ID

20108

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT00647790

Keywords

versioni (1)
  1. 06/02/17 06/02/17 -
Caricato su

6 febbraio 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00647790

Inglese

Eligibility Breast Cancer NCT00647790

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female patients
Descrizione

Gender

Tipo di dati

boolean

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

Age at diagnosis

Tipo di dati

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.
Descrizione

Invasive breast cancer or surgical excision

Tipo di dati

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).
Descrizione

Histopathologic confirmed diagnosis of invasive breast cancer

Tipo di dati

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.
Descrizione

Operative candidates

Tipo di dati

boolean

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

Bilateral breast cancer

Tipo di dati

boolean

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

Metastatic cancer

Tipo di dati

boolean

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

Sentinel node mapping

Tipo di dati

boolean

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

Informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

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

Previous or concurrent malignancy

Tipo di dati

boolean

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

Gynaecological status

Tipo di dati

boolean

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

PET

Tipo di dati

boolean

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

Active infection, autoimmune or inflammatory disease

Tipo di dati

boolean

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

Non invasive breast cancer

Tipo di dati

boolean

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

Prior radiation therapy

Tipo di dati

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.
Descrizione

Prior chemotherapy

Tipo di dati

boolean

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

Domestic setting

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0442519
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Similar models

Eligibility Breast Cancer NCT00647790

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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