ID
40558
Beschrijving
ICHOM Lung cancer data collection Version 2.3.1 Revised: April 10th, 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 Lung Cancer, the following conditions and treatment approaches (or interventions) are covered by our Standard Set. Conditions: Small Cell and Non-Small Cell Lung Cancer Treatment Approaches: Surgery | Radiotherapy | Chemotherapy | Targeted Therapy | Immunotherapy | Other This document contains Baseline - Clinical Form. It depicts first doctor's visit. Collecting Patient-Reported Outcome Measures: European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30). European Organization for Research and Treatment of Cancer Quality of Life Lung Cancer-Specific Questionnaire (EORTC QLQ-LC13). Both are free for all health care organizations, but a license is needed for use. http:// groups.eortc.be/qol/eortc-qlq-c30 is the official distribution site for EORTC QLQ-C30 and EORTC QLQ-LC13 questionnaire. Therefore only the total score will be included in this version of the standard set. Publication: Mak KS, van Bommel AC, Stowell C, et al. Defining a standard set of patient-centred outcomes for lung cancer. Eur Respir J. 2016;48(3):852–860. doi:10.1183/13993003.02049-2015 For this standard set ICHOM was supported by the Alliance of Dedicated Cancer Centers. For this version of the standard set, semantic annotation with UMLS CUIs has been added.
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- 15-05-19 15-05-19 -
- 16-05-19 16-05-19 -
- 30-04-20 30-04-20 - Sarah Riepenhausen
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ICHOM
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30 april 2020
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Creative Commons BY-NC 4.0
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ICHOM Lung Cancer
Baseline - Clinical Form
- StudyEvent: ODM
Beschrijving
Demographic factors
Alias
- UMLS CUI-1
- C1704791
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical or patient-‐reported Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0421451
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical or patient-‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0079399
Beschrijving
Baseline Clinical Factors
Alias
- UMLS CUI-1
- C0449440
- UMLS CUI-2
- C1442488
Beschrijving
Inclusion Criteria: Patients undergoing surgery Timing: Baseline Data Source: Clinical Type: Numerical value Response Options: Numerical value in liters 999 = Unknown
Datatype
float
Maateenheden
- L
Alias
- UMLS CUI [1,1]
- C0024119
- UMLS CUI [1,2]
- C0429706
Beschrijving
Inclusion Criteria: Patients undergoing surgery Timing: Baseline Data Source: Clinical Type: Numerical value Response Options: Numerical value of 0‐100 999 = Unknown
Datatype
float
Maateenheden
- %
Alias
- UMLS CUI [1,1]
- C0024119
- UMLS CUI [1,2]
- C0086715
Beschrijving
Baseline tumor factors
Alias
- UMLS CUI-1
- C0475752
- UMLS CUI-2
- C1442488
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2911685
- UMLS CUI [1,2]
- C0332140
- UMLS CUI [2,1]
- C2911685
- UMLS CUI [2,2]
- C1521733
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0019638
Beschrijving
Supporting Definition: If the test is not performed, unknown can be answered. Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0026882
- UMLS CUI [1,2]
- C0449438
- UMLS CUI [1,3]
- C0252409
- UMLS CUI [1,4]
- C0040715
Beschrijving
Supporting Definition: If the test is not performed, unknown can be answered. Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0026882
- UMLS CUI [1,2]
- C0449438
- UMLS CUI [1,3]
- C2984891
Beschrijving
Supporting Definition: Pathologic staging preferred, if available cT0: no primary tumor cT1: if not able to select T1a or T1b: Tumor ≤3 cm diameter, surrounded by lung or visceral pleura, without invasion more proximal than lobar bronchus cT1a: Tumor ≤2 cm in diameter cT1b: Tumor >2 cm but ≤3 cm in diameter cT2: if not able to select T2a or T2b: Tumor >3 cm but ≤7 cm, or tumor with any of the following features: Involves main bronchus, ≥2 cm distal to carina. Invades visceral pleura. Associated with atelectasis or obstructive pneumonitis that extends to the hilar region but does not involve the entire lung cT2a: Tumor >3 cm but ≤5 cm cT2b: Tumor >5 cm but ≤7 cm cT3: Tumor >7 cm or any of the following: Directly invades any of the following: chest wall, diaphragm, phrenic nerve, mediastinal pleura, parietal pericardium, main bronchus <2 cm from carina (without involvement of carina), Atelectasis or obstructive pneumonitis of the entire lung. Separate tumor nodules in the same lobe cT4: Tumor of any size that invades the mediastinum, heart, great vessels, trachea, recurrent laryngeal nerve, esophagus, vertebral body, carina, or with separate tumor nodules in a different ipsilateral lobe cTX: Primary tumor cannot be assessed Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C1300072
Beschrijving
Supporting Definition: Pathologic staging preferred, if available cN0: No regional lymph node metastases cN1: Metastasis in ipsilateral peribronchial and/or ipsilateral hilar lymph nodes and intrapulmonary nodes, including involvement by direct extension cN2: Metastasis in ipsilateral mediastinal and/or subcarinal lymph node(s) cN3: Metastasis in contralateral mediastinal, contralateral hilar, ipsilateral or contralateral scalene, or supraclavicular lymph node(s) cNX: Regional lymph nodes were not assessed Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0456532
- UMLS CUI [1,2]
- C0205210
Beschrijving
Supporting Definition: cM0: No distant metastasis cM1: Distant metastasis cM1a: Separate tumor nodule(s) in a contralateral lobe; tumor with pleural nodules or malignant pleural or pericardial effusion cM1b: Distant metastasis (in extrathoracic organs) cMX: Distant metastasis cannot be evaluated Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0456533
- UMLS CUI [1,2]
- C0205210
Beschrijving
Supporting Definition: pM0: No distant metastasis pM1: Distant metastasis pM1a: Separate tumor nodule(s) in a contralateral lobe; tumor with pleural nodules or malignant pleural or pericardial effusion pM1b: Distant metastasis (in extrathoracic organs) pMX: Distant metastasis cannot be evaluated Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1521733
- UMLS CUI [1,2]
- C0036525
- UMLS CUI [1,3]
- C1300072
Beschrijving
Degree of health
Alias
- UMLS CUI-1
- C0018759
Beschrijving
Supporting Definition: ECOG / WHO scale: - PS = 0 normal activity level; - PS = 1 restricted with strenuous activity, but can do light activity; - PS = 2 active >/= 50% of day; - PS = 3 spends >50% of day in chair or bed; - PS = 4 totally confined to bed Inclusion Criteria: All patients Timing: Baseline 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C1520224
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