Prostate cancer risk assessment (from TNM, GS and PSA)
Item
Intermediate-risk prostate cancer patients (T1/T2N0M0 with either GS < 7 and PSA between 10-20 ng/ml or GS 7 and PSA less than 20 ng/ml).
boolean
C0600139 (UMLS CUI [1,1])
C0086930 (UMLS CUI [1,2])
C1515169 (UMLS CUI [2])
C3203027 (UMLS CUI [3])
C0201544 (UMLS CUI [4])
planned for radical RT to the prostate with IMRT planning
Item
planned for radical RT to the prostate with IMRT planning (79Gy/39 fractions or 60 Gy/20 fractions)
boolean
C1301732 (UMLS CUI [1,1])
C0439807 (UMLS CUI [1,2])
C0033572 (UMLS CUI [1,3])
C1512814 (UMLS CUI [1,4])
C2169193 (UMLS CUI [2])
C0454266 (UMLS CUI [3])
no contraindications to diagnostic CT scanning
Item
no contraindications to diagnostic CT scanning
boolean
C0332197 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0040405 (UMLS CUI [1,3])
prostate volume
Item
prostate volumes will be less than 80 cc to control the planning dose volume histogram (DVH) as much as possible in terms of rectal and bladder volumes
boolean
C1441416 (UMLS CUI [1])
C3827011 (UMLS CUI [2,1])
C0034896 (UMLS CUI [2,2])
C3827011 (UMLS CUI [3,1])
C0005682 (UMLS CUI [3,2])
no known DNA repair disorders (e.g. AT, BRCA1/2, Li Fraumeni) or contraindications to radical pelvic RT
Item
no known DNA repair disorders (e.g. family history of AT, BRCA1/2 or Li Fraumeni syndrome) or contraindications to radical pelvic RT
boolean
C0332197 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
C0012899 (UMLS CUI [1,3])
C0332197 (UMLS CUI [2,1])
C0241889 (UMLS CUI [2,2])
C0004135 (UMLS CUI [2,3])
C0332197 (UMLS CUI [3,1])
C4543583 (UMLS CUI [3,2])
C0332197 (UMLS CUI [4,1])
C0241889 (UMLS CUI [4,2])
C0085390 (UMLS CUI [4,3])
C0332197 (UMLS CUI [5,1])
C0522473 (UMLS CUI [5,2])
C0439807 (UMLS CUI [5,3])
C1536155 (UMLS CUI [5,4])
inability to provide informed consent
Item
inability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
contraindications to diagnostic CT scan
Item
patient having contraindications to diagnostic CT scan
boolean
C1301624 (UMLS CUI [1,1])
C0040405 (UMLS CUI [1,2])
patients with unobtainable data regarding previous therapy and their clinical outcome
Item
patients who have unobtainable data regarding previous therapy and their clinical outcome
boolean
C2046401 (UMLS CUI [1,1])
C2114510 (UMLS CUI [1,2])
C2046401 (UMLS CUI [2,1])
C2114510 (UMLS CUI [2,2])
C1547647 (UMLS CUI [2,3])
Recent diagnostic X-rays or CAT scans
Item
Patients should not have any diagnostic X-rays or CAT scans 2 weeks prior to their enrollment into the study
boolean
C0043299 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
C0040405 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])