Non-Small Cell Lung Carcinoma TNM clinical staging
Item
patients who were diagnosed by the histologic, cytologic diagnosis of iv non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Age
Item
age from 18 to 70 years old
boolean
C0001779 (UMLS CUI [1])
Target Lesion Quantity Diameter Spiral CT | Target Lesion Quantity Diameter CT | Measurable lesion Imaging
Item
at least one target lesion diameter spiral ct ≥ 1 cm, or the common ct ≥ 2 cm, and can be measured by imaging tools
boolean
C2986546 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
C0860888 (UMLS CUI [1,4])
C2986546 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C1301886 (UMLS CUI [2,3])
C0040405 (UMLS CUI [2,4])
C1513041 (UMLS CUI [3,1])
C0079595 (UMLS CUI [3,2])
ECOG performance status
Item
ecog 0-1
boolean
C1520224 (UMLS CUI [1])
Life Expectancy
Item
expected life time longer than 12 weeks
boolean
C0023671 (UMLS CUI [1])
Normal Laboratory Test Result
Item
normal laboratory values:
boolean
C0438214 (UMLS CUI [1])
White Blood Cell Count procedure | Neutrophil count | Platelet Count measurement | Hemoglobin measurement | Alanine aminotransferase measurement | Aspartate aminotransferase measurement
Item
leucocyte≥ 4×109/l neutrophil≥ 1.5×109/l platelet≥100×109/l hemoglobin≥ 10g/l alt and ast
boolean
C0023508 (UMLS CUI [1])
C0200633 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
C0518015 (UMLS CUI [4])
C0201836 (UMLS CUI [5])
C0201899 (UMLS CUI [6])
Relationship Secondary malignant neoplasm of liver
Item
≤2.5×uln (≤5×uln if liver metastasis)
boolean
C0439849 (UMLS CUI [1,1])
C0494165 (UMLS CUI [1,2])
Pharmaceutical Preparations Inconsistent Study Protocol
Item
patients have not used drugs according to protocol
boolean
C0013227 (UMLS CUI [1,1])
C0442809 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
Hypersensitivity Pemetrexed | Cisplatin allergy
Item
patients were allergic to pemetrexed or cisplatin
boolean
C0020517 (UMLS CUI [1,1])
C0210657 (UMLS CUI [1,2])
C0570702 (UMLS CUI [2])
Therapeutic radiology procedure | Biological treatment
Item
patients received radiotherapy or other biological treatment 4 weeks before the trial
boolean
C1522449 (UMLS CUI [1])
C1531518 (UMLS CUI [2])
Hydrothorax Uncontrolled | Hydropericardium Uncontrolled
Item
uncontrolled hydrothorax or hydropericardium
boolean
C0020312 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0349077 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
Neuropathy Toxicity CTCAE Grades
Item
neuropathy toxicity ≥ ctc 3
boolean
C0442874 (UMLS CUI [1,1])
C0600688 (UMLS CUI [1,2])
C1516728 (UMLS CUI [1,3])
Heart Disease Symptomatic Severe
Item
severe symptomatic heart disease
boolean
C0018799 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
Peptic Ulcer Upper Gastrointestinal Tract | Dysfunction Digestive
Item
active upper gastrointestinal ulcer or digestive disfunction
boolean
C0030920 (UMLS CUI [1,1])
C3203348 (UMLS CUI [1,2])
C3887504 (UMLS CUI [2,1])
C0012238 (UMLS CUI [2,2])
Communicable Disease Severe | Dysfunction Metabolic
Item
severe infection or metabolic disfunction
boolean
C0009450 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3887504 (UMLS CUI [2,1])
C0311400 (UMLS CUI [2,2])
Cancer Other
Item
patients with other malignant tumor
boolean
C1707251 (UMLS CUI [1])
Metastatic malignant neoplasm to brain Uncontrolled
Item
uncontrolled brain metastases
boolean
C0220650 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Study Subject Participation Status
Item
patients have accepted other clinical trials
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Breast Feeding | Contraceptive methods Absent
Item
female patients during their pregnant and lactation period, or patients without contraception
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])