Inglés

Eligibility Non-Small Cell Lung Cancer NCT00881296

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of histologically confirmed stage iiib or iv non-small cell lung cancer
Descripción

Non-Small Cell Lung Carcinoma TNM clinical staging

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C3258246
good performance status (ecog 0-1)
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
no previous treatment
Descripción

Prior Therapy Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0332197
age 76 years and older
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
adequate bone marrow, liver and renal functions
Descripción

Bone Marrow function | Liver function | Renal function

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232804
no pregnant
Descripción

Pregnancy Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0332197
measurable disease, defined as at least one lesion whose longest diameter can be accurately measured as >=1.0 cm by spiral ct scan
Descripción

Measurable Disease | Lesion Quantity | Longest Diameter Spiral CT scan

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C0552406
UMLS CUI [3,2]
C0860888
provided written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe complications or a concomitant malignancy
Descripción

Severe medical complication | Cancer Other

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3495031
UMLS CUI [2]
C1707251
prior and other concurrent radiotherapy, chemotherapy, immunotherapy, egfr tyrosine kinase inhibitors
Descripción

Therapeutic radiology procedure | Chemotherapy | Immunotherapy | Epidermal growth factor receptor inhibitor

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1522449
UMLS CUI [2]
C0392920
UMLS CUI [3]
C0021083
UMLS CUI [4]
C1443775
interstitial pneumonia or lung fibrosis
Descripción

Pneumonia, Interstitial | Pulmonary Fibrosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0206061
UMLS CUI [2]
C0034069
contraindicated gemcitabine or carboplatin
Descripción

Medical contraindication Gemcitabine | Medical contraindication Carboplatin

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0045093
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0079083
inappropriate patients for entry to this study, judged by the physicians
Descripción

Study Subject Participation Status Inappropriate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
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Similar models

Eligibility Non-Small Cell Lung Cancer NCT00881296

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma TNM clinical staging
Item
diagnosis of histologically confirmed stage iiib or iv non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
ECOG performance status
Item
good performance status (ecog 0-1)
boolean
C1520224 (UMLS CUI [1])
Prior Therapy Absent
Item
no previous treatment
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Age
Item
age 76 years and older
boolean
C0001779 (UMLS CUI [1])
Bone Marrow function | Liver function | Renal function
Item
adequate bone marrow, liver and renal functions
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Pregnancy Absent
Item
no pregnant
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Measurable Disease | Lesion Quantity | Longest Diameter Spiral CT scan
Item
measurable disease, defined as at least one lesion whose longest diameter can be accurately measured as >=1.0 cm by spiral ct scan
boolean
C1513041 (UMLS CUI [1])
C0221198 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0552406 (UMLS CUI [3,1])
C0860888 (UMLS CUI [3,2])
Informed Consent
Item
provided written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Severe medical complication | Cancer Other
Item
severe complications or a concomitant malignancy
boolean
C3495031 (UMLS CUI [1])
C1707251 (UMLS CUI [2])
Therapeutic radiology procedure | Chemotherapy | Immunotherapy | Epidermal growth factor receptor inhibitor
Item
prior and other concurrent radiotherapy, chemotherapy, immunotherapy, egfr tyrosine kinase inhibitors
boolean
C1522449 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C0021083 (UMLS CUI [3])
C1443775 (UMLS CUI [4])
Pneumonia, Interstitial | Pulmonary Fibrosis
Item
interstitial pneumonia or lung fibrosis
boolean
C0206061 (UMLS CUI [1])
C0034069 (UMLS CUI [2])
Medical contraindication Gemcitabine | Medical contraindication Carboplatin
Item
contraindicated gemcitabine or carboplatin
boolean
C1301624 (UMLS CUI [1,1])
C0045093 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0079083 (UMLS CUI [2,2])
Study Subject Participation Status Inappropriate
Item
inappropriate patients for entry to this study, judged by the physicians
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
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