ID.1
Item
breast or colorectal primary tumor sites
boolean
C0678222|C0009402 (UMLS CUI [1])
ID.2
Item
considered incurable
boolean
C0175969 (UMLS CUI [1])
ID.3
Item
breast cancer patients must have disease progression after at least 2 different chemotherapy regimens (may include chemotherapy given as an adjuvant treatment)
boolean
C0392920 (UMLS CUI [1])
ID.4
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
ID.5
Item
age:
boolean
C0001779 (UMLS CUI [1])
ID.6
Item
18 and over
boolean
ID.7
Item
sex:
boolean
C0079399 (UMLS CUI [1])
ID.8
Item
male or female
boolean
ID.9
Item
performance status:
boolean
C1520224 (UMLS CUI [1])
ID.10
Item
ecog 0-2
boolean
ID.11
Item
life expectancy:
boolean
C0023671 (UMLS CUI [1])
ID.12
Item
more than 3 months
boolean
ID.13
Item
hepatic:
boolean
C0205054 (UMLS CUI [1])
ID.14
Item
bilirubin no greater than 3 times upper limit of normal (uln)
boolean
ID.15
Item
renal:
boolean
C0022646 (UMLS CUI [1])
ID.16
Item
calcium less than 1.2 times uln
boolean
ID.17
Item
other:
boolean
C0205394 (UMLS CUI [1])
ID.18
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
ID.19
Item
fertile patients must use effective contraception
boolean
C0015895 (UMLS CUI [1])
ID.20
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
ID.21
Item
chemotherapy:
boolean
C0392920 (UMLS CUI [1])
ID.22
Item
concurrent chemotherapy allowed
boolean
C0392920 (UMLS CUI [1,1])
C0009429 (UMLS CUI [1,2])
ID.23
Item
no concurrent participation in a cytotoxic chemotherapy clinical trial
boolean
C2348568 (UMLS CUI [1])
ID.24
Item
other:
boolean
C0205394 (UMLS CUI [1])
ID.25
Item
at least 60 days since prior shark cartilage
boolean