ID

37771

Beschrijving

Study ID: 104864/627 Clinical Study ID: 104864/627 Study Title: An Open-label, Multicenter, Non-Comparative Phase II Study of the Combination of Intravenous Topotecan and Gemcitabine Administered Once Weekly for Three Weeks Every 28 Days as Second-line Treatment in Patients With Recurrent Platinum Sensitive Ovarian Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00061308 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Topotecan, Gemcitabine Study Indication: Peritoneal Cancer, Ovarian Cancer, Neoplasms, Ovarian, Fallopian Tube Cancer

Trefwoorden

Versies (2)
  1. 23-08-19 23-08-19 -
  2. 23-08-19 23-08-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

23 augustus 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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Intravenous Topotecan and Gemcitabine as Second-line Treatment in Patients With Ovarian Cancer NCT00061308

Engels

Screening - Prior Ovarian Cancer Treatment; Laboratory Tests; Lesion Assessment Record

1 Formulieren  
Administrative
Beschrijving

Administrative

Alias
UMLS CUI-1
C1320722
Center Number
Beschrijving

Center Number

Datatype

text

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Patient Number
Beschrijving

Patient Number

Datatype

text

Alias
UMLS CUI [1]
C1709561
Patient ID
Beschrijving

Patient ID

Datatype

text

Alias
UMLS CUI [1]
C2348585
Prior Ovarian Cancer Treatment - Chemotherapy
Beschrijving

Prior Ovarian Cancer Treatment - Chemotherapy

Alias
UMLS CUI-1
C0029925
UMLS CUI-2
C0920425
UMLS CUI-3
C0392920
Line No.
Beschrijving

Line No.

Datatype

integer

Alias
UMLS CUI [1]
C0750480
Chemo Agent
Beschrijving

Chemo Agent

Datatype

text

Alias
UMLS CUI [1]
C0013216
Chemotherapy Start Date
Beschrijving

Chemotherapy Start Date

Datatype

date

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0808070
Chemotherapy End Date
Beschrijving

Chemotherapy End Date

Datatype

date

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0806020
Overall response
Beschrijving

Overall response

Datatype

integer

Alias
UMLS CUI [1]
C3272903
Has the patient received radiotherapy?
Beschrijving

Has the patient received radiotherapy?

Alias
UMLS CUI-1
C1522449
Has the patient received radiotherapy?
Beschrijving

If "Yes", please specify below.

Datatype

boolean

Alias
UMLS CUI [1]
C1522449
Prior Ovarian Cancer Treatment - Radiotherapy
Beschrijving

Prior Ovarian Cancer Treatment - Radiotherapy

Alias
UMLS CUI-1
C0029925
UMLS CUI-2
C0920425
UMLS CUI-3
C1522449
Line No.
Beschrijving

Line No.

Datatype

integer

Alias
UMLS CUI [1]
C0750480
Radiotherapy - Specify Area
Beschrijving

Radiotherapy - Specify Area

Datatype

text

Alias
UMLS CUI [1]
C1997599
Radiotherapy - Dose Received
Beschrijving

Radiotherapy - Dose Received

Datatype

text

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C3174092
Radiotherapy - Date
Beschrijving

Radiotherapy - Date

Datatype

date

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0011008
Has the patient received prior cancer-related surgery?
Beschrijving

Has the patient received prior cancer-related surgery?

Alias
UMLS CUI-1
C0543467
UMLS CUI-2
C0205156
UMLS CUI-3
C2826292
Has the patient received prior cancer-related surgery?
Beschrijving

If "Yes", please specify below.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0205156
UMLS CUI [1,3]
C2826292
Prior Ovarian Cancer Treatment - Surgical Treatment
Beschrijving

Prior Ovarian Cancer Treatment - Surgical Treatment

Alias
UMLS CUI-1
C0029925
UMLS CUI-2
C0920425
UMLS CUI-3
C0543467
Line No.
Beschrijving

Line No.

Datatype

integer

Alias
UMLS CUI [1]
C0750480
Surgery Type
Beschrijving

Surgery Type

Datatype

text

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0332307
Surgery Date
Beschrijving

Surgery Date

Datatype

date

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0011008
Has the patient received other cancer-related treatments?
Beschrijving

Has the patient received other cancer-related treatments?

Alias
UMLS CUI-1
C0920425
UMLS CUI-2
C0205394
Has the patient received other cancer-related treatments?
Beschrijving

If "Yes", please specify below.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C0205394
Other Cancer Related Treatments
Beschrijving

Other Cancer Related Treatments

Alias
UMLS CUI-1
C0920425
UMLS CUI-2
C0205394
Line No.
Beschrijving

Line No.

Datatype

integer

Alias
UMLS CUI [1]
C0750480
Treatment
Beschrijving

Treatment

Datatype

text

Alias
UMLS CUI [1]
C0087111
Treatment Start Date
Beschrijving

Treatment Start Date

Datatype

date

Alias
UMLS CUI [1]
C3173309
Treatment End Date
Beschrijving

Treatment End Date

Datatype

date

Alias
UMLS CUI [1]
C1531784
Laboratory Tests (within 7 days prior to Day 1) - Haematology
Beschrijving

Laboratory Tests (within 7 days prior to Day 1) - Haematology

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0474523
Haematology - Sample Date
Beschrijving

Haematology - Sample Date

Datatype

date

Alias
UMLS CUI [1,1]
C1302413
UMLS CUI [1,2]
C0018941
Haematology - Laboratory Name
Beschrijving

Haematology - Laboratory Name

Datatype

text

Alias
UMLS CUI [1,1]
C3258037
UMLS CUI [1,2]
C0018941
Laboratory Tests (within 7 days prior to Day 1) - Haematology
Beschrijving

Laboratory Tests (within 7 days prior to Day 1) - Haematology

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0474523
Haematology Test
Beschrijving

Haematology Test

Datatype

integer

Alias
UMLS CUI [1]
C0018941
Haematology - No Result
Beschrijving

Haematology - No Result

Datatype

integer

Alias
UMLS CUI [1,1]
C0018941
UMLS CUI [1,2]
C1274040
Haematology - Value
Beschrijving

Haematology - Value

Datatype

text

Alias
UMLS CUI [1]
C0474523
Haematology - Value out of range and NOT clinically significant
Beschrijving

Haematology - Value out of range and NOT clinically significant

Datatype

integer

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0438215
UMLS CUI [1,3]
C2826293
Haematology - Value out of range and clinically significant
Beschrijving

Haematology - Value out of range and clinically significant

Datatype

integer

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0438215
UMLS CUI [1,3]
C2826293
Laboratory Tests (within 7 days prior to Day 1) - Chemistry
Beschrijving

Laboratory Tests (within 7 days prior to Day 1) - Chemistry

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0008000
Chemistry - Sample Date
Beschrijving

Chemistry - Sample Date

Datatype

date

Alias
UMLS CUI [1,1]
C1302413
UMLS CUI [1,2]
C0008000
Chemistry - Laboratory Name
Beschrijving

Chemistry - Laboratory Name

Datatype

text

Alias
UMLS CUI [1,1]
C3258037
UMLS CUI [1,2]
C0008000
Laboratory Tests (within 7 days prior to Day 1) - Chemistry
Beschrijving

Laboratory Tests (within 7 days prior to Day 1) - Chemistry

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0008000
Chemistry - Test
Beschrijving

Chemistry - Test

Datatype

integer

Alias
UMLS CUI [1]
C0525044
Chemistry - No Result
Beschrijving

Chemistry - No Result

Datatype

integer

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C1274040
Chemistry - Value
Beschrijving

Chemistry - Value

Datatype

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C1274040
Chemistry - Value out of range and NOT clinically significant
Beschrijving

Chemistry - Value out of range and NOT clinically significant

Datatype

integer

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C1274040
UMLS CUI [1,3]
C0438215
UMLS CUI [1,4]
C2826293
Chemistry - Value out of range and NOT clinically significant
Beschrijving

Chemistry - Value out of range and NOT clinically significant

Datatype

integer

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C1274040
UMLS CUI [1,3]
C0438215
UMLS CUI [1,4]
C2826293
Lesion Assessment Record
Beschrijving

Lesion Assessment Record

Alias
UMLS CUI-1
C0221198
UMLS CUI-2
C1516048
Lesion No.
Beschrijving

Lesion No.

Datatype

integer

Alias
UMLS CUI [1,1]
C0237753
UMLS CUI [1,2]
C0221198
Lesion Site Code
Beschrijving

Lesion Site Code

Datatype

integer

Alias
UMLS CUI [1,1]
C0449695
UMLS CUI [1,2]
C0805701
Lesion Site Description
Beschrijving

Lesion Site Description

Datatype

text

Alias
UMLS CUI [1,1]
C0449695
UMLS CUI [1,2]
C0678257
Lesion Measurement - Method Code
Beschrijving

Lesion Measurement - Method Code

Datatype

integer

Alias
UMLS CUI [1,1]
C1299991
UMLS CUI [1,2]
C0221198
UMLS CUI [1,3]
C2911685
UMLS CUI [1,4]
C0805701
Lesion Measurement - Date Performed
Beschrijving

Lesion Measurement - Date Performed

Datatype

date

Alias
UMLS CUI [1,1]
C1299991
UMLS CUI [1,2]
C0221198
UMLS CUI [1,3]
C0011008
Measurable/ Non measurable Lesion Code
Beschrijving

Measurable/ Non measurable Lesion Code

Datatype

integer

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1513040
UMLS CUI [2]
C1334988
Lesion Size - 1. Diameter (cm)
Beschrijving

Lesion Size - 1. Diameter (cm)

Datatype

float

Maateenheden
  • cm
Alias
UMLS CUI [1,1]
C0449453
UMLS CUI [1,2]
C1301886
cm
Lesion Size - 2. Diameter (cm)
Beschrijving

Lesion Size - 2. Diameter (cm)

Datatype

float

Maateenheden
  • cm
Alias
UMLS CUI [1,1]
C0449453
UMLS CUI [1,2]
C1301886
cm
Lesion Non-Evaluable
Beschrijving

Lesion Non-Evaluable

Datatype

integer

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1883425
Lesion Non-Evaluable - Lesion Measurement Method Code
Beschrijving

Lesion Non-Evaluable - Lesion Measurement Method Code

Datatype

integer

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1883425
UMLS CUI [1,3]
C1299991
UMLS CUI [1,4]
C0805701
Lesion Non-Evaluable - Date Performed
Beschrijving

Lesion Non-Evaluable - Date Performed

Datatype

date

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1883425
UMLS CUI [1,3]
C0011008
Lesion Non-Evaluable Status
Beschrijving

Lesion Non-Evaluable Status

Datatype

integer

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1883425
UMLS CUI [1,3]
C0449438
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Similar models

Screening - Prior Ovarian Cancer Treatment; Laboratory Tests; Lesion Assessment Record

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Center Number
Item
Center Number
text
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Patient Number
Item
Patient Number
text
C1709561 (UMLS CUI [1])
Patient ID
Item
Patient ID
text
C2348585 (UMLS CUI [1])
Item Group
Prior Ovarian Cancer Treatment - Chemotherapy
C0029925 (UMLS CUI-1)
C0920425 (UMLS CUI-2)
C0392920 (UMLS CUI-3)
Line No.
Item
Line No.
integer
C0750480 (UMLS CUI [1])
Chemo Agent
Item
Chemo Agent
text
C0013216 (UMLS CUI [1])
Chemotherapy Start Date
Item
Chemotherapy Start Date
date
C0392920 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Chemotherapy End Date
Item
Chemotherapy End Date
date
C0392920 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item
Overall response
integer
C3272903 (UMLS CUI [1])
Overall response
Code List
Overall response
CL Item
None —> If “None", patient is not eligible for this study.  (1)
CL Item
Partial Response  (2)
CL Item
Complete Response (3)
Item Group
Has the patient received radiotherapy?
C1522449 (UMLS CUI-1)
Has the patient received radiotherapy?
Item
Has the patient received radiotherapy?
boolean
C1522449 (UMLS CUI [1])
Item Group
Prior Ovarian Cancer Treatment - Radiotherapy
C0029925 (UMLS CUI-1)
C0920425 (UMLS CUI-2)
C1522449 (UMLS CUI-3)
Line No.
Item
Line No.
integer
C0750480 (UMLS CUI [1])
Radiotherapy - Specify Area
Item
Radiotherapy - Specify Area
text
C1997599 (UMLS CUI [1])
Radiotherapy - Dose Received
Item
Radiotherapy - Dose Received
text
C0392920 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
Radiotherapy - Date
Item
Radiotherapy - Date
date
C0392920 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Has the patient received prior cancer-related surgery?
C0543467 (UMLS CUI-1)
C0205156 (UMLS CUI-2)
C2826292 (UMLS CUI-3)
Has the patient received prior cancer-related surgery?
Item
Has the patient received prior cancer-related surgery?
boolean
C0543467 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C2826292 (UMLS CUI [1,3])
Item Group
Prior Ovarian Cancer Treatment - Surgical Treatment
C0029925 (UMLS CUI-1)
C0920425 (UMLS CUI-2)
C0543467 (UMLS CUI-3)
Line No.
Item
Line No.
integer
C0750480 (UMLS CUI [1])
Surgery Type
Item
Surgery Type
text
C0543467 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Surgery Date
Item
Surgery Date
date
C0543467 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Has the patient received other cancer-related treatments?
C0920425 (UMLS CUI-1)
C0205394 (UMLS CUI-2)
Has the patient received other cancer-related treatments?
Item
Has the patient received other cancer-related treatments?
boolean
C0920425 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Item Group
Other Cancer Related Treatments
C0920425 (UMLS CUI-1)
C0205394 (UMLS CUI-2)
Line No.
Item
Line No.
integer
C0750480 (UMLS CUI [1])
Treatment
Item
Treatment
text
C0087111 (UMLS CUI [1])
Treatment Start Date
Item
Treatment Start Date
date
C3173309 (UMLS CUI [1])
Treatment End Date
Item
Treatment End Date
date
C1531784 (UMLS CUI [1])
Item Group
Laboratory Tests (within 7 days prior to Day 1) - Haematology
C0022885 (UMLS CUI-1)
C0474523 (UMLS CUI-2)
Haematology - Sample Date
Item
Haematology - Sample Date
date
C1302413 (UMLS CUI [1,1])
C0018941 (UMLS CUI [1,2])
Haematology - Laboratory Name
Item
Haematology - Laboratory Name
text
C3258037 (UMLS CUI [1,1])
C0018941 (UMLS CUI [1,2])
Item Group
Laboratory Tests (within 7 days prior to Day 1) - Haematology
C0022885 (UMLS CUI-1)
C0474523 (UMLS CUI-2)
Item
Haematology Test
integer
C0018941 (UMLS CUI [1])
Haematology Test
Code List
Haematology Test
CL Item
Hemoglobin  (1)
CL Item
Hematocrit  (2)
CL Item
RBC  (3)
CL Item
WBC  (4)
CL Item
Neutrophils  (5)
CL Item
Bands  (6)
CL Item
Lymphocytes  (7)
CL Item
Monocytes  (8)
CL Item
Eosinophils  (9)
CL Item
Basophils  (10)
CL Item
Platelets  (11)
CL Item
Granulocytes (12)
Item
Haematology - No Result
integer
C0018941 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Haematology - No Result
Code List
Haematology - No Result
CL Item
No Result (1)
Haematology - Value
Item
Haematology - Value
text
C0474523 (UMLS CUI [1])
Item
Haematology - Value out of range and NOT clinically significant
integer
C0474523 (UMLS CUI [1,1])
C0438215 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,3])
Haematology - Value out of range and NOT clinically significant
Code List
Haematology - Value out of range and NOT clinically significant
CL Item
Value out of range and NOT clinically significant (2)
Item
Haematology - Value out of range and clinically significant
integer
C0474523 (UMLS CUI [1,1])
C0438215 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,3])
Haematology - Value out of range and clinically significant
Code List
Haematology - Value out of range and clinically significant
CL Item
Value out of range and clinically significant (3)
Item Group
Laboratory Tests (within 7 days prior to Day 1) - Chemistry
C0022885 (UMLS CUI-1)
C0008000 (UMLS CUI-2)
Chemistry - Sample Date
Item
Chemistry - Sample Date
date
C1302413 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
Chemistry - Laboratory Name
Item
Chemistry - Laboratory Name
text
C3258037 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
Item Group
Laboratory Tests (within 7 days prior to Day 1) - Chemistry
C0022885 (UMLS CUI-1)
C0008000 (UMLS CUI-2)
Item
Chemistry - Test
integer
C0525044 (UMLS CUI [1])
Chemistry - Test
Code List
Chemistry - Test
CL Item
Total Protein  (1)
CL Item
Albumin  (2)
CL Item
Total Bilirubin  (3)
CL Item
SGPT (ALT)  (4)
CL Item
SGOT (AST)  (5)
CL Item
Alkaline Phosphatase  (6)
CL Item
Glucose  (7)
CL Item
LDH  (8)
CL Item
BUN  (9)
CL Item
Serum Creatinine  (10)
CL Item
Uric Acid  (11)
CL Item
Calcium  (12)
CL Item
Phosphorus  (13)
CL Item
Sodium  (14)
CL Item
Potassium  (15)
CL Item
Chloride  (16)
CL Item
Bicarbonate (17)
Item
Chemistry - No Result
integer
C0008000 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Chemistry - No Result
Code List
Chemistry - No Result
CL Item
No Result (1)
Chemistry - Value
Item
Chemistry - Value
text
C0008000 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Item
Chemistry - Value out of range and NOT clinically significant
integer
C0008000 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0438215 (UMLS CUI [1,3])
C2826293 (UMLS CUI [1,4])
Chemistry - Value out of range and NOT clinically significant
Code List
Chemistry - Value out of range and NOT clinically significant
CL Item
Value out of range and NOT clinically significant (2)
Item
Chemistry - Value out of range and NOT clinically significant
integer
C0008000 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0438215 (UMLS CUI [1,3])
C2826293 (UMLS CUI [1,4])
Chemistry - Value out of range and NOT clinically significant
Code List
Chemistry - Value out of range and NOT clinically significant
CL Item
Value out of range and clinically significant (3)
Item Group
Lesion Assessment Record
C0221198 (UMLS CUI-1)
C1516048 (UMLS CUI-2)
Lesion No.
Item
Lesion No.
integer
C0237753 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
Item
Lesion Site Code
integer
C0449695 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
Lesion Site Code
Code List
Lesion Site Code
CL Item
Abdominal/Pelvic  (01)
CL Item
Hepatic  (02)
CL Item
Pulmonary  (03)
CL Item
Lymph Node  (04)
CL Item
Chest Wall  (05)
CL Item
Other (99)
Lesion Site Description
Item
Lesion Site Description
text
C0449695 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
Item
Lesion Measurement - Method Code
integer
C1299991 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C2911685 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,4])
Method Code
Code List
Lesion Measurement - Method Code
CL Item
Physical Measurement  (01)
CL Item
CT scan  (02)
CL Item
MRI scan  (03)
CL Item
Radiography  (04)
CL Item
Chest X-Ray  (05)
CL Item
Radionuclide scan  (06)
CL Item
Other (99)
Lesion Measurement - Date Performed
Item
Lesion Measurement - Date Performed
date
C1299991 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
Measurable/ Non measurable Lesion Code
integer
C0221198 (UMLS CUI [1,1])
C1513040 (UMLS CUI [1,2])
C1334988 (UMLS CUI [2])
Measurable/ Non measurable Lesion Code
Code List
Measurable/ Non measurable Lesion Code
CL Item
Measurable (1)
CL Item
Non-measurable (2)
Lesion Size - 1. Diameter (cm)
Item
Lesion Size - 1. Diameter (cm)
float
C0449453 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
Lesion Size - 2. Diameter (cm)
Item
Lesion Size - 2. Diameter (cm)
float
C0449453 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
Item
Lesion Non-Evaluable
integer
C0221198 (UMLS CUI [1,1])
C1883425 (UMLS CUI [1,2])
Lesion Non-Evaluable
Code List
Lesion Non-Evaluable
CL Item
Ascites (1)
CL Item
Bone Metastases (2)
CL Item
Pleural Effusion (3)
Item
Lesion Non-Evaluable - Lesion Measurement Method Code
integer
C0221198 (UMLS CUI [1,1])
C1883425 (UMLS CUI [1,2])
C1299991 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,4])
Lesion Non-Evaluable - Lesion Measurement Method Code
Code List
Lesion Non-Evaluable - Lesion Measurement Method Code
CL Item
Physical Measurement  (01)
CL Item
CT scan  (02)
CL Item
MRI scan (03)
CL Item
Radiography (04)
CL Item
Chest X-Ray  (05)
CL Item
Radionuclide scan  (06)
CL Item
Other (99)
Lesion Non-Evaluable - Date Performed
Item
Lesion Non-Evaluable - Date Performed
date
C0221198 (UMLS CUI [1,1])
C1883425 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
Lesion Non-Evaluable Status
integer
C0221198 (UMLS CUI [1,1])
C1883425 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
Lesion Non-Evaluable Status
Code List
Lesion Non-Evaluable Status
CL Item
Not Done (1)
CL Item
Present (2)
CL Item
Absent (3)
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