NCCTG Study No
Item
Studie Nr.
string
C0008976 (UMLS CUI-1)
110465008 (SNOMED CT-1)
Numbers (Code-2)
C0237753 (UMLS CUI-2)
260299005 (SNOMED CT-2)
MTHU024869 (LOINC-2)
North Central Cancer Treatment Group (Code-3)
C1518419 (UMLS CUI-3)
Central Lab ID Number
Item
Labor Nr
string
Laboratory (Code-1)
C0022877 (UMLS CUI-1)
261904005 (SNOMED CT-1)
MTHU029808 (LOINC-1)
Numbers (Code-2)
C0237753 (UMLS CUI-2)
260299005 (SNOMED CT-2)
MTHU024869 (LOINC-2)
Institution Number
Item
Institutions-Nr.
string
C0021622 (UMLS CUI-1)
Numbers (Code-2)
C0237753 (UMLS CUI-2)
260299005 (SNOMED CT-2)
MTHU024869 (LOINC-2)
Patient Initials
Item
Patienteninitialien
string
Person Initials (Code-1)
C2986440 (UMLS CUI-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Institution
Item
Institution
string
C0021622 (UMLS CUI-1)
Coordinating Group Protocol Number (N063D)
Item
Gruppen-Protokoll Nr.
string
Group (Code-1)
C0441833 (UMLS CUI-1)
246261001 (SNOMED CT-1)
Protocols documentation (Code-2)
C0442711 (UMLS CUI-2)
258049002 (SNOMED CT-2)
Coordinating Group Code (NCCTG)
Item
Gruppen-Code
string
Group (Code-1)
C0441833 (UMLS CUI-1)
246261001 (SNOMED CT-1)
Code (Code-2)
C0805701 (UMLS CUI-2)
Protocol Title (ALTTO: Adjuvant Lapatinib and/or Trastuzumab Treatment Optimisation Trial)
Item
Protocol Titel
string
Study Protocol (Code-1)
C2348563 (UMLS CUI-1)
Patient Medical Record Number
Item
Nr. Krankenakte
string
Medical record number (Code-1)
C1301894 (UMLS CUI-1)
398225001 (SNOMED CT-1)
MTHU021237 (LOINC-1)
Participating Group Code
Item
Gruppen-Code Teilnehmer
string
Study Protocol Version Participating Organization Type Code (Code-1)
C2986314 (UMLS CUI-1)
Are data amended (check one if data are amended, please circle in red when using paper form)
Item
veränderte Daten
boolean
Amended (Code-1)
C1691222 (UMLS CUI-1)
Data (Code-2)
C1511726 (UMLS CUI-2)
Item
Registrierungs-Typ
integer
Type of registration (attribute) (Code-1)
C0449520 (UMLS CUI-1)
246243005 (SNOMED CT-1)
Code List
Registrierungs-Typ
CL Item
erste Einreichung (First Submission)
Submission (Code-1)
C1515023 (UMLS CUI-1)
First (Code-2)
C0205435 (UMLS CUI-2)
255216001 (SNOMED CT-2)
CL Item
zweite Einrichung (Second Submission )
Submission (Code-1)
C1515023 (UMLS CUI-1)
Second (Code-2)
C0205436 (UMLS CUI-2)
81170007 (SNOMED CT-2)
Item
erste Einreichung
integer
Submission (Code-1)
C1515023 (UMLS CUI-1)
First (Code-2)
C0205435 (UMLS CUI-2)
255216001 (SNOMED CT-2)
Code List
erste Einreichung
Last Name
Item
Nachname
string
Last Name (Code-1)
C1301584 (UMLS CUI-1)
397678008 (SNOMED CT-1)
MTHU020554 (LOINC-1)
contact person (Code-2)
C0337611 (UMLS CUI-2)
70862002 (SNOMED CT-2)
CON (HL7 V3-2)
Pathology (Code-3)
C0030664 (UMLS CUI-3)
394595002 (SNOMED CT-3)
First Name
Item
Vorname
string
First Name (Item-Info)
C1443235 (UMLS CUI-1)
408677003 (SNOMED CT-1)
MTHU020551 (LOINC-1)
contact person (Code-2)
C0337611 (UMLS CUI-2)
70862002 (SNOMED CT-2)
CON (HL7 V3-2)
Pathology (Code-3)
C0030664 (UMLS CUI-3)
394595002 (SNOMED CT-3)
Phone
Item
Telefon
string
Telephone Number (Code-1)
C1515258 (UMLS CUI-1)
MTHU039653 (LOINC-1)
contact person (Code-2)
C0337611 (UMLS CUI-2)
70862002 (SNOMED CT-2)
CON (HL7 V3-2)
Pathology (Code-3)
C0030664 (UMLS CUI-3)
394595002 (SNOMED CT-3)
Fax
Item
Fax
string
Fax Number (Code-1)
C1549619 (UMLS CUI-1)
contact person (Code-2)
C0337611 (UMLS CUI-2)
70862002 (SNOMED CT-2)
CON (HL7 V3-2)
Pathology (Code-3)
C0030664 (UMLS CUI-3)
394595002 (SNOMED CT-3)
E-Mail
Item
E-Mail
string
E-mail Address (Code-1)
C1705961 (UMLS CUI-1)
contact person (Code-2)
C0337611 (UMLS CUI-2)
70862002 (SNOMED CT-2)
CON (HL7 V3-2)
Pathology (Code-3)
C0030664 (UMLS CUI-3)
394595002 (SNOMED CT-3)
Item
Patienten-Geschlecht
integer
184100006 (SNOMED CT-1)
C0079399 (UMLS CUI)
Code List
Patienten-Geschlecht
Date of Birth
Item
Patienten-Geburtsdatum
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
ZIP Code
Item
Postleitzahl Patient
integer
C0421454 (UMLS CUI-1)
184102003 (SNOMED CT-1)
Country of Residence
Item
Wohnort
string
Country of residence (observable entity) (Code-1)
C1562954 (UMLS CUI-1)
416647007 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
Method of Payment
Item
integer
Item
Rasse
integer
Racial group (Code-1)
C0034510 (UMLS CUI-1)
103579009 (SNOMED CT-1)
MTHU009923 (LOINC-1)
CL Item
Kaukasier (White)
Caucasoid Race (Code-1)
C0007457 (UMLS CUI-1)
413773004 (SNOMED CT-1)
CL Item
Afroamerikaner (Black or African American)
African American (Code-1)
C0085756 (UMLS CUI-1)
15086000 (SNOMED CT-1)
CL Item
Pazifikinsulaner (Native Hawaiian or other Pacific Islander)
Pacific Island Americans (Code-1)
C0242191 (UMLS CUI-1)
CL Item
Asiate (Asian)
Asians (Code-1)
C0078988 (UMLS CUI-1)
413582008 (SNOMED CT-1)
2028-9 (HL7 V3-1)
CL Item
amerikaner Ureinwohner (American Indian or Alaska Native)
Native Americans (Code-1)
C0282204 (UMLS CUI-1)
413490006 (SNOMED CT-1)
1002-5 (HL7 V3-1)
CL Item
Nicht berichtet (Not Reported)
Not Stated (Code-1)
C1706613 (UMLS CUI-1)
CL Item
Unbekannt (Unknown)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Ethnische Gruppe
integer
Ethnic group (Code-1)
C0015031 (UMLS CUI-1)
364699009 (SNOMED CT-1)
Code List
Ethnische Gruppe
CL Item
keine Hispanoamerikanische Herkunft (NOT HISPANIC OR LATINO)
Negation (Code-1)
C1518422 (UMLS CUI-1)
Hispanics (Code-2)
C0086409 (UMLS CUI-2)
MTHU010274 (LOINC-2)
CL Item
Hispanoamerikanische Herkunft (HISPANIC OR LATINO)
Hispanics (Code-1)
C0086409 (UMLS CUI-1)
MTHU010274 (LOINC-1)
CL Item
Nicht berichtet (Not reported)
Not Stated (Code-1)
C1706613 (UMLS CUI-1)
CL Item
Unbekannt (Unknown)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Item
Einschlusskriterien
integer
Inclusion Criteria (Code-1)
C1512693 (UMLS CUI-1)
Code List
Einschlusskriterien
CL Item
Alter >= 18 (Age >= 18 years)
patient age (Code-1)
CL386174 (UMLS CUI-1)
CL Item
(Baseline LVEF > 50% measured by echocardiography or MUGA scan after completion of all anthracycline-based (neo-) adjuvant chemotherapy and prior to the targeted therapy(ies)
zu_spezielles_item (Item-Info)
Left Ventricular Ejection Fraction (Code-1)
CL433348 (UMLS CUI-1)
Complete (Code-2)
C0205197 (UMLS CUI-2)
255594003 (SNOMED CT-2)
CL Item
(Completion of all necessary baseline laboratory and radiological investigations)
CL Item
Eastern Cooperative Oncology Group (ecog) Performance Status < 1 (Eastern Cooperative Oncology Group (ECOG) performance status < 1)
Eastern Cooperative Oncology Group performance status - grade 0 (finding) (Code-1)
C1828078 (UMLS CUI-1)
425389002 (SNOMED CT-1)
CL Item
Hormon Rezeptor Status (Östrogen/Progesteron oder Östrogen alleine) (Known hormone receptor status (ER/PgR or ER alone))
Hormone Receptor (Code-1)
C0019929 (UMLS CUI-1)
CL Item
(Must have received at least four cycles of an approved anthracycline-based (neo-) adjuvant chemotherapy regimen)
CL Item
nicht metastasiertes operables Mamma-Karzinom (Non-metastatic operable primary invasive adenocarcinoma of the breast)
Breast Adenocarcinoma (Code-1)
C0858252 (UMLS CUI-1)
10006173 (MedDRA-1)
Operable (Code-2)
C0205188 (UMLS CUI-2)
76234009 (SNOMED CT-2)
Negative for metastatic tumor (finding) (Code-3)
C0332655 (UMLS CUI-3)
89474008 (SNOMED CT-3)
CL Item
Her2Neu positives Mamma-Karzinom (Overexpression and/or amplification of HER2 in the invasive component of the primary tumor)
HER2-positive carcinoma of breast (disorder) (Code-1)
C1960398 (UMLS CUI-1)
427685000 (SNOMED CT-1)
CL Item
Einverständniserklärung unterschrieben (Signed written informed consent)
Informed consent obtained (Code-1)
C0514044 (UMLS CUI-1)
Item
Ausschlusskriterien
integer
Exclusion Criteria (Code-1)
C0680251 (UMLS CUI-1)
Code List
Ausschlusskriterien
CL Item
((Neo-) or adjuvant chemotherapy using peripheral stem cell or bone marrow stem cell support)
CL Item
klinisches T4 Stadium (Any clinically staged T4 tumor, including inflammatory breast cancer)
T4 Stage Finding (Code-1)
C0475751 (UMLS CUI-1)
65565005 (SNOMED CT-1)
cT category (observable entity) (Code-2)
C1275863 (UMLS CUI-2)
399504009 (SNOMED CT-2)
CL Item
(Any of the following abnormal laboratory tests immediately prior to randomization (see list in instructions))
CL Item
(Any prior mediastinal irradiation except internal mammary node irradiation for the present)
CL Item
beidseitige Tumoren (Bilateral tumors)
Bilateral Breast Carcinoma (Code-1)
C0281267 (UMLS CUI-1)
CL Item
(Concomitant use of CYP3A4 inhibitors or inducers)
CL Item
(Concurrent anti-cancer treatment in another investigational trial with hormone therapy or immunotherapy)
CL Item
gleichzeitige Tumor-Therapie, außer Hormontherapie (Concurrent anti-cancer treatment, except hormonal therapy)
Cancer Therapeutic Procedure (Code-1)
C0920425 (UMLS CUI-1)
MTHU038130 (LOINC-1)
Concurrent (Code-2)
C0205420 (UMLS CUI-2)
68405009 (SNOMED CT-2)
Except for (attribute) (Code-3)
C0332300 (UMLS CUI-3)
5185003 (SNOMED CT-3)
Endocrine Therapy (Code-4)
C0279025 (UMLS CUI-4)
169413002 (SNOMED CT-4)
10065646 (MedDRA-4)
CL Item
Mammakarzinom in der Vorgeschichte (History of any prior (ipsi- and/or contralateral) invasive breast carcinoma)
Pre-existing Condition (Code-1)
C0521987 (UMLS CUI-1)
102478008 (SNOMED CT-1)
Invasive Breast Carcinoma (Code-2)
C0853879 (UMLS CUI-2)
10006190 (MedDRA-2)
CL Item
(Malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel, or person unable to swallow oral medication)
CL Item
(Maximum cumulative dose of doxorubicin >360mg/m2 or maximum cumulative dose of epirubicin >720mg/m2 or any prior anthracyclines unrelated to the present breast cancer)
CL Item
multifokaler Tumor (Multifocal tumors)
Multifocal tumor (finding) (Code-1)
C1302461 (UMLS CUI-1)
399506006 (SNOMED CT-1)
CL Item
(Other concurrent serious diseases that may interfere with planned treatment including severe pulmonary conditions/illness)
CL Item
(Past or current history of malignant neoplasms, except for curatively treated basal and squamous cell carcinoma of the skin or carcinoma in situ of the cervix)
CL Item
(Patients with positive or suspicious internal mammary nodes identified by sentinel node technique which have not been irradiated or will not be irradiated, or patients with supraclavicular lymph node involvement)
CL Item
Schwanger oder stillende Frau (Pregnant or lactating women)
Patient currently pregnant (finding) (Code-1)
C0549206 (UMLS CUI-1)
77386006 (SNOMED CT-1)
10036586 (MedDRA-1)
On examination - lactating breast (finding) (Code-2)
C0437092 (UMLS CUI-2)
163439005 (SNOMED CT-2)
CL Item
(Prior use of anti-HER2 therapy for any reason or other prior biologic or immunotherapy for breast cancer)
CL Item
(Serious cardiac illness or medical conditions (including...))
CL Item
(Unresolved or unstable serious adverse event from prior adjuvant chemotherapy or radiotherapy)
CL Item
(Women of childbearing potential including women whose last menstrual period was <1 year ago who are unable or unwilling to use adequate contraceptive measures during study treatment)
Date Informed consent signed
Item
Datum Einverstädniserklärung
date
Informed consent obtained (Code-1)
C0514044 (UMLS CUI-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Date of consent [for] pharmacogenetic research
Item
Datum Einverstädniserklärung für Pharmakogenetische Tests
date
Informed consent obtained (Code-1)
C0514044 (UMLS CUI-1)
Pharmacogenetic Test (Code-2)
C2347500 (UMLS CUI-2)
Date in time (Code-3)
C0011008 (UMLS CUI-3)
410671006 (SNOMED CT-3)
MTHU021546 (LOINC-3)
Did the patient consent to donate blood sample
Item
Datum Einverstädniserklärung für Blutproben
boolean
Blood Sample (Code-1)
C0178913 (UMLS CUI-1)
119297000 (SNOMED CT-1)
Informed consent obtained (Code-2)
C0514044 (UMLS CUI-2)
MTHU008888 (MedDRA-2)
Did the patient consent to tumor tissue
Item
Datum Einverstädniserklärung für Tumorgewebe
boolean
Tissue Collection (Code-1)
C0040278 (UMLS CUI-1)
Informed consent obtained (Code-2)
C0514044 (UMLS CUI-2)
MTHU008888 (MedDRA-2)
Did the patient consent to donate additional blood sample
Item
Datum Einverstädniserklärung für zusätzliche Blutproben
boolean
Additional (Code-1)
C1524062 (UMLS CUI-1)
Blood Sample (Code-2)
C0178913 (UMLS CUI-2)
119297000 (SNOMED CT-2)
Informed consent obtained (Code-3)
C0514044 (UMLS CUI-3)
MTHU008888 (MedDRA-3)
Did the patient consent to donate fresh/frozen tissue
Item
Datum Einverstädniserklärung für gefrorene Proben
boolean
Frozen Specimen (Code-1)
C1548793 (UMLS CUI-1)
Informed consent obtained (Code-2)
C0514044 (UMLS CUI-2)
MTHU008888 (MedDRA-2)
Item
Menopausenstatus
integer
Menopause finding (finding) (Code-1)
C0455962 (UMLS CUI-1)
276477006 (SNOMED CT-1)
Code List
Menopausenstatus
CL Item
Prämenopause (Pre (<6 mo since LMP AND no prior bilateral ovariectomy AND not on estrogen replacement))
Premenopausal state (finding) (Code-1)
C0232969 (UMLS CUI-1)
22636003 (SNOMED CT-1)
CL Item
Postmenopause (Post (prior bilateral ovariectomy OR >12 mo since LMP with no prior hysterectomy))
Postmenopausal (Code-1)
C0232970 (UMLS CUI-1)
76498008 (SNOMED CT-1)
CL Item
Kategorien nicht anwendbar, Alter unter 50 (Above categories not applicable AND Age < 50)
None or Not Applicable (Code-1)
CL413952 (UMLS CUI-1)
patient age (Code-2)
CL386174 (UMLS CUI-2)
CL Item
Kategorien nicht anwendbar, älter als 50 (Above categories not applicable AND Age >= 50)
None or Not Applicable (Code-1)
CL413952 (UMLS CUI-1)
patient age (Code-2)
CL386174 (UMLS CUI-2)
Date of last menstrual cycle
Item
Datum letzte Menstruation
date
Menstrual cycle (Code-1)
C0025329 (UMLS CUI-1)
78456001 (SNOMED CT-1)
Last (Code-2)
C1517741 (UMLS CUI-2)
Date in time (Code-3)
C0011008 (UMLS CUI-3)
410671006 (SNOMED CT-3)
MTHU021546 (LOINC-3)
Date of pregnancy test
Item
Datum Schwangerschaftstest
date
Pregnancy Tests (Code-1)
C0032976 (UMLS CUI-1)
74036000 (SNOMED CT-1)
10036572 (MedDRA-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Item
Schwangerschaftstest
integer
Pregnancy Tests (Code-1)
74036000 (SNOMED CT-1)
10036572 (MedDRA-1)
C0032976 (UMLS CUI)
Code List
Schwangerschaftstest
Has the patient had a hysterectomy?
Item
Hatte die Patientin eine Hysterektomie?
boolean
Hysterectomy (Code-1)
C0020699 (UMLS CUI-1)
236886002 (SNOMED CT-1)
10021151 (MedDRA-1)
Hysterectomy
Item
Datum Hysterektomie
date
Hysterectomy (Code-1)
C0020699 (UMLS CUI-1)
236886002 (SNOMED CT-1)
10021151 (MedDRA-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Unilateral ovariectomy/oophorectomy
Item
Einseitige Ovarektomie
boolean
Unilateral Oophorectomy (Code-1)
C0041687 (UMLS CUI-1)
33159007 (SNOMED CT-1)
10030344 (MedDRA-1)
65.3 (ICD-9-CM-1)
Item
Seite Ovarektomie
integer
C0441987 (UMLS CUI-1)
182353008 (SNOMED CT-1)
Unilateral Oophorectomy (Code-2)
C0041687 (UMLS CUI-2)
33159007 (SNOMED CT-2)
10030344 (MedDRA-2)
Code List
Seite Ovarektomie
CL Item
rechts (Right)
C0205090 (UMLS CUI-1)
24028007 (SNOMED CT-1)
CL Item
links (Left)
C0205091 (UMLS CUI-1)
7771000 (SNOMED CT-1)
Unilateral oophorectomy Date
Item
Datum Einseitige Ovarektomie
date
Unilateral Oophorectomy (Code-1)
C0041687 (UMLS CUI-1)
33159007 (SNOMED CT-1)
10030344 (MedDRA-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Date of Physical exam
Item
Datum körperliche Untersuchung
date
Physical Examination Date (Code-1)
C2826643 (UMLS CUI-1)
Item
körperliche Untersuchung
integer
C0031809 (UMLS CUI-1)
5880005 (SNOMED CT-1)
10034986 (MedDRA-1)
MTHU028014 (LOINC-1)
Code List
körperliche Untersuchung
CL Item
unauffällig (Normal)
Normal (Code-1)
C0205307 (UMLS CUI-1)
17621005 (SNOMED CT-1)
CL Item
auffällig, klinisch signifikant (Abnormal - Clinically significant)
Abnormal (Code-1)
C0205161 (UMLS CUI-1)
263654008 (SNOMED CT-1)
Clinically Significant Indicator (Code-2)
C2985739 (UMLS CUI-2)
CL Item
auffällig, klinisch nicht signifikant (Abnormal - Not clinically significant)
Abnormal (Code-1)
C0205161 (UMLS CUI-1)
263654008 (SNOMED CT-1)
Clinically Significant Indicator (Code-2)
C2985739 (UMLS CUI-2)
Negation (Code-3)
C1518422 (UMLS CUI-3)
Height
Item
Größe
float
cm (Item-Info)
Length of body (observable entity) (Code-1)
248334005 (SNOMED CT-1)
C0005890 (UMLS CUI-1)
Weight
Item
Körpergewicht
float
kg (Item-Info)
Body Weight (Code-1)
27113001 (SNOMED CT-1)
MTHU001885 (LOINC-1)
C0005910 (UMLS CUI-1)
BSA
Item
Körperoberfläche
float
m^2 (Item-Info)
Body Surface Area (Code-1)
301898006 (SNOMED CT-1)
10050311 (MedDRA-1)
C0005902 (UMLS CUI-1)
Systolic blood pressure
Item
Systolischer Blutdruck
integer
Systolic Blood Pressure (Code-1)
271649006 (SNOMED CT-1)
C0871470 (UMLS CUI-1)
Diastolic blood pressure
Item
Diastolischer Blutdruck
integer
Diastolic Blood Pressure (Code-1)
271650006 (SNOMED CT-1)
C0428883 (UMLS CUI-1)
Heart rate
Item
Herzfrequenz
integer
beats/min (Item-Info)
heart rate (Code-1)
364075005 (SNOMED CT-1)
10019299 (MedDRA-1)
MTHU003114 (LOINC-1)
C0018810 (UMLS CUI-1)
Item
ECOG Leistungszustand
integer
C1632812 (UMLS CUI-1)
Code List
ECOG Leistungszustand
CL Item
0 (0)
Eastern Cooperative Oncology Group performance status - grade 0 (finding) (Code-1)
C1828078 (UMLS CUI-1)
25389002 (SNOMED CT-1)
CL Item
1 (1)
Eastern Cooperative Oncology Group performance status - grade 1 (finding) (Code-1)
C1827388 (UMLS CUI-1)
422512005 (SNOMED CT-1)
CL Item
2 (2)
Eastern Cooperative Oncology Group performance status - grade 2 (finding) (Code-1)
C1828242 (UMLS CUI-1)
422894000 (SNOMED CT-1)
CL Item
3 (3)
Eastern Cooperative Oncology Group performance status - grade 3 (finding) (Code-1)
C1827126 (UMLS CUI-1)
423053003 (SNOMED CT-1)
CL Item
4 (4)
Eastern Cooperative Oncology Group performance status - grade 4 (finding) (Code-1)
C1827528 (UMLS CUI-1)
423237006 (SNOMED CT-1)
CL Item
5 (5)
Eastern Cooperative Oncology Group performance status - grade 5 (finding) (Code-1)
C1827926 (UMLS CUI-1)
423409001 (SNOMED CT-1)
LVEF date
Item
Datum Linksventrikuläre Ejektionsfraktion
date
Left Ventricular Ejection Fraction (Code-1)
Date in time (Code-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
C0428772 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
LVEF
Item
Linksventrikuläre Ejektionsfraktion
float
Left Ventricular Ejection Fraction (Code-1)
C0428772 (UMLS CUI-1)
Echocardiogramm
Item
Echokardiographie
boolean
changed_datatype (Code-Info)
Echocardiography (Code-1)
C0013516 (UMLS CUI-1)
40701008 (SNOMED CT-1)
10014113 (MedDRA-1)
88.72 (ICD-9-CM-1)
Muga Scan
Item
Radionuklidventrikulographie
boolean
changed_datatype (Code-Info)
Radionuclide Ventriculogram Scan (Code-1)
C0521317 (UMLS CUI-1)
404221001 (SNOMED CT-1)
10028211 (MedDRA-1)
Item
Ergebnis
integer
Result (Code-1)
C1274040 (UMLS CUI-1)
394617004 (SNOMED CT-1)
Left Ventricular Ejection Fraction (Code-2)
CL433348 (UMLS CUI-2)
CL Item
unauffällig (Normal)
Normal (Code-1)
C0205307 (UMLS CUI-1)
17621005 (SNOMED CT-1)
CL Item
auffällig, klinisch signifikant (Abnormal - Clinically significant)
Abnormal (Code-1)
C0205161 (UMLS CUI-1)
263654008 (SNOMED CT-1)
Clinically Significant Indicator (Code-2)
C2985739 (UMLS CUI-2)
CL Item
auffällig, klinisch nicht signifikant (Abnormal - Not clinically significant)
Abnormal (Code-1)
C0205161 (UMLS CUI-1)
263654008 (SNOMED CT-1)
Clinically Significant Indicator (Code-2)
C2985739 (UMLS CUI-2)
Negation (Code-3)
C1518422 (UMLS CUI-3)
Symptomatic CHF
Item
boolean
Item
text
C1275491 (UMLS CUI-1)
Code List
NYHA Classification
Code List
Staining Antibody
CL Item
nicht_sinnvoll_für_Untersuchung (Dako Herceptest [tm] )
CL Item
nicht_sinnvoll_für_Untersuchung (Dako A0485 )
CL Item
nicht_sinnvoll_für_Untersuchung (Cb-11/ventana Kit )
CL Item
nicht_sinnvoll_für_Untersuchung (Tab-250 )
CL Item
nicht_sinnvoll_für_Untersuchung (Ncl-c-erbb2-316 )
CL Item
nicht_sinnvoll_für_Untersuchung (other)
other
Item
nicht_sinnvoll_für_Untersuchung
string
Item
Her2/Neu Status
integer
Her2/Neu Status (Code-1)
C1512413 (UMLS CUI-1)
Code List
Her2/Neu Status
CL Item
positiv (Positive )
HER2-positive carcinoma of breast (disorder) (Code-1)
C1960398 (UMLS CUI-1)
427685000 (SNOMED CT-1)
CL Item
fraglich (Equivocal )
Equivocal result (qualifier value) (Code-1)
C0459423 (UMLS CUI-1)
280414007 (SNOMED CT-1)
CL Item
negativ (Negative )
HER2-negative breast cancer (Code-1)
CL412283 (UMLS CUI-1)
CL Item
Nicht auswertbar (Non-interpretable )
Unevaluable (Code-1)
C1883425 (UMLS CUI-1)
Percentage of invasive tumor cells with complete membrane staining
Item
integer
Code List
FISH Kit or Test Type
CL Item
nicht_sinnvoll_für_Untersuchung (Vysis/path Vysion[tm] )
CL Item
nicht_sinnvoll_für_Untersuchung (Other)
other
Item
nicht_sinnvoll_für_Untersuchung
string
Item
FisH-Test
integer
Fluorescent in Situ Hybridization (Code-1)
C0162789 (UMLS CUI-1)
426329006 (SNOMED CT-1)
10066931 (MedDRA-1)
CL Item
positiv (Amplified )
Positive Finding (Code-1)
C1446409 (UMLS CUI-1)
10828004 (SNOMED CT-1)
CL Item
fraglich (Equivocal )
Equivocal result (qualifier value) (Code-1)
C0459423 (UMLS CUI-1)
280414007 (SNOMED CT-1)
CL Item
negativ (Not Amplified )
Negative Finding (Code-1)
C0205160 (UMLS CUI-1)
260385009 (SNOMED CT-1)
FISH HER2/neu chromosome 17 Ratio
Item
integer
Code List
Chromosome 17 copy number
Sample test date
Item
Test Datum
date
Test Date (Code-1)
C2826247 (UMLS CUI-1)
Not done
Item
nicht durchgeführt
string
Not Done (Code-1)
C1272696 (UMLS CUI-1)
385660001 (SNOMED CT-1)
Her2/Neu Status (Code-2)
C1512413 (UMLS CUI-2)
Code List
CISH Kit or Test Type
CL Item
nicht_sinnvoll_für_Untersuchung (Ventana Inform)
CL Item
nicht_sinnvoll_für_Untersuchung (Other)
Other
Item
nicht_sinnvoll_für_Untersuchung
string
Item
CISH
integer
Cytokine-Inducible SH2-Containing Protein (Code-1)
C0299250 (UMLS CUI-1)
CL Item
positiv (Amplified )
Positive Finding (Code-1)
C1446409 (UMLS CUI-1)
10828004 (SNOMED CT-1)
CL Item
fraglich (Equivocal )
Equivocal result (qualifier value) (Code-1)
C0459423 (UMLS CUI-1)
280414007 (SNOMED CT-1)
CL Item
negativ (Not Amplified )
Negative Finding (Code-1)
C0205160 (UMLS CUI-1)
260385009 (SNOMED CT-1)
Code List
Chromosome 17 copy number
ER % cells stained positive
Item
Östrogenrezeptor-positive Zellen %
integer
Percentage unit (qualifier value) (Code-1)
C1532336 (UMLS CUI-1)
415067009 (SNOMED CT-1)
Estrogen receptor positive tumor (disorder) (Code-2)
C1562312 (UMLS CUI-2)
416053008 (SNOMED CT-2)
PgR % cells stained positive
Item
Progesteronrezeptor-positive Zellen %
integer
Percentage unit (qualifier value) (Code-1)
C1532336 (UMLS CUI-1)
415067009 (SNOMED CT-1)
Progesterone receptor positive tumor (disorder) (Code-2)
C1562928 (UMLS CUI-2)
416561008 (SNOMED CT-2)
Date of initial Pathologic Diagnosis
Item
Diagnosedatum
date
Date of diagnosis (Code-1)
C2316983 (UMLS CUI-1)
432213005 (SNOMED CT-1)
Tumor finding (finding) (Code-2)
C1274082 (UMLS CUI-2)
395557000 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Item
Körperseite Tumor
integer
C0441987 (UMLS CUI-1)
182353008 (SNOMED CT-1)
MTHU014973 (LOINC-1)
Tumor site (Code-2)
C0475445 (UMLS CUI-2)
263591006 (SNOMED CT-2)
MTHU015562 (LOINC-2)
Code List
Körperseite Tumor
CL Item
links (Left)
C0205091 (UMLS CUI-1)
7771000 (SNOMED CT-1)
CL Item
rechts (Right)
C0205090 (UMLS CUI-1)
24028007 (SNOMED CT-1)
Clinical Size of Tumor
Item
klinische Tumorgröße
integer
Tumor size (observable entity) (Code-1)
C0475440 (UMLS CUI-1)
263605001 (SNOMED CT-1)
Clinical (Code-2)
C0205210 (UMLS CUI-2)
58147004 (SNOMED CT-2)
Item
N - Stadium der regionalen Lymphknoten
integer
cN category (observable entity) (Code-1)
C1275865 (UMLS CUI-1)
399534004 (SNOMED CT-1)
Code List
N - Stadium der regionalen Lymphknoten
CL Item
N0 Stadium (N0)
N0 Stage Finding (Code-1)
C0441959 (UMLS CUI-1)
62455006 (SNOMED CT-1)
CL Item
N1 Stadium (N1)
N1 Stage Finding (Code-1)
C0441962 (UMLS CUI-1)
53623008 (SNOMED CT-1)
CL Item
N2 Stadium (N2)
N2 Stage Finding (Code-1)
C0441960 (UMLS CUI-1)
46059003 (SNOMED CT-1)
CL Item
N3 Stadium (N3)
N3 Stage Finding (Code-1)
C0441961 (UMLS CUI-1)
5856006 (SNOMED CT-1)
Pathologic Primary Tumor Size
Item
Tumorgröße
integer
Tumor size (observable entity) (Code-1)
C0475440 (UMLS CUI-1)
263605001 (SNOMED CT-1)
Margin involvement
Item
Schnittrand infiltiert durch Tumor
boolean
Surgical margin involved by malignant neoplasm (finding) (Code-1)
C1273678 (UMLS CUI-1)
384689007 (SNOMED CT-1)
Item
histologischer Typ
integer
Histologic Type (Code-1)
C0449574 (UMLS CUI-1)
263541007 (SNOMED CT-1)
MTHU020048 (LOINC-1)
Code List
histologischer Typ
CL Item
Duktales Karzinom (Ductal NOS)
Ductal Breast Carcinoma (Code-1)
C1527349 (UMLS CUI-1)
CL Item
invasives lobuläre Karzinom (Lobular )
Invasive Lobular Breast Carcinoma (Code-1)
CL029510 (UMLS CUI-1)
CL Item
Gemischt, duktal und lobulär (Mixed ductal and lobular)
Mixed Lobular and Ductal Breast Carcinoma (Code-1)
CL007210 (UMLS CUI-1)
CL Item
tubulär (Tubular (pure > or =90%))
Tubular Breast Carcinoma (Code-1)
C0279561 (UMLS CUI-1)
CL Item
apokrin (Apocrine )
Apocrine Breast Carcinoma (Code-1)
C1332316 (UMLS CUI-1)
10066206 (MedDRA-1)
CL Item
Tubulolobulär (Tubulolobular )
Invasive Lobular Breast Carcinoma, Tubulolobular Variant (Code-1)
CL429657 (UMLS CUI-1)
CL Item
Mikropapillär (Micropapillary )
Invasive Micropapillary Breast Carcinoma (Code-1)
C1334279 (UMLS CUI-1)
CL Item
Cribriform (Cribriform )
Invasive Cribriform Breast Carcinoma (Code-1)
C1334275 (UMLS CUI-1)
CL Item
Muzinöses Adenokarzinom (Mucinous)
Mucinous Adenocarcinoma (Code-1)
C0007130 (UMLS CUI-1)
72495009 (SNOMED CT-1)
10061564 (MedDRA-1)
CL Item
invasives Karzinom (Invasive NOS)
Invasive Breast Carcinoma (Code-1)
C0853879 (UMLS CUI-1)
10006190 (MedDRA-1)
CL Item
Medulläres Karzinom (Medullary)
Medullary Breast Carcinoma (Code-1)
C0860580 (UMLS CUI-1)
CL Item
andere (other)
Other (Code-1)
C0205394 (UMLS CUI-1)
74964007 (SNOMED CT-1)
other
Item
andere
string
Other (Code-1)
C0205394 (UMLS CUI-1)
74964007 (SNOMED CT-1)
Free Text Format (Code-2)
C2348713 (UMLS CUI-2)
Is carcinoma in situ present
Item
Carcinoma in Situ
boolean
Carcinoma in Situ (Code-1)
C0007099 (UMLS CUI-1)
109355002 (SNOMED CT-1)
10061450 (MedDRA-1)
D09.9 (ICD-10-CM-1)
234.9 (ICD-9-CM-1)
Item
histologischer Typ
integer
Histologic Type (Code-1)
C0449574 (UMLS CUI-1)
263541007 (SNOMED CT-1)
MTHU020048 (LOINC-1)
Code List
histologischer Typ
CL Item
DCIS (DCIS)
Noninfiltrating Intraductal Carcinoma (Code-1)
C0007124 (UMLS CUI-1)
86616005 (SNOMED CT-1)
10013806 (MedDRA-1)
D05.1 (ICD-10-CM-1)
CL Item
lobuläres Carcinoma in situ (LCIS)
Lobular carcinoma in situ of breast (Code-1)
C0279563 (UMLS CUI-1)
109888004 (SNOMED CT-1)
10024744 (MedDRA-1)
D05.0 (ICD-10-CM-1)
CL Item
Gemischt, duktales und lobuläres CIS (Mixed DCIS & LCIS)
Lobular carcinoma in situ of breast (Code-1)
C0279563 (UMLS CUI-1)
109888004 (SNOMED CT-1)
10024744 (MedDRA-1)
D05.0 (ICD-10-CM-1)
Noninfiltrating Intraductal Carcinoma (Code-2)
C0007124 (UMLS CUI-2)
86616005 (SNOMED CT-2)
10013806 (MedDRA-2)
D05.1 (ICD-10-CM-2)
Is Paget's disease of the nipple present?
Item
Morbus Paget der Mamille
boolean
Paget's Disease of the Nipple (Code-1)
C1704323 (UMLS CUI-1)
403946000 (SNOMED CT-1)
10033364 (MedDRA-1)
Item
Histopathologisches Grading
integer
C0919553 (UMLS CUI-1)
371469007 (SNOMED CT-1)
Code List
Histopathologisches Grading
CL Item
nicht bestimmbar (GX)
Grade cannot be determined (finding) (Code-1)
C1273714 (UMLS CUI-1)
384741006 (SNOMED CT-1)
CL Item
G1 gut differenziert (G1)
G1 grade (finding) (Code-1)
C0475269 (UMLS CUI-1)
54102005 (SNOMED CT-1)
CL Item
G2 mäßig differenziert (G2)
G2 grade (finding) (Code-1)
C0475270 (UMLS CUI-1)
1663004 (SNOMED CT-1)
CL Item
G3 schlecht differenziert (G3)
G3 grade (finding) (Code-1)
C0475271 (UMLS CUI-1)
61026006 (SNOMED CT-1)
Item
Lymphknotenbefall
integer
Lymph Node Involvement (Code-1)
C0806692 (UMLS CUI-1)
MTHU010351 (LOINC-1)
Code List
Lymphknotenbefall
CL Item
nicht anwendbar (Not Applicable)
Not Applicable (Code-1)
C1546968 (UMLS CUI-1)
385432009 (SNOMED CT-1)
NA (HL7 V3-1)
CL Item
(Node negative, no neoadjuvant chemotherapy)
CL Item
(1-3 positive nodes, no neoadjuvant chemotherapy)
CL Item
(>= 4 positive nodes, no neoadjuvant chemotherapy)
Code List
Timing of chemotherapy
CL Item
(Concurrently with targeted therapy)
Hematology And Biochemistry
Item
integer
Date of blood specimen collection
Item
date
CL Item
(Abnormal - Clinically significant)
CL Item
(Abnormal - Not clinically significant)
Laboratory Name
Item
Name Labor
string
Laboratory (Code-1)
C0022877 (UMLS CUI-1)
261904005 (SNOMED CT-1)
Item
Östrogen-Rezeptor
integer
Status of estrogen receptors of neoplasm (observable entity) (Code-1)
C2919271 (UMLS CUI-1)
445028008 (SNOMED CT-1)
Code List
Östrogen-Rezeptor
CL Item
positiv (Positive )
Estrogen receptor positive tumor (disorder) (Code-1)
C1562312 (UMLS CUI-1)
416053008 (SNOMED CT-1)
CL Item
negativ (Negative )
Estrogen receptor negative neoplasm (disorder) (Code-1)
C2584629 (UMLS CUI-1)
441117001 (SNOMED CT-1)
CL Item
unbekannt (Unknown)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Is estrogen receptor analysis result available
Item
Stauts Östrogenrezeptor im Tumor
boolean
Status of estrogen receptors of neoplasm (observable entity) (Code-1)
C2919271 (UMLS CUI-1)
445028008 (SNOMED CT-1)
Availability (Code-2)
C0470187 (UMLS CUI-2)
103328004 (SNOMED CT-2)
Estrogen receptor value
Item
Wert Östrogenrezeptor
integer
Estrogen Receptors (Code-1)
C0034804 (UMLS CUI-1)
23307004 (SNOMED CT-1)
MTHU004667 (LOINC-1)
Value (Code-2)
C1522609 (UMLS CUI-2)
Allred-Score
Item
integer
Remmle score
Item
integer
Item
Progesteron-Rezeptor
integer
Status of progesterone receptors of neoplasm (observable entity) (Code-1)
C2919590 (UMLS CUI-1)
445029000 (SNOMED CT-1)
Code List
Progesteron-Rezeptor
CL Item
positiv (Positive )
Progesterone receptor positive tumor (disorder) (Code-1)
C1562928 (UMLS CUI-1)
416561008 (SNOMED CT-1)
CL Item
negativ (Negative )
Progesterone receptor negative neoplasm (disorder) (Code-1)
C2584628 (UMLS CUI-1)
441118006 (SNOMED CT-1)
CL Item
unbekannt (Unknown)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
Is progesterone receptor analysis result available
Item
Stauts Progesteronrezeptor im Tumor
boolean
Status of progesterone receptors of neoplasm (observable entity) (Code-1)
C2919590 (UMLS CUI-1)
445029000 (SNOMED CT-1)
Availability (Code-2)
C0470187 (UMLS CUI-2)
103328004 (SNOMED CT-2)
Progesterone receptor value
Item
Wert Progesteronrezeptor
integer
Receptors, Progesterone (Code-1)
C0034833 (UMLS CUI-1)
61078009 (SNOMED CT-1)
MTHU002145 (LOINC-1)
Value (Code-2)
C1522609 (UMLS CUI-2)
Allred-Score
Item
integer
Remmle score
Item
integer
Was sentinel node sampling performed
Item
Durchführung Sentinellymphknotenbiopsie
boolean
Sentinel Lymph Node Biopsy (Code-1)
C0796693 (UMLS CUI-1)
396487001 (SNOMED CT-1)
Sentinel Node Biopsy Date
Item
Datum Sentinellymphknotenbiopsie
date
Sentinel Lymph Node Biopsy (Code-1)
C0796693 (UMLS CUI-1)
396487001 (SNOMED CT-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Item
Körperseite
integer
C0441987 (UMLS CUI-1)
182353008 (SNOMED CT-1)
MTHU014973 (LOINC-1)
Sentinel Lymph Node Biopsy (Code-2)
C0796693 (UMLS CUI-2)
396487001 (SNOMED CT-2)
CL Item
rechts (Left)
C0205090 (UMLS CUI-1)
24028007 (SNOMED CT-1)
CL Item
links (Right)
C0205091 (UMLS CUI-1)
7771000 (SNOMED CT-1)
Item
Sentinellymphknoten Biospie Axilla
integer
Sentinel Lymph Node Biopsy (Code-1)
C0796693 (UMLS CUI-1)
396487001 (SNOMED CT-1)
Axilla (Code-2)
C0004454 (UMLS CUI-2)
91470000 (SNOMED CT-2)
MTHU024430 (LOINC-2)
Code List
Sentinellymphknoten Biospie Axilla
CL Item
negativ (Negative)
Negative Finding (Code-1)
C0205160 (UMLS CUI-1)
260385009 (SNOMED CT-1)
CL Item
positiv (Positive )
Positive Finding (Code-1)
C1446409 (UMLS CUI-1)
10828004 (SNOMED CT-1)
Item
Sentinel Biopsie der internen Brustlymphknoten
integer
Internal mammary node (body structure) (Code-1)
C0447180 (UMLS CUI-1)
245340002 (SNOMED CT-1)
Sentinel Lymph Node Biopsy (Code-2)
C0796693 (UMLS CUI-2)
396487001 (SNOMED CT-2)
Code List
Sentinel Biopsie der internen Brustlymphknoten
CL Item
negativ (Negative)
Negative Finding (Code-1)
C0205160 (UMLS CUI-1)
260385009 (SNOMED CT-1)
CL Item
positiv (Positive )
Positive Finding (Code-1)
C1446409 (UMLS CUI-1)
10828004 (SNOMED CT-1)
Not done
Item
nicht durchgeführt
string
Not Done (Code-1)
C1272696 (UMLS CUI-1)
385660001 (SNOMED CT-1)
Sentinel Lymph Node Biopsy (Code-2)
C0796693 (UMLS CUI-2)
396487001 (SNOMED CT-2)
Date of Axillary Dissection
Item
Datum Axilladissektion
date
Axillary Lymph Node Dissection (Code-1)
C0193867 (UMLS CUI-1)
234254000 (SNOMED CT-1)
10068477 (MedDRA-1)
40.23 (ICD-9-CM-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Item
Seite
integer
Axillary Lymph Node Dissection (Code-1)
C0193867 (UMLS CUI-1)
234254000 (SNOMED CT-1)
10068477 (MedDRA-1)
Side (Code-2)
C0441987 (UMLS CUI-2)
182353008 (SNOMED CT-2)
MTHU014973 (LOINC-2)
CL Item
rechts (Right)
C0205090 (UMLS CUI-1)
24028007 (SNOMED CT-1)
CL Item
links (Left)
C0205091 (UMLS CUI-1)
7771000 (SNOMED CT-1)
Number of Lymph Nodes examinded
Item
Anzahl der untersuchten Lymphknoten
integer
C2733494 (UMLS CUI-1)
444025001 (SNOMED CT-1)
Number positive Lymph nodes
Item
Anzahl der beteiligten Lymphknoten
integer
Number of lymph nodes involved by malignant neoplasm (observable entity) (Code-1)
C2732750 (UMLS CUI-1)
443527007 (SNOMED CT-1)
Code List
Largest tumor deposit
CL Item
(Isolated Tumor Cells Alone)
CL Item
(Micrometastases)
CL Item
(Macrometastases)
Not done
Item
nicht durchgeführt
string
Not Done (Code-1)
C1272696 (UMLS CUI-1)
385660001 (SNOMED CT-1)
Operative Surgical Procedures (Code-2)
C0543467 (UMLS CUI-2)
387713003 (SNOMED CT-2)
10042609 (MedDRA-2)
MTHU007597 (LOINC-2)
Agent Name
Item
Chemotherapie Substanz
string
Chemotherapeutic agent (product) (Code-1)
C0729502 (UMLS CUI-1)
312059006 (SNOMED CT-1)
Total Dose
Item
kumulative Dosis
integer
C2986497 (UMLS CUI-1)
initial dose
Item
erste Dosis
integer
Initial (qualifier value) (Code-1)
C0205265 (UMLS CUI-1)
884001 (SNOMED CT-1)
Dosage (Code-2)
C0178602 (UMLS CUI-2)
277406006 (SNOMED CT-2)
Total No. Cycles
Item
Zyklen geplant
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)
Item
Intention - letzte Chemotherapie
integer
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Prior (Code-3)
C0332152 (UMLS CUI-3)
288556008 (SNOMED CT-3)
Code List
Intention - letzte Chemotherapie
CL Item
Neoadjuvant (Neoadjuvant)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
CL Item
Adjuvant (Adjuvant)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
Date Started
Item
Datum Beginn
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)
Date Stopped
Item
Datum Ende
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)
Has the patient suffered cardiovascular disease?
Item
nicht_sinnvoll_für_Untersuchung
boolean
Medical condition
Item
nicht_sinnvoll_für_Untersuchung
string
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
nicht_sinnvoll_für_Untersuchung
CL Item
nicht_sinnvoll_für_Untersuchung (Resolved)
CL Item
nicht_sinnvoll_für_Untersuchung (Current)
Treatment Required
Item
nicht_sinnvoll_für_Untersuchung
boolean
Has the patient been assessed for systemic disease
Item
nicht_sinnvoll_für_Untersuchung
boolean
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
nicht_sinnvoll_für_Untersuchung
CL Item
nicht_sinnvoll_für_Untersuchung (Abdominal CT-scan)
CL Item
nicht_sinnvoll_für_Untersuchung (Bilateral mammogram)
CL Item
nicht_sinnvoll_für_Untersuchung (Bone scan (scintigraphy))
CL Item
nicht_sinnvoll_für_Untersuchung (Bone X-ray)
CL Item
nicht_sinnvoll_für_Untersuchung (Chest CT-scan)
CL Item
nicht_sinnvoll_für_Untersuchung (Chest X-Ray)
CL Item
nicht_sinnvoll_für_Untersuchung (Left mammogram, only)
CL Item
nicht_sinnvoll_für_Untersuchung (Right mammogram, only)
CL Item
nicht_sinnvoll_für_Untersuchung (CT Scan)
CL Item
nicht_sinnvoll_für_Untersuchung (Endoscopy )
CL Item
nicht_sinnvoll_für_Untersuchung (Lymphangiogram )
CL Item
nicht_sinnvoll_für_Untersuchung (Mammography )
CL Item
nicht_sinnvoll_für_Untersuchung (MRI)
CL Item
nicht_sinnvoll_für_Untersuchung (Nuclear Scan )
CL Item
nicht_sinnvoll_für_Untersuchung (PET Scan)
CL Item
nicht_sinnvoll_für_Untersuchung (PET/CT scan)
CL Item
nicht_sinnvoll_für_Untersuchung (Transvaginal Ultrasound)
CL Item
nicht_sinnvoll_für_Untersuchung (Ultrasound )
CL Item
nicht_sinnvoll_für_Untersuchung (X-ray)
CL Item
nicht_sinnvoll_für_Untersuchung (Other )
Specify
Item
nicht_sinnvoll_für_Untersuchung
string
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
nicht_sinnvoll_für_Untersuchung
CL Item
nicht_sinnvoll_für_Untersuchung (Abdomen/abdominal Wall )
CL Item
nicht_sinnvoll_für_Untersuchung (Abdomen )
CL Item
nicht_sinnvoll_für_Untersuchung (Bone )
CL Item
nicht_sinnvoll_für_Untersuchung (Bladder )
CL Item
nicht_sinnvoll_für_Untersuchung (Breast )
CL Item
nicht_sinnvoll_für_Untersuchung (Colon )
CL Item
nicht_sinnvoll_für_Untersuchung (Colorectal )
CL Item
nicht_sinnvoll_für_Untersuchung (Central Nervous System (CNS))
CL Item
nicht_sinnvoll_für_Untersuchung (Chest )
CL Item
nicht_sinnvoll_für_Untersuchung (Cervix Uteri )
CL Item
nicht_sinnvoll_für_Untersuchung (Esophagus )
CL Item
nicht_sinnvoll_für_Untersuchung (Head And Neck )
CL Item
nicht_sinnvoll_für_Untersuchung (Heart )
CL Item
nicht_sinnvoll_für_Untersuchung (Kidney )
CL Item
nicht_sinnvoll_für_Untersuchung (Lung )
CL Item
nicht_sinnvoll_für_Untersuchung (Lymph Node )
CL Item
nicht_sinnvoll_für_Untersuchung (Liver )
CL Item
nicht_sinnvoll_für_Untersuchung (Mouth (Oral Cavity))
CL Item
nicht_sinnvoll_für_Untersuchung (Other )
CL Item
nicht_sinnvoll_für_Untersuchung (Ovary )
CL Item
nicht_sinnvoll_für_Untersuchung (Pleura )
CL Item
nicht_sinnvoll_für_Untersuchung (Peritoneum )
CL Item
nicht_sinnvoll_für_Untersuchung (Prostate Gland )
CL Item
nicht_sinnvoll_für_Untersuchung (Pancreas )
CL Item
nicht_sinnvoll_für_Untersuchung (Pelvis )
CL Item
nicht_sinnvoll_für_Untersuchung (Rectum )
CL Item
nicht_sinnvoll_für_Untersuchung (Stomach )
CL Item
nicht_sinnvoll_für_Untersuchung (Small Intestine)
CL Item
nicht_sinnvoll_für_Untersuchung (Skin )
CL Item
nicht_sinnvoll_für_Untersuchung (Spleen )
CL Item
nicht_sinnvoll_für_Untersuchung (Thyroid Gland (Thyroid))
CL Item
nicht_sinnvoll_für_Untersuchung (Testis (Testicle))
Date of test
Item
nicht_sinnvoll_für_Untersuchung
date
Are there any clinically significant abnormalites
Item
nicht_sinnvoll_für_Untersuchung
boolean
Specify
Item
nicht_sinnvoll_für_Untersuchung
string
Not done
Item
nicht_sinnvoll_für_Untersuchung
string
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
nicht_sinnvoll_für_Untersuchung
CL Item
nicht_sinnvoll_für_Untersuchung (FFPE tumor block)
CL Item
nicht_sinnvoll_für_Untersuchung (Blood Sample For Pgx)
CL Item
nicht_sinnvoll_für_Untersuchung (Tumor Tissue For Pgx)
CL Item
nicht_sinnvoll_für_Untersuchung (Additional Blood Sample For Ctc (circulating Tumor Cells) (Additional blood sample for CTC (circulating tumor cells)))
CL Item
nicht_sinnvoll_für_Untersuchung (Additional Blood Sample For Proteomics (Additional blood sample for Proteomics))
CL Item
nicht_sinnvoll_für_Untersuchung (Additional Fresh Frozen Tumor Samples (Additional fresh frozen tumor samples))
Date of blood specimen collection
Item
nicht_sinnvoll_für_Untersuchung
date
Was sample obtained
Item
nicht_sinnvoll_für_Untersuchung
boolean
Percentage greater than or equal to 3 Chromosome 17 signals
Item
string
NACA (No apparent Chromosome 17 anomaly)
Item
boolean
CL Item
nicht_sinnvoll_für_Untersuchung (Interductal Only )
CL Item
nicht_sinnvoll_für_Untersuchung (Hybridization Failure)
CL Item
nicht_sinnvoll_für_Untersuchung (Insufficient Tissue )
CL Item
nicht_sinnvoll_für_Untersuchung (No Cancer Tissue )
CL Item
nicht_sinnvoll_für_Untersuchung (Other)
CL Item
nicht_sinnvoll_für_Untersuchung (Duplication Of Her2 )
CL Item
nicht_sinnvoll_für_Untersuchung (Most Cells With No Centromere 17 )
CL Item
nicht_sinnvoll_für_Untersuchung (Negative Her2 )
CL Item
nicht_sinnvoll_für_Untersuchung (Normal Her2 )
CL Item
nicht_sinnvoll_für_Untersuchung (Not A Small Clone )
CL Item
nicht_sinnvoll_für_Untersuchung (Other )
CL Item
nicht_sinnvoll_für_Untersuchung (Small Clone Of Amplification )
Percentage of invasive tumor cells with complete membrane staining
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
Uniformity of staining
Code List
Homogeneous dark circumferential pattern
Item
Her-2/neu
integer
Her2/Neu Status (Code-1)
C1512413 (UMLS CUI-1)
CL Item
negativ (Negative - 0)
HER2-negative breast cancer (Code-1)
CL412283 (UMLS CUI-1)
CL Item
negativ (Negative - 1+)
HER2-negative breast cancer (Code-1)
CL412283 (UMLS CUI-1)
CL Item
borderline (Equivocal - 2+)
Borderline (Code-1)
C0205189 (UMLS CUI-1)
CL Item
positiv (Equivocal - 3+)
HER2-positive carcinoma of breast (disorder) (Code-1)
C1960398 (UMLS CUI-1)
427685000 (SNOMED CT-1)
CL Item
positiv (Positive - 3+)
HER2-positive carcinoma of breast (disorder) (Code-1)
C1960398 (UMLS CUI-1)
427685000 (SNOMED CT-1)
CL Item
nicht ausreichend Gewebe (Insufficient tissue/hybridization failure)
Insufficient tissue for diagnosis (finding) (Code-1)
C0332630 (UMLS CUI-1)
77289001 (SNOMED CT-1)
Is there vascular invasion
Item
Gefäßinvasion
boolean
Vascular invasion of tumor present (finding) (Code-1)
C1318569 (UMLS CUI-1)
372287009 (SNOMED CT-1)
Suitable for TMA
Item
boolean
prior Radiation Therapy
Item
Strahlentherapie durchgeführt
boolean
Therapeutic radiology procedure (Code-1)
C1522449 (UMLS CUI-1)
108290001 (SNOMED CT-1)
10037770 (MedDRA-1)
RT Site
Item
Ort der Bestrahlung
string
Organ target(s) (Code-1)
C0807185 (UMLS CUI-1)
Item
Körperseite
integer
C0441987 (UMLS CUI-1)
182353008 (SNOMED CT-1)
MTHU014973 (LOINC-1)
Tumor site (Code-2)
C0475445 (UMLS CUI-2)
263591006 (SNOMED CT-2)
MTHU015562 (LOINC-2)
CL Item
links (Left)
C0205091 (UMLS CUI-1)
7771000 (SNOMED CT-1)
CL Item
rechts (Right)
C0205090 (UMLS CUI-1)
24028007 (SNOMED CT-1)
RT Total Dose
Item
Gesamtdosis
integer
Total radiation dose delivered (observable entity) (Code-1)
C2919490 (UMLS CUI-1)
445461008 (SNOMED CT-1)
Item
Dosis - Einheit
integer
Code List
Dosis - Einheit
Radiation Therapy Start Date
Item
Beginn Strahlentherapie
date
Radiotherapy started (situation) (Code-1)
C0436382 (UMLS CUI-1)
168531007 (SNOMED CT-1)
Radiation Therapy End Date
Item
Ende Strahlentherapie
date
Radiotherapy completed (situation) (Code-1)
C0436385 (UMLS CUI-1)
168534004 (SNOMED CT-1)
Endocrine Therapy
Item
Hormon- / endokrine Therapie
boolean
169413002 (SNOMED CT-1)
10065646 (MedDRA-1)
C0279025 (UMLS CUI-1)
Name of treatment or surgical procedure
Item
Therapieart
string
C0087111 (UMLS CUI-1)
277132007 (SNOMED CT-1)
10053757 (MedDRA-1)
MTHU008880 (LOINC-1)
Free Text Format (Code-2)
C2348713 (UMLS CUI-2)
Dose
Item
Einzeldosis
integer
Single dose characteristic (observable entity) (Code-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
Item
Einheit
integer
C0565912 (UMLS CUI-1)
288462000 (SNOMED CT-1)
CL Item
Milligramm (mg)
C0439210 (UMLS CUI-1)
258684004 (SNOMED CT-1)
CL Item
nicht anwendbar (N/A)
None or Not Applicable (Code-1)
CL413952 (UMLS CUI-1)
Begin date
Item
Datum Therapiebeginn - endokrine Therapie
date
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)
End date
Item
Datum Therapieende - endokrine Therapie
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)
Item
fortlaufend am Studienende
integer
Continue (Code-1)
C0750536 (UMLS CUI-1)
Study End Date (Code-2)
C2983670 (UMLS CUI-2)
Endocrine Therapy (Code-3)
C0279025 (UMLS CUI-3)
169413002 (SNOMED CT-3)
Code List
fortlaufend am Studienende
CL Item
Ja (Yes)
C1298907 (UMLS CUI-1)
373066001 (SNOMED CT-1)
Name of treatment
Item
Name Nebentherapie
string
Concomitant Therapy (Code-1)
C1707479 (UMLS CUI-1)
Item
Intention
integer
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Concomitant Therapy (Code-2)
C1707479 (UMLS CUI-2)
CL Item
Prävention (Prophylaxis)
Prophylactic treatment (Code-1)
C0199176 (UMLS CUI-1)
129429009 (SNOMED CT-1)
10036898 (MedDRA-1)
CL Item
Kurativ (Curative)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
Date started
Item
Datum Therapiebeginn
date
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Concomitant Therapy (Code-2)
C1707479 (UMLS CUI-2)
Date stopped
Item
Datum Ende
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Concomitant Therapy (Code-2)
C1707479 (UMLS CUI-2)
Item
fortlaufend
integer
Continue (Code-1)
C0750536 (UMLS CUI-1)
Study End Date (Code-2)
C2983670 (UMLS CUI-2)
Concomitant Therapy (Code-3)
C1707479 (UMLS CUI-3)
CL Item
Ja (Yes)
C1298907 (UMLS CUI-1)
373066001 (SNOMED CT-1)
Date Agent Administered
Item
date
Dose
Item
Einzeldosis
integer
Single dose characteristic (observable entity) (Code-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
Total Dose
Item
kumulative Dosis
integer
C2986497 (UMLS CUI-1)
Was treatment delayed
Item
boolean
CL Item
(Hematologic Adverse Event )
CL Item
(Cardiac Adverse Event)
CL Item
(Adverse Event Other Than Hematologic Or Cardiac )
CL Item
(Subject Non-compliance)
CL Item
(Administrative Reasons )
Was dose reduced
Item
Dosislevel der Chemotherapie reduziert
boolean
C0861114 (UMLS CUI-1)
CL Item
(Hematologic Adverse Event )
CL Item
(Cardiac Adverse Event)
CL Item
(Adverse Event Other Than Hematologic Or Cardiac )
CL Item
(Subject Non-compliance)
CL Item
(Administrative Reasons )
Did the patient receive additional chemotherapy after recurrence of breast cancer or second primary malignancy of contralateral breast cancer
Item
Rezidivtherapie - Chemotherapie
boolean
relapse treatment (Code-1)
C0679868 (UMLS CUI-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Total No. Cycles
Item
integer
initial dose
Item
integer
Did the patient receive additional target therapy after recurrence of breast cancer or second primary malignancy of contralateral breast cancer
Item
boolean
Total No. Cycles
Item
integer
initial dose
Item
integer
Did the patient receive hormone therapy after recurrence of breast cancer or second primary malignancy of contralateral breast cancer
Item
Rezidivtherapie - Hormontherapie
boolean
relapse treatment (Code-1)
C0679868 (UMLS CUI-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
10065646 (MedDRA-2)
Total No. Cycles
Item
integer
initial dose
Item
integer
Did the patient receive radiotherapy after recurrence of breast cancer or second primary malignancy of contralateral breast cancer
Item
Rezidivtherapie - Bestrahlung
boolean
relapse treatment (Code-1)
C0679868 (UMLS CUI-1)
Therapeutic radiology procedure (Code-2)
C1522449 (UMLS CUI-2)
108290001 (SNOMED CT-2)
10037794 (MedDRA-2)
Radiation Therapy Site
Item
string
Radiation Therapy Start Date
Item
date
Radiation Therapy End Date
Item
date
Did the patient receive surgery after recurrence of breast cancer or second primary malignancy of contralateral breast cancer
Item
Rezidivtherapie - Operation
boolean
relapse treatment (Code-1)
C0679868 (UMLS CUI-1)
Operative Surgical Procedures (Code-2)
C0543467 (UMLS CUI-2)
387713003 (SNOMED CT-2)
10042609 (MedDRA-2)
MTHU007597 (LOINC-2)
Surgical site
Item
string
AE Name
Item
Name Adverse Event
integer
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Metabolic/laboratory Other (Metabolic/Laboratory-Other (Specify))
Item
Laborwerte
boolean
changed_datatype (Code-Info)
Other Metabolic and Laboratory Adverse Event (Code-1)
C1559945 (UMLS CUI-1)
MTHU117254 (CTCAE-1)
Renal/genitourinary Other (Renal/Genitourinary-Other (Specify))
Item
Gastrointestinaltrakt
boolean
changed_datatype (Code-Info)
Adverse Event Associated with the Gastrointestinal System (Code-1)
C1559265 (UMLS CUI-1)
MTHU112146 (CTCAE-1)
Niere/Blase
Item
Urogenital-System
boolean
changed_datatype (Code-Info)
Renal or Genitourinary Other Adverse Event (Code-1)
C1558061 (UMLS CUI-1)
MTHU117419 (CTCAE-1)
Dermatology/skin Other (Dermatology/Skin-Other (Specify))
Item
Haut
boolean
changed_datatype (Code-Info)
Other Dermatology or Skin Adverse Event (Code-1)
C1559104 (UMLS CUI-1)
MTHU117246 (CTCAE-1)
Allergy/immunology Other (Allergy/Immunology-Other (Specify))
Item
Allergie
boolean
changed_datatype (Code-Info)
Adverse Event Associated with Allergy and Immunology (Code-1)
C1560126 (UMLS CUI-1)
MTHU112125 (CTCAE-1)
Pyrexia (Fever (in the absence of neutropenia, where neutropenia is defined as ANC <1.0 x 10^9/L))
Item
Fieber
boolean
changed_datatype (Code-Info)
Fever Without Neutropenia Adverse Event (Code-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
Infection Nos (Infection-Other (Specify))
Item
Infektion
boolean
changed_datatype (Code-Info)
Adverse Event Associated with Infection (Code-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
Auditory/ear Other (Auditory/Ear-Other (Specify))
Item
Sinnesorgane
boolean
changed_datatype (Code-Info)
Adverse Event Associated with the Ear and Auditory System (Code-1)
C1560154 (UMLS CUI-1)
MTHU112144 (CTCAE-1)
Constitutional Symptoms Other (Constitutional Symptoms-Other (Specify))
Item
Allgemeinsymptome
boolean
changed_datatype (Code-Info)
Adverse Event Associated with Constitutional Symptoms (Code-1)
C1556354 (UMLS CUI-1)
MTHU112129 (CTCAE-1)
Pulmonary/upper Respiratory Other (Pulmonary/Upper Respiratory-Other (Specify))
Item
Lunge/Kehlkopf
boolean
changed_datatype (Code-Info)
Adverse Event Associated with Pulmonary and Upper Respiratory Systems (Code-1)
C1557628 (UMLS CUI-1)
MTHU112139 (CTCAE-1)
Endocrine Other (Endocrine-Other (Specify))
Item
Endokrines System
boolean
changed_datatype (Code-Info)
Adverse Event Associated with the Endocrine System (Code-1)
C1559198 (UMLS CUI-1)
MTHU112145 (CTCAE-1)
Cardiac General Other (Cardiac General-Other (Specify))
Item
Herz, allgemein
boolean
changed_datatype (Code-Info)
Adverse Event Associated with the Heart in General (Code-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
Haemoglobin Decreased (Hemoglobin)
Item
Hämoglobin
boolean
changed_datatype (Code-Info)
Hemoglobin Adverse Event (Code-1)
C2239101 (UMLS CUI-1)
MTHU116997 (CTCAE-1)
Aspartate Aminotransferase Increased (AST, SGOT (serum glutamic oxaloacetic transaminase))
Item
Aspartat-Transaminase
boolean
changed_datatype (Code-Info)
Serum Glutamic Oxaloacetic Transaminase Adverse Event (Code-1)
C1557198 (UMLS CUI-1)
MTHU117449 (CTCAE-1)
Alanine Aminotransferase Increased (ALT, SGPT (serum glutamic pyruvic transaminase))
Item
Alanin-Transaminase
boolean
changed_datatype (Code-Info)
Serum Glutamic Pyruvic Transaminase Adverse Event (Code-1)
C1557189 (UMLS CUI-1)
MTHU117450 (CTCAE-1)
Blood Creatinine Increased (Creatinine)
Item
Kreatinin
boolean
changed_datatype (Code-Info)
Creatinine Adverse Event (Code-1)
C1561535 (UMLS CUI-1)
MTHU116842 (CTCAE-1)
Neuralgia Nos (Pain - Neuralgia/peripheral nerve)
Item
Peripherer Nerv
boolean
changed_datatype (Code-Info)
Neuralgia and Peripheral Nerve Pain Adverse Event (Code-1)
C1557517 (UMLS CUI-1)
MTHU117196 (CTCAE-1)
Hemorrhage/bleeding Other (Hemorrhage/Bleeding-Other (Specify))
Item
Blutungen
boolean
changed_datatype (Code-Info)
Other Hemorrhage and Bleeding Adverse Event (Code-1)
C1556642 (UMLS CUI-1)
MTHU117250 (CTCAE-1)
Blood Bilirubin Increased (Bilirubin (hyperbilirubinemia))
Item
Bilirubin
boolean
changed_datatype (Code-Info)
Hyperbilirubinemia Adverse Event (Code-1)
C1557209 (UMLS CUI-1)
MTHU117008 (CTCAE-1)
Leucopenia Nos (Leukocytes (total WBC))
Item
Leukozyten
boolean
changed_datatype (Code-Info)
Leukocytes Adverse Event (Code-1)
C1560219 (UMLS CUI-1)
MTHU117099 (CTCAE-1)
Blood Alkaline Phosphatase Nos Increased (Alkaline phosphatase)
Item
Alkalische Phosphatase
boolean
changed_datatype (Code-Info)
Alkaline Phosphatase Adverse Event (Code-1)
C1561546 (UMLS CUI-1)
MTHU112158 (CTCAE-1)
Proteinuria Present (Proteinuria)
Item
Proteinurie
boolean
changed_datatype (Code-Info)
Proteinuria Adverse Event (Code-1)
C1962972 (UMLS CUI-1)
MTHU117382 (CTCAE-1)
Alopecia (Hair loss/Alopecia (scalp or body))
Item
Haar
boolean
changed_datatype (Code-Info)
Alopecia Adverse Event (Code-1)
C1559115 (UMLS CUI-1)
MTHU112161 (CTCAE-1)
Constipation (Constipation)
Item
Obstipation
boolean
changed_datatype (Code-Info)
Constipation Adverse Event (Code-1)
C1963087 (UMLS CUI-1)
MTHU116803 (CTCAE-1)
Diarrhoea Nos (Diarrhea)
Item
Diarrhoe
boolean
changed_datatype (Code-Info)
Diarrhea Adverse Event (Code-1)
C0232708 (UMLS CUI-1)
MTHU116856 (CTCAE-1)
Haematuria Present (Hemorrhage, GU - Urinary NOS)
Item
Hämaturie
boolean
changed_datatype (Code-Info)
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)
Pain Other (Pain-Other (Specify))
Item
Schmerzen
boolean
changed_datatype (Code-Info)
Other Pain Adverse Event (Code-1)
C1557623 (UMLS CUI-1)
MTHU117260 (CTCAE-1)
Platelet Count Decreased (Platelets)
Item
Thrombozyten
boolean
changed_datatype (Code-Info)
Platelets Adverse Event (Code-1)
C1963076 (UMLS CUI-1)
MTHU117353 (CTCAE-1)
Nausea (Nausea)
Item
Übelkeit
boolean
changed_datatype (Code-Info)
Nausea Adverse Event (Code-1)
C1963179 (UMLS CUI-1)
MTHU117189 (CTCAE-1)
Arrhythmia Nos (Cardiac Arrhythmia-Other (Specify))
Item
Herzrhythmus
boolean
changed_datatype (Code-Info)
Adverse Event Associated with Cardiac Arrhythmia (Code-1)
C1560249 (UMLS CUI-1)
MTHU112127 (CTCAE-1)
Pericarditis (Pericarditis)
Item
Perikarditis
boolean
changed_datatype (Code-Info)
Pericarditis Adverse Event (Code-1)
C1963211 (UMLS CUI-1)
MTHU117310 (CTCAE-1)
Depressed Level Of Consciousness (Somnolence/depressed level of consciousness)
Item
Bewusstsein
boolean
changed_datatype (Code-Info)
Somnolence and Depressed Level of Consciousness Adverse Event (Code-1)
C1557290 (UMLS CUI-1)
MTHU117503 (CTCAE-1)
Dyspnoea Nos (Dyspnea (shortness of breath))
Item
Dyspnoe
boolean
changed_datatype (Code-Info)
Dyspnea Adverse Event (Code-1)
C1963100 (UMLS CUI-1)
MTHU116873 (CTCAE-1)
Cystitis (Cystitis)
Item
Zystitis
boolean
changed_datatype (Code-Info)
Cystitis Adverse Event (Code-1)
C1963088 (UMLS CUI-1)
MTHU116844 (CTCAE-1)
Vomiting Nos (Vomiting)
Item
Vomiting
boolean
changed_datatype (Code-Info)
Vomiting Adverse Event (Code-1)
C1963281 (UMLS CUI-1)
MTHU117700 (CTCAE-1)
1024 more adverse events
Item
1024 more adverse events
integer
SAE reported
Item
boolean
CTCAE Begin Date
Item
date
CTC Adverse Event Grade
Item
Grad der Nebenwirkung
integer
Adverse Event Grade Code (Code-1)
C2985911 (UMLS CUI-1)
Code List
CTC Adverse Event Outcomme
CL Item
(resolved with sequelae)
Code List
Action Taken at Time of Adverse Event
CL Item
(protocol treatment discontinued)
CL Item
(study dose reduced)
CL Item
(protocol treatment delayed)
CL Item
(other treatment required)
relation to study drug
Item
boolean
Type of recurrence
Item
Rezdivtumor
string
Recurrent Malignant Neoplasm (Code-1)
C0549379 (UMLS CUI-1)
10038111 (SNOMED CT-1)
Date of First Recurrence or Progression
Item
date
Item
Medizinische Untersuchung
integer
C0582103 (UMLS CUI-1)
225886003 (SNOMED CT-1)
Recurrent Malignant Neoplasm (Code-2)
C0549379 (UMLS CUI-2)
10038111 (SNOMED CT-2)
Code List
Medizinische Untersuchung
CL Item
körperliche Untersuchung (Clinical)
C0031809 (UMLS CUI-1)
5880005 (SNOMED CT-1)
10034986 (MedDRA-1)
MTHU028014 (LOINC-1)
CL Item
radiologisch (Radiological)
Diagnostic radiologic examination (Code-1)
C0043299 (UMLS CUI-1)
363680008 (SNOMED CT-1)
Biopsy
Item
Biopsie
boolean
Biopsy (Code-1)
C0005558 (UMLS CUI-1)
86273004 (SNOMED CT-1)
10004720 (MedDRA-1)
MTHU028106 (LOINC-1)
Recurrent Malignant Neoplasm (Code-2)
C0549379 (UMLS CUI-2)
10038111 (SNOMED CT-2)
Biopsy Date
Item
Datum Biopsie
date
Biopsy (Code-1)
C0005558 (UMLS CUI-1)
86273004 (SNOMED CT-1)
10004720 (MedDRA-1)
MTHU028106 (LOINC-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Recurrent Malignant Neoplasm (Code-3)
C0549379 (UMLS CUI-3)
10038111 (SNOMED CT-3)
Specify other Histologic Type
Item
histologischer Typ
string
Histologic Type (Code-1)
C0449574 (UMLS CUI-1)
263541007 (SNOMED CT-1)
MTHU020048 (LOINC-1)
Recurrent Malignant Neoplasm (Code-2)
C0549379 (UMLS CUI-2)
10038111 (SNOMED CT-2)
Date of Physical Exam
Item
körperliche Untersuchung
date
C0031809 (UMLS CUI-1)
5880005 (SNOMED CT-1)
10034986 (MedDRA-1)
MTHU028014 (LOINC-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Not done
Item
nicht durchgeführt
string
Not Done (Code-1)
C1272696 (UMLS CUI-1)
385660001 (SNOMED CT-1)
Are there any changes since the previous assessment
Item
boolean
Code List
Are there any changes since the previous assessment
CL Item
Rezdivtumor (Recurrence of disease)
Recurrent Malignant Neoplasm (Code-1)
C0549379 (UMLS CUI-1)
10038111 (MedDRA-1)
CL Item
Zweittumor (Second primary malignancy or contralateral breast cancer)
Secondary Malignant Neoplasm (Code-1)
C0751623 (UMLS CUI-1)
10039801 (MedDRA-1)
CL Item
Herzerkrankung (Significant cardiac disease)
Heart Diseases (Code-1)
C0018799 (UMLS CUI-1)
56265001 (SNOMED CT-1)
10061024 (MedDRA-1)
I51.9 (ICD-10-CM-1)
429.9 (ICD-9-CM-1)
CL Item
(Adverse Event)
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
CL Item
Patient verstorben (Death )
Patient died (finding) (Code-1)
C1306577 (UMLS CUI-1)
397709008 (SNOMED CT-1)
10011906 (MedDRA-1)
CL Item
keine Nachuntersuchung erfolgt (Lost To Follow-up)
Lost To Follow-up (Code-1)
C1302313 (UMLS CUI-1)
399307001 (SNOMED CT-1)
CL Item
(Patient withdrew study consent)
Consent Withdrawn (Code-1)
C1707492 (UMLS CUI-1)
Date of last contact
Item
Datum des letzten Kontaktes
date
Date last contact (Code-1)
C0805839 (UMLS CUI-1)
MTHU010432 (LOINC-1)
Item
ECOG Leistungszustand
integer
C1632812 (UMLS CUI-1)
Code List
ECOG Leistungszustand
CL Item
0 (0)
Eastern Cooperative Oncology Group performance status - grade 0 (finding) (Code-1)
C1828078 (UMLS CUI-1)
25389002 (SNOMED CT-1)
CL Item
1 (1)
Eastern Cooperative Oncology Group performance status - grade 1 (finding) (Code-1)
C1827388 (UMLS CUI-1)
422512005 (SNOMED CT-1)
CL Item
2 (2)
Eastern Cooperative Oncology Group performance status - grade 2 (finding) (Code-1)
C1828242 (UMLS CUI-1)
422894000 (SNOMED CT-1)
CL Item
3 (3)
Eastern Cooperative Oncology Group performance status - grade 3 (finding) (Code-1)
C1827126 (UMLS CUI-1)
423053003 (SNOMED CT-1)
CL Item
4 (4)
Eastern Cooperative Oncology Group performance status - grade 4 (finding) (Code-1)
C1827528 (UMLS CUI-1)
423237006 (SNOMED CT-1)
CL Item
5 (5)
Eastern Cooperative Oncology Group performance status - grade 5 (finding) (Code-1)
C1827926 (UMLS CUI-1)
423409001 (SNOMED CT-1)
Blood Pressure, systolic
Item
Systolischer Blutdruck
integer
Systolic Blood Pressure (Code-1)
C0871470 (UMLS CUI-1)
271649006 (SNOMED CT-1)
Blood Pressure, diastolic
Item
Diastolischer Blutdruck
integer
Diastolic Blood Pressure (Code-1)
C0428883 (UMLS CUI-1)
271650006 (SNOMED CT-1)
Date of LVEF
Item
Datum Linksventrikuläre Ejektionsfraktion
date
Left Ventricular Ejection Fraction (Code-1)
CL433348 (UMLS CUI-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
LVEF
Item
Linksventrikuläre Ejektionsfraktion
string
Left Ventricular Ejection Fraction (Code-1)
CL433348 (UMLS CUI-1)
Echocardiogram
Item
Echokardiographie
boolean
changed_datatype (Code-Info)
Echocardiography (Code-1)
C0013516 (UMLS CUI-1)
40701008 (SNOMED CT-1)
10014113 (MedDRA-1)
88.72 (ICD-9-CM-1)
MUGA Scan
Item
Radionuklidventrikulographie
boolean
changed_datatype (Code-Info)
Radionuclide Ventriculogram Scan (Code-1)
C0521317 (UMLS CUI-1)
404221001 (SNOMED CT-1)
10028211 (MedDRA-1)
Item
Ergebnis
integer
Result (Code-1)
C1274040 (UMLS CUI-1)
394617004 (SNOMED CT-1)
Left Ventricular Ejection Fraction (Code-2)
CL433348 (UMLS CUI-2)
CL Item
unauffällig (Normal)
Normal (Code-1)
C0205307 (UMLS CUI-1)
17621005 (SNOMED CT-1)
CL Item
auffällig, klinisch signifikant (Abnormal - Clinically significant)
Abnormal (Code-1)
C0205161 (UMLS CUI-1)
263654008 (SNOMED CT-1)
Clinically Significant Indicator (Code-2)
C2985739 (UMLS CUI-2)
CL Item
auffällig, klinisch nicht signifikant (Abnormal - Not clinically significant)
Abnormal (Code-1)
C0205161 (UMLS CUI-1)
263654008 (SNOMED CT-1)
Clinically Significant Indicator (Code-2)
C2985739 (UMLS CUI-2)
Negation (Code-3)
C1518422 (UMLS CUI-3)
Symptomatic CHF
Item
boolean
Code List
New York Heart Association
Item
Mammogramm
integer
Mammography (Code-1)
C0024671 (UMLS CUI-1)
71651007 (SNOMED CT-1)
10026735 (MedDRA-1)
CL Item
rechts (Right)
C0205090 (UMLS CUI-1)
24028007 (SNOMED CT-1)
CL Item
links (Left)
C0205091 (UMLS CUI-1)
7771000 (SNOMED CT-1)
CL Item
beidseits (Bilateral)
C0238767 (UMLS CUI-1)
51440002 (SNOMED CT-1)
Date of Test
Item
Untersuchungsdatum
date
Mammography (Code-1)
C0024671 (UMLS CUI-1)
71651007 (SNOMED CT-1)
10026735 (MedDRA-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Not done
Item
nicht durchgeführt
string
Not Done (Code-1)
C1272696 (UMLS CUI-1)
385660001 (SNOMED CT-1)
Are there any clinically significant abnormalites
Item
boolean
Date of blood specimen collection
Item
date
CL Item
(Abnormal - Clinically significant)
CL Item
(Abnormal - Not clinically significant)
Item
Vitalstatus
integer
Vital status:Type:Point in time:^Patient:Nominal (Code-1)
C1146895 (UMLS CUI-1)
31210-8 (LOINC-1)
CL Item
lebend (Alive)
Alive (finding) (Code-1)
C2584946 (UMLS CUI-1)
438949009 (SNOMED CT-1)
CL Item
tot (Dead)
Patient died (finding) (Code-1)
C1306577 (UMLS CUI-1)
397709008 (SNOMED CT-1)
10011906 (MedDRA-1)
CL Item
keine Nachuntersuchung erfolgt (Lost To Follow-up)
Lost To Follow-up (Code-1)
C1302313 (UMLS CUI-1)
399307001 (SNOMED CT-1)
Dead
Item
Todesdatum
date
Date of death (Code-1)
C1148348 (UMLS CUI-1)
399753006 (SNOMED CT-1)
MTHU014693 (LOINC-1)
Date last contact (Code-2)
C0805839 (UMLS CUI-2)
MTHU010432 (LOINC-2)
Date of last contact
Item
Datum letzter Kontakt
date
extended_coding (Code-Info)
Date last contact (Code-1)
C0805839 (UMLS CUI-1)
MTHU010432 (LOINC-1)
Date last contact (Code-2)
C0805839 (UMLS CUI-2)
MTHU010432 (LOINC-2)
Investigator Signature
Item
Unterschrift Untersuchuer
string
Investigator Signature (Code-1)
C2346576 (UMLS CUI-1)
Date
Item
Datum
date
Date in time (Code-1)
C0011008 (UMLS CUI-1)
410671006 (SNOMED CT-1)
MTHU021546 (LOINC-1)
Investigator Signature (Code-2)
C2346576 (UMLS CUI-2)
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
nicht_sinnvoll_für_Untersuchung
CL Item
nicht_sinnvoll_für_Untersuchung (Yes)
CL Item
nicht_sinnvoll_für_Untersuchung (No)
CL Item
nicht_sinnvoll_für_Untersuchung (Not Applicable)
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
nicht_sinnvoll_für_Untersuchung
CL Item
nicht_sinnvoll_für_Untersuchung (Yes)
CL Item
nicht_sinnvoll_für_Untersuchung (No)
CL Item
nicht_sinnvoll_für_Untersuchung (Not Applicable)
Item
nicht_sinnvoll_für_Untersuchung
integer
Code List
nicht_sinnvoll_für_Untersuchung
CL Item
nicht_sinnvoll_für_Untersuchung (Yes)
CL Item
nicht_sinnvoll_für_Untersuchung (No)
CL Item
nicht_sinnvoll_für_Untersuchung (Not Applicable)
Item
Grund für Therapeabbruch
integer
Discontinue (Code-1)
C1444662 (UMLS CUI-1)
410546004 (SNOMED CT-1)
Indication of (contextual qualifier) (Code-2)
C0392360 (UMLS CUI-2)
410666004 (SNOMED CT-2)
MTHU008319 (LOINC-2)
Therapeutic procedure (Code-3)
C0087111 (UMLS CUI-3)
277132007 (SNOMED CT-3)
10053757 (MedDRA-3)
MTHU008880 (LOINC-3)
Code List
Grund für Therapeabbruch
CL Item
Adverse Event (Adverse Event)
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
CL Item
Verletzung des Protokolls (Protocol violation)
Protocol Violation (Code-1)
C1709750 (UMLS CUI-1)
CL Item
(Subject decided to withdraw from investigational product but is continuing to be followed per protocol)
CL Item
(Subject decided to withdraw from the study)
CL Item
Rediziverkrankung (Recurrence of disease)
extended_coding (Code-Info)
Recurrent Malignant Neoplasm (Code-1)
C0549379 (UMLS CUI-1)
10038111 (MedDRA-1)
CL Item
Zweittumor (second primary malignancy)
extended_coding (Code-Info)
Secondary Malignant Neoplasm (Code-1)
C0751623 (UMLS CUI-1)
10039801 (MedDRA-1)
CL Item
kontrallaterales Mammakarzinom (contralateral breast cancer)
extended_coding (Code-Info)
Contralateral Breast Carcinoma (Code-1)
CL433171 (UMLS CUI-1)
CL Item
Patient verstorben (Death )
Patient died (finding) (Code-1)
C1306577 (UMLS CUI-1)
397709008 (SNOMED CT-1)
10011906 (MedDRA-1)
CL Item
keine Nachuntersuchung erfolgt (Lost to follow-up)
Lost To Follow-up (Code-1)
C1302313 (UMLS CUI-1)
399307001 (SNOMED CT-1)
Date of last contact within treatment period
Item
Datum letzter Kontakt während Behandlungsperiode
date
Date last contact (Code-1)
C0805839 (UMLS CUI-1)
MTHU010432 (LOINC-1)
Therapeutic procedure (Code-2)
C0087111 (UMLS CUI-2)
277132007 (SNOMED CT-2)
10053757 (MedDRA-2)
MTHU008880 (LOINC-2)
Period (Code-3)
C1948053 (UMLS CUI-3)
CRF Page Number
Item
integer
Comments
Item
Kommentar
string
Comment (Code-1)
C0947611 (UMLS CUI-1)
Therapeutic procedure (Code-2)
C0087111 (UMLS CUI-2)
277132007 (SNOMED CT-2)
10053757 (MedDRA-2)
MTHU008880 (LOINC-2)
Investigator Signature
Item
Unterschrift Untersuchuer
string
Investigator Signature (Code-1)
C2346576 (UMLS CUI-1)
Date
Item
Datum
date
Investigator Signature (Code-1)
C2346576 (UMLS CUI-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Date of Death
Item
Todesdatum
date
C1148348 (UMLS CUI-1)
399753006 (SNOMED CT-1)
MTHU014693 (LOINC-1)
Item
Todesursache
integer
Cause of Death (Code-1)
C0007465 (UMLS CUI-1)
184305005 (SNOMED CT-1)
CL Item
Tumor Progression (Breast cancer progression)
Tumor Progression (Code-1)
C0178874 (UMLS CUI-1)
419835002 (SNOMED CT-1)
CL Item
Adverse Event während Studie (Adverse event during study)
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Clinical Trials (Code-2)
C0008976 (UMLS CUI-2)
110465008 (SNOMED CT-2)
During (Code-3)
C0347984 (UMLS CUI-3)
371881003 (SNOMED CT-3)
CL Item
Adverse Event während Therapie des Rezidiv (Adverse event during treatment given after recurrence)
Adverse event (Code-1)
C0877248 (UMLS CUI-1)
10060933 (MedDRA-1)
MTHU014542 (LOINC-1)
Therapeutic procedure (Code-2)
C0087111 (UMLS CUI-2)
277132007 (SNOMED CT-2)
10053757 (MedDRA-2)
MTHU008880 (LOINC-2)
During (Code-3)
C0347984 (UMLS CUI-3)
371881003 (SNOMED CT-3)
Recurrent Malignant Neoplasm (Code-4)
C0549379 (UMLS CUI-4)
10038111 (MedDRA-4)
CL Item
Todesursache tumorbedingt (Malignant disease other than breast cancer)
Malignant Neoplasms (Code-1)
C0006826 (UMLS CUI-1)
363346000 (SNOMED CT-1)
10028997 (MedDRA-1)
MTHU010328 (LOINC-1)
C00-C96 (ICD-10-CM-1)
Other (Code-2)
C0205394 (UMLS CUI-2)
74964007 (SNOMED CT-2)
CL Item
andere Todesursache (Other)
Other (Code-1)
C0205394 (UMLS CUI-1)
74964007 (SNOMED CT-1)
specify
Item
andere Todesursache
string
Other (Code-1)
C0205394 (UMLS CUI-1)
74964007 (SNOMED CT-1)
Cause of Death (Code-2)
C0007465 (UMLS CUI-2)
184305005 (SNOMED CT-2)
Item
Autopsie
integer
Autopsy (Code-1)
29240004 (SNOMED CT-1)
10050117 (MedDRA-1)
89.8 (ICD-10-CM-1)
C0004398 (UMLS CUI)
Please summarize findings
Item
string