ID.1
Item
to be included in this study, you must meet the following criteria:
boolean
Breast Carcinoma
Item
histologically proven breast cancer
boolean
C0678222 (UMLS CUI [1])
Gender | Age
Item
females, age greater than 18 years
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Performance of activities of daily living Ability | Assistance Minimal
Item
ability to perform activites of daily living with minimal assistance
boolean
C1821398 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
C0557034 (UMLS CUI [2,1])
C0547040 (UMLS CUI [2,2])
Cardiac function
Item
normal cardiac function
boolean
C0232164 (UMLS CUI [1])
Bone Marrow function | Liver function | Normal renal function
Item
adequate bone marrow, liver and kidney
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232805 (UMLS CUI [3])
Informed consent
Item
signed informed consent prior to beginning specific protocol procedures
boolean
C0021430 (UMLS CUI [1])
Study Subject Participation Status
Item
you cannot participate in this study if any of the following apply to you:
boolean
C2348568 (UMLS CUI [1])
cancer treatment Systemic Breast Carcinoma
Item
prior systemic anticancer therapy for breast cancer
boolean
C0920425 (UMLS CUI [1,1])
C0205373 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
Anthracyclines Chemotherapy Malignant Neoplasms | Taxanes Chemotherapy Malignant Neoplasms
Item
prior anthracycline or taxane based chemotherapy for any malignancy
boolean
C0282564 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
C0796419 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C0006826 (UMLS CUI [2,3])
Pregnancy | Breast Feeding
Item
pregnant or breast-feeding women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Toxicity Motor nerve Moderate to severe Pre-existing | Toxicity Sensory nerve Moderate to severe Pre-existing
Item
pre-existing moderate to severe motor or sensory neurotoxicity
boolean
C0600688 (UMLS CUI [1,1])
C0501384 (UMLS CUI [1,2])
C1299393 (UMLS CUI [1,3])
C2347662 (UMLS CUI [1,4])
C0600688 (UMLS CUI [2,1])
C0501385 (UMLS CUI [2,2])
C1299393 (UMLS CUI [2,3])
C2347662 (UMLS CUI [2,4])
Illness Serious | Other medical condition Serious
Item
other serious illness or medical condition
boolean
C0221423 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
criteria Additional | Study Subject Participation Status
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
boolean
C0243161 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2])