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Registration

1 forms  
  1. StudyEvent: SE
    1. Registration
Inclusion criteria
Description

Inclusion criteria

Newly diagnosed (Secondary malignancy) Non-Hodgkin lymphoma
Description

Newly diagnosed (Secondary malignancy) Non-Hodgkin lymphoma

Data type

integer

Alias
UMLS CUI [1,1]
C0024305
UMLS CUI [1,2]
C3266877
NHL subtype
Description

NHL subtype

Data type

integer

Alias
UMLS CUI [1,1]
C0024305
UMLS CUI [1,2]
C0449560
specify NHL subtype
Description

specify NHL subtype

Data type

text

Diagnosis and treatment in a participating center of the NHL-BFM group
Description

Diagnosis and treatment in a participating center of the NHL-BFM group

Data type

integer

Alias
UMLS CUI [1,1]
C0598048
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0039798
Patient age at diagnosis below 18 years
Description

Patient age at diagnosis below 18 years

Data type

integer

Alias
UMLS CUI [1]
C3173302
Signed informed consent for participation in the NHL-BFM Registry 2012 and data transfer
Description

Signed informed consent for participation in the NHL-BFM Registry 2012 and data transfer

Data type

integer

Alias
UMLS CUI [1]
C0021430
Date of signed informed consent
Description

Date consent

Data type

date

Follow-up is expected to be available for at least 2 years
Description

Follow-up is expected to be available for at least 2 years

Data type

integer

Alias
UMLS CUI [1]
C1522577
Personal data
Description

Personal data

Date when patient was added to Marvin
Description

Date of registration to Marvin

Data type

date

Alias
UMLS CUI [1]
C2985881
Patient ID
Description

Patient ID

Data type

text

Alias
UMLS CUI [1]
C2348585
Surname (or initial)
Description

Surname (or initial)

Data type

text

Alias
UMLS CUI [1]
C0421448
First name (or initial)
Description

First name (or initial)

Data type

text

Alias
UMLS CUI [1]
C0421447
Date of birth
Description

Date of birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

Sex

Data type

integer

Alias
UMLS CUI [1]
C0079399
Marvin-ID
Description

Marvin-ID

Data type

text

Alias
UMLS CUI [1]
C0552502
Identification
Description

Identification

Malig-ID (DKKR)
Description

Malig-ID (DKKR)

Data type

text

Alias
UMLS CUI [1]
C3897288
GPOH-PID
Description

GPOH-PID

Data type

text

Alias
UMLS CUI [1]
C2360808
Additional information
Description

Additional information

Maximum increase of LDH before start of therapy
Description

Maximum increase of LDH before start of therapy

Data type

integer

Measurement units
  • U/l
Alias
UMLS CUI [1,1]
C0442805
UMLS CUI [1,2]
C0202113
U/l
Upper normal limit of LDH in local laboratory
Description

Upper normal limit of LDH in local laboratory

Data type

integer

Measurement units
  • U/l
Alias
UMLS CUI [1,1]
C0202113
UMLS CUI [1,2]
C1519815
U/l
Involvement of central nervous system (CNS+)
Description

Involvement of central nervous system (CNS+)

Data type

integer

Alias
UMLS CUI [1]
C0449389
Involvement of bone marrow (BM+)
Description

Involvement of bone marrow (BM+)

Data type

integer

Alias
UMLS CUI [1]
C1517677
Therapy arm (for mature B-NHL only)
Description

Therapy arm (for mature B-NHL only)

Data type

integer

Alias
UMLS CUI [1]
C1522541
Date of treatment start
Description

Date of treatment start

Data type

date

Alias
UMLS CUI [1]
C3173309
Some data on anamnesis
Description

Some data on anamnesis

Chromosomal breakage syndrome, immunodeficiency, or HIV infection
Description

Chromosomal breakage syndrome, immunodeficiency, or HIV infection

Data type

integer

Alias
UMLS CUI [1]
C0398791
UMLS CUI [2]
C0019693
UMLS CUI [3]
C0021051
specify syndrome
Description

specify syndrome

Data type

text

Alias
UMLS CUI [1]
C1521902
Previous organ transplantation
Description

Previous organ transplantation

Data type

integer

Alias
UMLS CUI [1,1]
C0029216
UMLS CUI [1,2]
C0262926
specify TP
Description

specify TP

Data type

text

Alias
UMLS CUI [1]
C1521902
Previous malignancy/neoplasm
Description

Previous malignancy/neoplasm

Data type

integer

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0262926
specify previous malignancy
Description

specify previous malignancy

Data type

text

Alias
UMLS CUI [1]
C1521902
Other pre-existing disease prohibiting standard chemotherapy
Description

Other pre-existing disease prohibiting standard chemotherapy

Data type

integer

Alias
UMLS CUI [1]
C0009488
specify preexisting disease
Description

specify preexisting disease

Data type

text

Alias
UMLS CUI [1]
C1521902
Previous chemotherapy, radiotherapy, or systemic corticosteroid treatment
Description

Previous chemotherapy, radiotherapy, or systemic corticosteroid treatment

Data type

integer

Alias
UMLS CUI [1]
C0149783
UMLS CUI [2]
C0392920
UMLS CUI [3]
C1522449
specify previous therapy
Description

specify previous therapy

Data type

text

Alias
UMLS CUI [1]
C1521902
For female patients: Pregnancy or lactation period
Description

For female patients: Pregnancy or lactation period

Data type

integer

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
Simultaneous participation in a clinical study
Description

Simultaneous participation in a clinical study

Data type

integer

Alias
UMLS CUI [1]
C2348568
specify other study
Description

specify other study

Data type

text

Alias
UMLS CUI [1]
C1521902
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Similar models

Registration

1 forms
  1. StudyEvent: SE
    1. Registration
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item
Newly diagnosed (Secondary malignancy) Non-Hodgkin lymphoma
integer
C0024305 (UMLS CUI [1,1])
C3266877 (UMLS CUI [1,2])
NOYES
Code List
Newly diagnosed (Secondary malignancy) Non-Hodgkin lymphoma
CL Item
no (1)
CL Item
yes (2)
Item
NHL subtype
integer
C0024305 (UMLS CUI [1,1])
C0449560 (UMLS CUI [1,2])
SUBTYPE
Code List
NHL subtype
CL Item
lymphoblastic lymphoma (LBL) (1)
CL Item
mature B-cell lymphoma (B-NHL) (2)
CL Item
anaplastic large cell lymphoma (ALCL) (3)
CL Item
peripheral T-cell lymphoma (PTCL) (4)
CL Item
other NHL (9)
specify NHL subtype
Item
specify NHL subtype
text
Item
Diagnosis and treatment in a participating center of the NHL-BFM group
integer
C0598048 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0039798 (UMLS CUI [1,3])
NOYES
Code List
Diagnosis and treatment in a participating center of the NHL-BFM group
CL Item
no (1)
CL Item
yes (2)
Item
Patient age at diagnosis below 18 years
integer
C3173302 (UMLS CUI [1])
NOYES
Code List
Patient age at diagnosis below 18 years
CL Item
no (1)
CL Item
yes (2)
Item
Signed informed consent for participation in the NHL-BFM Registry 2012 and data transfer
integer
C0021430 (UMLS CUI [1])
NOYES
Code List
Signed informed consent for participation in the NHL-BFM Registry 2012 and data transfer
CL Item
no (1)
CL Item
yes (2)
Date consent
Item
Date of signed informed consent
date
Item
Follow-up is expected to be available for at least 2 years
integer
C1522577 (UMLS CUI [1])
NOYES
Code List
Follow-up is expected to be available for at least 2 years
CL Item
no (1)
CL Item
yes (2)
Item Group
Date of registration to Marvin
Item
Date when patient was added to Marvin
date
C2985881 (UMLS CUI [1])
Patient ID
Item
Patient ID
text
C2348585 (UMLS CUI [1])
Surname (or initial)
Item
Surname (or initial)
text
C0421448 (UMLS CUI [1])
First name (or initial)
Item
First name (or initial)
text
C0421447 (UMLS CUI [1])
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Sex
integer
C0079399 (UMLS CUI [1])
SEX
Code List
Sex
CL Item
male (1)
CL Item
female (2)
Marvin-ID
Item
Marvin-ID
text
C0552502 (UMLS CUI [1])
Item Group
Malig-ID (DKKR)
Item
Malig-ID (DKKR)
text
C3897288 (UMLS CUI [1])
GPOH-PID
Item
GPOH-PID
text
C2360808 (UMLS CUI [1])
Maximum increase of LDH before start of therapy
Item
Maximum increase of LDH before start of therapy
integer
C0442805 (UMLS CUI [1,1])
C0202113 (UMLS CUI [1,2])
Upper normal limit of LDH in local laboratory
Item
Upper normal limit of LDH in local laboratory
integer
C0202113 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
Item
Involvement of central nervous system (CNS+)
integer
C0449389 (UMLS CUI [1])
NOYESUN
Code List
Involvement of central nervous system (CNS+)
CL Item
no (1)
CL Item
yes (2)
CL Item
unclear / could not be clarified / (not interpretable) (3)
Item
Involvement of bone marrow (BM+)
integer
C1517677 (UMLS CUI [1])
NOYES
Code List
Involvement of bone marrow (BM+)
CL Item
no (1)
CL Item
yes (2)
Item
Therapy arm (for mature B-NHL only)
integer
C1522541 (UMLS CUI [1])
ARM
Code List
Therapy arm (for mature B-NHL only)
CL Item
R1 (1)
CL Item
R2 (2)
CL Item
R3 (3)
CL Item
R4 (4)
CL Item
R4 CNS pos. (5)
Date of treatment start
Item
Date of treatment start
date
C3173309 (UMLS CUI [1])
Item
Chromosomal breakage syndrome, immunodeficiency, or HIV infection
integer
C0398791 (UMLS CUI [1])
C0019693 (UMLS CUI [2])
C0021051 (UMLS CUI [3])
NOYES
Code List
Chromosomal breakage syndrome, immunodeficiency, or HIV infection
CL Item
no (1)
CL Item
yes (2)
specify syndrome
Item
specify syndrome
text
C1521902 (UMLS CUI [1])
Item
Previous organ transplantation
integer
C0029216 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
NOYES
Code List
Previous organ transplantation
CL Item
no (1)
CL Item
yes (2)
specify TP
Item
specify TP
text
C1521902 (UMLS CUI [1])
Item
Previous malignancy/neoplasm
integer
C0006826 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
NOYES
Code List
Previous malignancy/neoplasm
CL Item
no (1)
CL Item
yes (2)
specify previous malignancy
Item
specify previous malignancy
text
C1521902 (UMLS CUI [1])
Item
Other pre-existing disease prohibiting standard chemotherapy
integer
C0009488 (UMLS CUI [1])
NOYES
Code List
Other pre-existing disease prohibiting standard chemotherapy
CL Item
no (1)
CL Item
yes (2)
specify preexisting disease
Item
specify preexisting disease
text
C1521902 (UMLS CUI [1])
Item
Previous chemotherapy, radiotherapy, or systemic corticosteroid treatment
integer
C0149783 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
NOYES
Code List
Previous chemotherapy, radiotherapy, or systemic corticosteroid treatment
CL Item
no (1)
CL Item
yes (2)
specify previous therapy
Item
specify previous therapy
text
C1521902 (UMLS CUI [1])
Item
For female patients: Pregnancy or lactation period
integer
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
NOYES
Code List
For female patients: Pregnancy or lactation period
CL Item
no (1)
CL Item
yes (2)
Item
Simultaneous participation in a clinical study
integer
C2348568 (UMLS CUI [1])
NOYES
Code List
Simultaneous participation in a clinical study
CL Item
no (1)
CL Item
yes (2)
specify other study
Item
specify other study
text
C1521902 (UMLS CUI [1])
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