age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
who ps
Item
who ps 0-2
boolean
C1298650 (UMLS CUI [1])
histological or cytological confirmation of non-small cell lung cancer or an 18f-fdg-positive, growing mass on ct-thorax suggestive of nsclc
Item
histological or cytological confirmation of non-small cell lung cancer or an 18f-fdg-positive, growing mass on ct-thorax suggestive of nsclc.
boolean
C0007131 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C0019638 (UMLS CUI [1,3])
C0007131 (UMLS CUI [2,1])
C0750484 (UMLS CUI [2,2])
C0010819 (UMLS CUI [2,3])
C0007131 (UMLS CUI [3,1])
C0040405 (UMLS CUI [3,2])
C3641247 (UMLS CUI [3,3])
C1514241 (UMLS CUI [3,4])
tnm stage
Item
stage iiia or iiib
boolean
C1515169 (UMLS CUI [1,1])
C0475455 (UMLS CUI [1,2])
mediastinal lymph node involvement or large primary tumour size
Item
patients with extensive mediastinal lymph node involvement (such as n3), or large primary tumour size
boolean
C1515169 (UMLS CUI [1,1])
C0456532 (UMLS CUI [1,2])
C1515169 (UMLS CUI [2,1])
C0475455 (UMLS CUI [2,2])
adequate pulmonary function estimated by flow volume curves
Item
adequate pulmonary function estimated by flow volume curves
boolean
C0231921 (UMLS CUI [1,1])
C0205411 (UMLS CUI [1,2])
C0024119 (UMLS CUI [1,3])
life expectancy
Item
life expectancy of at least 6 months
boolean
C0023671 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol
Item
absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol; those conditions should be discussed with the patient before registration in the trial.
boolean
C0205486 (UMLS CUI [1,1])
C0348080 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C1292733 (UMLS CUI [1,4])
C0525058 (UMLS CUI [1,5])
C0241888 (UMLS CUI [2,1])
C0348080 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C1292733 (UMLS CUI [2,4])
C0525058 (UMLS CUI [2,5])
C3850138 (UMLS CUI [3,1])
C0348080 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C1292733 (UMLS CUI [3,4])
C0525058 (UMLS CUI [3,5])
C0017444 (UMLS CUI [4,1])
C0348080 (UMLS CUI [4,2])
C0332197 (UMLS CUI [4,3])
C1292733 (UMLS CUI [4,4])
C0525058 (UMLS CUI [4,5])
planned radiotherapy with concomitant chemotherapy
Item
planned for 25 x 2.4 gy, with concomitant chemotherapy
boolean
C1522449 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
C1707479 (UMLS CUI [1,4])
written informed consent
Item
before patient registration, written informed consent will be obtained.
boolean
C0021430 (UMLS CUI [1])
mri contra-indications
Item
presence of contra-indications for undergoing mri
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])