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- StudyEvent: E1900 Long-Term Follow-up Form
Name
 Type
 Description | Question | Decode (Coded Value) 
 Data type
 Alias
  Protocol ID ECOG 
 Item
 ECOG Protocol No.
 text
  C3274381 (UMLS CUI-1)
C1512162 (UMLS CUI-2)
 
 C1512162 (UMLS CUI-2)
 ECOG Patient ID 
 Item
 ECOG Patient ID
 text
  C2348585 (UMLS CUI-1)
C1512162 (UMLS CUI-2)
 
 C1512162 (UMLS CUI-2)
 Registration Step 
 Item
 Registration Step
 text
  C1514821 (UMLS CUI-1)
 
  Patient Name 
 Item
 Patient's Name
 text
  C1299487 (UMLS CUI-1)
 
  Protocol ID Participating Group 
 Item
 Participating Group Protocol No.
 text
  C3274381 (UMLS CUI-1)
C2347449 (UMLS CUI-2)
 
 C2347449 (UMLS CUI-2)
 Patient ID Participating Group 
 Item
 Participating Group Patient ID
 text
  C2348585 (UMLS CUI-1)
C2347449 (UMLS CUI-2)
 
 C2347449 (UMLS CUI-2)
 Institution 
 Item
 Institution/Affiliate
 text
  C1301943 (UMLS CUI-1)
 
  Data amended 
 Item
 Are data amended?
 boolean
  C25474 (NCI Thesaurus ObjectClass)
C25416 (NCI Thesaurus Property)
C1511726 (UMLS CUI-1)
C1691222 (UMLS CUI-2)
 
 C25416 (NCI Thesaurus Property)
C1511726 (UMLS CUI-1)
C1691222 (UMLS CUI-2)
 Reporting Period Start Date 
 Item
 Reporting Period Start Date
 date
  C2361257 (UMLS CUI-1)
 
  Reporting Period End Date 
 Item
 Reporting Period End Date
 date
  C2361259 (UMLS CUI-1)
 
  Comments 
 Item
 Comments
 text
  C0947611 (UMLS CUI-1)
 
  Investigator Signature 
 Item
 Investigator Signature
 text
  C25678 (NCI Thesaurus Property)
C17089 (NCI Thesaurus ObjectClass)
C2346576 (UMLS CUI-1)
 
 C17089 (NCI Thesaurus ObjectClass)
C2346576 (UMLS CUI-1)
 Investigator Signature Date 
 Item
 Investigator Signature Date
 date
  C2346576 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
 
 C0011008 (UMLS CUI-2)
CL Item
 Alive (Alive)
  CL Item
 Dead (Dead)
   Date of Last Contact or Death 
 Item
 Date of Last Contact or Death
 date
  C0805839 (UMLS CUI-1)
C1148348 (UMLS CUI-2)
 
 C1148348 (UMLS CUI-2)
CL Item
 Due To Protocol Treatment (Due to protocol treatment)
  CL Item
 Due To This Disease (Due to this disease)
  CL Item
 Due To Other Cause, Specify (Due to other cause)
  CL Item
 Unknown (Unknown)
   C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
 
 C0439673 (UMLS 2011AA)
 Death Reason, Specify 
 Item
 Describe cause of death
 text
  C0007465 (UMLS CUI-1)
C1521902 (UMLS CUI-2)
 
 C1521902 (UMLS CUI-2)
 Follow-Up Cancer 
 Item
 Has the patient had a documented clinical assessment for this cancer (since submission of the previous follow-up form)?
 boolean
  C1522577 (UMLS CUI-1)
C0006826 (UMLS CUI-2)
 
 C0006826 (UMLS CUI-2)
 Follow-up Date Cancer 
 Item
 Date of last clinical cancer assessment (If yes)
 date
  C2991 (NCI Thesaurus ObjectClass)
C25365 (NCI Thesaurus Property)
C3694716 (UMLS CUI-1)
C0006826 (UMLS CUI-2)
 
 C25365 (NCI Thesaurus Property)
C3694716 (UMLS CUI-1)
C0006826 (UMLS CUI-2)
 Tumor Progression 
 Item
 Has the patient developed a first relapse that has not been previously reported?
 boolean
  C0178874 (UMLS CUI-1)
 
  Date of Relapse 
 Item
 Date of relapse
 date
  C0035020 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
 
 C0011008 (UMLS CUI-2)
 Relapse certain 
 Item
 Did a physician make a formal diagnosis of relapse? (If no or unknown, specify basis of PD in Comments)
 boolean
  C38148 (NCI Thesaurus ValueDomain)
C25741 (NCI Thesaurus ObjectClass)
C25254 (NCI Thesaurus Property)
C15220 (NCI Thesaurus Property-2)
C0035020 (UMLS CUI-1)
C0205423 (UMLS CUI-2)
 
 C25741 (NCI Thesaurus ObjectClass)
C25254 (NCI Thesaurus Property)
C15220 (NCI Thesaurus Property-2)
C0035020 (UMLS CUI-1)
C0205423 (UMLS CUI-2)
 New Primary Cancer 
 Item
 Has a new primary cancer or MDS been diagnosed that has not been previously reported?
 boolean
  C0751623 (UMLS CUI-1)
 
  New Primary Cancer Site 
 Item
 Site(s) of new primary
 text
  C0751623 (UMLS CUI-1)
C1515974 (UMLS CUI-2)
 
 C1515974 (UMLS CUI-2)
 Toxicity, long-term 
 Item
 Has the patient experienced any severe (Grade >= 3) long term toxicity that has not been previously reported?
 boolean
  C0040539 (UMLS CUI-1)
C0443252 (UMLS CUI-2)
 
 C0443252 (UMLS CUI-2)
 Non-protocol Therapy 
 Item
 Has the patient received any non-protocol cancer therapy prior to first relapse (not previously reported)?
 boolean
  C38148 (NCI Thesaurus ValueDomain)
C1518384 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
 
 C1518384 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
 Platelet Transfusion 
 Item
 Number of platlet transfusions (this reporting period)
 integer
  C44278 (NCI Thesaurus ValueDomain)
C25639 (NCI Thesaurus Property)
C25463 (NCI Thesaurus ValueDomain-2)
C15366 (NCI Thesaurus ObjectClass)
C0086818 (UMLS CUI-1)
 
 C25639 (NCI Thesaurus Property)
C25463 (NCI Thesaurus ValueDomain-2)
C15366 (NCI Thesaurus ObjectClass)
C0086818 (UMLS CUI-1)
 Platelet Transfusion, recent date 
 Item
 Date of most recent platelet transfusion
 date
  C25164 (NCI Thesaurus ValueDomain)
C25639 (NCI Thesaurus Property)
C15366 (NCI Thesaurus ObjectClass)
C25577 (NCI Thesaurus ValueDomain-2)
C0086818 (UMLS CUI-1)
C0332185 (UMLS CUI-2)
 
 C25639 (NCI Thesaurus Property)
C15366 (NCI Thesaurus ObjectClass)
C25577 (NCI Thesaurus ValueDomain-2)
C0086818 (UMLS CUI-1)
C0332185 (UMLS CUI-2)
 Red Blood Cell Transfusion 
 Item
 Number of RBC transfusions (this reporting period)
 integer
  C44278 (NCI Thesaurus ValueDomain)
C25639 (NCI Thesaurus Property)
C25463 (NCI Thesaurus ValueDomain-2)
C15409 (NCI Thesaurus ObjectClass)
C0086252 (UMLS CUI-1)
 
 C25639 (NCI Thesaurus Property)
C25463 (NCI Thesaurus ValueDomain-2)
C15409 (NCI Thesaurus ObjectClass)
C0086252 (UMLS CUI-1)
 Red Blood Cell Transfusion, recent date 
 Item
 Date of most recent RBC transfusion
 date
  C25164 (NCI Thesaurus ValueDomain)
C25639 (NCI Thesaurus Property)
C15409 (NCI Thesaurus ObjectClass)
C25577 (NCI Thesaurus ValueDomain-2)
C0086252 (UMLS CUI-1)
C0332185 (UMLS CUI-2)
 
 C25639 (NCI Thesaurus Property)
C15409 (NCI Thesaurus ObjectClass)
C25577 (NCI Thesaurus ValueDomain-2)
C0086252 (UMLS CUI-1)
C0332185 (UMLS CUI-2)