ID

39315

Description

1st Line Treatment of Bevacizumab-Taxane vs Bevacizumab-Exemestane in Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01303679

Link

https://clinicaltrials.gov/show/NCT01303679

Keywords

  1. 12/18/19 12/18/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

December 18, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility First Line Metastatic Breast Cancer NCT01303679

Eligibility First Line Metastatic Breast Cancer NCT01303679

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 18 ans.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
metastatic breast cancer or locally advanced
Description

Secondary malignant neoplasm of female breast | Locally advanced breast cancer

Data type

boolean

Alias
UMLS CUI [1]
C0346993
UMLS CUI [2]
C3495949
re+, her2-
Description

Estrogen receptor positive | HER2 Negative

Data type

boolean

Alias
UMLS CUI [1]
C0279754
UMLS CUI [2]
C2348908
patient receiving paclitaxel-bevacizumab first line chemotherapy
Description

Chemotherapeutics regimen first line of treatment | Paclitaxel | bevacizumab

Data type

boolean

Alias
UMLS CUI [1]
C2045825
UMLS CUI [2]
C0144576
UMLS CUI [3]
C0796392
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous treatment by exemestane (both in adjuvant or metastatic treatment).
Description

Prior Adjuvant Therapy | exemestane | Prior Therapy metastatic

Data type

boolean

Alias
UMLS CUI [1]
C1514456
UMLS CUI [2]
C0851344
UMLS CUI [3,1]
C1514463
UMLS CUI [3,2]
C1522484
1st line of chemotherapy different thaan paclitaxel-bevacizumab.
Description

Cemotherapeutics regimen first line of treatment | Except Paclitaxel | Except Bevacizumab

Data type

boolean

Alias
UMLS CUI [1]
C2045825
UMLS CUI [2,1]
C0332300
UMLS CUI [2,2]
C0144576
UMLS CUI [3,1]
C0332300
UMLS CUI [3,2]
C0796392
treatment by paclitaxel-bevacizumab > 18 weeks.
Description

Prior Therapy | Paclitaxel | bevacizumab

Data type

boolean

Alias
UMLS CUI [1]
C1514463
UMLS CUI [2]
C0144576
UMLS CUI [3]
C0796392
her2 positifs et/ou récepteurs aux oestrogènes négatifs.
Description

HER2 Positive | Estrogen receptor negative

Data type

boolean

Alias
UMLS CUI [1]
C2348909
UMLS CUI [2]
C0279756
previous thrombosis event within the 6 months before inclusion .
Description

Thrombosis Event Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C0040053
UMLS CUI [1,2]
C0441471
UMLS CUI [1,3]
C0205156
previous significant surgery within the 28 days before treatment start
Description

Prior surgery

Data type

boolean

Alias
UMLS CUI [1]
C0455610
previuous coagulopathy.
Description

Blood Coagulation Disorder Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0205156

Similar models

Eligibility First Line Metastatic Breast Cancer NCT01303679

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age > 18 ans.
boolean
C0001779 (UMLS CUI [1])
Secondary malignant neoplasm of female breast | Locally advanced breast cancer
Item
metastatic breast cancer or locally advanced
boolean
C0346993 (UMLS CUI [1])
C3495949 (UMLS CUI [2])
Estrogen receptor positive | HER2 Negative
Item
re+, her2-
boolean
C0279754 (UMLS CUI [1])
C2348908 (UMLS CUI [2])
Chemotherapeutics regimen first line of treatment | Paclitaxel | bevacizumab
Item
patient receiving paclitaxel-bevacizumab first line chemotherapy
boolean
C2045825 (UMLS CUI [1])
C0144576 (UMLS CUI [2])
C0796392 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Prior Adjuvant Therapy | exemestane | Prior Therapy metastatic
Item
previous treatment by exemestane (both in adjuvant or metastatic treatment).
boolean
C1514456 (UMLS CUI [1])
C0851344 (UMLS CUI [2])
C1514463 (UMLS CUI [3,1])
C1522484 (UMLS CUI [3,2])
Cemotherapeutics regimen first line of treatment | Except Paclitaxel | Except Bevacizumab
Item
1st line of chemotherapy different thaan paclitaxel-bevacizumab.
boolean
C2045825 (UMLS CUI [1])
C0332300 (UMLS CUI [2,1])
C0144576 (UMLS CUI [2,2])
C0332300 (UMLS CUI [3,1])
C0796392 (UMLS CUI [3,2])
Prior Therapy | Paclitaxel | bevacizumab
Item
treatment by paclitaxel-bevacizumab > 18 weeks.
boolean
C1514463 (UMLS CUI [1])
C0144576 (UMLS CUI [2])
C0796392 (UMLS CUI [3])
HER2 Positive | Estrogen receptor negative
Item
her2 positifs et/ou récepteurs aux oestrogènes négatifs.
boolean
C2348909 (UMLS CUI [1])
C0279756 (UMLS CUI [2])
Thrombosis Event Previous
Item
previous thrombosis event within the 6 months before inclusion .
boolean
C0040053 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
Prior surgery
Item
previous significant surgery within the 28 days before treatment start
boolean
C0455610 (UMLS CUI [1])
Blood Coagulation Disorder Previous
Item
previuous coagulopathy.
boolean
C0005779 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])

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