ID

26628

Description

Anastrozole or Fulvestrant in Treating Postmenopausal Patients With Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00871858

Link

https://clinicaltrials.gov/show/NCT00871858

Keywords

Versions (1)
  1. 10/22/17 10/22/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

October 22, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00871858

English

Eligibility Breast Cancer NCT00871858

1 forms  
Criteria
Description

Criteria

histologically confirmed invasive breast cancer, meeting 1 of the following criteria:
Description

Invasive carcinoma of breast

Data type

boolean

Alias
UMLS CUI [1]
C0853879
sbr grade i-ii disease (patients < 65 years of age)
Description

Disease Scarff-Bloom-Richardson Grading System | Age

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3828224
UMLS CUI [2]
C0001779
sbr grade i-iii disease (patients > 65 years of age)
Description

Disease Scarff-Bloom-Richardson Grading System | Age

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3828224
UMLS CUI [2]
C0001779
t2 (2-5 cm), t3, or t4b, and n0-1 disease
Description

Disease TNM Breast tumor staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0474926
no metastatic disease
Description

Neoplasm Metastasis Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C2828389
breast lesion not amenable to breast-conserving resection
Description

Lesion of breast | Breast-Conserving Surgery Unsuccessful

Data type

boolean

Alias
UMLS CUI [1]
C0567489
UMLS CUI [2,1]
C0917927
UMLS CUI [2,2]
C1272705
no inflammatory breast cancer
Description

Inflammatory Breast Carcinoma Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0278601
UMLS CUI [1,2]
C2828389
no prior breast cancer
Description

Breast Carcinoma Previous Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205156
UMLS CUI [1,3]
C2828389
hormone receptor status:
Description

Hormone Receptor Status

Data type

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
estrogen receptor- and/or progesterone receptor-positive
Description

Estrogen receptor positive | Progesterone receptor positive

Data type

boolean

Alias
UMLS CUI [1]
C0279754
UMLS CUI [2]
C0279759
patient characteristics:
Description

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
postmenopausal
Description

Postmenopausal state

Data type

boolean

Alias
UMLS CUI [1]
C0232970
no other cancer within the past 5 years except for adequately treated skin carcinoma or carcinoma in situ of the cervix
Description

Exclusion Cancer Other | Exception Skin carcinoma Treated | Exception Carcinoma in situ of uterine cervix Treated

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C1707251
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
UMLS CUI [2,3]
C1522326
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0851140
UMLS CUI [3,3]
C1522326
no contraindication to anti-hormonal treatment
Description

Exclusion Medical contraindication Hormone Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C0279025
no psychological, familial, social, or geographical reasons that would preclude follow up
Description

Exclusion Condition Preventing Follow-up

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0348080
UMLS CUI [1,3]
C1292733
UMLS CUI [1,4]
C3274571
prior concurrent therapy:
Description

Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1]
C0087111
at least 8 days since prior hormone replacement therapy
Description

Hormone replacement therapy

Data type

boolean

Alias
UMLS CUI [1]
C0282402
no concurrent anti-vitamin k treatment
Description

Exclusion Therapeutic procedure Against Vitamin K

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0521124
UMLS CUI [1,4]
C0042878
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Similar models

Eligibility Breast Cancer NCT00871858

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Invasive carcinoma of breast
Item
histologically confirmed invasive breast cancer, meeting 1 of the following criteria:
boolean
C0853879 (UMLS CUI [1])
Disease Scarff-Bloom-Richardson Grading System | Age
Item
sbr grade i-ii disease (patients < 65 years of age)
boolean
C0012634 (UMLS CUI [1,1])
C3828224 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Disease Scarff-Bloom-Richardson Grading System | Age
Item
sbr grade i-iii disease (patients > 65 years of age)
boolean
C0012634 (UMLS CUI [1,1])
C3828224 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Disease TNM Breast tumor staging
Item
t2 (2-5 cm), t3, or t4b, and n0-1 disease
boolean
C0012634 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
Neoplasm Metastasis Excluded
Item
no metastatic disease
boolean
C0027627 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
Lesion of breast | Breast-Conserving Surgery Unsuccessful
Item
breast lesion not amenable to breast-conserving resection
boolean
C0567489 (UMLS CUI [1])
C0917927 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
Inflammatory Breast Carcinoma Excluded
Item
no inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
Breast Carcinoma Previous Excluded
Item
no prior breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
Hormone Receptor Status
Item
hormone receptor status:
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Estrogen receptor positive | Progesterone receptor positive
Item
estrogen receptor- and/or progesterone receptor-positive
boolean
C0279754 (UMLS CUI [1])
C0279759 (UMLS CUI [2])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Postmenopausal state
Item
postmenopausal
boolean
C0232970 (UMLS CUI [1])
Exclusion Cancer Other | Exception Skin carcinoma Treated | Exception Carcinoma in situ of uterine cervix Treated
Item
no other cancer within the past 5 years except for adequately treated skin carcinoma or carcinoma in situ of the cervix
boolean
C2828389 (UMLS CUI [1,1])
C1707251 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
C1522326 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0851140 (UMLS CUI [3,2])
C1522326 (UMLS CUI [3,3])
Exclusion Medical contraindication Hormone Therapy
Item
no contraindication to anti-hormonal treatment
boolean
C2828389 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0279025 (UMLS CUI [1,3])
Exclusion Condition Preventing Follow-up
Item
no psychological, familial, social, or geographical reasons that would preclude follow up
boolean
C2828389 (UMLS CUI [1,1])
C0348080 (UMLS CUI [1,2])
C1292733 (UMLS CUI [1,3])
C3274571 (UMLS CUI [1,4])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Hormone replacement therapy
Item
at least 8 days since prior hormone replacement therapy
boolean
C0282402 (UMLS CUI [1])
Exclusion Therapeutic procedure Against Vitamin K
Item
no concurrent anti-vitamin k treatment
boolean
C2828389 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0521124 (UMLS CUI [1,3])
C0042878 (UMLS CUI [1,4])
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