non-small cell lung cancer
Item
presumed histological or cytological diagnosis of non-small cell lung cancer
boolean
C0019638 (UMLS CUI [1,1])
C0007131 (UMLS CUI [1,2])
C0010819 (UMLS CUI [2,1])
C0007131 (UMLS CUI [2,2])
biopsy
Item
diagnosis to be confirmed upon study entry to collect biopsy material for correlative studies
boolean
C0005558 (UMLS CUI [1])
tumor stage
Item
stage i-iiia disease
boolean
C1300072 (UMLS CUI [1])
ecog
Item
ecog performance status of 0-2
boolean
C1520224 (UMLS CUI [1])
creatinine
Item
serum creatinine ≤ 1.5 mg/dl
boolean
C0201976 (UMLS CUI [1])
granulocyte count
Item
granulocytes ≥ 1,500/mm^3
boolean
C0857490 (UMLS CUI [1])
platelet count
Item
platelets ≥ 100,000/mm^3
boolean
C0032181 (UMLS CUI [1])
ast
Item
ast ≤ 3 times normal
boolean
C0201899 (UMLS CUI [1])
bilirubin
Item
bilirubin ≤ 1.5 mg/dl
boolean
C1278039 (UMLS CUI [1])
pregnancy, lactation
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
contraception
Item
fertile patients must use effective contraception
boolean
C0700589 (UMLS CUI [1])
infection
Item
no active unresolved infection
boolean
C0009450 (UMLS CUI [1])
ID.14
Item
prior concurrent therapy:
boolean
cox-2 inhibitors
Item
at least 7 days since prior and no concurrent non-steroidal anti-inflammatory agents or other cyclo-oxygenase-2 inhibitors
boolean
C1257954 (UMLS CUI [1])
antibiotics
Item
at least 7 days since prior parenteral antibiotics
boolean
C0003232 (UMLS CUI [1,1])
C0021441 (UMLS CUI [1,2])
chemotherapy, radiotherapy
Item
no prior systemic chemotherapy or radiotherapy
boolean
C0392920 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])