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Eligibility Breast Cancer NCT00191243

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically verified diagnosis of breast carcinoma, at first diagnosis
Description

ID.1

Data type

boolean

Alias
UMLS CUI [1,1]
C0019638
UMLS CUI [1,2]
C0678222
restricted previous adjuvant chemotherapy (completed >6 months prior the study)
Description

ID.2

Data type

boolean

Alias
UMLS CUI [1]
C0085533
measurable and/or non-measurable disease
Description

ID.3

Data type

boolean

Alias
UMLS CUI [1]
C1513041
previous radiotherapy is allowed if:terminated at least 10 days prior the sudy therapy, at least one target lesion for evaluation of tumor response has not been irradiated
Description

ID.4

Data type

boolean

Alias
UMLS CUI [1]
C1522449
performance status 0-2 (who, zubrod)
Description

ID.5

Data type

boolean

Alias
UMLS CUI [1]
C1520224
adequate bone marrow reserve defined
Description

ID.6

Data type

boolean

Alias
UMLS CUI [1]
C0005956
adequate liver / renal functions defined
Description

ID.7

Data type

boolean

Alias
UMLS CUI [1]
C0023895|C0022658
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any prior systematic chemotherapy for metastatic breast cancer
Description

ID.8

Data type

boolean

Alias
UMLS CUI [1]
C1514457
expected survival time less than 12 weeks
Description

ID.9

Data type

boolean

Alias
UMLS CUI [1]
C0023671
past or current history of malignant neoplasm other than breast carcinoma
Description

ID.10

Data type

boolean

Alias
UMLS CUI [1]
C0085183
except for cured non-melanoma skin cancer or curatively treated in situ carcinoma of the cervix uteri
Description

ID.11

Data type

boolean

Alias
UMLS CUI [1,1]
C1880198
UMLS CUI [1,2]
C0037286|C0851140
known brain metastases/leptomeningeal involvement
Description

ID.12

Data type

boolean

Alias
UMLS CUI [1]
C0220650
active uncontrolled infection
Description

ID.13

Data type

boolean

Alias
UMLS CUI [1]
C3714514
symptomatic peripheral neuropathy > grade 2 according to nci
Description

ID.14

Data type

boolean

Alias
UMLS CUI [1]
C0031117
patients whose lesions are assessable only by radionuclide scan or patients with sclerotic bone lesions as the only site of disease
Description

ID.15

Data type

boolean

Alias
UMLS CUI [1,1]
C0032743|C0748541
UMLS CUI [1,2]
C0748541
concomitant illness that is contraindication to the use of corticosteroids
Description

ID.16

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0038317
other concomitant serious illness or medical condition, which may worsen due to the treatment
Description

ID.17

Data type

boolean

Alias
UMLS CUI [1]
C0009488
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Similar models

Eligibility Breast Cancer NCT00191243

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
histologically verified diagnosis of breast carcinoma, at first diagnosis
boolean
C0019638 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
ID.2
Item
restricted previous adjuvant chemotherapy (completed >6 months prior the study)
boolean
C0085533 (UMLS CUI [1])
ID.3
Item
measurable and/or non-measurable disease
boolean
C1513041 (UMLS CUI [1])
ID.4
Item
previous radiotherapy is allowed if:terminated at least 10 days prior the sudy therapy, at least one target lesion for evaluation of tumor response has not been irradiated
boolean
C1522449 (UMLS CUI [1])
ID.5
Item
performance status 0-2 (who, zubrod)
boolean
C1520224 (UMLS CUI [1])
ID.6
Item
adequate bone marrow reserve defined
boolean
C0005956 (UMLS CUI [1])
ID.7
Item
adequate liver / renal functions defined
boolean
C0023895|C0022658 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.8
Item
any prior systematic chemotherapy for metastatic breast cancer
boolean
C1514457 (UMLS CUI [1])
ID.9
Item
expected survival time less than 12 weeks
boolean
C0023671 (UMLS CUI [1])
ID.10
Item
past or current history of malignant neoplasm other than breast carcinoma
boolean
C0085183 (UMLS CUI [1])
ID.11
Item
except for cured non-melanoma skin cancer or curatively treated in situ carcinoma of the cervix uteri
boolean
C1880198 (UMLS CUI [1,1])
C0037286|C0851140 (UMLS CUI [1,2])
ID.12
Item
known brain metastases/leptomeningeal involvement
boolean
C0220650 (UMLS CUI [1])
ID.13
Item
active uncontrolled infection
boolean
C3714514 (UMLS CUI [1])
ID.14
Item
symptomatic peripheral neuropathy > grade 2 according to nci
boolean
C0031117 (UMLS CUI [1])
ID.15
Item
patients whose lesions are assessable only by radionuclide scan or patients with sclerotic bone lesions as the only site of disease
boolean
C0032743|C0748541 (UMLS CUI [1,1])
C0748541 (UMLS CUI [1,2])
ID.16
Item
concomitant illness that is contraindication to the use of corticosteroids
boolean
C1301624 (UMLS CUI [1,1])
C0038317 (UMLS CUI [1,2])
ID.17
Item
other concomitant serious illness or medical condition, which may worsen due to the treatment
boolean
C0009488 (UMLS CUI [1])
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