ID

9770

Descripción

S0100 FOLLOW UP FORM Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=AEB52E43-75AF-43F2-E034-0003BA12F5E7

Link

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=AEB52E43-75AF-43F2-E034-0003BA12F5E7

Palabras clave

  1. 25/5/12 25/5/12 -
  2. 22/1/15 22/1/15 - Martin Dugas
Subido en

22 de enero de 2015

DOI

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Licencia

Creative Commons BY-NC 3.0 Legacy

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FOLLOW UP FORM (S0100)

No Instruction available.

  1. StudyEvent: S0100 FOLLOW UP FORM
    1. No Instruction available.
Vital Status
Descripción

Vital Status

Alias
UMLS CUI-1
C1148433
Vital Status
Descripción

Patient'sVitalStatus

Tipo de datos

text

Alias
UMLS CUI-1
C3846084
Date of last contact or death
Descripción

DeathDate/LastContactDate

Tipo de datos

date

Disease Follow Up Status
Descripción

Disease Follow Up Status

Alias
UMLS CUI-1
C1522577
Has the patient had a documented clinical assessment for this cancer since submission of the previous follow-up form? (If Yes, )
Descripción

CancerFollow-upStatusInd

Tipo de datos

boolean

Date of Last Clinical Assessment
Descripción

CancerFollow-upStatusDate

Tipo de datos

date

Alias
NCI Thesaurus ObjectClass
C2991
UMLS 2011AA ObjectClass
C0012634
NCI Thesaurus Property
C25365
UMLS 2011AA Property
C0678257
Notice Of First Relapse Or Progression
Descripción

Notice Of First Relapse Or Progression

Has the patient developed a first relapse or progression that has not been previously reported? (If Yes)
Descripción

Hasthepatientdevelopedafirstrelapseorprogressionthathasnotbeenpreviouslyreported?

Tipo de datos

boolean

Alias
UMLS CUI-1
C0242656
Date of Relapse or Progression
Descripción

DateofRelapseorProgression

Tipo de datos

text

Site(s) of Relapse or Progression
Descripción

Site(s)ofRelapseorProgression

Tipo de datos

text

Notice Of New Primary
Descripción

Notice Of New Primary

Has a new primary cancer or myelodysplastic syndrome (MDS) been diagnosed that has not been previously reported? (If Yes,)
Descripción

NewPrimaryCancerInd

Tipo de datos

boolean

New Primary Site
Descripción

NewPrimarySite

Tipo de datos

text

Non-protocol Treatment
Descripción

Non-protocol Treatment

Has the patient received any non-protocol cancer therapy (prior to progression/relapse) not previously reported? (If Yes)
Descripción

Non-ProtocolTherapyInd

Tipo de datos

boolean

Date of First Non-Protocol Therapy
Descripción

Non-ProtocolTherapyDate,First

Tipo de datos

date

Agents
Descripción

AgentName

Tipo de datos

text

Long Term Toxicity
Descripción

Long Term Toxicity

Has the patient experienced (prior to treatment for progression or relapse or a second primary, and prior to non-protocol treatment) any severe (grade 3) long term toxicity that has not been previously reported? (If Yes,)
Descripción

LateAdverseEventInd

Tipo de datos

boolean

Toxicities and Grades
Descripción

CTCAdverseEventTerm

Tipo de datos

text

Notes
Descripción

Comments

Tipo de datos

text

Ccrr Module For S0100 Follow Up Form
Descripción

Ccrr Module For S0100 Follow Up Form

SWOG Patient ID
Descripción

SWOGPatientID

Tipo de datos

text

SWOG Study No.
Descripción

SWOGStudyNo.

Tipo de datos

text

Registration Step
Descripción

RegistrationStep

Tipo de datos

text

Patient Initials (L, F, M)
Descripción

PatientInitials

Tipo de datos

text

Institution/Affiliate
Descripción

MainMemberInstitution/Affiliate

Tipo de datos

text

Physician
Descripción

TreatingPhysician

Tipo de datos

text

Alias
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
NCI Thesaurus ObjectClass
C25741
UMLS 2011AA ObjectClass
C0031831
NCI Thesaurus ObjectClass-2
C25705
UMLS 2011AA ObjectClass-2
C1522326
Group Name
Descripción

GroupName

Tipo de datos

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS 2011AA ValueDomain
C1547383
NCI Thesaurus ObjectClass
C17005
UMLS 2011AA ObjectClass
C1257890
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
Study No.
Descripción

StudyNo.

Tipo de datos

text

Pt. ID
Descripción

Pt.ID

Tipo de datos

text

Similar models

No Instruction available.

  1. StudyEvent: S0100 FOLLOW UP FORM
    1. No Instruction available.
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Vital Status
C1148433 (UMLS CUI-1)
Item
Vital Status
text
C3846084 (UMLS CUI-1)
Code List
Vital Status
CL Item
Alive (Alive)
C2584946 (UMLS CUI-1)
CL Item
Dead (Dead)
C0011065 (UMLS CUI-1)
DeathDate/LastContactDate
Item
Date of last contact or death
date
Item Group
Disease Follow Up Status
C1522577 (UMLS CUI-1)
CancerFollow-upStatusInd
Item
Has the patient had a documented clinical assessment for this cancer since submission of the previous follow-up form? (If Yes, )
boolean
CancerFollow-upStatusDate
Item
Date of Last Clinical Assessment
date
C2991 (NCI Thesaurus ObjectClass)
C0012634 (UMLS 2011AA ObjectClass)
C25365 (NCI Thesaurus Property)
C0678257 (UMLS 2011AA Property)
Item Group
Notice Of First Relapse Or Progression
Progression
Item
Has the patient developed a first relapse or progression that has not been previously reported? (If Yes)
boolean
C0242656 (UMLS CUI-1)
DateofRelapseorProgression
Item
Date of Relapse or Progression
text
Site(s)ofRelapseorProgression
Item
Site(s) of Relapse or Progression
text
Item Group
Notice Of New Primary
NewPrimaryCancerInd
Item
Has a new primary cancer or myelodysplastic syndrome (MDS) been diagnosed that has not been previously reported? (If Yes,)
boolean
NewPrimarySite
Item
New Primary Site
text
Item Group
Non-protocol Treatment
Non-ProtocolTherapyInd
Item
Has the patient received any non-protocol cancer therapy (prior to progression/relapse) not previously reported? (If Yes)
boolean
Non-ProtocolTherapyDate,First
Item
Date of First Non-Protocol Therapy
date
AgentName
Item
Agents
text
Item Group
Long Term Toxicity
LateAdverseEventInd
Item
Has the patient experienced (prior to treatment for progression or relapse or a second primary, and prior to non-protocol treatment) any severe (grade 3) long term toxicity that has not been previously reported? (If Yes,)
boolean
CTCAdverseEventTerm
Item
Toxicities and Grades
text
Comments
Item
Notes
text
Item Group
Ccrr Module For S0100 Follow Up Form
SWOGPatientID
Item
SWOG Patient ID
text
SWOGStudyNo.
Item
SWOG Study No.
text
RegistrationStep
Item
Registration Step
text
PatientInitials
Item
Patient Initials (L, F, M)
text
MainMemberInstitution/Affiliate
Item
Institution/Affiliate
text
TreatingPhysician
Item
Physician
text
C25364 (NCI Thesaurus Property)
C0600091 (UMLS 2011AA Property)
C25741 (NCI Thesaurus ObjectClass)
C0031831 (UMLS 2011AA ObjectClass)
C25705 (NCI Thesaurus ObjectClass-2)
C1522326 (UMLS 2011AA ObjectClass-2)
GroupName
Item
Group Name
text
C25191 (NCI Thesaurus ValueDomain)
C1547383 (UMLS 2011AA ValueDomain)
C17005 (NCI Thesaurus ObjectClass)
C1257890 (UMLS 2011AA ObjectClass)
C25364 (NCI Thesaurus Property)
C0600091 (UMLS 2011AA Property)
StudyNo.
Item
Study No.
text
Pt.ID
Item
Pt. ID
text

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