Non-Small Cell Lung Carcinoma
Item
histologic or cytologic diagnosis of nsclc
boolean
C0007131 (UMLS CUI [1])
TNM clinical staging
Item
presence of stage iiib or stage iv disease
boolean
C3258246 (UMLS CUI [1])
Systemic Chemotherapy
Item
patients must have received no prior systemic chemotherapy
boolean
C1883256 (UMLS CUI [1])
Measurable Disease 2-Dimensional Quantity | Circumscribed lesion | Diameter Perpendicular Quantity | Plain chest X-ray | X-Ray Computed Tomography | Palpation | Disease Progression | prior radiation therapy
Item
patients must have at least one bi-dimensionally measurable lesion with clearly defined margins and two perpendicular diameters that are clearly measurable by any of the following: chest x-ray, with at least one diameter 1.0 cm or greater, ct, with both diameters greater than the distance between cuts of the imaging study, palpation, with both diameters 2.0 cm or greater, or disease progressing in areas of prior radiation therapy may be included
boolean
C1513041 (UMLS CUI [1,1])
C1705052 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1268666 (UMLS CUI [2])
C1301886 (UMLS CUI [3,1])
C3272860 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C0039985 (UMLS CUI [4])
C0040405 (UMLS CUI [5])
C0030247 (UMLS CUI [6])
C0242656 (UMLS CUI [7])
C0279134 (UMLS CUI [8])
Radiotherapy Target Organ Alignment | Therapeutic radiology procedure | Toxic effect Due to Therapeutic procedure | Patient Recovered
Item
no prior radiotherapy for the target organ, no other radiotherapy for at least 2 weeks prior to study enrollment and the patient must have fully recovered from all acute toxic effects of the treatment.
boolean
C3179063 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C0600688 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0087111 (UMLS CUI [3,3])
C0030705 (UMLS CUI [4,1])
C0521108 (UMLS CUI [4,2])
Research Personnel Affiliated Study | Immediate family Research Personnel Affiliated Study
Item
are investigator site personnel directly affiliated with the study, or are immediate family of investigator site personnel directly affiliated with the study. immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted.
boolean
C0035173 (UMLS CUI [1,1])
C1510826 (UMLS CUI [1,2])
C2603343 (UMLS CUI [1,3])
C2371717 (UMLS CUI [2,1])
C0035173 (UMLS CUI [2,2])
C1510826 (UMLS CUI [2,3])
C2603343 (UMLS CUI [2,4])
lilly Employed | lilly Employee Immediate family | Study Subject Participation Status
Item
are employed by lilly (that is, employees, temporary contract workers, or designees responsible for the conduct the study). immediate family of lilly employees may participate in lilly sponsored clinical trials, but are not permitted to participate at a lilly facility. immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted.
boolean
C0331851 (UMLS CUI [1,1])
C0557351 (UMLS CUI [1,2])
C0331851 (UMLS CUI [2,1])
C0599987 (UMLS CUI [2,2])
C2371717 (UMLS CUI [2,3])
C2348568 (UMLS CUI [3])
Non-Prescription Drugs Indication Any
Item
have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.
boolean
C0013231 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
Study Subject Participation Status | gemcitabine
Item
have previously completed or withdrawn from this study or any other study investigating gemcitabine.
boolean
C2348568 (UMLS CUI [1])
C0045093 (UMLS CUI [2])