ID

22666

Beskrivning

Induction Erlotinib Therapy in Stage III A (N2) Non-Small Cell Lung Cancer (NSCLC); ODM derived from: https://clinicaltrials.gov/show/NCT00600587

Länk

https://clinicaltrials.gov/show/NCT00600587

Nyckelord

  1. 2017-06-09 2017-06-09 -
Uppladdad den

9 juni 2017

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Carcinoma, Non-Small-Cell Lung NCT00600587

Eligibility Carcinoma, Non-Small-Cell Lung NCT00600587

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
written informed consent
Beskrivning

ID.1

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
histological or cytological documented
Beskrivning

ID.2

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0449575
UMLS CUI [1,2]
C0205471
UMLS CUI [1,3]
C0007131
resectable nsclc of stage iiia-n2 confirmed by mediastinoscopy or pet
Beskrivning

ID.3

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C1300072
naive therapy nsclc
Beskrivning

ID.4

Datatyp

boolean

Alias
UMLS CUI [1]
C0919936
candidates should be tolerated with induction therapy and thoracotomy with ecog performance status 0-2, adequate haematological and hepatic- renal function and qualified lung function
Beskrivning

ID.5

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1520224
UMLS CUI [1,2]
C0678852
UMLS CUI [1,3]
C0857127
enough tissue samples to perform gene analysis
Beskrivning

ID.6

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3267141
UMLS CUI [1,2]
C0475358
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
small cell lung cancer
Beskrivning

ID.7

Datatyp

boolean

Alias
UMLS CUI [1]
C0149925
pregnant or breast-feeding women
Beskrivning

ID.8

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0549206
UMLS CUI [1,2]
C0006147
any unstable systemic disease
Beskrivning

ID.9

Datatyp

boolean

Alias
UMLS CUI [1]
C1385002
patients with exposure to investigational drug therapy or other concurrent anticancer therapy outside of this trial
Beskrivning

ID.10

Datatyp

boolean

Alias
UMLS CUI [1]
C0008976

Similar models

Eligibility Carcinoma, Non-Small-Cell Lung NCT00600587

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
ID.2
Item
histological or cytological documented
boolean
C0449575 (UMLS CUI [1,1])
C0205471 (UMLS CUI [1,2])
C0007131 (UMLS CUI [1,3])
ID.3
Item
resectable nsclc of stage iiia-n2 confirmed by mediastinoscopy or pet
boolean
C0007131 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
ID.4
Item
naive therapy nsclc
boolean
C0919936 (UMLS CUI [1])
ID.5
Item
candidates should be tolerated with induction therapy and thoracotomy with ecog performance status 0-2, adequate haematological and hepatic- renal function and qualified lung function
boolean
C1520224 (UMLS CUI [1,1])
C0678852 (UMLS CUI [1,2])
C0857127 (UMLS CUI [1,3])
ID.6
Item
enough tissue samples to perform gene analysis
boolean
C3267141 (UMLS CUI [1,1])
C0475358 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
ID.7
Item
small cell lung cancer
boolean
C0149925 (UMLS CUI [1])
ID.8
Item
pregnant or breast-feeding women
boolean
C0549206 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
ID.9
Item
any unstable systemic disease
boolean
C1385002 (UMLS CUI [1])
ID.10
Item
patients with exposure to investigational drug therapy or other concurrent anticancer therapy outside of this trial
boolean
C0008976 (UMLS CUI [1])

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