Informationen:
Fehler:
ID
21234
Beschreibung
Studying Biopsy Samples in Women Undergoing First-Line Chemotherapy for Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00870168
Link
https://clinicaltrials.gov/show/NCT00870168
Stichworte
Versionen (1)
- 14.04.17 14.04.17 -
Hochgeladen am
14. April 2017
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00870168
Eligibility Breast Cancer NCT00870168
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT00870168
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
adenocarcinoma of the breast, histologically confirmed
Item
histologically confirmed adenocarcinoma of the breast
boolean
C0858252 (UMLS CUI [1,1])
C0019638 (UMLS CUI [1,2])
C0019638 (UMLS CUI [1,2])
metastatic adenocarcinoma of the breast
Item
metastatic disease
boolean
C0858252 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
C0027627 (UMLS CUI [1,2])
inflammatory breast cancer
Item
no inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
adenocarcinoma of the breast, measurable disease
Item
measurable disease according to recist criteria
boolean
C0858252 (UMLS CUI [1,1])
C1513041 (UMLS CUI [1,2])
C1513041 (UMLS CUI [1,2])
adenocarcinoma of the breast, hormone receptor status
Item
hormone receptor status:
boolean
C0858252 (UMLS CUI [1,1])
C0019929 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
C0019929 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
adenocarcinoma of the breast, estrogen and progesterone receptor immunhis
Item
estrogen receptor- and/or progesterone receptor-negative by ihc
boolean
C0858252 (UMLS CUI [1,1])
C0034804 (UMLS CUI [1,2])
C0034833 (UMLS CUI [1,3])
C0021044 (UMLS CUI [1,4])
C0034804 (UMLS CUI [1,2])
C0034833 (UMLS CUI [1,3])
C0021044 (UMLS CUI [1,4])
patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
menopausal status
Item
menopausal status not specified
boolean
C0455962 (UMLS CUI [1])
who performance status
Item
who performance status 0-2
boolean
C1298650 (UMLS CUI [1])
life expectancy
Item
life expectancy > 3 months
boolean
C0023671 (UMLS CUI [1])
absolute neutrophile count
Item
anc > 1.5 x 10^9/l
boolean
C0948762 (UMLS CUI [1])
platelet count
Item
platelet count > 100 x 10^9/l
boolean
C0005821 (UMLS CUI [1])
liver transaminases
Item
liver transaminases ≤ 3 times upper limit of normal (uln)
boolean
C0002594 (UMLS CUI [1])
alkaline phosphatase
Item
alkaline phosphatase ≤ 3 times uln
boolean
C0201850 (UMLS CUI [1])
bilirubin
Item
bilirubin ≤ 1.5 times uln
boolean
C1278039 (UMLS CUI [1])
creatinine
Item
creatinine ≤ 2 times uln
boolean
C0201976 (UMLS CUI [1])
pregnancy, breast feeding
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
fertile patients with effective contraception
Item
fertile patients must use effective contraception
boolean
C1960468 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
xylocaine allergy
Item
no allergy to xylocaine
boolean
C0699094 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0020517 (UMLS CUI [1,2])
heart failure, kidney insuffiency, bone marrow insufficiency, respiratory insufficiency, liver insufficiency
Item
no heart failure, or kidney, bone marrow, respiratory, or liver insufficiency
boolean
C0018801 (UMLS CUI [1])
C1565489 (UMLS CUI [2])
C0005953 (UMLS CUI [3,1])
C0231179 (UMLS CUI [3,2])
C0035229 (UMLS CUI [4])
C1306571 (UMLS CUI [5])
C1565489 (UMLS CUI [2])
C0005953 (UMLS CUI [3,1])
C0231179 (UMLS CUI [3,2])
C0035229 (UMLS CUI [4])
C1306571 (UMLS CUI [5])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
first-line treatment for metastatic disease
Item
no prior first-line treatment for metastatic disease
boolean
C0027627 (UMLS CUI [1,1])
C1708063 (UMLS CUI [1,2])
C1708063 (UMLS CUI [1,2])