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Eligibility Breast Cancer NCT01674842

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
primary tumor is triple negative breast cancer
Description

Primary tumor | Triple Negative Breast Neoplasm

Data type

boolean

Alias
UMLS CUI [1]
C0677930
UMLS CUI [2]
C3539878
breast-conserving surgery or mastectomy with surgical excision of all gross disease with negative surgical margins
Description

Breast-Conserving Surgery | Mastectomy | Excision Disease Gross | Negative Surgical Margin

Data type

boolean

Alias
UMLS CUI [1]
C0917927
UMLS CUI [2]
C0024881
UMLS CUI [3,1]
C0728940
UMLS CUI [3,2]
C0012634
UMLS CUI [3,3]
C0439806
UMLS CUI [4]
C1709157
pathologic or clinical stage ii or iii disease
Description

Disease Pathologic TNM stage | Disease TNM Breast tumor staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1319019
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0474926
at least 3 week interval from last chemotherapy administration/breast surgery to radiation (no more than 8 weeks)
Description

Interval | Chemotherapy | Operation on breast | Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1]
C1272706
UMLS CUI [2]
C0392920
UMLS CUI [3]
C3714726
UMLS CUI [4]
C1522449
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or breastfeeding
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
prior radiation to breast or ipsilateral regional nodes
Description

Irradiation of breast Previous | Irradiation of lymph nodes regional ipsilateral previous

Data type

boolean

Alias
UMLS CUI [1,1]
C2148528
UMLS CUI [1,2]
C0205156
UMLS CUI [2,1]
C2169077
UMLS CUI [2,2]
C0205147
UMLS CUI [2,3]
C0441989
UMLS CUI [2,4]
C0205156
ongoing therapy with other investigational agents
Description

Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C0013230
hormonal therapy
Description

Hormone Therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279025
significant co-morbidity
Description

Comorbidity Significant

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0750502
pathologic complete response following preoperative chemotherapy
Description

Pathologic Complete Response Following Preoperative Chemotherapy

Data type

boolean

Alias
UMLS CUI [1,1]
C4050242
UMLS CUI [1,2]
C0332282
UMLS CUI [1,3]
C2347669
biopsy proven metastatic disease
Description

Neoplasm Metastasis

Data type

boolean

Alias
UMLS CUI [1]
C0027627
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Similar models

Eligibility Breast Cancer NCT01674842

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Primary tumor | Triple Negative Breast Neoplasm
Item
primary tumor is triple negative breast cancer
boolean
C0677930 (UMLS CUI [1])
C3539878 (UMLS CUI [2])
Breast-Conserving Surgery | Mastectomy | Excision Disease Gross | Negative Surgical Margin
Item
breast-conserving surgery or mastectomy with surgical excision of all gross disease with negative surgical margins
boolean
C0917927 (UMLS CUI [1])
C0024881 (UMLS CUI [2])
C0728940 (UMLS CUI [3,1])
C0012634 (UMLS CUI [3,2])
C0439806 (UMLS CUI [3,3])
C1709157 (UMLS CUI [4])
Disease Pathologic TNM stage | Disease TNM Breast tumor staging
Item
pathologic or clinical stage ii or iii disease
boolean
C0012634 (UMLS CUI [1,1])
C1319019 (UMLS CUI [1,2])
C0012634 (UMLS CUI [2,1])
C0474926 (UMLS CUI [2,2])
Interval | Chemotherapy | Operation on breast | Therapeutic radiology procedure
Item
at least 3 week interval from last chemotherapy administration/breast surgery to radiation (no more than 8 weeks)
boolean
C1272706 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C3714726 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Irradiation of breast Previous | Irradiation of lymph nodes regional ipsilateral previous
Item
prior radiation to breast or ipsilateral regional nodes
boolean
C2148528 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C2169077 (UMLS CUI [2,1])
C0205147 (UMLS CUI [2,2])
C0441989 (UMLS CUI [2,3])
C0205156 (UMLS CUI [2,4])
Investigational New Drugs
Item
ongoing therapy with other investigational agents
boolean
C0013230 (UMLS CUI [1])
Hormone Therapy
Item
hormonal therapy
boolean
C0279025 (UMLS CUI [1])
Comorbidity Significant
Item
significant co-morbidity
boolean
C0009488 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Pathologic Complete Response Following Preoperative Chemotherapy
Item
pathologic complete response following preoperative chemotherapy
boolean
C4050242 (UMLS CUI [1,1])
C0332282 (UMLS CUI [1,2])
C2347669 (UMLS CUI [1,3])
Neoplasm Metastasis
Item
biopsy proven metastatic disease
boolean
C0027627 (UMLS CUI [1])
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