Eligibility Breast Neoplasms NCT00386087

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
clinical diagnosis of metastatic breast cancer or recurrent breast cancer where surgery can not be done for curative intent
Descrizione

Secondary malignant neoplasm of female breast Inoperable Curative | Breast cancer recurrent Inoperable Curative

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0346993
UMLS CUI [1,2]
C0205187
UMLS CUI [1,3]
C1276305
UMLS CUI [2,1]
C0278493
UMLS CUI [2,2]
C0205187
UMLS CUI [2,3]
C1276305
have received prior therapy with an anthracycline (class of drugs) and a taxane (class of drugs).
Descrizione

Anthracyclines Class of Trial Agent | taxane Class of Trial Agent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0282564
UMLS CUI [1,2]
C2983595
UMLS CUI [2,1]
C0215136
UMLS CUI [2,2]
C2983595
tumors must not be positive for her2, but if positive, the treatment plan should not include further treatment with the drug herceptin.
Descrizione

HER2-positive carcinoma of breast Herceptin Excluded

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1960398
UMLS CUI [1,2]
C0338204
UMLS CUI [1,3]
C2828389
disease that can be definitely measured on cat scans or other radiological tests.
Descrizione

Measurable Disease X-Ray Computed Tomography | Radiology test

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C0040405
UMLS CUI [2]
C0807679
may have received high dose chemotherapy for autologous stem cell support greater than or equal to 6 months of starting this study.
Descrizione

High-Dose Chemotherapy with Autologous Stem Cell Transplant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1512429
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
more than 2 chemotherapy regimens for metastatic or locally recurrent disease.
Descrizione

Chemotherapy Regimen Quantity Neoplasm Metastasis | Chemotherapy Regimen Quantity Recurrent disease Local

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0027627
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0277556
UMLS CUI [2,4]
C0205276
have brain cancer from breast cancer
Descrizione

Malignant neoplasm of brain Due to Breast Carcinoma

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0153633
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0678222
pregnant or breastfeeding
Descrizione

Pregnancy | Breast Feeding

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
have an inability to swallow tablets
Descrizione

Able to swallow Tablets

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2712086
UMLS CUI [1,2]
C0039225
within 6 months have had a serious heart condition
Descrizione

Heart condition Serious

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3842523
UMLS CUI [1,2]
C0205404

Similar models

Eligibility Breast Neoplasms NCT00386087

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Secondary malignant neoplasm of female breast Inoperable Curative | Breast cancer recurrent Inoperable Curative
Item
clinical diagnosis of metastatic breast cancer or recurrent breast cancer where surgery can not be done for curative intent
boolean
C0346993 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C1276305 (UMLS CUI [1,3])
C0278493 (UMLS CUI [2,1])
C0205187 (UMLS CUI [2,2])
C1276305 (UMLS CUI [2,3])
Anthracyclines Class of Trial Agent | taxane Class of Trial Agent
Item
have received prior therapy with an anthracycline (class of drugs) and a taxane (class of drugs).
boolean
C0282564 (UMLS CUI [1,1])
C2983595 (UMLS CUI [1,2])
C0215136 (UMLS CUI [2,1])
C2983595 (UMLS CUI [2,2])
HER2-positive carcinoma of breast Herceptin Excluded
Item
tumors must not be positive for her2, but if positive, the treatment plan should not include further treatment with the drug herceptin.
boolean
C1960398 (UMLS CUI [1,1])
C0338204 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
Measurable Disease X-Ray Computed Tomography | Radiology test
Item
disease that can be definitely measured on cat scans or other radiological tests.
boolean
C1513041 (UMLS CUI [1,1])
C0040405 (UMLS CUI [1,2])
C0807679 (UMLS CUI [2])
High-Dose Chemotherapy with Autologous Stem Cell Transplant
Item
may have received high dose chemotherapy for autologous stem cell support greater than or equal to 6 months of starting this study.
boolean
C1512429 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Chemotherapy Regimen Quantity Neoplasm Metastasis | Chemotherapy Regimen Quantity Recurrent disease Local
Item
more than 2 chemotherapy regimens for metastatic or locally recurrent disease.
boolean
C0392920 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0027627 (UMLS CUI [1,3])
C0392920 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0277556 (UMLS CUI [2,3])
C0205276 (UMLS CUI [2,4])
Malignant neoplasm of brain Due to Breast Carcinoma
Item
have brain cancer from breast cancer
boolean
C0153633 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Able to swallow Tablets
Item
have an inability to swallow tablets
boolean
C2712086 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Heart condition Serious
Item
within 6 months have had a serious heart condition
boolean
C3842523 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])