ID

37931

Descrição

Patterns of Care in Hormone-receptor Positive, Advanced Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01277926

Link

https://clinicaltrials.gov/show/NCT01277926

Palavras-chave

  1. 01/09/2019 01/09/2019 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

1 de setembro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01277926

Eligibility Breast Cancer NCT01277926

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
histological or cytological diagnosis of breast cancer
Descrição

Breast Carcinoma

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0678222
postmenopausal status at the time of enrolment, according to the following definitions:
Descrição

Postmenopausal state

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0232970
history of bilateral oophorectomy at any age
Descrição

Bilateral oophorectomy | Age Any

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0278321
UMLS CUI [2,1]
C0001779
UMLS CUI [2,2]
C1552551
proven hormonal menopause
Descrição

Menopause present

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0567312
positive estrogen receptor (er) and/or progesterone receptor (pr) by immuno
Descrição

Estrogen receptor positive Immunohistochemistry | Progesterone receptor positive Immunohistochemistry

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0279754
UMLS CUI [1,2]
C0021044
UMLS CUI [2,1]
C0279759
UMLS CUI [2,2]
C0021044
failure of one previous endocrine therapy in the adjuvant or metastatic setting
Descrição

Hormone Therapy Quantity failed | Adjuvant therapy | Neoplasm Metastasis

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0231175
UMLS CUI [2]
C0677850
UMLS CUI [3]
C0027627
use of no more than one previous chemotherapy regimen in the neoadjuvant or adjuvant setting
Descrição

Prior Chemotherapy Quantity | Neoadjuvant Therapy | Adjuvant therapy

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C1265611
UMLS CUI [2]
C0600558
UMLS CUI [3]
C0677850
indication to receive chemotherapy or endocrine therapy
Descrição

Indication Chemotherapy | Indication Hormone Therapy

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0392920
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0279025
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
inability to comply with the study protocol
Descrição

Protocol Compliance Unable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
use of more than one previous endocrine therapy, regardless of the setting; --
Descrição

Prior Hormone Therapy Quantity

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1514460
UMLS CUI [1,2]
C1265611
previous use of chemotherapy for metastatic disease
Descrição

Prior Chemotherapy Neoplasm Metastasis

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0027627
use of neoadjuvant endocrine therapy as the only previous type of endocrine therapy
Descrição

Neoadjuvant Hormone Therapy

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C0279025
serious medical, surgical or psychiatric comorbidity that, upon investigator's discretion, should preclude participation in the study.
Descrição

Comorbidity Serious | Operative Surgical Procedure Serious | Serious mental illness | Study Subject Participation Status Excluded

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205404
UMLS CUI [2,1]
C0543467
UMLS CUI [2,2]
C0205404
UMLS CUI [3]
C3841614
UMLS CUI [4,1]
C2348568
UMLS CUI [4,2]
C0332196

Similar models

Eligibility Breast Cancer NCT01277926

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma
Item
histological or cytological diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
Postmenopausal state
Item
postmenopausal status at the time of enrolment, according to the following definitions:
boolean
C0232970 (UMLS CUI [1])
Bilateral oophorectomy | Age Any
Item
history of bilateral oophorectomy at any age
boolean
C0278321 (UMLS CUI [1])
C0001779 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
Menopause present
Item
proven hormonal menopause
boolean
C0567312 (UMLS CUI [1])
Estrogen receptor positive Immunohistochemistry | Progesterone receptor positive Immunohistochemistry
Item
positive estrogen receptor (er) and/or progesterone receptor (pr) by immuno
boolean
C0279754 (UMLS CUI [1,1])
C0021044 (UMLS CUI [1,2])
C0279759 (UMLS CUI [2,1])
C0021044 (UMLS CUI [2,2])
Hormone Therapy Quantity failed | Adjuvant therapy | Neoplasm Metastasis
Item
failure of one previous endocrine therapy in the adjuvant or metastatic setting
boolean
C0279025 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0677850 (UMLS CUI [2])
C0027627 (UMLS CUI [3])
Prior Chemotherapy Quantity | Neoadjuvant Therapy | Adjuvant therapy
Item
use of no more than one previous chemotherapy regimen in the neoadjuvant or adjuvant setting
boolean
C1514457 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0600558 (UMLS CUI [2])
C0677850 (UMLS CUI [3])
Indication Chemotherapy | Indication Hormone Therapy
Item
indication to receive chemotherapy or endocrine therapy
boolean
C3146298 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0279025 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Protocol Compliance Unable
Item
inability to comply with the study protocol
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Prior Hormone Therapy Quantity
Item
use of more than one previous endocrine therapy, regardless of the setting; --
boolean
C1514460 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Prior Chemotherapy Neoplasm Metastasis
Item
previous use of chemotherapy for metastatic disease
boolean
C1514457 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
Neoadjuvant Hormone Therapy
Item
use of neoadjuvant endocrine therapy as the only previous type of endocrine therapy
boolean
C0600558 (UMLS CUI [1,1])
C0279025 (UMLS CUI [1,2])
Comorbidity Serious | Operative Surgical Procedure Serious | Serious mental illness | Study Subject Participation Status Excluded
Item
serious medical, surgical or psychiatric comorbidity that, upon investigator's discretion, should preclude participation in the study.
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C3841614 (UMLS CUI [3])
C2348568 (UMLS CUI [4,1])
C0332196 (UMLS CUI [4,2])

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