Comorbidity number
Item
Comorbidity number
integer
C0009488 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Comorbidity description
Item
Comorbidity description
text
C0678257 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
Begin
Item
Begin
date
C0808070 (UMLS CUI [1])
End
Item
End
date
C0806020 (UMLS CUI [1])
Ongoing
Item
Ongoing
integer
C0549178 (UMLS CUI [1])
Therapy
Item
Therapy
integer
C0087111 (UMLS CUI [1])
Therapy begin
Item
Therapy begin
date
C0087111 (UMLS CUI [1,1])
C0439659 (UMLS CUI [1,2])
Therapy end
Item
Therapy end
integer
C0087111 (UMLS CUI [1,1])
C0444930 (UMLS CUI [1,2])
Therapy ongoing
Item
Therapy ongoing
integer
C0549178 (UMLS CUI [1,1])
C0039798 (UMLS CUI [1,2])
Death date
Item
Death date
date
C1148348 (UMLS CUI [1])
Discontinuation date
Item
Discontinuation date
date
C1444662 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Time of premature discontinuation
integer
C0457454 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Code List
Time of premature discontinuation
CL Item
Cycle (2)
C1302181 (UMLS CUI-1)
CL Item
Arm A, cycle (3)
C1522541 (UMLS CUI-1)
CL Item
Arm B, cycle (4)
C1522541 (UMLS CUI-1)
CL Item
DHAP, cycle (5)
C0057634 (UMLS CUI-1)
CL Item
ESHAP, cycle (6)
C0285858 (UMLS CUI-1)
CL Item
Follow-up (7)
C1522577 (UMLS CUI-1)
CL Item
BEAM-R, cycle (8)
Item
Reason for premature discontinuation of trial participation
integer
C0457454 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
Reason for premature discontinuation of trial participation
CL Item
unknown (1)
C0439673 (UMLS CUI-1)
CL Item
death (2)
C0011065 (UMLS CUI-1)
CL Item
Lymphoma aftermath (3)
C0024299 (UMLS CUI-1)
CL Item
disease progression (4)
C0242656 (UMLS CUI-1)
CL Item
toxicity (5)
C0013221 (UMLS CUI-1)
CL Item
protocol violation (6)
C1709750 (UMLS CUI-1)
CL Item
non-compliance (7)
C0457432 (UMLS CUI-1)
CL Item
lost to follow-up (8)
C1302313 (UMLS CUI-1)
CL Item
patient wish (9)
C0747309 (UMLS CUI-1)
CL Item
Physician Decision (10)
C1709536 (UMLS CUI-1)
Adverse event number
Item
Adverse event number
integer
C0877248 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Begin
Item
Begin
date
C0808070 (UMLS CUI [1])
End
Item
End
date
C0806020 (UMLS CUI [1])
Adverse event
Item
Adverse event
text
C0877248 (UMLS CUI [1])
Item
Adverse event frequency
integer
C0877248 (UMLS CUI [1,1])
C0439603 (UMLS CUI [1,2])
Code List
Adverse event frequency
Item
Adverse Event: Severity
integer
C1710066 (UMLS CUI [1])
Code List
Adverse Event: Severity
CL Item
Mild (Mild)
C2945599 (UMLS CUI-1)
CL Item
Moderate (Moderate)
C0205081 (UMLS CUI-1)
CL Item
Severe (Severe)
C0205082 (UMLS CUI-1)
CL Item
Life threatening (4)
C2826244 (UMLS CUI-1)
CL Item
Death (5)
C0011065 (UMLS CUI-1)
Item
Adverse Event Action Code
integer
C0877248 (UMLS CUI [1,1])
C0441472 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
Code List
Adverse Event Action Code
CL Item
Agent Withdrawn (1)
C2349954 (UMLS CUI-1)
CL Item
Agent Dose Reduced (2)
C0441610 (UMLS CUI-1)
CL Item
Agent Dose Increased (3)
C0442805 (UMLS CUI-1)
CL Item
Agent Dose Not Changed (4)
C0443172 (UMLS CUI-1)
CL Item
Unknown (5)
C0439673 (UMLS CUI-1)
CL Item
Not Applicable (6)
C1272460 (UMLS CUI-1)
Item
Correlation with trial procedure
integer
C1707520 (UMLS CUI [1])
Code List
Correlation with trial procedure
CL Item
no correlation (5)
CL Item
can not be assessed (6)
Item
Result of adverse event
integer
C2985628 (UMLS CUI [1])
Code List
Result of adverse event
CL Item
Patient restored (1)
C0846605 (UMLS CUI-1)
CL Item
Ongoing (2)
C0549178 (UMLS CUI-1)
CL Item
permanent damage (3)
C3640792 (UMLS CUI-1)
CL Item
malformation (4)
C0302142 (UMLS CUI-1)
CL Item
death (5)
C0011065 (UMLS CUI-1)
CL Item
unknown (6)
C0439673 (UMLS CUI-1)
Comment
Item
Comment
text
C0947611 (UMLS CUI [1])
Date of processing
Item
Date of processing
date
C1709694 (UMLS CUI [1])
Signature clinical investigator
Item
Signature clinical investigator
boolean
C0008961 (UMLS CUI [1])