Registration

  1. StudyEvent: SE
    1. Registration
Inclusion criteria
Beschrijving

Inclusion criteria

Newly diagnosed (Secondary malignancy) Non-Hodgkin lymphoma
Beschrijving

Newly diagnosed (Secondary malignancy) Non-Hodgkin lymphoma

Datatype

integer

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

NHL subtype

Datatype

integer

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

specify NHL subtype

Datatype

text

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

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

Datatype

integer

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

Patient age at diagnosis below 18 years

Datatype

integer

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

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

Datatype

integer

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

Date consent

Datatype

date

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

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

Datatype

integer

Alias
UMLS CUI [1]
C1522577
Personal data
Beschrijving

Personal data

Date of registration to Marvin
Beschrijving

Date of registration to Marvin

Datatype

date

Alias
UMLS CUI [1]
C2985881
Patient ID
Beschrijving

Patient ID

Datatype

text

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

Surname (or initial)

Datatype

text

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

First name (or initial)

Datatype

text

Alias
UMLS CUI [1]
C0421447
Date of birth
Beschrijving

Date of birth

Datatype

date

Alias
UMLS CUI [1]
C0421451
Sex
Beschrijving

Sex

Datatype

integer

Alias
UMLS CUI [1]
C0079399
Marvin-ID
Beschrijving

Marvin-ID

Datatype

text

Alias
UMLS CUI [1]
C0552502
Identification
Beschrijving

Identification

Malig-ID (DKKR)
Beschrijving

Malig-ID (DKKR)

Datatype

text

Alias
UMLS CUI [1]
C3897288
GPOH-PID
Beschrijving

GPOH-PID

Datatype

text

Alias
UMLS CUI [1]
C2360808
Additional information
Beschrijving

Additional information

Maximum increase of LDH before start of therapy
Beschrijving

Maximum increase of LDH before start of therapy

Datatype

integer

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

Upper normal limit of LDH in local laboratory

Datatype

integer

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

Involvement of central nervous system (CNS+)

Datatype

integer

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

Involvement of bone marrow (BM+)

Datatype

integer

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

Therapy arm (for mature B-NHL only)

Datatype

integer

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

Date of treatment start

Datatype

date

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

Some data on anamnesis

Chromosomal breakage syndrome, immunodeficiency, or HIV infection
Beschrijving

Chromosomal breakage syndrome, immunodeficiency, or HIV infection

Datatype

integer

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

specify syndrome

Datatype

text

Alias
UMLS CUI [1]
C1521902
Previous organ transplantation
Beschrijving

Previous organ transplantation

Datatype

integer

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

specify TP

Datatype

text

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

Previous malignancy/neoplasm

Datatype

integer

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

specify previous malignancy

Datatype

text

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

Other pre-existing disease prohibiting standard chemotherapy

Datatype

integer

Alias
UMLS CUI [1]
C0009488
specify preexisting disease
Beschrijving

specify preexisting disease

Datatype

text

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

Previous chemotherapy, radiotherapy, or systemic corticosteroid treatment

Datatype

integer

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

specify previous therapy

Datatype

text

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

For female patients: Pregnancy or lactation period

Datatype

integer

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

Simultaneous participation in a clinical study

Datatype

integer

Alias
UMLS CUI [1]
C2348568
specify other study
Beschrijving

specify other study

Datatype

text

Alias
UMLS CUI [1]
C1521902

Similar models

Registration

  1. StudyEvent: SE
    1. Registration
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item
Newly diagnosed (Secondary malignancy) Non-Hodgkin lymphoma
integer
C0024305 (UMLS CUI [1,1])
C3266877 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])