Study Coordinating Center, Identification number
Item
Center number
integer
C2825181 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Patient number
Item
Patient Number
integer
C1830427 (UMLS CUI [1])
Person Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Item
Cause of Death
text
C0007465 (UMLS CUI [1])
CL Item
Progressive Disease (1)
CL Item
Toxicity: Hematologic (2)
CL Item
Toxicity: Non-Hematologic (3)
CL Item
Other, specify (4)
Cause of Death
Item
Specify
text
C0007465 (UMLS CUI [1])
Date of death
Item
Date of Death
date
C1148348 (UMLS CUI [1])
Cessation of life, Autopsy
Item
Was a post-mortem done?
boolean
C0011065 (UMLS CUI [1,1])
C0004398 (UMLS CUI [1,2])
Cessation of life, Autopsy, Finding
Item
If 'Yes' please summarize findings (include diagnosis)
text
C0011065 (UMLS CUI [1,1])
C0004398 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,3])
Cessation of life, Signature of responsible attending physician on file
Item
Physician's Signature
text
C0011065 (UMLS CUI [1,1])
C0807938 (UMLS CUI [1,2])
Cessation of life, Signature of responsible attending physician on file, Date in time
Item
Date
date
C0011065 (UMLS CUI [1,1])
C0807938 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])