DATE
Item
Date of last contact:
date
C0011008 (UMLS CUI-1)
Item
Subject disease status:
text
C0332307 (UMLS CUI-1)
C0012634 (UMLS CUI-2)
C0678257 (UMLS CUI-3)
Code List
Subject disease status:
CL Item
Alive, no evidence of disease (1)
CL Item
Alive, with disease (2)
CL Item
Alive, disease status unknown (3)
CL Item
Lost to follow-up (4)
toxicity
Item
Does subject still have a prior toxicity related to study drug?
boolean
C0040539 (UMLS CUI-1)
disease progression
Item
Did the subject's disease progress since the last report?
boolean
C0242656 (UMLS CUI-1)
DATE
Item
Date of recent progression:
date
C0011008 (UMLS CUI-1)
SUBJECT STATUS
Item
Will the subject continue to be followed?
boolean
C2348568 (UMLS CUI-1)
Item
If no, please indicate the primary reason:
text
C0392360 (UMLS CUI-1)
Code List
If no, please indicate the primary reason:
CL Item
Subject withdrew consent (Specify) (1)
CL Item
Lost to follow-up (3)
CL Item
Other (Specify) (4)
DATE
Item
In case of "Lost to follow-up", please mention the date of last contact:
date
C0011008 (UMLS CUI-1)
Specification
Item
For the reasons with "Specify", please mention the details:
text
C2348235 (UMLS CUI-1)
EQ-5D
Item
Evaluation of EQ-5D:
text
C2733251 (UMLS CUI [1])