (w/o previous chemotherapy, hormonal drugs and radiotherapy).
boolean
C0030705 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0013227 (UMLS CUI [3,1])
C0458083 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C1522449 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Cancer Other Location Absent
Item
5. patient without other cancer locations
boolean
C1707251 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Healthy Volunteers Control Group
Item
inclusion criteria for presumably healthy subjects for control group:
boolean
C1708335 (UMLS CUI [1,1])
C0009932 (UMLS CUI [1,2])
Age
Item
1. subjects over the age of 40.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
2. subjects who are willing to participate as evidenced by signing the written informed consent form.
boolean
C0021430 (UMLS CUI [1])
Absence Symptoms Breast Diseases | Family history of breast cancer Absent | Breast Disease out ruling
Item
3. subjects who are presumably healthy and without breast pathologies' symptoms and family history of breast cancer, i.e., breast disease (except history of functional breast problems, e.g., mastitis within lactation period) has been ruled out based on physician anamnesis
boolean
C0332197 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0006145 (UMLS CUI [1,3])
C0559119 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0006145 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
Screening mammography Result Negative
Item
4. subjects with negative results of screening mammography.
boolean
C0203028 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C1513916 (UMLS CUI [1,3])
Pharmaceutical Preparations Hormonal Absent
Item
5. subjects without taking of any hormonal medicines
boolean
C0013227 (UMLS CUI [1,1])
C0458083 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Cancer Other Organ Internal
Item
1. subjects with any known cancer in other internal organs or systems.
boolean
C1707251 (UMLS CUI [1,1])
C0178784 (UMLS CUI [1,2])
C0205102 (UMLS CUI [1,3])
High fever
Item
2. subjects with high fever presentation (more than 38.5).
boolean
C0743973 (UMLS CUI [1])
Therapy Breast Disease
Item
3. subjects with known breast disease undergoing treatment for the disease.
boolean
C0087111 (UMLS CUI [1,1])
C0006145 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
4. pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])