Informatie:
Fout:
ID
24530
Beschrijving
Development of a Model to Predict Progression-Free Survival After Erlotinib in Patients With Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00897533
Link
https://clinicaltrials.gov/show/NCT00897533
Trefwoorden
Versies (1)
- 05-08-17 05-08-17 -
Geüploaded op
5 augustus 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Lung Cancer NCT00897533
Eligibility Lung Cancer NCT00897533
- StudyEvent: Eligibility
Similar models
Eligibility Lung Cancer NCT00897533
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Non-Small Cell Lung Carcinoma | Non-Small Cell Lung Carcinoma Subtype
Item
diagnosis of non-small cell lung cancer, including any of the following subtypes:
boolean
C0007131 (UMLS CUI [1])
C0007131 (UMLS CUI [2,1])
C0449560 (UMLS CUI [2,2])
C0007131 (UMLS CUI [2,1])
C0449560 (UMLS CUI [2,2])
Adenocarcinoma
Item
adenocarcinoma
boolean
C0001418 (UMLS CUI [1])
Squamous cell carcinoma
Item
squamous cell carcinoma
boolean
C0007137 (UMLS CUI [1])
Bronchioloalveolar carcinoma
Item
bronchoalveolar carcinoma
boolean
C0007120 (UMLS CUI [1])
Carcinoid
Item
carcinoid
boolean
C0007095 (UMLS CUI [1])
TNM clinical staging | Recurrent disease
Item
stage iiib or iv or recurrent disease
boolean
C3258246 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
C0277556 (UMLS CUI [2])
Erlotinib Hydrochloride
Item
must have received treatment with erlotinib hydrochloride on clinical trial ecog-e3503
boolean
C1533491 (UMLS CUI [1])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.11
Item
see disease characteristics
boolean