Non-Small Cell Lung Carcinoma | Squamous cell carcinoma of lung | Adenocarcinoma of lung | Large cell carcinoma of lung
Item
histologically proven (biopsy or cytology) nsclc (scc, adenocarcinoma, large cell)
boolean
C0007131 (UMLS CUI [1])
C0149782 (UMLS CUI [2])
C0152013 (UMLS CUI [3])
C0345958 (UMLS CUI [4])
TNM clinical staging Inoperable | TNM clinical staging unresectable | Pleural effusion Absent
Item
tnm clinical non-operable stage i/ii and non-resectable stage iiia/b without pleural effusion
boolean
C3258246 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C3258246 (UMLS CUI [2,1])
C1519810 (UMLS CUI [2,2])
C0032227 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Measurable Disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Malignant Neoplasms | Skin carcinoma | Interval Disease Free of
Item
no other malignancy, except non-melanomatous skin cancer, within 5 years prior to participation in this study; the disease-free interval from any prior carcinoma must be continuous
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2])
C1272706 (UMLS CUI [3,1])
C0012634 (UMLS CUI [3,2])
C0332296 (UMLS CUI [3,3])
Patient suitable Conformal Radiotherapy Radical
Item
patient suitable for radical 3-dcrt
boolean
C0030705 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C0600521 (UMLS CUI [1,3])
C0439807 (UMLS CUI [1,4])
ECOG performance status | Karnofsky Performance Status
Item
ecog-performance status ≤ 2 / kps > or equal to 60
boolean
C1520224 (UMLS CUI [1])
C0206065 (UMLS CUI [2])
Weight decreased Percentage
Item
weight loss <10% within the 3 months prior to diagnosis
boolean
C1262477 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
Radiotherapy to thorax Absent
Item
no prior radiotherapy to the thorax
boolean
C4038705 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Patient suitable Immobilization Lung Board
Item
patient is suitable for lung-board immobilisation
boolean
C0030705 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C0020944 (UMLS CUI [1,3])
C0024109 (UMLS CUI [1,4])
C0972401 (UMLS CUI [1,5])
Chemotherapy Absent | PET/CT scan Planned
Item
no chemotherapy received prior to planning pet-ct scan
boolean
C0392920 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1699633 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Age
Item
age 18 and over
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
provision of written informed consent
boolean
C0021430 (UMLS CUI [1])
Disease Study Subject Participation Status Unfavorable | Laboratory finding Study Subject Participation Status Unfavorable | Disease Protocol Compliance Unlikely | Laboratory finding Protocol Compliance Unlikely
Item
evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the trial or if it is felt by the research / medical team that the patient may not be able to comply with the protocol.
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C3640815 (UMLS CUI [1,3])
C0587081 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C3640815 (UMLS CUI [2,3])
C0012634 (UMLS CUI [3,1])
C0525058 (UMLS CUI [3,2])
C0750558 (UMLS CUI [3,3])
C0587081 (UMLS CUI [4,1])
C0525058 (UMLS CUI [4,2])
C0750558 (UMLS CUI [4,3])
PULMONARY FUNCTION TEST FEV1
Item
fev1 < 1
boolean
C0748133 (UMLS CUI [1])