Non-Small Cell Lung Carcinoma Advanced TNM clinical staging | Secondary malignant neoplasm of lymph node Supraclavicular | Pleural effusion | Non-Small Cell Lung Carcinoma TNM clinical staging
Item
histologic or cytologic confirmation of advanced nsclc (stage iiib with supraclavicular lymph node metastases or pleural effusion or stage iv) on entry into study
boolean
C0007131 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0686619 (UMLS CUI [2,1])
C1550301 (UMLS CUI [2,2])
C0032227 (UMLS CUI [3])
C0007131 (UMLS CUI [4,1])
C3258246 (UMLS CUI [4,2])
Measurable lesion Quantity | Longest Diameter Spiral CT scan | Longest Diameter Technique conventional
Item
one or more measurable lesions at least 10 mm in the longest diameter (ld) by spiral ct scan or 20 mm with conventional techniques according to recist criteria
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0552406 (UMLS CUI [2,1])
C0860888 (UMLS CUI [2,2])
C0552406 (UMLS CUI [3,1])
C0449851 (UMLS CUI [3,2])
C0439858 (UMLS CUI [3,3])
Chemotherapy naive | Adjuvant Chemotherapy Previous Completed
Item
chemotherapy-naïve (prior chemotherapy in the adjuvant setting completed more than 3 months before the trial entry is accepted).
boolean
C0392920 (UMLS CUI [1,1])
C0919936 (UMLS CUI [1,2])
C0085533 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0205197 (UMLS CUI [2,3])
Age
Item
female or male aged 70 years or above
boolean
C0001779 (UMLS CUI [1])
Cancer treatment Previous | Exception Adjuvant therapy
Item
patients must not have received prior anti-cancer therapy except in the adjuvant setting
boolean
C0920425 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0677850 (UMLS CUI [2,2])
Organ function Inadequate | Systemic disease Severe | Systemic disease Uncontrolled | Condition Study Subject Participation Status Unfavorable
Item
inadequate end-organ function or evidence of severe or uncontrolled systemic disease or any concurrent condition which in the investigator's opinion makes it undesirable for the patient to participate in the trial
boolean
C0678852 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
C0442893 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0442893 (UMLS CUI [3,1])
C0205318 (UMLS CUI [3,2])
C0348080 (UMLS CUI [4,1])
C2348568 (UMLS CUI [4,2])
C3640815 (UMLS CUI [4,3])
Cardiovascular event | Myocardial Infarction | Superior Vena Cava Syndrome | Heart Disease New York Heart Association Classification
Item
significant cardiovascular event (e.g. myocardial infarction, superior vena cava [svc] syndrome, new york heart association [nyha] classification of heart disease ³2) within 3 months before entry, or presence of cardiac disease that in the opinion of
boolean
C1320716 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0038833 (UMLS CUI [3])
C0018799 (UMLS CUI [4,1])
C1275491 (UMLS CUI [4,2])
Cardiac Arrhythmia | QTc Bazett formula Measurement Unsuccessful | ECG QTc interval Bazett formula
Item
history of arrhythmia or qtc with bazett's correction unmeasurable or ≥ 480 msec on screening ecg
boolean
C0003811 (UMLS CUI [1])
C0860814 (UMLS CUI [2,1])
C4038411 (UMLS CUI [2,2])
C0242485 (UMLS CUI [2,3])
C1272705 (UMLS CUI [2,4])
C2216079 (UMLS CUI [3,1])
C4038411 (UMLS CUI [3,2])