ID

37931

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01277926

Nyckelord

Versioner (1)
  1. 2019-09-01 2019-09-01 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

1 september 2019

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01277926

Engelsk

Eligibility Breast Cancer NCT01277926

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

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

Breast Carcinoma

Datatyp

boolean

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

Postmenopausal state

Datatyp

boolean

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

Bilateral oophorectomy | Age Any

Datatyp

boolean

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

Menopause present

Datatyp

boolean

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

Estrogen receptor positive Immunohistochemistry | Progesterone receptor positive Immunohistochemistry

Datatyp

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
Beskrivning

Hormone Therapy Quantity failed | Adjuvant therapy | Neoplasm Metastasis

Datatyp

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
Beskrivning

Prior Chemotherapy Quantity | Neoadjuvant Therapy | Adjuvant therapy

Datatyp

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
Beskrivning

Indication Chemotherapy | Indication Hormone Therapy

Datatyp

boolean

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

Exclusion Criteria

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

Protocol Compliance Unable

Datatyp

boolean

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

Prior Hormone Therapy Quantity

Datatyp

boolean

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

Prior Chemotherapy Neoplasm Metastasis

Datatyp

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
Beskrivning

Neoadjuvant Hormone Therapy

Datatyp

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.
Beskrivning

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

Datatyp

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
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Similar models

Eligibility Breast Cancer NCT01277926

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

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