Tumor assessment of Chronic Lymphocytic Leukemia NCT00090051 BO17072

Tumor assessment at screening
Beschrijving

Tumor assessment at screening

Date of Assessment
Beschrijving

Assessment Date

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2985720
dd/mm/yy
Indicator lesions
Beschrijving

Indicator lesions

Code of origin
Beschrijving

Code of origin

Datatype

integer

Alias
UMLS CUI [1]
C2986125
extra nodal or other specification
Beschrijving

extra nodal or other specification

Datatype

text

Alias
UMLS CUI [1]
C1517067
Side of lesion
Beschrijving

Side of lesion

Datatype

text

Alias
UMLS CUI [1]
C0441987
Dimensions
Beschrijving

Dimensions

Datatype

text

Maateenheden
  • mm x mm
Alias
UMLS CUI [1]
C0439534
mm x mm
Method of assessment
Beschrijving

Method of assessment

Datatype

text

Alias
UMLS CUI [1]
C2598110
Other specification
Beschrijving

Other specification

Datatype

text

Non-indicator lesions
Beschrijving

Non-indicator lesions

Alias
UMLS CUI-1
C0221198
Code of origin
Beschrijving

Code of origin

Datatype

integer

Alias
UMLS CUI [1]
C2986125
extra nodal or other specification
Beschrijving

extra nodal or other specification

Datatype

text

Alias
UMLS CUI [1]
C1517067
Side of lesion
Beschrijving

Side of lesion

Datatype

text

Alias
UMLS CUI [1]
C0441987
Liver and spleen examination
Beschrijving

Liver and spleen examination

Date of Assessment
Beschrijving

Date of Assessment

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2985720
dd/mm/yy
Examination type
Beschrijving

Examination type

Datatype

integer

Alias
UMLS CUI [1]
C0031809
specify other examination
Beschrijving

specify other examination

Datatype

text

Alias
UMLS CUI [1]
C0582103
Hepatomegaly
Beschrijving

Hepatomegaly

Datatype

boolean

Alias
UMLS CUI [1]
C0019209
Splenomegaly
Beschrijving

Splenomegaly

Datatype

boolean

Alias
UMLS CUI [1]
C0038002
Tumor assessment after Cycle 3 and 6
Beschrijving

Tumor assessment after Cycle 3 and 6

Assessment Date
Beschrijving

Date of Assessment

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2985720
dd/mm/yy
Indicator lesions
Beschrijving

Indicator lesions

Code of origin
Beschrijving

Code of origin

Datatype

text

Alias
UMLS CUI [1]
C2986125
extra nodal or other specification
Beschrijving

extra nodal or other specification

Datatype

integer

Alias
UMLS CUI [1]
C1517067
Side of lesion
Beschrijving

Side of lesion

Datatype

integer

Alias
UMLS CUI [1]
C1285236
Dimensions
Beschrijving

Dimensions

Datatype

integer

Maateenheden
  • mm x mm
Alias
UMLS CUI [1]
C0439534
mm x mm
Method of assessment
Beschrijving

Method of assessment

Datatype

integer

Alias
UMLS CUI [1]
C2598110
Other specification
Beschrijving

Other specification

Datatype

integer

Alias
UMLS CUI [1]
C2348235
Non-indicator lesions
Beschrijving

Non-indicator lesions

Code of origin
Beschrijving

Code of origin

Datatype

text

extra nodal or other specification
Beschrijving

extra nodal or other specification

Datatype

text

Alias
UMLS CUI [1]
C1517067
Side of lesion
Beschrijving

Side of lesion

Datatype

integer

Alias
UMLS CUI [1]
C1285236
Presence
Beschrijving

Presence

Datatype

boolean

Alias
UMLS CUI [1]
C0150312
Liver and spleen examination after Cycle 3 and 6
Beschrijving

Liver and spleen examination after Cycle 3 and 6

Date of Assessment
Beschrijving

Date of Assessment

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2985720
dd/mm/yy
Examination type
Beschrijving

Examination type

Datatype

integer

Alias
UMLS CUI [1]
C0031809
specify other examination
Beschrijving

specify other examination

Datatype

text

Alias
UMLS CUI [1]
C0260879
Hepatomegaly
Beschrijving

Hepatomegaly

Datatype

boolean

Alias
UMLS CUI [1]
C0019209
Status since last visit
Beschrijving

Status since last visit

Datatype

integer

Alias
UMLS CUI [1]
C0449438
Splenomegaly
Beschrijving

Splenomegaly

Datatype

boolean

Alias
UMLS CUI [1]
C0038002
Status since last visit
Beschrijving

Status since last visit

Datatype

integer

Alias
UMLS CUI [1]
C0449438
Response assessment after cycle 3
Beschrijving

Response assessment after cycle 3

Date of Assessment
Beschrijving

Assessment Date

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2985720
dd/mm/yy
Are there any new lesions?
Beschrijving

New lesions

Datatype

boolean

Alias
UMLS CUI [1]
C0221198
Was there unequivocal progression in the size of non-indicator lesions?
Beschrijving

Non-indicator lesions

Datatype

boolean

Alias
UMLS CUI [1]
C3272925
Overall response
Beschrijving

Overall response

Datatype

integer

Alias
UMLS CUI [1]
C3272903
Does patient fulfill the criteria for a CR but have persistent anemia or thrombocytopenia?
Beschrijving

Partial response

Datatype

boolean

Alias
UMLS CUI [1]
C0741008
Response assessment after Cycle 6
Beschrijving

Response assessment after Cycle 6

Assessment Date
Beschrijving

Date of Assessment

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2985720
dd/mm/yy
Are there any new lesions?
Beschrijving

New lesions

Datatype

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0205314
Was there unequivocal progression in the size of non-indicator lesions?
Beschrijving

Non-indicator lesions

Datatype

boolean

Overall response
Beschrijving

Overall response

Datatype

integer

Alias
UMLS CUI [1]
C3272903
Was complete response confirmed with a bone marrow biopsy?
Beschrijving

Complete response

Datatype

integer

Alias
UMLS CUI [1]
C0677874
Is patient in complete remission but has bone marrow nodules that can be identified histologically?
Beschrijving

Partial response

Datatype

integer

Alias
UMLS CUI [1]
C0229654
Does patient fulfill the criteria for a CR but have persistent anemia or thrombocytopenia?
Beschrijving

Partial response

Datatype

boolean

Alias
UMLS CUI [1]
C0741008

Similar models

Tumor assessment of Chronic Lymphocytic Leukemia NCT00090051 BO17072

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Tumor assessment at screening
Assessment Date
Item
Date of Assessment
date
C2985720 (UMLS CUI [1])
Item Group
Indicator lesions
Code of origin
Item
Code of origin
integer
C2986125 (UMLS CUI [1])
extra nodal or other specification
Item
text
C1517067 (UMLS CUI [1])
Side of lesion
Item
text
C0441987 (UMLS CUI [1])
Dimensions
Item
text
C0439534 (UMLS CUI [1])
Method of assessment
Item
text
C2598110 (UMLS CUI [1])
Other specification
Item
text
Item Group
Non-indicator lesions
C0221198 (UMLS CUI-1)
Code of origin
Item
Code of origin
integer
C2986125 (UMLS CUI [1])
extra nodal or other specification
Item
text
C1517067 (UMLS CUI [1])
Side of lesion
Item
text
C0441987 (UMLS CUI [1])
Item Group
Liver and spleen examination
Date of Assessment
Item
date
C2985720 (UMLS CUI [1])
Item
integer
C0031809 (UMLS CUI [1])
Code List
Examination type
CL Item
CT scan (1)
C0040405 (UMLS CUI-1)
CL Item
physical examination (2)
C0031809 (UMLS CUI-1)
CL Item
other (3)
C0205394 (UMLS CUI-1)
specify other examination
Item
specify other examination
text
C0582103 (UMLS CUI [1])
Hepatomegaly
Item
Hepatomegaly
boolean
C0019209 (UMLS CUI [1])
Splenomegaly
Item
Splenomegaly
boolean
C0038002 (UMLS CUI [1])
Item Group
Tumor assessment after Cycle 3 and 6
Assessment Date
Item
date
C2985720 (UMLS CUI [1])
Item Group
Indicator lesions
Code of origin
Item
Code of origin
text
C2986125 (UMLS CUI [1])
extra nodal or other specification
Item
extra nodal or other specification
integer
C1517067 (UMLS CUI [1])
Side of lesion
Item
Side of lesion
integer
C1285236 (UMLS CUI [1])
Dimensions
Item
Dimensions
integer
C0439534 (UMLS CUI [1])
Method of assessment
Item
Method of assessment
integer
C2598110 (UMLS CUI [1])
Other specification
Item
Other specification
integer
C2348235 (UMLS CUI [1])
Item Group
Non-indicator lesions
Code of origin
Item
text
extra nodal or other specification
Item
text
C1517067 (UMLS CUI [1])
Side of lesion
Item
Side of lesion
integer
C1285236 (UMLS CUI [1])
Presence
Item
Presence
boolean
C0150312 (UMLS CUI [1])
Item Group
Liver and spleen examination after Cycle 3 and 6
Date of Assessment
Item
Date of Assessment
date
C2985720 (UMLS CUI [1])
Item
Examination type
integer
C0031809 (UMLS CUI [1])
Code List
Examination type
CL Item
CT scan (1)
C0040405 (UMLS CUI-1)
CL Item
physical examination (2)
C0031809 (UMLS CUI-1)
CL Item
other (3)
C0205394 (UMLS CUI-1)
specify other examination
Item
specify other examination
text
C0260879 (UMLS CUI [1])
Hepatomegaly
Item
Hepatomegaly
boolean
C0019209 (UMLS CUI [1])
Item
Status since last visit
integer
C0449438 (UMLS CUI [1])
Code List
Status since last visit
CL Item
no change (1)
C0442739 (UMLS CUI-1)
CL Item
decrease (2)
C0547047 (UMLS CUI-1)
CL Item
increase (3)
C0442805 (UMLS CUI-1)
Splenomegaly
Item
boolean
C0038002 (UMLS CUI [1])
Item
integer
C0449438 (UMLS CUI [1])
Code List
Status since last visit
CL Item
no change (1)
C0442739 (UMLS CUI-1)
CL Item
decrease (2)
C0547047 (UMLS CUI-1)
CL Item
increase (3)
C0442805 (UMLS CUI-1)
Item Group
Response assessment after cycle 3
Assessment Date
Item
Date of Assessment
date
C2985720 (UMLS CUI [1])
New lesions
Item
Are there any new lesions?
boolean
C0221198 (UMLS CUI [1])
Non-indicator lesions
Item
Was there unequivocal progression in the size of non-indicator lesions?
boolean
C3272925 (UMLS CUI [1])
Item
Overall response
integer
C3272903 (UMLS CUI [1])
Code List
Overall response
CL Item
complete response (1)
C0677874 (UMLS CUI-1)
CL Item
partial response (2)
C1521726 (UMLS CUI-1)
CL Item
stable disease (3)
C0677946 (UMLS CUI-1)
CL Item
pregressive disease (4)
C1335499 (UMLS CUI-1)
Partial response
Item
Does patient fulfill the criteria for a CR but have persistent anemia or thrombocytopenia?
boolean
C0741008 (UMLS CUI [1])
Item Group
Response assessment after Cycle 6
Assessment Date
Item
date
C2985720 (UMLS CUI [1])
New lesions
Item
Are there any new lesions?
boolean
C0221198 (UMLS CUI [1,1])
C0205314 (UMLS CUI [1,2])
Non-indicator lesions
Item
Was there unequivocal progression in the size of non-indicator lesions?
boolean
Item
Overall response
integer
C3272903 (UMLS CUI [1])
Code List
Overall response
CL Item
complete response (1)
C0677874 (UMLS CUI-1)
CL Item
partial response (2)
C1521726 (UMLS CUI-1)
CL Item
stable disease (3)
C0677946 (UMLS CUI-1)
CL Item
pregressive disease (4)
C1335499 (UMLS CUI-1)
Item
Was complete response confirmed with a bone marrow biopsy?
integer
C0677874 (UMLS CUI [1])
Code List
Was complete response confirmed with a bone marrow biopsy?
CL Item
yes (1)
C1705108 (UMLS CUI-1)
CL Item
no (2)
C1298908 (UMLS CUI-1)
CL Item
not applicable (3)
C1272460 (UMLS CUI-1)
Item
Is patient in complete remission but has bone marrow nodules that can be identified histologically?
integer
C0229654 (UMLS CUI [1])
Code List
Is patient in complete remission but has bone marrow nodules that can be identified histologically?
CL Item
yes (1)
C1705108 (UMLS CUI-1)
CL Item
no (2)
C1298908 (UMLS CUI-1)
CL Item
not applicable (3)
C1272460 (UMLS CUI-1)
Partial response
Item
Does patient fulfill the criteria for a CR but have persistent anemia or thrombocytopenia?
boolean
C0741008 (UMLS CUI [1])