ID

44065

Description

base-dataset from ADT - systemic therapy, ODM derived from http://www.tumorzentren.de/tl_files/dokumente/adt_basis.pdf

Link

http://www.tumorzentren.de/tl_files/dokumente/adt_basis.pdf

Keywords

Versions (3)
  1. 8/1/13 8/1/13 -
  2. 3/15/21 3/15/21 - Dr. rer. medic Philipp Neuhaus
  3. 9/20/21 9/20/21 -
Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY-NC 3.0 Legacy
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quality management ADT-systemic therapy cancer

German English

quality management

1 forms  
  1. StudyEvent: quality management
    1. quality management
Patient data
Description

Patient data

patient number
Description

Patientenidentifikationsnummer

Data type

string

Alias
Code-1
Patients
UMLS CUI-1
C0030705
SNOMED CT-1
116154003
Code-2
Identification number
UMLS CUI-2
C1300638
SNOMED CT-2
396278008
Health Insurance
Description

Krankenkasse

Data type

string

Alias
UMLS CUI-1
C0021682
Patient telephone number
Description

Telefon

Data type

string

Alias
UMLS CUI-1
C0421455
SNOMED CT-1
184103008
Patient surname
Description

Name

Data type

string

Alias
UMLS CUI-1
C0421448
SNOMED CT-1
184096005
Maiden Name
Description

Geburtsname

Data type

string

Alias
UMLS CUI-1
C0806887
SNOMED CT-1
423203003
LOINC-1
MTHU010481
Code-2
Patients
UMLS CUI-2
C0030705
SNOMED CT-2
116154003
Patient forename
Description

Vorname

Data type

string

Alias
UMLS CUI-1
C0421447
SNOMED CT-1
184095009
Patient sex
Description

Geschlecht

Data type

integer

Alias
UMLS CUI-1
C0150831
SNOMED CT-1
184100006
Patient date of birth
Description

Geburtsdatum

Data type

date

Alias
UMLS CUI-1
C0421451
SNOMED CT-1
184099003
Ethnicity / related nationality data
Description

Staatsangehörigkeit

Data type

string

Alias
UMLS CUI-1
C0438960
SNOMED CT-1
186034007
Code-2
Patients
UMLS CUI-2
C0030705
SNOMED CT-2
116154003
Patient address
Description

Patient address

Street Address
Description

Straße

Data type

string

Alias
UMLS CUI-1
C1301826
SNOMED CT-1
398099009
Code-2
Patient address
UMLS CUI-2
C0421449
SNOMED CT-2
184097001
Patient postal code
Description

PLZ

Data type

integer

Alias
UMLS CUI-1
C0421454
SNOMED CT-1
184102003
City of residence
Description

Ort

Data type

string

Alias
UMLS CUI-1
C2316883
SNOMED CT-1
433178008
Code-2
Patient address
UMLS CUI-2
C0421449
SNOMED CT-2
184097001
treatment classification
Description

treatment classification

Chemotherapy Regimen
Description

Chemotherapie

Data type

boolean

Alias
UMLS CUI-1
C0392920
SNOMED CT-1
69960004
MedDRA-1
10061758
Endocrine Therapy
Description

Hormontherapie

Data type

boolean

Alias
UMLS CUI-1
C0279025
SNOMED CT-1
169413002
Immunotherapy
Description

Antikörper/Immuntherapie

Data type

boolean

Alias
UMLS CUI-1
C0021083
SNOMED CT-1
76334006
Intent - chemotherapy
Description

Intention - Chemotherapie

Data type

integer

Alias
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Chemotherapy Regimen
UMLS CUI-2
C0392920
SNOMED CT-2
69960004
MedDRA-2
10061758
Intent - endocrine therapy
Description

Intention - endokrine Therapie

Data type

integer

Alias
Code-Info
extended_coding
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Endocrine Therapy
UMLS CUI-2
C0279025
SNOMED CT-2
169413002
Intent - immunotherapy
Description

Intention - Immuntherapie

Data type

integer

Alias
Code-Info
extended_coding
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Immunotherapy
UMLS CUI-2
C0021083
SNOMED CT-2
76334006
Therapeutic procedure
Description

Therapeutic procedure

Chemotherapy Protocols, Antineoplastic
Description

Protokoll

Data type

string

Alias
UMLS CUI-1
C0949219
planned cycles
Description

Zyklen geplant

Data type

integer

Alias
Code-1
Plan
UMLS CUI-1
C1301732
SNOMED CT-1
397943006
Code-2
Chemotherapy cycle (procedure)
UMLS CUI-2
C1302181
SNOMED CT-2
399042005
executed cycles
Description

Zyklen durchgeführt

Data type

integer

Alias
Code-1
Execution
UMLS CUI-1
C1705848
Code-2
Chemotherapy cycle (procedure)
UMLS CUI-2
C1302181
SNOMED CT-2
399042005
Date treatment started - chemotherapy
Description

Beginn - Chemotherapie

Data type

date

Alias
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Chemotherapy Regimen
UMLS CUI-2
C0392920
SNOMED CT-2
69960004
MedDRA-2
10061758
Date treatment started - endocrine therapy
Description

Beginn - endokrine Therapie

Data type

date

Alias
Code-Info
extended_coding
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Endocrine Therapy
UMLS CUI-2
C0279025
SNOMED CT-2
169413002
Date treatment started - immunotherapy
Description

Beginn - Immuntherapie

Data type

date

Alias
Code-Info
extended_coding
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Immunotherapy
UMLS CUI-2
C0021083
SNOMED CT-2
76334006
Chemotherapeutic agent
Description

Substanzen

Data type

string

Alias
Code-1
Chemotherapeutic agent (product)
UMLS CUI-1
C0729502
SNOMED CT-1
312059006
Chemotherapeutic drug level decreased
Description

Dosisreduktion

Data type

boolean

Alias
UMLS CUI-1
C0861114
Single dose characteristic
Description

Einzeldosis

Data type

integer

Alias
Code-1
Single dose characteristic (observable entity)
UMLS CUI-1
C1960417
SNOMED CT-1
426146003
Cumulative Dose
Description

Menge der Absolutdosis

Data type

integer

Alias
UMLS CUI-1
C2986497
Unit type
Description

Einheit

Data type

string

Alias
Code-1
Unit type (qualifier value)
UMLS CUI-1
C0565912
SNOMED CT-1
288462000
Date treatment stopped - interruption
Description

Unterbrechung vom:

Data type

date

Alias
Code-1
Date treatment stopped (observable entity)
UMLS CUI-1
C1531784
SNOMED CT-1
413947000
Code-2
Interruption
UMLS CUI-2
C1512900
Date treatment started after interruption
Description

Unterbrechung bis:

Data type

date

Alias
Code-1
Date treatment started (observable entity)
UMLS CUI-1
C3173309
SNOMED CT-1
413946009
Code-2
Post
UMLS CUI-2
C0231290
SNOMED CT-2
237679004
Code-3
Interruption
UMLS CUI-3
C1512900
Reason for Treatment Interruption
Description

Gründe der Unterbrechung

Data type

string

Alias
UMLS CUI-1
CL436968
Termination systemic therapy
Description

Termination systemic therapy

Date treatment stopped - chemotherapy
Description

Therapieende Chemo

Data type

date

Alias
Code-1
Date treatment stopped (observable entity)
UMLS CUI-1
C1531784
SNOMED CT-1
413947000
Code-2
Chemotherapy Regimen
UMLS CUI-2
C0392920
SNOMED CT-2
69960004
MedDRA-2
10061758
Date treatment stopped - endocrine therapy
Description

Therapieende endokrine Therape

Data type

date

Alias
Code-1
Date treatment stopped (observable entity)
UMLS CUI-1
C1531784
SNOMED CT-1
413947000
Code-2
Endocrine Therapy
UMLS CUI-2
C0279025
SNOMED CT-2
169413002
Date treatment stopped - immunotherapy
Description

Therapieende Immuntherapie

Data type

date

Alias
Code-1
Date treatment stopped (observable entity)
UMLS CUI-1
C1531784
SNOMED CT-1
413947000
Code-2
Immunotherapy
UMLS CUI-2
C0021083
SNOMED CT-2
76334006
Termination systemic therapy
Description

Beendigung der Systemischen Therapie

Data type

integer

Alias
Code-Info
for_compare
Code-1
Termination - action (qualifier value)
UMLS CUI-1
C1283212
SNOMED CT-1
360239007
Code-2
Systemic Therapy
UMLS CUI-2
C1515119
other reason
Description

sonstige Gründe

Data type

string

Alias
Code-1
Indication of (contextual qualifier)
UMLS CUI-1
C0392360
SNOMED CT-1
230165009
LOINC-1
MTHU008319
Code-2
Other
UMLS CUI-2
C0205395
SNOMED CT-2
74964008
Treatment outcome
Description

Treatment outcome

Tumor Status
Description

Gesamtbeurteilung des Tumorstatus

Data type

integer

Alias
Code-Info
for_compare
UMLS CUI-1
C0475752
SNOMED CT-1
277058005
Adverse event
Description

Adverse event

Adverse event
Description

Nebenwirkungen

Data type

boolean

Alias
Code-Info
for_compare
UMLS CUI-1
C0877248
MedDRA-1
10060933
LOINC-1
MTHU014542
Hemoglobin
Description

HB

Data type

integer

Alias
Code-1
Hemoglobin Adverse Event
UMLS CUI-1
C2239101
CTCAE-1
MTHU116997
Aspartate Transaminase
Description

GOT

Data type

integer

Alias
Code-1
Serum Glutamic Oxaloacetic Transaminase Adverse Event
UMLS CUI-1
C1557198
CTCAE-1
MTHU117449
Alanine Transaminase
Description

GPT

Data type

integer

Alias
Code-1
Serum Glutamic Pyruvic Transaminase Adverse Event
UMLS CUI-1
C1557189
CTCAE-1
MTHU117450
Creatinine
Description

Kreatinin

Data type

integer

Alias
Code-1
Creatinine Adverse Event
UMLS CUI-1
C1561535
CTCAE-1
MTHU116842
Skin
Description

Haut

Data type

integer

Alias
Code-1
Other Dermatology or Skin Adverse Event
UMLS CUI-1
C1559104
CTCAE-1
MTHU117246
Peripheral Nerves
Description

Periph. Nerven

Data type

integer

Alias
Code-1
Neuralgia and Peripheral Nerve Pain Adverse Event
UMLS CUI-1
C1557517
CTCAE-1
MTHU117196
Hemorrhage
Description

Blutungen

Data type

integer

Alias
Code-1
Other Hemorrhage and Bleeding Adverse Event
UMLS CUI-1
C1556642
CTCAE-1
MTHU117250
Bilirubin
Description

Bilirubin

Data type

integer

Alias
Code-1
Hyperbilirubinemia Adverse Event
UMLS CUI-1
C1557209
CTCAE-1
MTHU117008
Leukocytes
Description

Leuko

Data type

integer

Alias
Code-1
Leukocytes Adverse Event
UMLS CUI-1
C1560219
CTCAE-1
MTHU117099
Alkaline Phosphatase
Description

AP

Data type

integer

Alias
Code-1
Alkaline Phosphatase Adverse Event
UMLS CUI-1
C1561546
CTCAE-1
MTHU112158
Proteinuria
Description

Proteinurie

Data type

integer

Alias
Code-1
Proteinuria Adverse Event
UMLS CUI-1
C1962972
CTCAE-1
MTHU117382
Hair
Description

Haar

Data type

integer

Alias
Code-1
Alopecia Adverse Event
UMLS CUI-1
C1559115
CTCAE-1
MTHU112161
Obstipation
Description

Obstipation

Data type

integer

Alias
Code-1
Constipation Adverse Event
UMLS CUI-1
C1963087
CTCAE-1
MTHU116803
Diarrhea
Description

Diarrhoe

Data type

integer

Alias
Code-1
Diarrhea Adverse Event
UMLS CUI-1
C0232708
CTCAE-1
MTHU116856
Urea
Description

Harnstoff

Data type

integer

Alias
Code-1
Urea
UMLS CUI-1
C0041942
SNOMED CT-1
387092000
LOINC-1
MTHU009413
neutrophil
Description

Granuloz

Data type

integer

Alias
Code-1
Neutrophils and Granulocytes Adverse Event
UMLS CUI-1
C1560233
CTCAE-1
MTHU117202
Mucous Membrane
Description

Schleimh.

Data type

integer

Alias
Code-1
Mucositis and Stomatitis Adverse Event by Functional and Symptomatic Classification
UMLS CUI-1
C1556411
CTCAE-1
MTHU117173
Hematuria
Description

Hämaturie

Data type

integer

Alias
UMLS CUI-1
C0018965
SNOMED CT-1
34436003
MedDRA-1
10018867
ICD-10-CM-1
R31.9
ICD-9-CM-1
599.7
CTCAE-1
E13000
Infection
Description

Infektionen

Data type

integer

Alias
Code-1
Adverse Event Associated with Infection
UMLS CUI-1
C1556682
CTCAE-1
MTHU112135
Pain
Description

Schmerzen

Data type

integer

Alias
Code-1
Other Pain Adverse Event (CUI C1557623)
CTCAE-1
MTHU117260
Fever
Description

Fieber

Data type

integer

Alias
Code-1
Fever Without Neutropenia Adverse Event
UMLS CUI-1
C1556366
CTCAE-1
MTHU116933
Allergic Reaction
Description

Allergie

Data type

integer

Alias
Code-1
Adverse Event Associated with Allergy and Immunology
UMLS CUI-1
C1560126
CTCAE-1
MTHU112125
Blood Platelets
Description

Thrombo

Data type

integer

Alias
Code-1
Platelets Adverse Event
UMLS CUI-1
C1963076
CTCAE-1
MTHU117353
Nausea
Description

Übelkeit

Data type

integer

Alias
Code-1
Nausea Adverse Event
UMLS CUI-1
C1963179
CTCAE-1
MTHU117189
Lung
Description

Lunge

Data type

integer

Alias
UMLS CUI-1
C0024109
SNOMED CT-1
39607008
LOINC-1
MTHU008683
Heart Rhythm
Description

Herzrhythmus

Data type

integer

Alias
Code-1
Adverse Event Associated with Cardiac Arrhythmia
UMLS CUI-1
C1560249
CTCAE-1
MTHU112127
Cardiac function
Description

Herzfunktion

Data type

integer

Alias
Code-1
Adverse Event Associated with the Heart in General
UMLS CUI-1
C1556247
CTCAE-1
MTHU112147
Pericarditis
Description

Perikarditis

Data type

integer

Alias
Code-1
Pericarditis Adverse Event
UMLS CUI-1
C1963211
CTCAE-1
MTHU117310
Conscious
Description

Bewusstsein

Data type

integer

Alias
Code-1
Somnolence and Depressed Level of Consciousness Adverse Event
UMLS CUI-1
C1557290
CTCAE-1
MTHU117503
Therapeutic radiology procedure
Description

Gleichzeitig Strahlentherapie?

Data type

boolean

Alias
UMLS CUI-1
C1522449
SNOMED CT-1
108290001
MedDRA-1
10037770
Code-2
Concurrent (qualifier value)
UMLS CUI-2
C0205420
SNOMED CT-2
68405009
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Similar models

quality management

1 forms
  1. StudyEvent: quality management
    1. quality management
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patient data
Patientenidentifikationsnummer
Item
patient number
string
Patients (Code-1)
C0030705 (UMLS CUI-1)
116154003 (SNOMED CT-1)
Identification number (Code-2)
C1300638 (UMLS CUI-2)
396278008 (SNOMED CT-2)
Krankenkasse
Item
Health Insurance
string
C0021682 (UMLS CUI-1)
Telefon
Item
Patient telephone number
string
C0421455 (UMLS CUI-1)
184103008 (SNOMED CT-1)
Name
Item
Patient surname
string
C0421448 (UMLS CUI-1)
184096005 (SNOMED CT-1)
Geburtsname
Item
Maiden Name
string
C0806887 (UMLS CUI-1)
423203003 (SNOMED CT-1)
MTHU010481 (LOINC-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Vorname
Item
Patient forename
string
C0421447 (UMLS CUI-1)
184095009 (SNOMED CT-1)
Item
Patient sex
integer
C0150831 (UMLS CUI-1)
184100006 (SNOMED CT-1)
Geschlecht
Code List
Patient sex
CL Item
Female (weiblich)
C0086287 (UMLS CUI-1)
1086007 (SNOMED CT-1)
CL Item
Male gender (männlich)
C0086582 (UMLS CUI-1)
10052007 (SNOMED CT-1)
Geburtsdatum
Item
Patient date of birth
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
Staatsangehörigkeit
Item
Ethnicity / related nationality data
string
C0438960 (UMLS CUI-1)
186034007 (SNOMED CT-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Item Group
Patient address
Straße
Item
Street Address
string
C1301826 (UMLS CUI-1)
398099009 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
PLZ
Item
Patient postal code
integer
C0421454 (UMLS CUI-1)
184102003 (SNOMED CT-1)
Ort
Item
City of residence
string
C2316883 (UMLS CUI-1)
433178008 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
Item Group
treatment classification
Chemotherapie
Item
Chemotherapy Regimen
boolean
C0392920 (UMLS CUI-1)
69960004 (SNOMED CT-1)
10061758 (MedDRA-1)
Hormontherapie
Item
Endocrine Therapy
boolean
C0279025 (UMLS CUI-1)
169413002 (SNOMED CT-1)
Antikörper/Immuntherapie
Item
Immunotherapy
boolean
C0021083 (UMLS CUI-1)
76334006 (SNOMED CT-1)
Item
Intent - chemotherapy
integer
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Intention - Chemotherapie
Code List
Intent - chemotherapy
CL Item
Curative - procedure intent  (kurativ)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent  (palliativ)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent  (neoadjuvant)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item
Intent - endocrine therapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
Intention - endokrine Therapie
Code List
Intent - endocrine therapy
CL Item
Curative - procedure intent  (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent  (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent  (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item
Intent - immunotherapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
Intention - Immuntherapie
Code List
Intent - immunotherapy
CL Item
Curative - procedure intent  (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent  (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent  (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item Group
Therapeutic procedure
Protokoll
Item
Chemotherapy Protocols, Antineoplastic
string
C0949219 (UMLS CUI-1)
Zyklen geplant
Item
planned cycles
integer
Plan (Code-1)
C1301732 (UMLS CUI-1)
397943006 (SNOMED CT-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
Zyklen durchgeführt
Item
executed cycles
integer
Execution (Code-1)
C1705848 (UMLS CUI-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
Beginn - Chemotherapie
Item
Date treatment started - chemotherapy
date
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Beginn - endokrine Therapie
Item
Date treatment started - endocrine therapy
date
extended_coding (Code-Info)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
Beginn - Immuntherapie
Item
Date treatment started - immunotherapy
date
extended_coding (Code-Info)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
Substanzen
Item
Chemotherapeutic agent
string
Chemotherapeutic agent (product) (Code-1)
C0729502 (UMLS CUI-1)
312059006 (SNOMED CT-1)
Dosisreduktion
Item
Chemotherapeutic drug level decreased
boolean
C0861114 (UMLS CUI-1)
Einzeldosis
Item
Single dose characteristic
integer
Single dose characteristic (observable entity) (Code-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
Menge der Absolutdosis
Item
Cumulative Dose
integer
C2986497 (UMLS CUI-1)
Einheit
Item
Unit type
string
Unit type (qualifier value) (Code-1)
C0565912 (UMLS CUI-1)
288462000 (SNOMED CT-1)
Unterbrechung vom:
Item
Date treatment stopped - interruption
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Interruption (Code-2)
C1512900 (UMLS CUI-2)
Unterbrechung bis:
Item
Date treatment started after interruption
date
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Post (Code-2)
C0231290 (UMLS CUI-2)
237679004 (SNOMED CT-2)
Interruption (Code-3)
C1512900 (UMLS CUI-3)
Gründe der Unterbrechung
Item
Reason for Treatment Interruption
string
CL436968 (UMLS CUI-1)
Item Group
Termination systemic therapy
Therapieende Chemo
Item
Date treatment stopped - chemotherapy
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Therapieende endokrine Therape
Item
Date treatment stopped - endocrine therapy
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
Therapieende Immuntherapie
Item
Date treatment stopped - immunotherapy
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
Item
Termination systemic therapy
integer
for_compare (Code-Info)
Termination - action (qualifier value) (Code-1)
C1283212 (UMLS CUI-1)
360239007 (SNOMED CT-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
Beendigung der Systemischen Therapie
Code List
Termination systemic therapy
CL Item
regular End of Therapy (reguläres Ende)
changed_datatype (Code-Info)
Regular (Code-1)
C0449581 (UMLS CUI-1)
17854005 (SNOMED CT-1)
End (Code-2)
C1272693 (UMLS CUI-2)
385656004 (SNOMED CT-2)
CL Item
Discontinue because of adverse effects (Abbruch wegen Nebenwirkung)
changed_datatype (Code-Info)
Adverse effects (Code-1)
C0879626 (UMLS CUI-1)
281647001 (SNOMED CT-1)
10067484 (MedDRA-1)
Discontinue (Code-2)
C1444662 (UMLS CUI-2)
410546004 (SNOMED CT-2)
Indication of (contextual qualifier) (Code-3)
C0392360 (UMLS CUI-3)
230165009 (SNOMED CT-3)
MTHU008319 (LOINC-3)
CL Item
Refusal of Treatment (Patient verweigert Therapie)
changed_datatype (Code-Info)
C0040809 (UMLS CUI-1)
105480006 (SNOMED CT-1)
10056407 (MedDRA-1)
sonstige Gründe
Item
other reason
string
Indication of (contextual qualifier) (Code-1)
C0392360 (UMLS CUI-1)
230165009 (SNOMED CT-1)
MTHU008319 (LOINC-1)
Other (Code-2)
C0205395 (UMLS CUI-2)
74964008 (SNOMED CT-2)
Item Group
Treatment outcome
Item
Tumor Status
integer
for_compare (Code-Info)
C0475752 (UMLS CUI-1)
277058005 (SNOMED CT-1)
Gesamtbeurteilung des Tumorstatus
Code List
Tumor Status
CL Item
In complete remission  (Vollremission)
changed_datatype (Code-Info)
C0677874 (UMLS CUI-1)
103338009 (SNOMED CT-1)
CL Item
partial response  (Teilremission)
changed_datatype (Code-Info)
C1521726 (UMLS CUI-1)
103337004 (SNOMED CT-1)
CL Item
Stable Disease (keine Änderung)
changed_datatype (Code-Info)
C0677946 (UMLS CUI-1)
CL Item
Tumor Progression (Progression)
changed_datatype (Code-Info)
C0178874 (UMLS CUI-1)
419835002 (SNOMED CT-1)
CL Item
Cannot Be Assessed (nicht beurteilbar)
Cannot Be Assessed (Code-1)
C1707258 (UMLS CUI-1)
CL Item
Unknown  (unbekannt)
changed_datatype (Code-Info)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item Group
Adverse event
Nebenwirkungen
Item
Adverse event
boolean
for_compare (Code-Info)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Item
Hemoglobin
integer
Hemoglobin Adverse Event (Code-1)
C2239101 (UMLS CUI-1)
MTHU116997 (CTCAE-1)
HB
Code List
Hemoglobin
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Hemoglobin Adverse Event (Code-2)
C2239101 (UMLS CUI-2)
MTHU116997 (CTCAE-2)
Item
Aspartate Transaminase
integer
Serum Glutamic Oxaloacetic Transaminase Adverse Event (Code-1)
C1557198 (UMLS CUI-1)
MTHU117449 (CTCAE-1)
GOT
Code List
Aspartate Transaminase
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
only in connection with GPT (only in connection with GPT)
Item
Alanine Transaminase
integer
Serum Glutamic Pyruvic Transaminase Adverse Event (Code-1)
C1557189 (UMLS CUI-1)
MTHU117450 (CTCAE-1)
GPT
Code List
Alanine Transaminase
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
only in connection with GPT (only in connection with GPT)
Item
Creatinine
integer
Creatinine Adverse Event (Code-1)
C1561535 (UMLS CUI-1)
MTHU116842 (CTCAE-1)
Kreatinin
Code List
Creatinine
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Skin
integer
Other Dermatology or Skin Adverse Event (Code-1)
C1559104 (UMLS CUI-1)
MTHU117246 (CTCAE-1)
Haut
Code List
Skin
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Peripheral Nerves
integer
Neuralgia and Peripheral Nerve Pain Adverse Event (Code-1)
C1557517 (UMLS CUI-1)
MTHU117196 (CTCAE-1)
Periph. Nerven
Code List
Peripheral Nerves
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Hemorrhage
integer
Other Hemorrhage and Bleeding Adverse Event (Code-1)
C1556642 (UMLS CUI-1)
MTHU117250 (CTCAE-1)
Blutungen
Code List
Hemorrhage
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Bilirubin
integer
Hyperbilirubinemia Adverse Event (Code-1)
C1557209 (UMLS CUI-1)
MTHU117008 (CTCAE-1)
Bilirubin
Code List
Bilirubin
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Leukocytes
integer
Leukocytes Adverse Event (Code-1)
C1560219 (UMLS CUI-1)
MTHU117099 (CTCAE-1)
Leuko
Code List
Leukocytes
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Alkaline Phosphatase
integer
Alkaline Phosphatase Adverse Event (Code-1)
C1561546 (UMLS CUI-1)
MTHU112158 (CTCAE-1)
AP
Code List
Alkaline Phosphatase
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Proteinuria
integer
Proteinuria Adverse Event (Code-1)
C1962972 (UMLS CUI-1)
MTHU117382 (CTCAE-1)
Proteinurie
Code List
Proteinuria
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Hair
integer
Alopecia Adverse Event (Code-1)
C1559115 (UMLS CUI-1)
MTHU112161 (CTCAE-1)
Haar
Code List
Hair
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Obstipation
integer
Constipation Adverse Event (Code-1)
C1963087 (UMLS CUI-1)
MTHU116803 (CTCAE-1)
Obstipation
Code List
Obstipation
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Diarrhea
integer
Diarrhea Adverse Event (Code-1)
C0232708 (UMLS CUI-1)
MTHU116856 (CTCAE-1)
Diarrhoe
Code List
Diarrhea
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Urea
integer
Urea (Code-1)
C0041942 (UMLS CUI-1)
387092000 (SNOMED CT-1)
MTHU009413 (LOINC-1)
Harnstoff
Code List
Urea
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
neutrophil
integer
Neutrophils and Granulocytes Adverse Event (Code-1)
C1560233 (UMLS CUI-1)
MTHU117202 (CTCAE-1)
Granuloz
Code List
neutrophil
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Mucous Membrane
integer
Mucositis and Stomatitis Adverse Event by Functional and Symptomatic Classification (Code-1)
C1556411 (UMLS CUI-1)
MTHU117173 (CTCAE-1)
Schleimh.
Code List
Mucous Membrane
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Hematuria
integer
C0018965 (UMLS CUI-1)
34436003 (SNOMED CT-1)
10018867 (MedDRA-1)
R31.9 (ICD-10-CM-1)
599.7 (ICD-9-CM-1)
E13000 (CTCAE-1)
Hämaturie
Code List
Hematuria
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Infection
integer
Adverse Event Associated with Infection (Code-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
Infektionen
Code List
Infection
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Pain
integer
Other Pain Adverse Event (CUI C1557623) (Code-1)
MTHU117260 (CTCAE-1)
Schmerzen
Code List
Pain
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Fever
integer
Fever Without Neutropenia Adverse Event (Code-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
Fieber
Code List
Fever
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Allergic Reaction
integer
Adverse Event Associated with Allergy and Immunology (Code-1)
C1560126 (UMLS CUI-1)
MTHU112125 (CTCAE-1)
Allergie
Code List
Allergic Reaction
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Blood Platelets
integer
Platelets Adverse Event (Code-1)
C1963076 (UMLS CUI-1)
MTHU117353 (CTCAE-1)
Thrombo
Code List
Blood Platelets
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Nausea
integer
Nausea Adverse Event (Code-1)
C1963179 (UMLS CUI-1)
MTHU117189 (CTCAE-1)
Übelkeit
Code List
Nausea
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Lung
integer
C0024109 (UMLS CUI-1)
39607008 (SNOMED CT-1)
MTHU008683 (LOINC-1)
Lunge
Code List
Lung
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Heart Rhythm
integer
Adverse Event Associated with Cardiac Arrhythmia (Code-1)
C1560249 (UMLS CUI-1)
MTHU112127 (CTCAE-1)
Herzrhythmus
Code List
Heart Rhythm
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Cardiac function
integer
Adverse Event Associated with the Heart in General (Code-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
Herzfunktion
Code List
Cardiac function
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Pericarditis
integer
Pericarditis Adverse Event (Code-1)
C1963211 (UMLS CUI-1)
MTHU117310 (CTCAE-1)
Perikarditis
Code List
Pericarditis
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Conscious
integer
Somnolence and Depressed Level of Consciousness Adverse Event (Code-1)
C1557290 (UMLS CUI-1)
MTHU117503 (CTCAE-1)
Bewusstsein
Code List
Conscious
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = Geringe Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = Allgemeinbefinden verschlechtert)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = Unterbrechung notwendig)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Stationäre Krankenhausbehandlung notwendig)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Gleichzeitig Strahlentherapie?
Item
Therapeutic radiology procedure
boolean
C1522449 (UMLS CUI-1)
108290001 (SNOMED CT-1)
10037770 (MedDRA-1)
Concurrent (qualifier value) (Code-2)
C0205420 (UMLS CUI-2)
68405009 (SNOMED CT-2)
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