ECOG performance status
Item
performance status of 0 to 1 on the eastern cooperative oncology group (ecog) scale.
boolean
C1520224 (UMLS CUI [1])
Squamous cell carcinoma of lung Untreated Inoperable TNM clinical staging | Pericardial effusion Excluded | Pleural effusion Excluded | Hilar lymph nodes Contralateral Excluded | Supraclavicular lymph nodes Contralateral Excluded
Item
previously untreated, histological documented, inoperable stage iiia or iiib squamous cell carcinoma of lung, excluding those with pericardial, pleural effusion, and those with contralateral hilar or contralateral supraclavicular lymph nodes.
boolean
C0149782 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0205187 (UMLS CUI [1,3])
C3258246 (UMLS CUI [1,4])
C0031039 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0032227 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C1305372 (UMLS CUI [4,1])
C0441988 (UMLS CUI [4,2])
C0332196 (UMLS CUI [4,3])
C0229730 (UMLS CUI [5,1])
C0441988 (UMLS CUI [5,2])
C0332196 (UMLS CUI [5,3])
Measurable Disease | Neoplasm Appropriate Radiation Field
Item
patients must have measurable disease according to recist criteria, and all detectable tumor can be encompassed by radiation therapy fields.
boolean
C1513041 (UMLS CUI [1])
C0027651 (UMLS CUI [2,1])
C1548787 (UMLS CUI [2,2])
C1882536 (UMLS CUI [2,3])
Weight loss Percentage Timespan
Item
weight loss ≦ 5% in the previous six months.
boolean
C1262477 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C0872291 (UMLS CUI [1,3])
Hematologic function | Liver function | Pulmonary function | Renal function
Item
patient must have adequate blood, liver, lungs and kidney function within the requirements of this study.
boolean
C0221130 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0231921 (UMLS CUI [3])
C0232804 (UMLS CUI [4])
Childbearing Potential Serum pregnancy test negative | Gender Contraceptive methods
Item
female patients of child-bearing potential must test negative for pregnancy at the time of enrollment based on a serum pregnancy test. male and female patients must agree to use a reliable method of birth control during and for 3 months following the last dose of study drug.
boolean
C3831118 (UMLS CUI [1,1])
C0430061 (UMLS CUI [1,2])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Informed Consent
Item
patients must sign a study-specific informed consent form prior to study entry.
boolean
C0021430 (UMLS CUI [1])
Complete excision Neoplasm | Recurrent disease | Eligibility Operative Surgical Procedure Definitive
Item
complete tumor resection, recurrent disease, or those patients eligible for definitive surgery.
boolean
C0015250 (UMLS CUI [1,1])
C0027651 (UMLS CUI [1,2])
C0277556 (UMLS CUI [2])
C1548635 (UMLS CUI [3,1])
C0543467 (UMLS CUI [3,2])
C0443196 (UMLS CUI [3,3])
Prior Chemotherapy Carcinoma of lung | Biological Response Modifiers Carcinoma of lung
Item
previous chemotherapy or previous biologic response modifiers for current lung cancer.
boolean
C1514457 (UMLS CUI [1,1])
C0684249 (UMLS CUI [1,2])
C0005525 (UMLS CUI [2,1])
C0684249 (UMLS CUI [2,2])
Radiotherapy to thorax
Item
patient has previously had thoracic radiation therapy.
boolean
C4038705 (UMLS CUI [1])
Malignant Neoplasms | Exception Skin carcinoma | Exception Disease Free Duration
Item
prior or concurrent malignancy except non-melanomatous skin cancer unless disease-free for five years or more.
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0012634 (UMLS CUI [3,2])
C0332296 (UMLS CUI [3,3])
C0449238 (UMLS CUI [3,4])
Comorbidity Serious compromises Patient safety | Comorbidity Serious compromises Completion of clinical trial
Item
serious concomitant disorders that would compromise the safety of the patient, or compromise the patient's ability to complete the study, at the discretion of the investigator.
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C2945640 (UMLS CUI [1,3])
C1113679 (UMLS CUI [1,4])
C0009488 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C2945640 (UMLS CUI [2,3])
C2732579 (UMLS CUI [2,4])
Nervous system disorder | Mental disorders | Seizures | Dementia
Item
history of significant neurological or mental disorder, including seizures or dementia.
boolean
C0027765 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0036572 (UMLS CUI [3])
C0497327 (UMLS CUI [4])