Information:
Error:
ID
19663
Description
A Study of Perjeta (Pertuzumab) in Combination With Herceptin in Patients With Metastatic Breast Cancer.; ODM derived from: https://clinicaltrials.gov/show/NCT01674062
Link
https://clinicaltrials.gov/show/NCT01674062
Keywords
Versions (2)
- 1/20/17 1/20/17 -
- 1/20/17 1/20/17 -
Uploaded on
January 20, 2017
DOI
To request one please log in.
License
Creative Commons BY 4.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Eligibility Breast Cancer NCT01674062
Eligibility Breast Cancer NCT01674062
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01674062
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Adult | Age | HER2-positive carcinoma of breast
Item
adult patients, >=18 years of age, with histologically-confirmed her2-positive breast cancer
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C1960398 (UMLS CUI [3])
C0001779 (UMLS CUI [2])
C1960398 (UMLS CUI [3])
Secondary malignant neoplasm of female breast | Disease Progression | Therapeutic procedure Herceptin Based Neoplasm Metastasis
Item
metastatic breast cancer, with progression on herceptin-based therapy as last treatment for metastatic disease
boolean
C0346993 (UMLS CUI [1])
C0242656 (UMLS CUI [2])
C0087111 (UMLS CUI [3,1])
C0338204 (UMLS CUI [3,2])
C1705938 (UMLS CUI [3,3])
C0027627 (UMLS CUI [3,4])
C0242656 (UMLS CUI [2])
C0087111 (UMLS CUI [3,1])
C0338204 (UMLS CUI [3,2])
C1705938 (UMLS CUI [3,3])
C0027627 (UMLS CUI [3,4])
Chemotherapy Regimen Quantity
Item
<=3 chemotherapy regimens prior to study entry
boolean
C0392920 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
Herceptin Dose | pertuzumab
Item
last herceptin dose <=9 weeks before study entry for patients reciving pertuzumab +
boolean
C0338204 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1328025 (UMLS CUI [2])
C0178602 (UMLS CUI [1,2])
C1328025 (UMLS CUI [2])
Herceptin | pertuzumab
Item
herceptin, and >=4 weeks for patients receiving pertuzumab monotherapy
boolean
C0338204 (UMLS CUI [1])
C1328025 (UMLS CUI [2])
C1328025 (UMLS CUI [2])
Left ventricular ejection fraction
Item
lvef>= 55% at study entry
boolean
C0428772 (UMLS CUI [1])
Vaccines Against Malignant Neoplasms | Targeted Therapy | Herceptin
Item
previous treatment with an anti-cancer vaccine or any targeted therapy other than herceptin
boolean
C0042210 (UMLS CUI [1,1])
C0521124 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
C2985566 (UMLS CUI [2])
C0338204 (UMLS CUI [3])
C0521124 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
C2985566 (UMLS CUI [2])
C0338204 (UMLS CUI [3])
Metastatic malignant neoplasm to brain
Item
brain metastases
boolean
C0220650 (UMLS CUI [1])
Adverse event cardiac Herceptin Related
Item
history of any cardiac ae related to herceptin therapy
boolean
C0877248 (UMLS CUI [1,1])
C0018787 (UMLS CUI [1,2])
C0338204 (UMLS CUI [1,3])
C0439849 (UMLS CUI [1,4])
C0018787 (UMLS CUI [1,2])
C0338204 (UMLS CUI [1,3])
C0439849 (UMLS CUI [1,4])
Malignant Neoplasms | Basal cell carcinoma | Carcinoma in situ of uterine cervix
Item
any other malignancy in the last 5 years, except for basal cell cancer or cancer in situ of the cervix
boolean
C0006826 (UMLS CUI [1])
C0007117 (UMLS CUI [2])
C0851140 (UMLS CUI [3])
C0007117 (UMLS CUI [2])
C0851140 (UMLS CUI [3])