Non-Small Cell Lung Carcinoma | Adenocarcinoma Histology
Item
pathologically confirmed diagnosis of nsclc of adenocarcinoma histology
boolean
C0007131 (UMLS CUI [1])
C0001418 (UMLS CUI [2,1])
C4048239 (UMLS CUI [2,2])
TNM clinical staging
Item
stage ia-b, iia-b, or iiia by the american joint committee on cancer 7th edition staging criteria
boolean
C3258246 (UMLS CUI [1])
Excision Curative
Item
patients must have undergone surgical resection with curative intent within 6 months of enrollment
boolean
C0728940 (UMLS CUI [1,1])
C1276305 (UMLS CUI [1,2])
Availability of Tumor tissue Sufficient | EGFR gene mutation Analysis
Item
sufficient tumor tissue available for egfr mutation analysis
boolean
C0470187 (UMLS CUI [1,1])
C0475358 (UMLS CUI [1,2])
C0205410 (UMLS CUI [1,3])
C3266992 (UMLS CUI [2,1])
C0002778 (UMLS CUI [2,2])
Client Characteristics | EGFR exon 19 deletion | Point mutation in exon 21 (L858R) | Gender | Never smoked tobacco | Asians
Item
at least one of the following patient characteristics: previously detected deletion 19 or l858r egfr mutation, female sex, history of never smoking, or asian/pacific rim ethnicity (to be enrolled in the screening portion of trial).
boolean
C0815172 (UMLS CUI [1])
C3889117 (UMLS CUI [2])
C3888903 (UMLS CUI [3])
C0079399 (UMLS CUI [4])
C0425293 (UMLS CUI [5])
C0078988 (UMLS CUI [6])
Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Tumor tissue sample EGFR exon 19 deletion | Tumor tissue sample Point mutation in exon 21 (L858R)
Item
tumor samples must have either exon 19 deletion mutations or the exon 21 l858r point mutation
boolean
C0475358 (UMLS CUI [1,1])
C3889117 (UMLS CUI [1,2])
C0475358 (UMLS CUI [2,1])
C3888903 (UMLS CUI [2,2])
ECOG performance status
Item
ecog performance status of 0,1, or 2
boolean
C1520224 (UMLS CUI [1])
Organ function
Item
adequate organ function as outlined in protocol
boolean
C0678852 (UMLS CUI [1])
Non-small cell lung cancer recurrent Radiography | erlotinib
Item
radiographic evidence of recurrent nsclc prior to erlotinib treatment
boolean
C0278517 (UMLS CUI [1,1])
C0034571 (UMLS CUI [1,2])
C1135135 (UMLS CUI [2])
EGFR T790M Resistance Mutation | Tumor tissue sample Primary
Item
confirmed t790m resistance mutation in the primary tumor sample
boolean
C3274192 (UMLS CUI [1,1])
C1514892 (UMLS CUI [1,2])
C0026882 (UMLS CUI [1,3])
C0475358 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
Exposure to EGFR Tyrosine Kinase Inhibitors
Item
prior exposure to egfr tyrosine kinase inhibitors
boolean
C0332157 (UMLS CUI [1,1])
C1443775 (UMLS CUI [1,2])
Hypersensitivity Erlotinib | Hypersensitivity Gefitinib | Hypersensitivity Pharmaceutical Preparations Related
Item
known hypersensitivity to erlotinib, gefitinib, or any closely related drug
boolean
C0020517 (UMLS CUI [1,1])
C1135135 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1122962 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0013227 (UMLS CUI [3,2])
C0439849 (UMLS CUI [3,3])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Lung Diseases, Interstitial
Item
any evidence of clinically active interstitial lung disease
boolean
C0206062 (UMLS CUI [1])
Antiepileptic Agents Enzyme Inducing | Carbamazepine | oxcarbazepine | Phenytoin | fosphenytoin | Phenobarbital | Primidone
Item
current use of enzyme-inducing anti-epileptic drugs, including carbamazepine, oxcarbazepine, phenytoin, fosphenytoin, phenobarbital, and primidone
boolean
C0003299 (UMLS CUI [1,1])
C0014442 (UMLS CUI [1,2])
C0205263 (UMLS CUI [1,3])
C0006949 (UMLS CUI [2])
C0069751 (UMLS CUI [3])
C0031507 (UMLS CUI [4])
C0244656 (UMLS CUI [5])
C0031412 (UMLS CUI [6])
C0033148 (UMLS CUI [7])
Disease Study Subject Participation Status Unfavorable | Laboratory finding Study Subject Participation Status Unfavorable
Item
evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the study
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C3640815 (UMLS CUI [1,3])
C0587081 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C3640815 (UMLS CUI [2,3])
Drugs, Non-Prescription | Investigational New Drugs | Side effects Pharmaceutical Preparations Recovery failed
Item
use of any non-fda approved or investigational agent within 2 weeks of enrolling onto the trial, or failure to recover from the side effects of any of these agents
boolean
C0013231 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C0879626 (UMLS CUI [3,1])
C0013227 (UMLS CUI [3,2])
C2004454 (UMLS CUI [3,3])
C0231175 (UMLS CUI [3,4])