Follow-up Number
Item
Follow-up Number
integer
C1522577 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Date of Follow-up
Item
Date of Follow-up:
date
C0011008 (UMLS CUI [1,1])
C1522577 (UMLS CUI [1,2])
Item
Patient Status
integer
C3846084 (UMLS CUI [1])
CL Item
Lost to follow-up (2)
Date last known to be alive
Item
If patient alive: Date last known to be alive
date
C0805839 (UMLS CUI [1])
Relapse
Item
If patient alive: Has the patient had a relapse of NSCLC since the last assessment?
boolean
C0277556 (UMLS CUI [1])
Anticancer Treatment for NSCLC
Item
If patient alive: Has the patient received new anticancer treatment for NSCLC since the last assessment?
boolean
C0087111 (UMLS CUI [1,1])
C0007131 (UMLS CUI [1,2])
Date of last contact
Item
If lost to follow-up: Date of last patient contact:
date
C0805839 (UMLS CUI [1])
Follow-up attempts
Item
If lost to follow-up: What attempts were made to follow up on the patient status?
text
C1302313 (UMLS CUI [1])
Date of death
Item
If patient deceased: Date of death
date
C1148348 (UMLS CUI [1])
Item
If patient deceased: Primary Cause of Death
integer
C0007465 (UMLS CUI [1])
Code List
If patient deceased: Primary Cause of Death
CL Item
NSCLC Relapse (Complete Relapse Report page, if not previously reported) (1)
CL Item
Protocol-related toxicity (specify) (2)
CL Item
lntercurrent illness (specify) (3)
CL Item
Other (specify) (4)
Cause of Death
Item
Please specify cause of death:
text
C0007465 (UMLS CUI [1])
Item
If patient deceased: Was an autopsy performed?
integer
C0004398 (UMLS CUI [1])
Code List
If patient deceased: Was an autopsy performed?
CL Item
Yes (If Yes, append a copy of the autopsy report) (1)
Item
Was a chest/upper abdomen CT scan performed?
integer
C0202823 (UMLS CUI [1])
C1627748 (UMLS CUI [2])
Code List
Was a chest/upper abdomen CT scan performed?
Date chest/upper abdomen CT scan
Item
Date chest/upper abdomen CT scan performed:
date
C0011008 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1627748 (UMLS CUI [2,2])
Relapse
Item
If Yes, was relapse documented?
boolean
C0277556 (UMLS CUI [1])
Radiologic Examination
Item
Was any other radiological disease assessment performed?
boolean
C0043299 (UMLS CUI [1])
Date of assessment
Item
Date of assessment
date
C2985720 (UMLS CUI [1])
Evaluation Method
Item
Specify type of assessment:
text
C2911685 (UMLS CUI [1])
Relapse
Item
If Yes, was relapse documented?
boolean
C0277556 (UMLS CUI [1])
Chest X-ray
Item
Did the ''Other'' radiological assessment performed include X-Ray imaging of the chest?
boolean
C0039985 (UMLS CUI [1])
Chest CT
Item
Did the ''Other'' radiological assessment performed include CT imaging of the chest?
boolean
C0202823 (UMLS CUI [1])
CT of the chest/upper abdomen
Item
Did the ''Other'' radiological assessment performed include CT imaging of the chest/upper abdomen?
boolean
C0202823 (UMLS CUI [1])
C1627748 (UMLS CUI [2])
Adverse Events
Item
Did any Adverse Events occur?
boolean
C0877248 (UMLS CUI [1])
Adverse Events
Item
Sign/Symptom or Adverse Event
text
C0877248 (UMLS CUI [1])
Item
Severity (CTC Grade)
integer
C1710066 (UMLS CUI [1])
Code List
Severity (CTC Grade)
Adverse Event Start Date
Item
Start Date
date
C2697888 (UMLS CUI [1])
Adverse Event End Date
Item
Stop Date
date
C2697886 (UMLS CUI [1])
Seriousness of Adverse Event
Item
Serious
boolean
C1710056 (UMLS CUI [1])