ID

26604

Beschrijving

A Study of Avastin (Bevacizumab) in Combination With Taxane-based Chemotherapy as First Line Treatment in Patients With HER-2 Negative Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00846027

Link

https://clinicaltrials.gov/show/NCT00846027

Trefwoorden

  1. 21-10-17 21-10-17 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

21 oktober 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00846027

Eligibility Breast Cancer NCT00846027

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
female patients, ≥ 18 years of age.
Beschrijving

Gender | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
breast cancer, with measurable, locally recurrent or metastatic lesions, or patients with bone metastasis only.
Beschrijving

Breast Carcinoma | Measurable Disease | Lesion Recurrent Local | Metastatic Lesion | Secondary malignant neoplasm of bone

Datatype

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2]
C1513041
UMLS CUI [3,1]
C0221198
UMLS CUI [3,2]
C2945760
UMLS CUI [3,3]
C0205276
UMLS CUI [4]
C1513183
UMLS CUI [5]
C0153690
her-2 negative disease.
Beschrijving

Disease HER2 negative

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C4087376
candidates for chemotherapy.
Beschrijving

Indication Chemotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0392920
eastern cooperative oncology group (ecog) performance status ≤ 2.
Beschrijving

ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous chemotherapy for metastatic or locally advanced breast cancer.
Beschrijving

Chemotherapy Secondary malignant neoplasm of female breast | Chemotherapy Locally advanced breast cancer

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0346993
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C3495949
previous radiotherapy for treatment of metastatic breast cancer.
Beschrijving

Therapeutic radiology procedure Secondary malignant neoplasm of female breast

Datatype

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0346993
any prior adjuvant treatment with anthracyclines completed < 6 months prior to enrollment.
Beschrijving

Anthracyclines Adjuvant therapy Completed

Datatype

boolean

Alias
UMLS CUI [1,1]
C0282564
UMLS CUI [1,2]
C0677850
UMLS CUI [1,3]
C0205197
chronic daily treatment with corticosteroids (≥ 10 mg/day), aspirin (> 325 mg/day) or clopidogrel (> 75mg/day).
Beschrijving

Adrenal Cortex Hormones chronic U/day | Aspirin chronic U/day | Clopidogrel chronic U/day

Datatype

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C0205191
UMLS CUI [1,3]
C0456683
UMLS CUI [2,1]
C0004057
UMLS CUI [2,2]
C0205191
UMLS CUI [2,3]
C0456683
UMLS CUI [3,1]
C0070166
UMLS CUI [3,2]
C0205191
UMLS CUI [3,3]
C0456683

Similar models

Eligibility Breast Cancer NCT00846027

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
female patients, ≥ 18 years of age.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Breast Carcinoma | Measurable Disease | Lesion Recurrent Local | Metastatic Lesion | Secondary malignant neoplasm of bone
Item
breast cancer, with measurable, locally recurrent or metastatic lesions, or patients with bone metastasis only.
boolean
C0678222 (UMLS CUI [1])
C1513041 (UMLS CUI [2])
C0221198 (UMLS CUI [3,1])
C2945760 (UMLS CUI [3,2])
C0205276 (UMLS CUI [3,3])
C1513183 (UMLS CUI [4])
C0153690 (UMLS CUI [5])
Disease HER2 negative
Item
her-2 negative disease.
boolean
C0012634 (UMLS CUI [1,1])
C4087376 (UMLS CUI [1,2])
Indication Chemotherapy
Item
candidates for chemotherapy.
boolean
C3146298 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status ≤ 2.
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Chemotherapy Secondary malignant neoplasm of female breast | Chemotherapy Locally advanced breast cancer
Item
previous chemotherapy for metastatic or locally advanced breast cancer.
boolean
C0392920 (UMLS CUI [1,1])
C0346993 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C3495949 (UMLS CUI [2,2])
Therapeutic radiology procedure Secondary malignant neoplasm of female breast
Item
previous radiotherapy for treatment of metastatic breast cancer.
boolean
C1522449 (UMLS CUI [1,1])
C0346993 (UMLS CUI [1,2])
Anthracyclines Adjuvant therapy Completed
Item
any prior adjuvant treatment with anthracyclines completed < 6 months prior to enrollment.
boolean
C0282564 (UMLS CUI [1,1])
C0677850 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Adrenal Cortex Hormones chronic U/day | Aspirin chronic U/day | Clopidogrel chronic U/day
Item
chronic daily treatment with corticosteroids (≥ 10 mg/day), aspirin (> 325 mg/day) or clopidogrel (> 75mg/day).
boolean
C0001617 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0456683 (UMLS CUI [1,3])
C0004057 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0456683 (UMLS CUI [2,3])
C0070166 (UMLS CUI [3,1])
C0205191 (UMLS CUI [3,2])
C0456683 (UMLS CUI [3,3])

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