Description

Supporting Definition: 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 Data Source: Administrative or clinical Type: Numerical Response Options: According to institution

Data type

integer

Alias

UMLS CUI [1]

C2348585

Description

Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical or patient-­‐reported Type: Date by DD/MM/YYYY

Data type

date

Measurement units

• DD/MM/YYYY

Alias

UMLS CUI [1]

C0421451

Description

Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical or patient-­‐reported Type: Single answer

Data type

integer

Alias

UMLS CUI [1]

C0079399

Description

Inclusion Criteria: Patients undergoing surgery Timing: Baseline Data Source: Clinical Type: Numerical value Response Options: Numerical value in liters 999 = Unknown

Data type

float

Measurement units

• L

Alias

UMLS CUI [1,1]

C0024119

UMLS CUI [1,2]

C0429706

Description

Inclusion Criteria: Patients undergoing surgery Timing: Baseline Data Source: Clinical Type: Numerical value Response Options: Numerical value of 0‐100 999 = Unknown

Data type

float

Measurement units

• %

Alias

UMLS CUI [1,1]

C0024119

UMLS CUI [1,2]

C0086715

Description

Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer

Data type

integer

Alias

UMLS CUI [1,1]

C2911685

UMLS CUI [1,2]

C0332140

UMLS CUI [2,1]

C2911685

UMLS CUI [2,2]

C1521733

Description

Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer

Data type

integer

Alias

UMLS CUI [1]

C0019638

Description

Supporting Definition: If the test is not performed, unknown can be answered. Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer

Data type

integer

Alias

UMLS CUI [1,1]

C0026882

UMLS CUI [1,2]

C0449438

UMLS CUI [1,3]

C0252409

UMLS CUI [1,4]

C0040715

Description

Supporting Definition: If the test is not performed, unknown can be answered. Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer

Data type

integer

Alias

UMLS CUI [1,1]

C0026882

UMLS CUI [1,2]

C0449438

UMLS CUI [1,3]

C2984891

Description

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

Data type

integer

Alias

UMLS CUI [1,1]

C0205210

UMLS CUI [1,2]

C1300072

Description

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

Data type

integer

Alias

UMLS CUI [1,1]

C0456532

UMLS CUI [1,2]

C0205210

Description

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

Data type

integer

Alias

UMLS CUI [1,1]

C0456533

UMLS CUI [1,2]

C0205210

Description

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

Data type

integer

Alias

UMLS CUI [1,1]

C1521733

UMLS CUI [1,2]

C0036525

UMLS CUI [1,3]

C1300072

Description

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

Data type

integer

Alias

UMLS CUI [1]

C1520224