Non-Small Cell Lung Carcinoma TNM clinical staging | CT with intravenous contrast Chest | Imaging other
Item
patient with any stage non-small cell lung cancer (nsclc) who will undergo imaging with ct of the chest with intravenous contrast as standard of care. other imaging tests will be performed as clinically indicated.
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0202653 (UMLS CUI [2,1])
C0817096 (UMLS CUI [2,2])
C0025086 (UMLS CUI [3])
Systemic therapy | Chemotherapy | Investigational New Drugs | Therapeutic radiology procedure | Adjuvant therapy Absent | Therapeutic procedure Postoperative Absent | Neoadjuvant Therapy allowed
Item
patient should be receiving, or planning to receive, or have received systemic therapy (chemotherapy and/or novel agents) treatment with or without radiotherapy. patients should not be receiving adjuvant or postoperative treatment but neoadjuvant treatment is allowed.
boolean
C1515119 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C0013230 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
C0677850 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C0087111 (UMLS CUI [6,1])
C0032790 (UMLS CUI [6,2])
C0332197 (UMLS CUI [6,3])
C0600558 (UMLS CUI [7,1])
C0683607 (UMLS CUI [7,2])
Non-Small Cell Lung Carcinoma
Item
histologically or cytologically proven nsclc.
boolean
C0007131 (UMLS CUI [1])
Measurable Disease Primary Size Quantity | Lesion thorax | Lesion supraclavicular | Lesion Malignant Biopsy | Lesion Malignant Imaging study
Item
at least one measurable primary or other intrathoracic/supraclavicular lesion ≥ 1 cm, according to response evaluation criteria in solid tumors (recist); this lesion should be either proven to be malignant by biopsy or be considered malignant based on its evolution on previous imaging studies. a scan within 3-6 months prior to registration can be used as the baseline scan.
boolean
C1513041 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
C1406924 (UMLS CUI [2])
C0221198 (UMLS CUI [3,1])
C0446461 (UMLS CUI [3,2])
C0221198 (UMLS CUI [4,1])
C0205282 (UMLS CUI [4,2])
C0005558 (UMLS CUI [4,3])
C0221198 (UMLS CUI [5,1])
C0205282 (UMLS CUI [5,2])
C1881134 (UMLS CUI [5,3])
Age | Informed Consent
Item
age 18 years or older and ability to provide informed consent.
boolean
C0001779 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
Sexually active Contraceptive methods | Childbearing Potential Pregnancy Absent | Childbearing Potential Breast Feeding Absent
Item
subjects must use medically appropriate contraception if sexually active; women of childbearing potential must not be pregnant or breastfeeding
boolean
C0241028 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C3831118 (UMLS CUI [2,1])
C0032961 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C3831118 (UMLS CUI [3,1])
C0006147 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Renal function | Kidney Function Tests | Administration Intravenous contrast | Renal Insufficiency | Glomerular Filtration Rate Body Surface Area | Creatinine measurement, serum
Item
subjects must have normal renal function to participate. standard laboratory testing to evaluate renal function will be performed prior to administering iv contrast and will be available as standard of care. renal impairment is defined as a glomerular filtration rate of less than 60 ml/min/1.73 m2 bsa, derived from the patients' serum creatinine concentration.
boolean
C0232804 (UMLS CUI [1])
C0022662 (UMLS CUI [2])
C1533734 (UMLS CUI [3,1])
C4072741 (UMLS CUI [3,2])
C1565489 (UMLS CUI [4])
C0017654 (UMLS CUI [5,1])
C0005902 (UMLS CUI [5,2])
C0201976 (UMLS CUI [6])
Reproductive potential Sexually active Contraceptive methods Unwilling | Reproductive potential Sexually active Contraceptive methods Unable | Pregnancy | Breast Feeding
Item
subjects of reproductive potential, who are sexually active but unwilling and/or unable to use medically appropriate contraception, or women who are pregnant or breastfeeding;
boolean
C4034483 (UMLS CUI [1,1])
C0241028 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
C0558080 (UMLS CUI [1,4])
C4034483 (UMLS CUI [2,1])
C0241028 (UMLS CUI [2,2])
C0700589 (UMLS CUI [2,3])
C1299582 (UMLS CUI [2,4])
C0032961 (UMLS CUI [3])
C0006147 (UMLS CUI [4])
Iodine contrast allergy
Item
established allergy to iodine containing contrast media
boolean
C4022917 (UMLS CUI [1])