Informed Consent
Item
ability to understand and the willingness to sign a written informed consent document.
boolean
C0021430 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma TNM clinical staging
Item
histologically or cytologically confirmed non-small cell cancer, stage iiib or iv.
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Age
Item
age should be 18 years or above.
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ecog should be in 0-1 range.
boolean
C1520224 (UMLS CUI [1])
Absolute neutrophil count
Item
absolute neutrophil count ≥ 1,00,000/mm3
boolean
C0948762 (UMLS CUI [1])
Hemoglobin measurement
Item
hemoglobin ≥ 9.0g/dl
boolean
C0518015 (UMLS CUI [1])
Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Relationship Secondary malignant neoplasm of liver
Item
ast and alt ≤ 2.5 times upper limit of normal (uln)range of institution (5times uln if liver metastasis present).
boolean
C0201899 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0439849 (UMLS CUI [3,1])
C0494165 (UMLS CUI [3,2])
Serum total bilirubin measurement | Relationship Involvement with Liver
Item
bilirubin not greater than 1.5 times uln range of institution (3 times uln if liver involvement).
boolean
C1278039 (UMLS CUI [1])
C0439849 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C0023884 (UMLS CUI [2,3])
Creatinine measurement, serum
Item
creatinine ≤ upper limit of normal (uln) range of institution.
boolean
C0201976 (UMLS CUI [1])
Childbearing Potential Pregnancy test negative
Item
negative pregnancy test for women of child bearing potential prior to entry into the trial.
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
Cytotoxic Chemotherapy | Therapeutic radiology procedure
Item
patient who have cytotoxic chemotherapy or radiotherapy prior to entering the study
boolean
C0677881 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Metastatic malignant neoplasm to brain systematic
Item
patient with systematic brain metastasis.
boolean
C0220650 (UMLS CUI [1,1])
C0220922 (UMLS CUI [1,2])
Paclitaxel allergy | Cisplatin allergy | Allergic Reaction Mycobacterium w | Allergic Reaction Paclitaxel Ingredient | Allergic Reaction Cisplatin Ingredient | Allergic Reaction Mycobacterium w Ingredient
Item
history of allergic reaction attributed to paclitaxel, cisplatin or mycobacterium w or any of their ingredients.
boolean
C0570707 (UMLS CUI [1])
C0570702 (UMLS CUI [2])
C1527304 (UMLS CUI [3,1])
C1940778 (UMLS CUI [3,2])
C1527304 (UMLS CUI [4,1])
C0144576 (UMLS CUI [4,2])
C1550600 (UMLS CUI [4,3])
C1527304 (UMLS CUI [5,1])
C0008838 (UMLS CUI [5,2])
C1550600 (UMLS CUI [5,3])
C1527304 (UMLS CUI [6,1])
C1940778 (UMLS CUI [6,2])
C1550600 (UMLS CUI [6,3])
Pregnancy | Breast Feeding
Item
pregnant women or nursing women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Comorbidity Uncontrolled | Protocol Compliance Limited
Item
uncontrolled intercurrent illness that would limit compliance with study requirements.
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
HIV Seropositivity
Item
hiv positive patients.
boolean
C0019699 (UMLS CUI [1])
Splenectomy
Item
previous splenectomy.
boolean
C0037995 (UMLS CUI [1])