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])
Bronchogenic Carcinoma Non-small cell
Item
non-small cell bronchogenic carcinoma
boolean
C0007121 (UMLS CUI [1,1])
C0445128 (UMLS CUI [1,2])
Carcinoma unresectable | TNM clinical staging
Item
newly diagnosed unresectable stage iiib or stage iv disease
boolean
C0007097 (UMLS CUI [1,1])
C1519810 (UMLS CUI [1,2])
C3258246 (UMLS CUI [2])
TNM clinical staging | Patients Ineligible Combined Modality Therapy
Item
patients with stage iiib disease should be ineligible for combined therapy
boolean
C3258246 (UMLS CUI [1])
C0030705 (UMLS CUI [2,1])
C1512714 (UMLS CUI [2,2])
C0009429 (UMLS CUI [2,3])
Measurable Disease | roentgenography | X-Ray Computed Tomography
Item
patients must have measurable lesion definable by x-ray or ct scan.
boolean
C1513041 (UMLS CUI [1])
C0034571 (UMLS CUI [2])
C0040405 (UMLS CUI [3])
Chemotherapy Carcinoma of lung
Item
no prior antineoplastic chemotherapy for lung cancer prior to study entry
boolean
C0392920 (UMLS CUI [1,1])
C0684249 (UMLS CUI [1,2])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Aids to daily living Minimal
Item
able to perform activities of daily living with minimal assistance
boolean
C1283236 (UMLS CUI [1,1])
C1524031 (UMLS CUI [1,2])
Bone Marrow function | Liver function | Renal function
Item
adequate bone marrow, liver and kidney function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Informed Consent
Item
written informed consent must be obtained prior to study entry
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
patients must be available for treatment and followup.
boolean
C0525058 (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 patient pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Heart Disease
Item
history of heart disease
boolean
C0018799 (UMLS CUI [1])
Communicable Disease Serious
Item
serious active infection at the time of treatment
boolean
C0009450 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Other medical condition Serious
Item
other serious underlying medical condition
boolean
C3843040 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Metastatic malignant neoplasm to brain
Item
brain metastasis
boolean
C0220650 (UMLS CUI [1])
Measurable Disease Lacking
Item
patients without measurable disease
boolean
C1513041 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Diabetic - poor control | Random blood glucose level result
Item
uncontrolled diabetes mellitus defined as random blood sugar > 250mg/dl
boolean
C0421258 (UMLS CUI [1])
C1261429 (UMLS CUI [2])
Dementia | Mental state altered Significant
Item
dementia or significantly altered mental status
boolean
C0497327 (UMLS CUI [1])
C0278060 (UMLS CUI [2,1])
C0392747 (UMLS CUI [2,2])
C0750502 (UMLS CUI [2,3])
Peripheral Neuropathy Significant | Physical Examination
Item
significant peripheral neuropathy by history or physical examination.
boolean
C0031117 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0031809 (UMLS CUI [2])
criteria Study Protocol | Study Subject Participation Status
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
C0243161 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2])