breast or colorectal primary tumor
Item
breast or colorectal primary tumor sites
boolean
C0678222 (UMLS CUI [1])
C0009402 (UMLS CUI [2])
incurable tumor
Item
considered incurable
boolean
C0175969 (UMLS CUI [1])
disease progression under chemotherapy
Item
breast cancer patients must have disease progression after at least 2 different chemotherapy regimens (may include chemotherapy given as an adjuvant treatment)
boolean
C0242656 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
18 and over
Item
18 and over
boolean
C0001779 (UMLS CUI [1])
male or female
Item
male or female
boolean
C0079399 (UMLS CUI [1])
ECOG 0-2
Item
ECOG 0-2
boolean
C1512162 (UMLS CUI [1])
more than 3 months
Item
more than 3 months
boolean
C0023671 (UMLS CUI [1])
bilirubin no greater than 3 times upper limit of normal (uln)
Item
bilirubin no greater than 3 times upper limit of normal (uln)
boolean
C0005437 (UMLS CUI [1])
calcium less than 1.2 times uln
Item
calcium less than 1.2 times uln
boolean
C0201925 (UMLS CUI [1])
pregnant or nursing
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
contraception
Item
fertile patients must use effective contraception
boolean
C0700589 (UMLS CUI [1])
prior concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
chemotherapy
Item
chemotherapy:
boolean
C0392920 (UMLS CUI [1])
concurrent chemotherapy
Item
concurrent chemotherapy allowed
boolean
C0392920 (UMLS CUI [1,1])
C0009429 (UMLS CUI [1,2])
concurrent clinical trial participation
Item
no concurrent participation in a cytotoxic chemotherapy clinical trial
boolean
C2348568 (UMLS CUI [1])
prior shark cartilage therapy
Item
at least 60 days since prior shark cartilage
boolean
C1514463 (UMLS CUI [1,1])
C1883024 (UMLS CUI [1,2])