Age | Non-Small Cell Lung Carcinoma TNM clinical staging
Item
patients aged greater than 18 years with a diagnosis of stage iii non-small cell lung cancer.
boolean
C0001779 (UMLS CUI [1])
C0007131 (UMLS CUI [2,1])
C3258246 (UMLS CUI [2,2])
Chemoradiotherapy Planned | Chemoradiotherapy Preoperative Planned | Excision Planned
Item
planned treatment with either definitive chemoradiotherapy or preoperative chemoradiotherapy followed by surgical resection.
boolean
C0436307 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0436307 (UMLS CUI [2,1])
C0445204 (UMLS CUI [2,2])
C1301732 (UMLS CUI [2,3])
C0728940 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
PET/CT Study | DECT Study
Item
pet-ct study within 4 weeks of next available dect study.
boolean
C1699633 (UMLS CUI [1,1])
C2603343 (UMLS CUI [1,2])
C4055114 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
Measurable Disease Primary | Disorder of lymph node Primary | Primary lesion Size Quantity | Lymph node Primary lesion Size Quantity
Item
patients must have measurable primary and nodal disease, defined by at least one lesion (primary and lymph node) greater than 1 cm.
boolean
C1513041 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0272394 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
C1402294 (UMLS CUI [3,1])
C0456389 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C0024204 (UMLS CUI [4,1])
C1402294 (UMLS CUI [4,2])
C0456389 (UMLS CUI [4,3])
C1265611 (UMLS CUI [4,4])
Renal function | CT iodinated contrast dye
Item
kidney function sufficient to tolerate iodine-based ct contrast.
boolean
C0232804 (UMLS CUI [1])
C0040405 (UMLS CUI [2,1])
C0879373 (UMLS CUI [2,2])
Iodine contrast allergy Absent
Item
no allergy to iodine-based contrast.
boolean
C4022917 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
ability to understand and the willingness to sign informed consent.
boolean
C0021430 (UMLS CUI [1])
Radiotherapy to thorax
Item
participants with a prior history of thoracic radiotherapy.
boolean
C4038705 (UMLS CUI [1])
Investigational New Drugs
Item
participants may not be receiving any other study agents.
boolean
C0013230 (UMLS CUI [1])
CT scan contrast Receive Unable
Item
inability to tolerate ct contrast
boolean
C0742919 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Pregnancy | Breast Feeding To be stopped
Item
pregnant women are excluded from this study because radiotherapy has the potential for teratogenic or abortifacient effects. because there is an unknown but potential risk of adverse events in nursing infants secondary to treatment of the mother with radiotherapy, breastfeeding should be discontinued if the mother is treated with radiotherapy. these potential risks may also apply to other agents used in this study.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2,1])
C1272691 (UMLS CUI [2,2])