Criteria Fulfill
Item
to be included in this study, you must meet the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Non-Small Cell Lung Carcinoma
Item
histologically confirmed non-small cell bronchogenic carcinoma
boolean
C0007131 (UMLS CUI [1])
Newly Diagnosed Disease TNM clinical staging | Recurrent disease unresectable TNM clinical staging
Item
newly diagnosed or recurrent unresectable stage iii or stage iv disease
boolean
C1334965 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0277556 (UMLS CUI [2,1])
C1519810 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
Mixed Neoplasm Anaplastic Cell Absent
Item
no mixed tumors with small cell anaplastic elements
boolean
C1368354 (UMLS CUI [1,1])
C1515964 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Measurable Disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Carcinoma of lung Chemotherapy Absent
Item
must not have received any prior antineoplastic chemotherapy for lung cancer
boolean
C0684249 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Activities of Daily Living Perform Able
Item
able to perform activities of daily living with little or no assistance
boolean
C0001288 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Bone Marrow function | Liver function | Renal function
Item
adequate bone marrow, liver and kidney
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Informed Consent
Item
understand the nature of this study and give written informed consent.
boolean
C0021430 (UMLS CUI [1])
Study Subject Participation Status
Item
you cannot participate in this study if any of the following apply to you:
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
female patients who are pregnant or are lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Cardiovascular Disease Serious
Item
history of serious cardiovascular disease within the previous six months
boolean
C0007222 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Communicable Disease Serious
Item
serious active infection at the time of treatment
boolean
C0009450 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Comorbidity Serious
Item
other serious underlying medical condition
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Clinical Trial Eligibility Criteria Additional
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
boolean
C1516637 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])