ID

31379

Description

Study ID: 104507 Clinical Study ID: BEX104507 Study Title: Phase II Study of Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphoma Patients who have Previously Received Rituximab Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00996593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Keywords

Versions (2)
  1. 7/31/18 7/31/18 -
  2. 8/18/18 8/18/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 18, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593

English

Long Term Follow- Up for Survival and Disease Status

1 forms  
Patient Status
Description

Patient Status

Alias
UMLS CUI-1
C0449437
Patient Status
Description

Patient Status

Data type

text

Alias
UMLS CUI [1]
C0449437
Date of status
Description

Date of status

Data type

date

Alias
UMLS CUI [1,1]
C0449437
UMLS CUI [1,2]
C0011008
How was contact made?
Description

How was contact made

Data type

text

Alias
UMLS CUI [1]
C1705415
If other type of contact, please specify
Description

Communication Contact; Other; Specification

Data type

text

Alias
UMLS CUI [1,1]
C1705415
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C2348235
Does the patient have an ongoing response to Iodine-131 Tositumomab?
Description

iodine-131-tositumomab; Response to treatment; Continuous

Data type

boolean

Alias
UMLS CUI [1,1]
C0768182
UMLS CUI [1,2]
C0521982
UMLS CUI [1,3]
C0549178
Since the time the last LTFU was completed...
Description

Since the time the last LTFU was completed...

Alias
UMLS CUI-1
C1517942
UMLS CUI-2
C3872643
Has any additional therapy for NHL been administered?
Description

If yes, specify below and provide applicable data.

Data type

boolean

Alias
UMLS CUI [1,1]
C1706712
UMLS CUI [1,2]
C0024305
Subsequent NHL Therapy since last LTFU
Description

Subsequent NHL Therapy since last LTFU

Alias
UMLS CUI-1
C0024305
UMLS CUI-2
C0087111
UMLS CUI-3
C1514923
Subsequent NHL Therapy since last LTFU
Description

Subsequent NHL Therapy since last LTFU

Data type

text

Alias
UMLS CUI [1,1]
C0024305
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C1514923
Start Date Subsequent NHL Therapy
Description

Start Date Subsequent NHL Therapy

Data type

date

Alias
UMLS CUI [1,1]
C0024305
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C1514923
UMLS CUI [1,4]
C0808070
Subsequent NHL Therapy Stop Date
Description

Subsequent NHL Therapy Stop Date

Data type

date

Alias
UMLS CUI [1,1]
C0024305
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C1514923
UMLS CUI [1,4]
C0806020
Total number of cycles
Description

Total number of cycles

Data type

integer

Alias
UMLS CUI [1]
C2045831
Diagnosis of malignancy
Description

Diagnosis of malignancy

Alias
UMLS CUI-1
C0006826
UMLS CUI-2
C0011900
Has the patient had a documented diagnosis of myelodysplasia?
Description

myelodysplasia

Data type

boolean

Alias
UMLS CUI [1]
C0026985
If diagnosis of myelodysplasia, date of diagnosis
Description

Myelodysplasia; Date of diagnosis

Data type

date

Alias
UMLS CUI [1,1]
C0026985
UMLS CUI [1,2]
C2316983
Has the patient had a documented diagnosis of AML?
Description

Leukemia, Myelocytic, Acute

Data type

boolean

Alias
UMLS CUI [1]
C0023467
If diagnosis of AML, date of diagnosis
Description

Leukemia, Myelocytic, Acute; Date of diagnosis

Data type

text

Alias
UMLS CUI [1,1]
C0023467
UMLS CUI [1,2]
C2316983
Has the patient had a diagnosis of another malignancy?
Description

Malignant Neoplasms; Diagnosis; Other

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0205394
If diagnosis of other malignancy, date of diagnosis
Description

Malignant Neoplasms; Diagnosis; Other; Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0011008
If diagnosis of other malignancy, type of malignancy
Description

Malignant Neoplasms; Diagnosis; Other; Type - attribute

Data type

text

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0332307
Laboratory
Description

Laboratory

Alias
UMLS CUI-1
C0022885
TSH Date
Description

Thyroid stimulating hormone measurement; Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0202230
UMLS CUI [1,2]
C0011008
TSH Result
Description

TSH Result

Data type

float

Measurement units
  • u[iU]/mL
Alias
UMLS CUI [1,1]
C0202230
UMLS CUI [1,2]
C1274040
u[iU]/mL
TSH not done
Description

TSH not done

Data type

text

Alias
UMLS CUI [1,1]
C0202230
UMLS CUI [1,2]
C1272696
Has the patient begun thyroid replacement therapy since last LTFU?
Description

Thyroid hormone replacement therapy; Long-term Follow-up; Since last encounter

Data type

boolean

Alias
UMLS CUI [1,1]
C2242640
UMLS CUI [1,2]
C1517942
UMLS CUI [1,3]
C3872643
Thyroid replacement therapy start date
Description

Thyroid replacement therapy start date

Data type

date

Alias
UMLS CUI [1,1]
C2242640
UMLS CUI [1,2]
C0808070
Thyroid replacement therapy Drug name
Description

Thyroid replacement therapy Drug name

Data type

text

Alias
UMLS CUI [1,1]
C2242640
UMLS CUI [1,2]
C2360065
Was a HAMA obtained since the last LTFU?
Description

Human anti-mouse antibody; Long-term Follow-up; Since last encounter

Data type

text

Alias
UMLS CUI [1,1]
C1291910
UMLS CUI [1,2]
C1517942
UMLS CUI [1,3]
C3872643
If HAMA was obtained, enter accession number
Description

Human anti-mouse antibody; Accession Number (identifier)

Data type

text

Alias
UMLS CUI [1,1]
C1291910
UMLS CUI [1,2]
C1510755
Administrative
Description

Administrative

Alias
UMLS CUI-1
C1320722
Investigator Signature
Description

Investigator Signature

Data type

text

Alias
UMLS CUI [1]
C2346576
Date of evaluation
Description

Assessment Date

Data type

date

Alias
UMLS CUI [1]
C2985720
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Similar models

Long Term Follow- Up for Survival and Disease Status

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patient Status
C0449437 (UMLS CUI-1)
Item
Patient Status
text
C0449437 (UMLS CUI [1])
Patient Status
Code List
Patient Status
CL Item
Alive (1)
CL Item
Dead (Complete "Notification of Patient Death" Form (2)
CL Item
Lost to Follow- Up (3)
Date of status
Item
Date of status
date
C0449437 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
How was contact made?
text
C1705415 (UMLS CUI [1])
How was contact made
Code List
How was contact made?
CL Item
Tumor registry (1)
CL Item
Contact with patient (2)
CL Item
Contact with MD (3)
CL Item
Contact with family (4)
CL Item
Other (5)
Communication Contact; Other; Specification
Item
If other type of contact, please specify
text
C1705415 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
iodine-131-tositumomab; Response to treatment; Continuous
Item
Does the patient have an ongoing response to Iodine-131 Tositumomab?
boolean
C0768182 (UMLS CUI [1,1])
C0521982 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
Item Group
Since the time the last LTFU was completed...
C1517942 (UMLS CUI-1)
C3872643 (UMLS CUI-2)
Additional Therapy; Lymphoma, Non-Hodgkin
Item
Has any additional therapy for NHL been administered?
boolean
C1706712 (UMLS CUI [1,1])
C0024305 (UMLS CUI [1,2])
Item Group
Subsequent NHL Therapy since last LTFU
C0024305 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C1514923 (UMLS CUI-3)
Subsequent NHL Therapy since last LTFU
Item
Subsequent NHL Therapy since last LTFU
text
C0024305 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C1514923 (UMLS CUI [1,3])
Start Date Subsequent NHL Therapy
Item
Start Date Subsequent NHL Therapy
date
C0024305 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C1514923 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,4])
Subsequent NHL Therapy Stop Date
Item
Subsequent NHL Therapy Stop Date
date
C0024305 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C1514923 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,4])
Total number of cycles
Item
Total number of cycles
integer
C2045831 (UMLS CUI [1])
Item Group
Diagnosis of malignancy
C0006826 (UMLS CUI-1)
C0011900 (UMLS CUI-2)
myelodysplasia
Item
Has the patient had a documented diagnosis of myelodysplasia?
boolean
C0026985 (UMLS CUI [1])
Myelodysplasia; Date of diagnosis
Item
If diagnosis of myelodysplasia, date of diagnosis
date
C0026985 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
Leukemia, Myelocytic, Acute
Item
Has the patient had a documented diagnosis of AML?
boolean
C0023467 (UMLS CUI [1])
Leukemia, Myelocytic, Acute; Date of diagnosis
Item
If diagnosis of AML, date of diagnosis
text
C0023467 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
Malignant Neoplasms; Diagnosis; Other
Item
Has the patient had a diagnosis of another malignancy?
boolean
C0006826 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Malignant Neoplasms; Diagnosis; Other; Date in time
Item
If diagnosis of other malignancy, date of diagnosis
date
C0006826 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Malignant Neoplasms; Diagnosis; Other; Type - attribute
Item
If diagnosis of other malignancy, type of malignancy
text
C0006826 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,4])
Item Group
Laboratory
C0022885 (UMLS CUI-1)
Thyroid stimulating hormone measurement; Date in time
Item
TSH Date
date
C0202230 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
TSH Result
Item
TSH Result
float
C0202230 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Item
TSH not done
text
C0202230 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
TSH not done
Code List
TSH not done
CL Item
not done (1)
Thyroid hormone replacement therapy; Long-term Follow-up; Since last encounter
Item
Has the patient begun thyroid replacement therapy since last LTFU?
boolean
C2242640 (UMLS CUI [1,1])
C1517942 (UMLS CUI [1,2])
C3872643 (UMLS CUI [1,3])
Thyroid replacement therapy start date
Item
Thyroid replacement therapy start date
date
C2242640 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Thyroid replacement therapy Drug name
Item
Thyroid replacement therapy Drug name
text
C2242640 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Item
Was a HAMA obtained since the last LTFU?
text
C1291910 (UMLS CUI [1,1])
C1517942 (UMLS CUI [1,2])
C3872643 (UMLS CUI [1,3])
undefined item
Code List
Was a HAMA obtained since the last LTFU?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not applicable (3)
Human anti-mouse antibody; Accession Number (identifier)
Item
If HAMA was obtained, enter accession number
text
C1291910 (UMLS CUI [1,1])
C1510755 (UMLS CUI [1,2])
Item Group
Administrative
C1320722 (UMLS CUI-1)
Investigator Signature
Item
Investigator Signature
text
C2346576 (UMLS CUI [1])
Assessment Date
Item
Date of evaluation
date
C2985720 (UMLS CUI [1])
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