ID

20108

Description

Positron Emission Tomography (PET) Using Hormone Receptor Ligands in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00647790

Link

https://clinicaltrials.gov/show/NCT00647790

Keywords

Versions (1)
  1. 2/6/17 2/6/17 -
Uploaded on

February 6, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00647790

English

Eligibility Breast Cancer NCT00647790

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female patients
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
aged 18 or older at the time of breast cancer diagnosis
Description

Age at diagnosis

Data type

boolean

Alias
UMLS CUI [1]
C1828181
patients with invasive breast cancer at least 1 cm in size. patients who have had a prior surgical excision are eligible provided there is a residual of at least a 1 cm area suspected on imaging studies.
Description

Invasive breast cancer or surgical excision

Data type

boolean

Alias
UMLS CUI [1]
C0853879
UMLS CUI [2]
C0728940
histopathologic review at mskcc confirming diagnosis of invasive breast cancer (ductal, lobular, or inflammatory breast cancer).
Description

Histopathologic confirmed diagnosis of invasive breast cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0677043
UMLS CUI [1,2]
C0853879
patients who are operative candidates. patient will have surgery to include either mastectomy or lumpectomy. radiologic assisted excisions such as needle localization are also eligible.
Description

Operative candidates

Data type

boolean

Alias
UMLS CUI [1,1]
C1882154
UMLS CUI [1,2]
C1518601
patients with bilateral breast cancer are eligible.
Description

Bilateral breast cancer

Data type

boolean

Alias
UMLS CUI [1]
C0281267
patients with metastatic cancer, provided they need surgical biopsy.
Description

Metastatic cancer

Data type

boolean

Alias
UMLS CUI [1]
C0027627
patients who are undergoing sentinel node mapping (day before or sameday mapping).
Description

Sentinel node mapping

Data type

boolean

Alias
UMLS CUI [1]
C1519247
patient must sign informed consent.
Description

Informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous or concurrent malignancy (except basal and squamous skin cancer and stage 0 cervical cancer)
Description

Previous or concurrent malignancy

Data type

boolean

Alias
UMLS CUI [1]
C0006826
patients who are pregnant or nursing
Description

Gynaecological status

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients unable to tolerate pet or pet/ct
Description

PET

Data type

boolean

Alias
UMLS CUI [1]
C0032743
patients with known active infection, autoimmune or inflammatory disease such as sarcoidosis, and rheumatoid arthritis.
Description

Active infection, autoimmune or inflammatory disease

Data type

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0004364
UMLS CUI [3]
C1290884
patients with non invasive breast cancer such as dcis.
Description

Non invasive breast cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0205303
UMLS CUI [1,2]
C0006142
patients who have received prior radiation therapy to the affected breast.
Description

Prior radiation therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0332152
patients who have received prior chemotherapy, including neoadjuvant chemotherapy or hormonal therapy for breast cancer.
Description

Prior chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1514457
patients living in a residential care or correctional facility.
Description

Domestic setting

Data type

boolean

Alias
UMLS CUI [1]
C0442519
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Similar models

Eligibility Breast Cancer NCT00647790

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
male and female patients
boolean
C0079399 (UMLS CUI [1])
Age at diagnosis
Item
aged 18 or older at the time of breast cancer diagnosis
boolean
C1828181 (UMLS CUI [1])
Invasive breast cancer or surgical excision
Item
patients with invasive breast cancer at least 1 cm in size. patients who have had a prior surgical excision are eligible provided there is a residual of at least a 1 cm area suspected on imaging studies.
boolean
C0853879 (UMLS CUI [1])
C0728940 (UMLS CUI [2])
Histopathologic confirmed diagnosis of invasive breast cancer
Item
histopathologic review at mskcc confirming diagnosis of invasive breast cancer (ductal, lobular, or inflammatory breast cancer).
boolean
C0677043 (UMLS CUI [1,1])
C0853879 (UMLS CUI [1,2])
Operative candidates
Item
patients who are operative candidates. patient will have surgery to include either mastectomy or lumpectomy. radiologic assisted excisions such as needle localization are also eligible.
boolean
C1882154 (UMLS CUI [1,1])
C1518601 (UMLS CUI [1,2])
Bilateral breast cancer
Item
patients with bilateral breast cancer are eligible.
boolean
C0281267 (UMLS CUI [1])
Metastatic cancer
Item
patients with metastatic cancer, provided they need surgical biopsy.
boolean
C0027627 (UMLS CUI [1])
Sentinel node mapping
Item
patients who are undergoing sentinel node mapping (day before or sameday mapping).
boolean
C1519247 (UMLS CUI [1])
Informed consent
Item
patient must sign informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Previous or concurrent malignancy
Item
previous or concurrent malignancy (except basal and squamous skin cancer and stage 0 cervical cancer)
boolean
C0006826 (UMLS CUI [1])
Gynaecological status
Item
patients who are pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
PET
Item
patients unable to tolerate pet or pet/ct
boolean
C0032743 (UMLS CUI [1])
Active infection, autoimmune or inflammatory disease
Item
patients with known active infection, autoimmune or inflammatory disease such as sarcoidosis, and rheumatoid arthritis.
boolean
C0009450 (UMLS CUI [1])
C0004364 (UMLS CUI [2])
C1290884 (UMLS CUI [3])
Non invasive breast cancer
Item
patients with non invasive breast cancer such as dcis.
boolean
C0205303 (UMLS CUI [1,1])
C0006142 (UMLS CUI [1,2])
Prior radiation therapy
Item
patients who have received prior radiation therapy to the affected breast.
boolean
C1522449 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
Prior chemotherapy
Item
patients who have received prior chemotherapy, including neoadjuvant chemotherapy or hormonal therapy for breast cancer.
boolean
C1514457 (UMLS CUI [1])
Domestic setting
Item
patients living in a residential care or correctional facility.
boolean
C0442519 (UMLS CUI [1])
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