ID

40621

Beschreibung

ICHOM Breast Cancer data collection Version 1.0.1 Revised: March 30, 2017 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. For Breast Cancer, the following treatment approaches (or interventions) are covered by our Standard Set. Conditions*: All patients (men and women) with newly pathologically diagnosed invasive breast cancer (stage I-IV) and ductal carcinoma in situ (DCIS). *Excluded Conditions: Rare tumors (e.g. phyllodes tumor), lobular carcinoma in situ (LCIS) and patients with recurrent disease at baseline will be excluded. Treatment approaches: (Reconstructive) Surgery | Radiotherapy | Chemotherapy | Hormonal Therapy | Targeted Therapy | This document contains the Baseline - Clinical-reported form. It has to be filled in at first doctor's visit of patient and repeated at the beginning of therapies or in case of recurrence. Collecting Patient-Reported Outcome Measures: European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30, EORTC QLQ-BR23, EORTC QLQ-LMC21). As a permission is needed for use of these questionnaires, only the total score of each will be included in this version of the standard set. More information can be found at http://groups.eortc.be/qol/eortc-qlq-c30 BREAST-Q Patient Reported Outcomes Instrument (BREAST-Q). As a license is needed for use of this questionnaire, only the total score will be included in this version of the standard set. For more information, please visit: https:// eprovide.mapi-trust.org/instruments/ breast-q#contact_and_conditions_of_ use Functional Assessment of Cancer Therapy Endocrine Subscale (FACT-ES). As a permission is needed for use of this questionnaire, only the total score of each will be included in this version of the standard set. For more information see http://www.facit.org/facitorg/ questionnaires. Reference: Ong WL, Schouwenburg MG, van Bommel AC, et al. A Standard Set of Value-Based Patient-Centered Outcomes for Breast Cancer: The International Consortium for Health Outcomes Measurement (ICHOM) Initiative. JAMA Oncol. 2017;3(5):677–685. doi:10.1001/jamaoncol.2016.4851 The Standard set of ICHOM was supported by the Dutch Dnstitute for Clinical Auditing, Onderlinge Waarborgmaatschappij Centrale Zorgverzekeraars group, Ramsay Health Care and Karolinska Institute. For this version of the standard set, semantic annotation with UMLS CUIs has been added.

Link

http://www.ichom.org/

Stichworte

Versionen (5)
  1. 05.07.19 05.07.19 -
  2. 05.07.19 05.07.19 -
  3. 22.07.19 22.07.19 -
  4. 26.07.19 26.07.19 - Sarah Riepenhausen
  5. 30.04.20 30.04.20 - Sarah Riepenhausen
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ICHOM

Hochgeladen am

30. April 2020

DOI

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Creative Commons BY-NC 4.0
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ICHOM Breast Cancer

Englisch

Baseline - Clinical-reported

1 Formulare  
Administrative Data
Beschreibung

Administrative Data

Alias
UMLS CUI-1
C1320722
Indicate the patient's medical record number
Beschreibung

This number will not be shared with ICHOM. In the case patient-level data is submitted to ICHOM for benchmarking or research purposes, a separate ICHOM Patient Identifier will be created and cross-linking between the ICHOM Patient Identifier and the medical record number will only be known at the treating institution INCLUSION CRITERIA: All patients TIMING: On all forms REPORTING SOURCE: Administrative or clinical RESPONSE OPTIONS: According to institution

Datentyp

integer

Alias
UMLS CUI [1]
C1269815
Patient's last name:
Beschreibung

The patients' name will not be shared with ICHOM.  INCLUSION CRITERIA: All patients TIMING: On all forms REPORTING SOURCE: Administrative or clinical

Datentyp

text

Alias
UMLS CUI [1]
C1299487
Time Relative to Baseline
Beschreibung

This Item does not exist in the original standard set, instead it is asked to do the following: Please timestamp all variables. Some Standard Set variables are collected at multiple timepoints, and we will ask you to submit these variables in a concatenated VARIABLEID_TIMESTAMP form for future analyses. For example, VARIABLEID_AT (After treatment); VARIABLEID_AS (After surgery); VARIABLEID_UPDATE (Update at least annually), etc.

Datentyp

text

Alias
UMLS CUI [1,1]
C0439564
UMLS CUI [1,2]
C1442488
Demographic factors
Beschreibung

Demographic factors

Alias
UMLS CUI-1
C1704791
What is your date of birth?
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported and clinical TYPE: Single answer

Datentyp

date

Maßeinheiten
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C0421451
DD/MM/YYYY
Baseline clinical factors
Beschreibung

Baseline clinical factors

Alias
UMLS CUI-1
C0449440
UMLS CUI-2
C1442488
Indicate height in centimeters or inches
Beschreibung

Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of height in cm or in

Datentyp

float

Alias
UMLS CUI [1]
C0005890
Indicate units of height
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0005890
UMLS CUI [1,2]
C1519795
Indicate weight in kilograms or pounds
Beschreibung

Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer RESPONSE OPTIONS: Numerical value of weight in kg or lbs

Datentyp

float

Alias
UMLS CUI [1]
C0005910
Indicate units of weight
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0005910
UMLS CUI [1,2]
C1519795
Indicate the laterality of breast cancer:
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0925205
UMLS CUI [1,2]
C0678222
Indicate if this is first breast cancer or new cancer on contralateral or ipsilateral breast:
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C3172269
Baseline tumor factors
Beschreibung

Baseline tumor factors

Alias
UMLS CUI-1
C0475752
UMLS CUI-2
C1442488
Initial date of histological diagnosis
Beschreibung

SUPPORTING DEFINITION: The first time that histology of the tumoris examined, after biopsy or surgery, whichever came first  INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Date by DD/MM/YYYY

Datentyp

date

Maßeinheiten
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0679557
UMLS CUI [1,2]
C0011008
DD/MM/YYYY
Indicate histologic type of the tumor (select all that apply) 0 = Ductal carcinoma in situ
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

boolean

Alias
UMLS CUI [1]
C0449574
UMLS CUI [2]
C1527349
Indicate histologic type of the tumor (select all that apply) 1 = Invasive ductal carcinoma
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

boolean

Alias
UMLS CUI [1]
C0449574
UMLS CUI [2]
C1134719
Indicate histologic type of the tumor (select all that apply) 2 = Invasive lobular carcinoma
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

boolean

Alias
UMLS CUI [1]
C0449574
UMLS CUI [2]
C0279565
Indicate histologic type of the tumor (select all that apply) 3 = Other
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

boolean

Alias
UMLS CUI [1]
C0449574
UMLS CUI [2]
C0205394
Indicate histologic type of the tumor (select all that apply) 999 = Unknown
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

boolean

Alias
UMLS CUI [1]
C0449574
UMLS CUI [2]
C0439673
Indicate if the patient carries a genetic mutation predisposing breast cancer:
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline and after 1 year REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0314657
UMLS CUI [1,2]
C0678222
Indicate grade of invasive component of tumor:
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1]
C1269955
Indicate tumor grade of DCIS component of tumor:
Beschreibung

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0007124
UMLS CUI [1,2]
C0919553
Clinical tumor stage (per AJCC 5th - 7th Ed.)
Beschreibung

SUPPORTING DEFINITION: Tumor stage (AJCC 5th -7th edition): TX: primary tumor cannot be assessed T0: no evidence of primary tumor Tis: intraepithelial or invasion of lamina propria T1: tumor confined to the submucosa T2: tumor has grown into (but not through) the muscularis propria T3: tumor has grown into (but not through) the serosa T4: tumor has penetrated through the serosa and the peritoneal surface. INCLUSION CRITERIA: All patients that received neoadjuvant therapy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0205210
UMLS CUI [1,2]
C1300072
Clinical nodal stage (per AJCC 5th - 7th Ed.)
Beschreibung

SUPPORTING DEFINITION: Nodal stage (AJCC 5th -7th edition): NX: lymph nodes were not assessed N0: no lymph nodes contain tumor cells N1: there are tumor cells in up to 3 regional lymph nodes N2: there are tumor cells in 4 or more regional lymph nodes INCLUSION CRITERIA: All patients that received neoadjuvant therapy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0456532
UMLS CUI [1,2]
C0205210
Clinical distant metastasis (per AJCC 5th - 7th Ed.)
Beschreibung

SUPPORTING DEFINITION: Distant metastasis (AJCC 5th- 7th edition): Mx: presence of metastasis cannot be assessed M0: no metastasis to distant organs M1: metastasis to distant organs INCLUSION CRITERIA: All patients that received neoadjuvant therapy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1]
C1275856
Pathological tumor stage (per AJCC 5th - 7th Ed.)
Beschreibung

SUPPORTING DEFINITION: Tumor stage (AJCC 5th -7th edition): TX: primary tumor cannot be assessed T0: no evidence of primary tumor Tis: intraepithelial or invasion of lamina propria T1: tumor confined to the submucosa T2: tumor has grown into (but not through) the muscularis propria T3: tumor has grown into (but not through) the serosa T4: tumor has penetrated through the serosa and the peritoneal surface. INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C1300072
UMLS CUI [1,2]
C1521733
Pathological nodal stage (per AJCC 5th - 7th Ed.)
Beschreibung

SUPPORTING DEFINITION: Nodal stage (AJCC 5th -7th edition): NX: lymph nodes were not assessed N0: no lymph nodes contain tumor cells N1: there are tumor cells in up to 3 regional lymph nodes N2: there are tumor cells in 4 or more regional lymph nodes INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0456532
UMLS CUI [1,2]
C1300072
UMLS CUI [1,3]
C0205469
Pathological distant metastasis (per AJCC 5th - 7th Ed.)
Beschreibung

SUPPORTING DEFINITION: Distant metastasis (AJCC 5th- 7th edition): Mx: presence of metastasis cannot be assessed M0: no metastasis to distant organs M1: metastasis to distant organs INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Datentyp

integer

Alias
UMLS CUI [1,1]
C0807944
UMLS CUI [1,2]
C1521733
Indicate size of invasive component of tumor (in mm):  
Beschreibung

INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Numerical value; Please enter "999" if size of invasive component is unknown.

Datentyp

integer

Maßeinheiten
  • mm
Alias
UMLS CUI [1]
C0475440
mm
Number of lymph nodes resected: 
Beschreibung

INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Numerical value; Please enter "999" if size of invasive component is unknown.

Datentyp

integer

Alias
UMLS CUI [1,1]
C0024204
UMLS CUI [1,2]
C0728940
Number of lymph nodes involved according to the TNM stage AJCC 7th Ed.: 
Beschreibung

INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Numerical value; Please enter "999" if size of invasive component is unknown.

Datentyp

integer

Alias
UMLS CUI [1]
C0806692
Indicate if the estrogen receptor status is positive:
Beschreibung

INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer

Datentyp

integer

Alias
UMLS CUI [1]
C1516974
Indicate if the progesterone receptor status is positive:
Beschreibung

INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer

Datentyp

integer

Alias
UMLS CUI [1]
C1514471
Indicate if the HER2 receptor status is positive:
Beschreibung

SUPPORTING DEFINITION: By immunohistochemistry or ISH, whichever was considered most definitive INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer

Datentyp

integer

Alias
UMLS CUI [1]
C1512413
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Ähnliche Modelle

Baseline - Clinical-reported

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Patient ID
Item
Indicate the patient's medical record number
integer
C1269815 (UMLS CUI [1])
Patient's last name
Item
Patient's last name:
text
C1299487 (UMLS CUI [1])
Time Relative to Baseline
Item
Time Relative to Baseline
text
C0439564 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
Item Group
Demographic factors
C1704791 (UMLS CUI-1)
Date of birth
Item
What is your date of birth?
date
C0421451 (UMLS CUI [1])
Item Group
Baseline clinical factors
C0449440 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
Height
Item
Indicate height in centimeters or inches
float
C0005890 (UMLS CUI [1])
Item
Indicate units of height
integer
C0005890 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Height units
Code List
Indicate units of height
CL Item
centimeters (1)
C0475210 (UMLS CUI-1)
(Comment:en)
CL Item
inches (2)
C0439204 (UMLS CUI-1)
(Comment:en)
Weight
Item
Indicate weight in kilograms or pounds
float
C0005910 (UMLS CUI [1])
Item
Indicate units of weight
integer
C0005910 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Weight units
Code List
Indicate units of weight
CL Item
kilograms (1)
C0439209 (UMLS CUI-1)
(Comment:en)
CL Item
pounds (2)
C0439219 (UMLS CUI-1)
(Comment:en)
Item
Indicate the laterality of breast cancer:
integer
C0925205 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Laterality
Code List
Indicate the laterality of breast cancer:
CL Item
Left breast (0)
C0222601 (UMLS CUI-1)
(Comment:en)
CL Item
Right breast (1)
C0222600 (UMLS CUI-1)
(Comment:en)
CL Item
Both breasts (3)
C1706086 (UMLS CUI-1)
C0006141 (UMLS CUI-2)
(Comment:en)
Item
Indicate if this is first breast cancer or new cancer on contralateral or ipsilateral breast:
integer
C0678222 (UMLS CUI [1,1])
C3172269 (UMLS CUI [1,2])
First breast cancer
Code List
Indicate if this is first breast cancer or new cancer on contralateral or ipsilateral breast:
CL Item
Primary tumor (0)
C0677930 (UMLS CUI-1)
(Comment:en)
CL Item
New ipsilateral (1)
C0205314 (UMLS CUI-1)
C0441989 (UMLS CUI-2)
C0006826 (UMLS CUI-3)
(Comment:en)
CL Item
New contralateral (2)
C0205314 (UMLS CUI-1)
C0441988 (UMLS CUI-2)
C0006826 (UMLS CUI-3)
(Comment:en)
Item Group
Baseline tumor factors
C0475752 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
Histological diagnosis
Item
Initial date of histological diagnosis
date
C0679557 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Histological type: Ductal carcinoma in situ
Item
Indicate histologic type of the tumor (select all that apply) 0 = Ductal carcinoma in situ
boolean
C0449574 (UMLS CUI [1])
C1527349 (UMLS CUI [2])
Histological type: Invasive ductal carcinoma
Item
Indicate histologic type of the tumor (select all that apply) 1 = Invasive ductal carcinoma
boolean
C0449574 (UMLS CUI [1])
C1134719 (UMLS CUI [2])
Histological type: Invasive lobular carcinoma
Item
Indicate histologic type of the tumor (select all that apply) 2 = Invasive lobular carcinoma
boolean
C0449574 (UMLS CUI [1])
C0279565 (UMLS CUI [2])
Histological type: Other
Item
Indicate histologic type of the tumor (select all that apply) 3 = Other
boolean
C0449574 (UMLS CUI [1])
C0205394 (UMLS CUI [2])
Histological type: Unknown
Item
Indicate histologic type of the tumor (select all that apply) 999 = Unknown
boolean
C0449574 (UMLS CUI [1])
C0439673 (UMLS CUI [2])
Item
Indicate if the patient carries a genetic mutation predisposing breast cancer:
integer
C0314657 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Genetic mutation
Code List
Indicate if the patient carries a genetic mutation predisposing breast cancer:
CL Item
No mutation (0)
C1298908 (UMLS CUI-1)
C0026882 (UMLS CUI-2)
(Comment:en)
CL Item
BRCA 1 (1)
C1511022 (UMLS CUI-1)
(Comment:en)
CL Item
BRCA 2 (2)
C1511024 (UMLS CUI-1)
(Comment:en)
CL Item
Other mutation (3)
C0205394 (UMLS CUI-1)
C0026882 (UMLS CUI-2)
(Comment:en)
CL Item
Not tested (4)
C3640292 (UMLS CUI-1)
(Comment:en)
Item
Indicate grade of invasive component of tumor:
integer
C1269955 (UMLS CUI [1])
Invasion grade
Code List
Indicate grade of invasive component of tumor:
CL Item
Grade 1 (0)
C1269955 (UMLS CUI-1)
C0687695 (UMLS CUI-2)
(Comment:en)
CL Item
Grade 2 (1)
C1269955 (UMLS CUI-1)
C1522446 (UMLS CUI-2)
(Comment:en)
CL Item
Grade 3 (2)
C1269955 (UMLS CUI-1)
C0450094 (UMLS CUI-2)
(Comment:en)
CL Item
Not reported (3)
C1549114 (UMLS CUI-1)
(Comment:en)
Item
Indicate tumor grade of DCIS component of tumor:
integer
C0007124 (UMLS CUI [1,1])
C0919553 (UMLS CUI [1,2])
Tumor grade
Code List
Indicate tumor grade of DCIS component of tumor:
CL Item
Low (0)
C0205251 (UMLS CUI-1)
(Comment:en)
CL Item
Intermediate (1)
C0205103 (UMLS CUI-1)
(Comment:en)
CL Item
High (2)
C0205250 (UMLS CUI-1)
(Comment:en)
CL Item
Not reported (3)
C1549114 (UMLS CUI-1)
(Comment:en)
Item
Clinical tumor stage (per AJCC 5th - 7th Ed.)
integer
C0205210 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
Clinical tumor stage
Code List
Clinical tumor stage (per AJCC 5th - 7th Ed.)
CL Item
cTX (0)
C0332377 (UMLS CUI-1)
C1275863 (UMLS CUI-2)
(Comment:en)
CL Item
cT0 (1)
C0475371 (UMLS CUI-1)
C1275863 (UMLS CUI-2)
(Comment:en)
CL Item
cTis (2)
C0475413 (UMLS CUI-1)
C1275863 (UMLS CUI-2)
(Comment:en)
CL Item
cT1 (3)
C0475372 (UMLS CUI-1)
C1275863 (UMLS CUI-2)
(Comment:en)
CL Item
cT2 (4)
C0475373 (UMLS CUI-1)
C1275863 (UMLS CUI-2)
(Comment:en)
CL Item
cT3 (5)
C0475374 (UMLS CUI-1)
C1275863 (UMLS CUI-2)
(Comment:en)
CL Item
cT4 (6)
C0475751 (UMLS CUI-1)
C1275863 (UMLS CUI-2)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Clinical nodal stage (per AJCC 5th - 7th Ed.)
integer
C0456532 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
Clinical nodal stage
Code List
Clinical nodal stage (per AJCC 5th - 7th Ed.)
CL Item
cNX (0)
C1275865 (UMLS CUI-1)
C0445085 (UMLS CUI-2)
(Comment:en)
CL Item
cN0 (1)
C1275865 (UMLS CUI-1)
C0441959 (UMLS CUI-2)
(Comment:en)
CL Item
cN1 (2)
C1275865 (UMLS CUI-1)
C0441962 (UMLS CUI-2)
(Comment:en)
CL Item
cN2 (3)
C1275865 (UMLS CUI-1)
C0441960 (UMLS CUI-2)
(Comment:en)
CL Item
cN3 (4)
C1275865 (UMLS CUI-1)
C0441961 (UMLS CUI-2)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Clinical distant metastasis (per AJCC 5th - 7th Ed.)
integer
C1275856 (UMLS CUI [1])
Clinical distant metastatsis
Code List
Clinical distant metastasis (per AJCC 5th - 7th Ed.)
CL Item
cMX (0)
C0445039 (UMLS CUI-1)
C1275856 (UMLS CUI-2)
(Comment:en)
CL Item
cM0 (1)
C0445034 (UMLS CUI-1)
C1275856 (UMLS CUI-2)
(Comment:en)
CL Item
cM1 (2)
C0441971 (UMLS CUI-1)
C1275856 (UMLS CUI-2)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Pathological tumor stage (per AJCC 5th - 7th Ed.)
integer
C1300072 (UMLS CUI [1,1])
C1521733 (UMLS CUI [1,2])
Pathological tumor stage
Code List
Pathological tumor stage (per AJCC 5th - 7th Ed.)
CL Item
pTX (0)
C0332395 (UMLS CUI-1)
(Comment:en)
CL Item
pT0 (1)
C0332390 (UMLS CUI-1)
(Comment:en)
CL Item
pTis (2)
C0332389 (UMLS CUI-1)
(Comment:en)
CL Item
pT1 (3)
C0332391 (UMLS CUI-1)
(Comment:en)
CL Item
pT2 (4)
C0332392 (UMLS CUI-1)
(Comment:en)
CL Item
pT3 (5)
C0332393 (UMLS CUI-1)
(Comment:en)
CL Item
pT4 (6)
C0332394 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Pathological nodal stage (per AJCC 5th - 7th Ed.)
integer
C0456532 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
C0205469 (UMLS CUI [1,3])
Pathological nodal stage
Code List
Pathological nodal stage (per AJCC 5th - 7th Ed.)
CL Item
pNX (0)
C0332401 (UMLS CUI-1)
(Comment:en)
CL Item
pN0 (1)
C0332396 (UMLS CUI-1)
(Comment:en)
CL Item
pN1 (2)
C0332397 (UMLS CUI-1)
(Comment:en)
CL Item
pN2 (3)
C0332398 (UMLS CUI-1)
(Comment:en)
CL Item
pN3 (4)
C0332399 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Pathological distant metastasis (per AJCC 5th - 7th Ed.)
integer
C0807944 (UMLS CUI [1,1])
C1521733 (UMLS CUI [1,2])
Pathological distant metastasis
Code List
Pathological distant metastasis (per AJCC 5th - 7th Ed.)
CL Item
pMx (0)
C0332404 (UMLS CUI-1)
(Comment:en)
CL Item
pM0 (1)
C0332402 (UMLS CUI-1)
(Comment:en)
CL Item
pM1 (2)
C0456957 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Size of invasive tumor
Item
Indicate size of invasive component of tumor (in mm):  
integer
C0475440 (UMLS CUI [1])
Lymph nodes resected
Item
Number of lymph nodes resected: 
integer
C0024204 (UMLS CUI [1,1])
C0728940 (UMLS CUI [1,2])
Lymph nodes involved
Item
Number of lymph nodes involved according to the TNM stage AJCC 7th Ed.: 
integer
C0806692 (UMLS CUI [1])
Item
Indicate if the estrogen receptor status is positive:
integer
C1516974 (UMLS CUI [1])
Estrogen receptor status
Code List
Indicate if the estrogen receptor status is positive:
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Not performed (2)
C0445106 (UMLS CUI-1)
(Comment:en)
CL Item
Unkown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate if the progesterone receptor status is positive:
integer
C1514471 (UMLS CUI [1])
Estrogen receptor status
Code List
Indicate if the progesterone receptor status is positive:
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Not performed (2)
C0445106 (UMLS CUI-1)
(Comment:en)
CL Item
Unkown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate if the HER2 receptor status is positive:
integer
C1512413 (UMLS CUI [1])
HER2 receptor status
Code List
Indicate if the HER2 receptor status is positive:
CL Item
Negative (0)
C0205160 (UMLS CUI-1)
(Comment:en)
CL Item
Positive (1)
C1446409 (UMLS CUI-1)
(Comment:en)
CL Item
Equivocal (2)
C0332241 (UMLS CUI-1)
(Comment:en)
CL Item
Not performed (3)
C0445106 (UMLS CUI-1)
(Comment:en)
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