End of Study Date
Item
End of Study Date
date
C2983670 (UMLS CUI-1)
Item
Reason for End of Study
integer
C2348577 (UMLS CUI-1)
Code List
Reason for End of Study
CL Item
regular End of Study (0)
C0205272 (UMLS CUI-1)
CL Item
no CR after Induction (Progressive Disease) (1)
C1335499 (UMLS CUI-1)
CL Item
exzessive extramedullary medical toxicity (2)
C0013221 (UMLS CUI-1)
CL Item
dead (3)
C1306577 (UMLS CUI-1)
CL Item
relapse after CR (4)
C0035020 (UMLS CUI-1)
CL Item
Withdrawal of informed consent (5)
C1710677 (UMLS CUI-1)
CL Item
Protocol deviation (6)
C1705236 (UMLS CUI-1)
CL Item
other (7)
C0205394 (UMLS CUI-1)
Specify if Reason for End of Study = 6 or 7
Item
Specify if Reason for End of Study = 6 or 7
text
Induction therapy I administered
Item
Induction therapy I administered
boolean
C0857127 (UMLS CUI-1)
C0205447 (UMLS CUI-2)
Induction therapy II administered
Item
Induction therapy II administered
boolean
C0857127 (UMLS CUI-1)
C0205448 (UMLS CUI-2)
Consolidation therapy I administered
Item
Consolidation therapy I administered
boolean
C1511484 (UMLS CUI-1)
C0205447 (UMLS CUI-2)
Consolidation therapy II administered
Item
Consolidation therapy II administered
boolean
C1511484 (UMLS CUI-1)
C0205448 (UMLS CUI-2)
Consolidation therapy III administered
Item
Consolidation therapy III administered
boolean
C1511484 (UMLS CUI-1)
C0205449 (UMLS CUI-2)
Consolidation therapy IV administered
Item
Consolidation therapy IV administered
boolean
C1511484 (UMLS CUI-1)
C0205450 (UMLS CUI-2)
Maintenance therapy administered
Item
Maintenance therapy administered
boolean
C0677908 (UMLS CUI-1)
Date
Item
Date
date
C0011008 (UMLS CUI-1)
Name of Investigator
Item
Name of Investigator
text
C2826892 (UMLS CUI-1)
Signature of investigator
Item
Signature of investigator
text
C2346576 (UMLS CUI-1)