ID.1
Item
meets 1 of the following criteria:
boolean
ID.2
Item
pathologically confirmed invasive breast cancer (patient)
boolean
C0678222 (UMLS CUI [1])
ID.3
Item
no ductal carcinoma in situ
boolean
C1527349 (UMLS CUI [1])
ID.4
Item
affected or unaffected sibling
boolean
C0037047 (UMLS CUI [1])
ID.5
Item
affected sibling must have had (or currently has) breast cancer only
boolean
C0037047 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
ID.6
Item
unaffected sibling must be female
boolean
C0037047 (UMLS CUI [1,1])
C0015780 (UMLS CUI [1,2])
ID.7
Item
no deceased siblings
boolean
C0037047 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
ID.8
Item
must be a full-blood related sibling
boolean
C0037047 (UMLS CUI [1,1])
C1266852 (UMLS CUI [1,2])
ID.9
Item
patients receiving treatment on clinical trial ecog-e1y97 or ecog-e3y92 are not eligible
boolean
C1520224 (UMLS CUI [1])
ID.10
Item
patient characteristics:
boolean
ID.11
Item
not specified
boolean
ID.12
Item
prior concurrent therapy:
boolean
ID.13
Item
not specified
boolean