Eligibility Breast Cancer NCT00935558

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with histological proven metastatic or locally advanced er+/pgr+ breast cancer in progression after receiving 1. line endocrine therapy.
Description

Secondary malignant neoplasm of female breast Estrogen receptor positive Progressive | Secondary malignant neoplasm of female breast Progesterone receptor positive Progressive | Locally advanced breast cancer Estrogen receptor positive Progressive | Locally advanced breast cancer Progesterone receptor positive Progressive | Hormone Therapy First line

Data type

boolean

Alias
UMLS CUI [1,1]
C0346993
UMLS CUI [1,2]
C0279754
UMLS CUI [1,3]
C0205329
UMLS CUI [2,1]
C0346993
UMLS CUI [2,2]
C0279759
UMLS CUI [2,3]
C0205329
UMLS CUI [3,1]
C3495949
UMLS CUI [3,2]
C0279754
UMLS CUI [3,3]
C0205329
UMLS CUI [4,1]
C3495949
UMLS CUI [4,2]
C0279759
UMLS CUI [4,3]
C0205329
UMLS CUI [5,1]
C0279025
UMLS CUI [5,2]
C1708063
further inclusion criteria: p53+ tumour, ps≤1, postmenopausal. age >18, ps ≤ 1 and acceptable cbc and blood chemistry results
Description

Neoplasm Protein p53 Positive | performance status | Postmenopausal state | Age | Full blood count normal | Blood chemistry normal

Data type

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C0080055
UMLS CUI [1,3]
C1514241
UMLS CUI [2]
C1518965
UMLS CUI [3]
C0232970
UMLS CUI [4]
C0001779
UMLS CUI [5]
C0427692
UMLS CUI [6]
C0438257
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a history of any other neoplastic disease less than 5 years ago (excepting treated carcinoma in situ of the cervix and basal/squamous carcinoma of the skin)
Description

Neoplastic disease | Exception Carcinoma in situ of uterine cervix Treated | Exception Basal cell carcinoma Treated | Exception Squamous cell carcinoma of skin Treated

Data type

boolean

Alias
UMLS CUI [1]
C1882062
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0851140
UMLS CUI [2,3]
C1522326
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0007117
UMLS CUI [3,3]
C1522326
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0553723
UMLS CUI [4,3]
C1522326
patients with metastatic disease in the central nervous system
Description

CNS metastases

Data type

boolean

Alias
UMLS CUI [1]
C0686377
patients with other significant illness including severe allergy, asthma, dm, angina pectoris or congestive heart failure
Description

Illness | Severe allergy | Asthma | Diabetes Mellitus | Angina Pectoris | Congestive heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0221423
UMLS CUI [2]
C2945656
UMLS CUI [3]
C0004096
UMLS CUI [4]
C0011849
UMLS CUI [5]
C0002962
UMLS CUI [6]
C0018802
patients with acute or chronic infection including hiv, hepatitis og tb
Description

Communicable Disease | Chronic infectious disease | HIV Infection | Hepatitis | Tuberculosis

Data type

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0151317
UMLS CUI [3]
C0019693
UMLS CUI [4]
C0019158
UMLS CUI [5]
C0041296
patients who received antineoplastic therapy including chemotherapy, radiation, immunotherapy or other agents, less than 4 weeks before the beginning of the trial
Description

Antineoplastic Drug/Agent Therapy | Chemotherapy | Therapeutic radiology procedure | Immunotherapy | Pharmaceutical Preparations

Data type

boolean

Alias
UMLS CUI [1]
C2346834
UMLS CUI [2]
C0392920
UMLS CUI [3]
C1522449
UMLS CUI [4]
C0021083
UMLS CUI [5]
C0013227
patients who received corticosteroids or other immunosuppressive agents
Description

Adrenal Cortex Hormones | Immunosuppressive Agents

Data type

boolean

Alias
UMLS CUI [1]
C0001617
UMLS CUI [2]
C0021081
patients with active autoimmune diseases such as lupus erythematosus, rheumatoid arthritis or thyroiditis
Description

Autoimmune Diseases | Lupus Erythematosus | Rheumatoid Arthritis | Thyroiditis

Data type

boolean

Alias
UMLS CUI [1]
C0004364
UMLS CUI [2]
C0409974
UMLS CUI [3]
C0003873
UMLS CUI [4]
C0040147
severe hypercalcemia
Description

Hypercalcemia Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C0020437
UMLS CUI [1,2]
C0205082

Similar models

Eligibility Breast Cancer NCT00935558

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Secondary malignant neoplasm of female breast Estrogen receptor positive Progressive | Secondary malignant neoplasm of female breast Progesterone receptor positive Progressive | Locally advanced breast cancer Estrogen receptor positive Progressive | Locally advanced breast cancer Progesterone receptor positive Progressive | Hormone Therapy First line
Item
patients with histological proven metastatic or locally advanced er+/pgr+ breast cancer in progression after receiving 1. line endocrine therapy.
boolean
C0346993 (UMLS CUI [1,1])
C0279754 (UMLS CUI [1,2])
C0205329 (UMLS CUI [1,3])
C0346993 (UMLS CUI [2,1])
C0279759 (UMLS CUI [2,2])
C0205329 (UMLS CUI [2,3])
C3495949 (UMLS CUI [3,1])
C0279754 (UMLS CUI [3,2])
C0205329 (UMLS CUI [3,3])
C3495949 (UMLS CUI [4,1])
C0279759 (UMLS CUI [4,2])
C0205329 (UMLS CUI [4,3])
C0279025 (UMLS CUI [5,1])
C1708063 (UMLS CUI [5,2])
Neoplasm Protein p53 Positive | performance status | Postmenopausal state | Age | Full blood count normal | Blood chemistry normal
Item
further inclusion criteria: p53+ tumour, ps≤1, postmenopausal. age >18, ps ≤ 1 and acceptable cbc and blood chemistry results
boolean
C0027651 (UMLS CUI [1,1])
C0080055 (UMLS CUI [1,2])
C1514241 (UMLS CUI [1,3])
C1518965 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
C0001779 (UMLS CUI [4])
C0427692 (UMLS CUI [5])
C0438257 (UMLS CUI [6])
Item Group
C0680251 (UMLS CUI)
Neoplastic disease | Exception Carcinoma in situ of uterine cervix Treated | Exception Basal cell carcinoma Treated | Exception Squamous cell carcinoma of skin Treated
Item
patients with a history of any other neoplastic disease less than 5 years ago (excepting treated carcinoma in situ of the cervix and basal/squamous carcinoma of the skin)
boolean
C1882062 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0851140 (UMLS CUI [2,2])
C1522326 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0007117 (UMLS CUI [3,2])
C1522326 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0553723 (UMLS CUI [4,2])
C1522326 (UMLS CUI [4,3])
CNS metastases
Item
patients with metastatic disease in the central nervous system
boolean
C0686377 (UMLS CUI [1])
Illness | Severe allergy | Asthma | Diabetes Mellitus | Angina Pectoris | Congestive heart failure
Item
patients with other significant illness including severe allergy, asthma, dm, angina pectoris or congestive heart failure
boolean
C0221423 (UMLS CUI [1])
C2945656 (UMLS CUI [2])
C0004096 (UMLS CUI [3])
C0011849 (UMLS CUI [4])
C0002962 (UMLS CUI [5])
C0018802 (UMLS CUI [6])
Communicable Disease | Chronic infectious disease | HIV Infection | Hepatitis | Tuberculosis
Item
patients with acute or chronic infection including hiv, hepatitis og tb
boolean
C0009450 (UMLS CUI [1])
C0151317 (UMLS CUI [2])
C0019693 (UMLS CUI [3])
C0019158 (UMLS CUI [4])
C0041296 (UMLS CUI [5])
Antineoplastic Drug/Agent Therapy | Chemotherapy | Therapeutic radiology procedure | Immunotherapy | Pharmaceutical Preparations
Item
patients who received antineoplastic therapy including chemotherapy, radiation, immunotherapy or other agents, less than 4 weeks before the beginning of the trial
boolean
C2346834 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
C0021083 (UMLS CUI [4])
C0013227 (UMLS CUI [5])
Adrenal Cortex Hormones | Immunosuppressive Agents
Item
patients who received corticosteroids or other immunosuppressive agents
boolean
C0001617 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
Autoimmune Diseases | Lupus Erythematosus | Rheumatoid Arthritis | Thyroiditis
Item
patients with active autoimmune diseases such as lupus erythematosus, rheumatoid arthritis or thyroiditis
boolean
C0004364 (UMLS CUI [1])
C0409974 (UMLS CUI [2])
C0003873 (UMLS CUI [3])
C0040147 (UMLS CUI [4])
Hypercalcemia Severe
Item
severe hypercalcemia
boolean
C0020437 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])