ID
40614
Description
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 Follow-up, 6 month, 3-10 years post treatment - Patient-reported form. It has to be filled in 6 month and annually for 3-10 years after each begin of a new therapy. Annual follow-up reassessed from date of surgery or start of a new therapy (e.g. due to recurrence) so that it will run parallel with annual outpatient visit. At least 10 years post surgery/start of other therapy. Distinction for long-term follow-up: Local disease: Up to 10 years follow-up; Metastatic disease: Annually for life 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.
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Keywords
Versions (4)
- 7/25/19 7/25/19 -
- 7/30/19 7/30/19 -
- 8/2/19 8/2/19 - Sarah Riepenhausen
- 4/30/20 4/30/20 - Sarah Riepenhausen
Copyright Holder
ICHOM
Uploaded on
April 30, 2020
DOI
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License
Creative Commons BY-NC 4.0
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ICHOM Breast Cancer
Follow-up, 6 month, 3-10 years post treatment - Patient-reported
- StudyEvent: ODM
Description
Baseline clinical factors
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1298908
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0018799
- UMLS CUI [3]
- C0002962
- UMLS CUI [4]
- C0027051
- UMLS CUI [5]
- C0018801
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0020538
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1306889
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0024115
- UMLS CUI [3]
- C0004096
- UMLS CUI [4]
- C0008677
- UMLS CUI [5]
- C0034067
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011849
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0022658
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0023895
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2,1]
- C0038454
- UMLS CUI [2,2]
- C0678227
- UMLS CUI [2,3]
- C0033213
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0027765
- UMLS CUI [3]
- C0030567
- UMLS CUI [4]
- C0026769
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1707251
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011581
Description
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0003864
Description
Treatment variables
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1298908
- UMLS CUI [1,2]
- C0543467
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0085076
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0024881
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0193867
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0439673
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Date by DD/MM/YYYY; Please enter "999" if date is unknown
Data type
date
Measurement units
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1624150
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1515119
- UMLS CUI [1,2]
- C2003901
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2746065
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0392920
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C2985566
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0279025
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Data type
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0439673
Description
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Date by DD/MM/YYYY; Please enter "999" if date is unknown
Data type
date
Measurement units
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1515119
- UMLS CUI [1,2]
- C3173309
Description
Degree of health
Description
As a permission is needed for use of this questionnaire, the actual 30 questions are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: EORTC QLQ-C30_Q01 to EORTC QLQ-C30_Q30. INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C4055104
- UMLS CUI [1,2]
- C2964552
Description
As a permission is needed for use of this questionnaire, the actual 23 questions are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: EORTCQLQBR23_Q31 to EORTCQLQBR23_Q53. INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C4724921
- UMLS CUI [1,2]
- C0451149
- UMLS CUI [1,3]
- C2964552
Description
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-LMC21): A license is needed for use of this questionnaire as well, however only one question is used. The ICHOM OID's is: EORTC QLQ-LMC21 INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0451149
- UMLS CUI [1,2]
- C2116350
- UMLS CUI [1,3]
- C0347984
- UMLS CUI [1,4]
- C2987125
- UMLS CUI [2,1]
- C0451149
- UMLS CUI [2,2]
- C2116331
- UMLS CUI [2,3]
- C0347984
- UMLS CUI [2,4]
- C2987125
Description
As a permission is needed for use of this questionnaire, the actual 6 questions are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: FACTES_Q01 (BRM1), FACTES_Q02 to FACTES_Q06 (ES4-ES8) INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C3889662
- UMLS CUI [1,2]
- C0449820
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