Inclusion criteria Fulfill
Item
patients must meet all of the following inclusion criteria to be eligible for enrolment into the trial:
boolean
C1512693 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Invasive carcinoma of breast TNM clinical staging
Item
1. histologically or cytologically proven diagnosis of invasive breast cancer (stage i-iii).
boolean
C0853879 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
BRCA1 Germ-Line Mutation
Item
2. documentation of the presence of a germ-line brca1 mutation
boolean
C0376571 (UMLS CUI [1,1])
C0206530 (UMLS CUI [1,2])
Measurable Disease Size Mammography | Measurable Disease Size Ultrasonography
Item
3. measurable disease of any size by mammography or ultrasound.
boolean
C1513041 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
C0024671 (UMLS CUI [1,3])
C1513041 (UMLS CUI [2,1])
C0456389 (UMLS CUI [2,2])
C0041618 (UMLS CUI [2,3])
Gender | Breast Carcinoma | Age
Item
4. female diagnosed with breast cancer between the ages of 20 to 70.
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
ECOG performance status
Item
5. eastern cooperative oncology group [ecog] performance status of 0 and 1.
boolean
C1520224 (UMLS CUI [1])
Liver function | Bone Marrow function | Renal function
Item
6. evidence of adequate organ function (liver, bone marrow, kidney)
boolean
C0232741 (UMLS CUI [1])
C0005953 (UMLS CUI [2,1])
C0031843 (UMLS CUI [2,2])
C0232804 (UMLS CUI [3])
Informed Consent | Informed Consent Patient Representative
Item
7. signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrolment.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
Protocol Compliance
Item
8. willingness and ability to comply with scheduled visits, treatment plans laboratory tests, and other study procedures.
boolean
C0525058 (UMLS CUI [1])
Resident Polish
Item
9. polish resident.
boolean
C2347958 (UMLS CUI [1,1])
C0220896 (UMLS CUI [1,2])
Exclusion Criteria Fulfill
Item
patients presenting with any of the following will not be included in the trial:
boolean
C0680251 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Prior Chemotherapy Malignant Neoplasms
Item
1. previous chemotherapy for current cancer.
boolean
C1514457 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
Malignant Neoplasms | Exception Basal cell carcinoma Treated | Exception Squamous cell carcinoma of skin Treated | Exception Carcinoma in situ of uterine cervix Treated
Item
2. previous or current diagnosis of any other malignancy except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix.
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])
C1522326 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0553723 (UMLS CUI [3,2])
C1522326 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0851140 (UMLS CUI [4,2])
C1522326 (UMLS CUI [4,3])
Pharmaceutical Preparations Affecting Renal function
Item
3. receiving any medication that may markedly affect renal function.
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
4. pregnant or breastfeeding women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Comorbidity Uncontrolled Protocol Compliance Limited | Communicable Diseases | Symptomatic congestive heart failure | Angina, Unstable | Cardiac Arrhythmia | Mental disorders
Item
5. uncontrolled inter-current illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness that would limit compliance with study requirements.
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,4])
C0009450 (UMLS CUI [2])
C0742758 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C0003811 (UMLS CUI [5])
C0004936 (UMLS CUI [6])