Informações:
Falhas:
ID
19583
Descrição
A Study of Avastin (Bevacizumab) in Women With HER2 Negative Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00333775
Link
https://clinicaltrials.gov/show/NCT00333775
Palavras-chave
Versões (1)
- 12/01/2017 12/01/2017 -
Transferido a
12 de janeiro de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00333775
Eligibility Breast Cancer NCT00333775
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00333775
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Gender | Age
Item
female patients >= 18 years of age;
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Human epidermal growth factor 2 negative carcinoma of breast | Recurrent disease Locally | Neoplasm Metastasis Chemotherapy suitable
Item
her2 negative cancer of the breast with locally recurrent or metastatic disease, suitable for chemotherapy;
boolean
C2316304 (UMLS CUI [1])
C0277556 (UMLS CUI [2,1])
C1517927 (UMLS CUI [2,2])
C0027627 (UMLS CUI [3,1])
C0392920 (UMLS CUI [3,2])
C3900053 (UMLS CUI [3,3])
C0277556 (UMLS CUI [2,1])
C1517927 (UMLS CUI [2,2])
C0027627 (UMLS CUI [3,1])
C0392920 (UMLS CUI [3,2])
C3900053 (UMLS CUI [3,3])
Chemotherapy, Adjuvant | Chemotherapy Taxane Based
Item
no adjuvant chemotherapy within 6 months before randomization, and no taxane-based chemotherapy within 12 months before randomization;
boolean
C0085533 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C0215136 (UMLS CUI [2,2])
C1705938 (UMLS CUI [2,3])
C0392920 (UMLS CUI [2,1])
C0215136 (UMLS CUI [2,2])
C1705938 (UMLS CUI [2,3])
ECOG performance status
Item
ecog performance status 0-1.
boolean
C1520224 (UMLS CUI [1])
Chemotherapy Secondary malignant neoplasm of female breast | Chemotherapy Breast cancer recurrent Locally
Item
previous chemotherapy for metastatic or locally recurrent breast cancer;
boolean
C0392920 (UMLS CUI [1,1])
C0346993 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0278493 (UMLS CUI [2,2])
C1517927 (UMLS CUI [2,3])
C0346993 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0278493 (UMLS CUI [2,2])
C1517927 (UMLS CUI [2,3])
Therapeutic radiology procedure Neoplasm Metastasis
Item
radiotherapy for treatment of metastatic disease;
boolean
C1522449 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
C0027627 (UMLS CUI [1,2])
primary tumor | Basal cell carcinoma Limited Controlled | Squamous cell carcinoma of skin Limited Controlled | Carcinoma in situ of uterine cervix
Item
other primary tumors within last 5 years, except for controlled limited basal cell or squamous cancer of the skin, or cancer in situ of the cervix;
boolean
C0677930 (UMLS CUI [1])
C0007117 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C2587213 (UMLS CUI [2,3])
C0553723 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
C2587213 (UMLS CUI [3,3])
C0851140 (UMLS CUI [4])
C0007117 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C2587213 (UMLS CUI [2,3])
C0553723 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
C2587213 (UMLS CUI [3,3])
C0851140 (UMLS CUI [4])
Compression of spinal cord | Metastatic malignant neoplasm to brain
Item
spinal cord compression or brain metastases;
boolean
C0037926 (UMLS CUI [1])
C0220650 (UMLS CUI [2])
C0220650 (UMLS CUI [2])
major surgery | open biopsy | Traumatic injury Significant
Item
major surgical procedure, open biopsy or significant traumatic injury within 28 days prior to randomization;
boolean
C0679637 (UMLS CUI [1])
C0184922 (UMLS CUI [2])
C3263723 (UMLS CUI [3,1])
C0750502 (UMLS CUI [3,2])
C0184922 (UMLS CUI [2])
C3263723 (UMLS CUI [3,1])
C0750502 (UMLS CUI [3,2])
Bone Marrow function | Liver function | Renal function
Item
inadequate bone marrow, liver or renal function;
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Uncontrolled hypertension
Item
uncontrolled hypertension.
boolean
C1868885 (UMLS CUI [1])