Participant has a confirmed diagnosis of non-B-cell acute lymphoblastic leukemia (ALL)
Item
Participant has a confirmed diagnosis of non-B-cell acute lymphoblastic leukemia (ALL)
boolean
C1512693 (UMLS CUI [1,1])
C0023492 (UMLS CUI [1,2])
C0023449 (UMLS CUI [1,3])
Participant is less than or equal to 18 years of age
Item
Participant is less than or equal to 18 years of age
boolean
C1512693 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
Written, informed consent following NCI, IRB, FDA, and OPRR Guidelines
Item
Written, informed consent following NCI, IRB, FDA, and OPRR Guidelines
boolean
C1512693 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Patient received high-dose methotrexate as part of protocol-directed therapy for ALL
Item
Patient received high-dose methotrexate as part of protocol-directed therapy for ALL
boolean
C1512693 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0444956 (UMLS CUI [1,3])
C0025677 (UMLS CUI [1,4])