ID

11393

Beschrijving

Form 6 - Final Report NCT00049543 Gefitinib in Treating Patients With Non-Small Cell Lung Cancer That Has Been Surgically Removed Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=A1AD599A-E8FC-3686-E034-080020C9C0E0

Link

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=A1AD599A-E8FC-3686-E034-080020C9C0E0

Trefwoorden

Versies (3)
  1. 19-09-12 19-09-12 -
  2. 09-01-15 09-01-15 - Martin Dugas
  3. 03-07-15 03-07-15 -
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3 juli 2015

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Form 6 - Final Report NCT00049543

Engels

No Instruction available.

1 Formulieren  
  1. StudyEvent: Form 6 - Final Report
    1. No Instruction available.
1. Patient Information
Beschrijving

1. Patient Information

Pt. Serial #
Beschrijving

PatientStudyID,CoordinatingGroup

Datatype

text

Hospital #
Beschrijving

PatientMedicalRecordNumber

Datatype

text

Pt. Initials
Beschrijving

Patient Initials

Datatype

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Intergroup Patient Serial #
Beschrijving

PatientStudyID,ParticipatingGroup

Datatype

text

Site #
Beschrijving

NCIInstitutionNumber

Datatype

text

Patient's Social Security # (USA only)
Beschrijving

PatientSocialSecurityNumber

Datatype

float

Institution
Beschrijving

InstitutionName

Datatype

text

Investigator
Beschrijving

RegisteredInvestigator

Datatype

text

2. Cause Of Death
Beschrijving

2. Cause Of Death

Date of death
Beschrijving

DeathDocumentedDate

Datatype

date

Cause of Death
Beschrijving

DeathReason

Datatype

text

other primary malignancy (specify & send report)
Beschrijving

OtherPrimaryMalignantNeoplasmPresentStatus

Datatype

text

Alias
NCI Thesaurus ObjectClass
C17649
UMLS 2011AA ObjectClass
C0205394
NCI Thesaurus ObjectClass-2
C25251
UMLS 2011AA ObjectClass-2
C0205225
NCI Thesaurus ObjectClass-3
C9305
UMLS 2011AA ObjectClass-3
C0006826
NCI Thesaurus Property
C25626
UMLS 2011AA Property
C0150312
NCI Thesaurus ValueDomain
C25688
UMLS 2011AA ValueDomain
C0449438
NCIC CTG use only code
Beschrijving

NCICCTGuseonlycode

Datatype

text

Describe
Beschrijving

DeathReason,Specify

Datatype

text

Status of NSCLC at Time of Death
Beschrijving

StatusofNSCLCatTimeofDeath

Datatype

text

3. Autopsy
Beschrijving

3. Autopsy

Autopsy performed
Beschrijving

AutopsyInd

Datatype

text

NCIC CTG Use only: Received
Beschrijving

NCICCTGUseonly:Received

Datatype

text

4. Other Malignancies Or Marrow Dysplasia
Beschrijving

4. Other Malignancies Or Marrow Dysplasia

Have any other malignancies or myelodysplastic syndrome (MDS) been diagnosed?
Beschrijving

NewPrimaryCancerInd

Datatype

boolean

Date of diagnosis
Beschrijving

NewPrimaryCancerDate

Datatype

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
Site of new primary
Beschrijving

NewPrimarySite

Datatype

text

Describe (An Adverse Event Report must be sent to NCIC CTG within 15 working days that diagnosis is known to the investigator. See protocol section 11.0 for details.)
Beschrijving

NewPrimaryDetail

Datatype

text

Ncic Ctg Use
Beschrijving

Ncic Ctg Use

Malignancy Type
Beschrijving

NewPrimaryMalignancyType

Datatype

text

Ncic Ctg Use Only
Beschrijving

Ncic Ctg Use Only

Logged
Beschrijving

LoggedEntryInitials

Datatype

text

Header
Beschrijving

LoggedEntryDate

Datatype

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
Study Coord
Beschrijving

CoordinatorReviewInitials

Datatype

text

Coordinator Review Date
Beschrijving

Coordinator Review Date

Datatype

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS CUI-1
C0011008
Phy
Beschrijving

PhysicianReviewInitials

Datatype

text

Data Ent'd
Beschrijving

DataEntryInitials

Datatype

text

Verified
Beschrijving

DataVerificationInitials

Datatype

text

5. Treatment Given Since Last Report To Ncic Ctg
Beschrijving

5. Treatment Given Since Last Report To Ncic Ctg

Is the patient receiving any non-protocol cancer therapy not previously reported? (if yes, specify below)
Beschrijving

Non-ProtocolTherapyInd

Datatype

boolean

Non-Protocol Hormonal Therapy? (include medical and surgical)
Beschrijving

Non-ProtocolHormonalTherapyInd

Datatype

boolean

Non-Protocol Chemotherapy?
Beschrijving

Non-ProtocolChemotherapyInd

Datatype

boolean

Non-Protocol Immunotherapy?
Beschrijving

Non-ProtocolImmunotherapyInd

Datatype

boolean

Non-Protocol Biologic Response Modifier?
Beschrijving

Non-ProtocolBRMInd

Datatype

boolean

Non-Protocol High Dose Chemotherapy/ Autologous Stem Cell Transplant?
Beschrijving

Non-ProtocolHDC/ASCTInd

Datatype

boolean

Non-Protocol Radiation Therapy?
Beschrijving

Non-ProtocolRTInd

Datatype

boolean

Non-Protocol Surgery?
Beschrijving

Non-protocolSurgeryPerformedInd-3

Datatype

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
NCI Thesaurus Property
C38000
UMLS 2011AA Property
C0884358
NCI Thesaurus ObjectClass
C15329
UMLS 2011AA ObjectClass
C0543467
NCI Thesaurus ObjectClass-2
C25590
UMLS 2011AA ObjectClass-2
C1518384
Other Non-Protocol Therapy?
Beschrijving

OtherTherapyInd

Datatype

boolean

(specify)
Beschrijving

OtherNon-ProtocolTherapyName

Datatype

text

First ever chemotherapy or EGFR inhibitor given: (specify)
Beschrijving

Non-ProtocolFirstChemotherapyAgentName

Datatype

text

Alias
NCI Thesaurus ObjectClass
C25590
UMLS 2011AA ObjectClass
C1518384
NCI Thesaurus ObjectClass-2
C2167
UMLS 2011AA ObjectClass-2
C1443775
NCI Thesaurus Property
C25382
UMLS 2011AA Property
C1521801
Date started
Beschrijving

Non-ProtocolFirstChemotherapyBeginDate

Datatype

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
NCI Thesaurus ValueDomain-2
C25431
UMLS 2011AA ValueDomain-2
C0439659
Second ever chemotherapy or EGFR inhibitor given: (specify)
Beschrijving

Non-ProtocolSecondChemotherapyAgentName

Datatype

text

Alias
NCI Thesaurus ObjectClass
C25590
UMLS 2011AA ObjectClass
C1518384
NCI Thesaurus ObjectClass-2
C2167
UMLS 2011AA ObjectClass-2
C1443775
NCI Thesaurus Property
C25382
UMLS 2011AA Property
C1521801
Date started(2nd)
Beschrijving

Non-ProtocolSecondChemotherapyBeginDate

Datatype

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
Ncic Ctg Use2
Beschrijving

Ncic Ctg Use2

1st line
Beschrijving

1stline

Datatype

text

2nd line
Beschrijving

2ndline

Datatype

text

6. Delayed Toxicity/adverse Event/intercurrent Illness
Beschrijving

6. Delayed Toxicity/adverse Event/intercurrent Illness

NCIC CTG use only
Beschrijving

NCICCTGuseonly

Datatype

text

Did the patient experience any long term toxicities of protocol treatment that has not yet been reported? (if yes, please complete form below)
Beschrijving

LateAdverseEventInd

Datatype

boolean

Late Toxicity Term
Beschrijving

CTCAdverseEventTerm

Datatype

text

Category Code*
Beschrijving

CTCAdverseEventCategory

Datatype

text

NCIC CTG use only Tox Code
Beschrijving

NCICCTGuseonlyToxCode

Datatype

text

Worst Severity/Grade* (0=None NA=Not Assessed * Code/grade according to Common Toxicity Criteria, Version 2.0)
Beschrijving

CTCAdverseEventGrade

Datatype

text

Relation to Protocol Therapy
Beschrijving

CTCAdverseEventAttributionCode

Datatype

text

COMMENTS
Beschrijving

Comments

Datatype

text

7. Comments
Beschrijving

7. Comments

8. Have You Attached Copies Of
Beschrijving

8. Have You Attached Copies Of

8. HAVE YOU ATTACHED COPIES OF (please _)
Beschrijving

HAVEYOUATTACHEDCOPIESOF

Datatype

text

9. Investigator Signature
Beschrijving

9. Investigator Signature

Signature of Responsible Investigator
Beschrijving

InvestigatorSignature

Datatype

text

Alias
NCI Thesaurus Property
C25678
UMLS 2011AA Property
C1519316
NCI Thesaurus ObjectClass
C17089
UMLS 2011AA ObjectClass
C0035173
Name of Clinical Research Associate
Beschrijving

PersonCompletingForm,LastName

Datatype

text

Date
Beschrijving

FormCompletionDate,Original

Datatype

date

Ccrr Module For Form 6 - Final Report
Beschrijving

Ccrr Module For Form 6 - Final Report

Person Completing Form, First Name
Beschrijving

PersonCompletingForm,FirstName

Datatype

text

Alias
NCI Thesaurus ObjectClass
C25190
UMLS 2011AA ObjectClass
C0027361
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
CTC Adverse Event Term, Other
Beschrijving

CTCAdverseEventTerm,Other

Datatype

text

Non-Protocol EGFR Inhibitor Ind
Beschrijving

Non-ProtocolEpidermalGrowthFactorReceptorTyrosineKinaseInhibitorAdministeredInd-3

Datatype

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
NCI Thesaurus ObjectClass
C25590
UMLS 2011AA ObjectClass
C1518384
NCI Thesaurus ObjectClass-2
C2167
UMLS 2011AA ObjectClass-2
C1443775
NCI Thesaurus Property
C25382
UMLS 2011AA Property
C1521801
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No Instruction available.

1 Formulieren
  1. StudyEvent: Form 6 - Final Report
    1. No Instruction available.
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
1. Patient Information
PatientStudyID,CoordinatingGroup
Item
Pt. Serial #
text
PatientMedicalRecordNumber
Item
Hospital #
text
Patient Initials
Item
Pt. Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
PatientStudyID,ParticipatingGroup
Item
Intergroup Patient Serial #
text
NCIInstitutionNumber
Item
Site #
text
PatientSocialSecurityNumber
Item
Patient's Social Security # (USA only)
float
InstitutionName
Item
Institution
text
RegisteredInvestigator
Item
Investigator
text
Item Group
2. Cause Of Death
DeathDocumentedDate
Item
Date of death
date
Item
Cause of Death
text
CL.1
Code List
Cause of Death
CL Item
Due To This Disease (NSCLC)
CL Item
Unknown (UNKNOWN)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
CL Item
Due To Protocol Treatment (protocol treatment complication)
CL Item
combination NSCLC and protocol treatment complication (combination NSCLC and protocol treatment complication)
CL Item
non-protocol treatment complication (non-protocol treatment complication)
CL Item
combination NSCLC and non-protocol treatment complication (combination NSCLC and non-protocol treatment complication)
CL Item
other primary malignancy (other primary malignancy)
CL Item
Due To Other Cause (other condition or circumstance)
OtherPrimaryMalignantNeoplasmPresentStatus
Item
other primary malignancy (specify & send report)
text
C17649 (NCI Thesaurus ObjectClass)
C0205394 (UMLS 2011AA ObjectClass)
C25251 (NCI Thesaurus ObjectClass-2)
C0205225 (UMLS 2011AA ObjectClass-2)
C9305 (NCI Thesaurus ObjectClass-3)
C0006826 (UMLS 2011AA ObjectClass-3)
C25626 (NCI Thesaurus Property)
C0150312 (UMLS 2011AA Property)
C25688 (NCI Thesaurus ValueDomain)
C0449438 (UMLS 2011AA ValueDomain)
NCICCTGuseonlycode
Item
NCIC CTG use only code
text
DeathReason,Specify
Item
Describe
text
Item
Status of NSCLC at Time of Death
text
CL.2
Code List
Status of NSCLC at Time of Death
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Unknown (Unknown)
Item Group
3. Autopsy
Item
Autopsy performed
text
CL.3
Code List
Autopsy performed
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (UNKNOWN)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
NCICCTGUseonly:Received
Item
NCIC CTG Use only: Received
text
Item Group
4. Other Malignancies Or Marrow Dysplasia
NewPrimaryCancerInd
Item
Have any other malignancies or myelodysplastic syndrome (MDS) been diagnosed?
boolean
NewPrimaryCancerDate
Item
Date of diagnosis
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
NewPrimarySite
Item
Site of new primary
text
NewPrimaryDetail
Item
Describe (An Adverse Event Report must be sent to NCIC CTG within 15 working days that diagnosis is known to the investigator. See protocol section 11.0 for details.)
text
Item Group
Ncic Ctg Use
NewPrimaryMalignancyType
Item
Malignancy Type
text
Item Group
Ncic Ctg Use Only
LoggedEntryInitials
Item
Logged
text
LoggedEntryDate
Item
Header
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
CoordinatorReviewInitials
Item
Study Coord
text
CoordinatorReviewDate
Item
Coordinator Review Date
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS CUI-1)
PhysicianReviewInitials
Item
Phy
text
DataEntryInitials
Item
Data Ent'd
text
DataVerificationInitials
Item
Verified
text
Item Group
5. Treatment Given Since Last Report To Ncic Ctg
Non-ProtocolTherapyInd
Item
Is the patient receiving any non-protocol cancer therapy not previously reported? (if yes, specify below)
boolean
Non-ProtocolHormonalTherapyInd
Item
Non-Protocol Hormonal Therapy? (include medical and surgical)
boolean
Non-ProtocolChemotherapyInd
Item
Non-Protocol Chemotherapy?
boolean
Non-ProtocolImmunotherapyInd
Item
Non-Protocol Immunotherapy?
boolean
Non-ProtocolBRMInd
Item
Non-Protocol Biologic Response Modifier?
boolean
Non-ProtocolHDC/ASCTInd
Item
Non-Protocol High Dose Chemotherapy/ Autologous Stem Cell Transplant?
boolean
Non-ProtocolRTInd
Item
Non-Protocol Radiation Therapy?
boolean
Non-protocolSurgeryPerformedInd-3
Item
Non-Protocol Surgery?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
C38000 (NCI Thesaurus Property)
C0884358 (UMLS 2011AA Property)
C15329 (NCI Thesaurus ObjectClass)
C0543467 (UMLS 2011AA ObjectClass)
C25590 (NCI Thesaurus ObjectClass-2)
C1518384 (UMLS 2011AA ObjectClass-2)
OtherTherapyInd
Item
Other Non-Protocol Therapy?
boolean
OtherNon-ProtocolTherapyName
Item
(specify)
text
Non-ProtocolFirstChemotherapyAgentName
Item
First ever chemotherapy or EGFR inhibitor given: (specify)
text
C25590 (NCI Thesaurus ObjectClass)
C1518384 (UMLS 2011AA ObjectClass)
C2167 (NCI Thesaurus ObjectClass-2)
C1443775 (UMLS 2011AA ObjectClass-2)
C25382 (NCI Thesaurus Property)
C1521801 (UMLS 2011AA Property)
Non-ProtocolFirstChemotherapyBeginDate
Item
Date started
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C25431 (NCI Thesaurus ValueDomain-2)
C0439659 (UMLS 2011AA ValueDomain-2)
Non-ProtocolSecondChemotherapyAgentName
Item
Second ever chemotherapy or EGFR inhibitor given: (specify)
text
C25590 (NCI Thesaurus ObjectClass)
C1518384 (UMLS 2011AA ObjectClass)
C2167 (NCI Thesaurus ObjectClass-2)
C1443775 (UMLS 2011AA ObjectClass-2)
C25382 (NCI Thesaurus Property)
C1521801 (UMLS 2011AA Property)
Non-ProtocolSecondChemotherapyBeginDate
Item
Date started(2nd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
Item Group
Ncic Ctg Use2
1stline
Item
1st line
text
2ndline
Item
2nd line
text
Item Group
6. Delayed Toxicity/adverse Event/intercurrent Illness
Item
NCIC CTG use only
text
CL.14
Code List
NCIC CTG use only
CL Item
Acute Toxicity Database (Acute toxicity database)
CL Item
Delayed Toxicity Database (Delayed toxicity database)
LateAdverseEventInd
Item
Did the patient experience any long term toxicities of protocol treatment that has not yet been reported? (if yes, please complete form below)
boolean
Item
Late Toxicity Term
text
CL.16
Code List
Late Toxicity Term
CL Item
Anorexia (Anorexia)
C2875 (NCI Thesaurus)
C0003123 (UMLS 2011AA)
CL Item
Chest Pain (Chest Pain (non-cardiac and non-pleuritic))
C38665 (NCI Thesaurus)
C0008031 (UMLS 2011AA)
CL Item
Constipation (CONSTIPATION)
C37930 (NCI Thesaurus)
C0009806 (UMLS 2011AA)
CL Item
Diarrhea For Patients Without Colostomy (Diarrhea (patients without colostomy))
CL Item
Dry Skin (Dry skin)
C0151908 (NCI Metathesaurus)
CL Item
Vomiting (Vomiting)
C3442 (NCI Thesaurus)
C0042963 (UMLS 2011AA)
CL Item
Fatigue (Fatigue (lethargy, malaise, asthenia))
C3036 (NCI Thesaurus)
C0015672 (UMLS 2011AA)
CL Item
Infection Without Neutropenia (Infection (without neutropenia))
CL Item
Nausea (Nausea)
C3258 (NCI Thesaurus)
C0027497 (UMLS 2011AA)
CL Item
Pruritus (Pruritus)
C3344 (NCI Thesaurus)
C0033774 (UMLS 2011AA)
CL Item
Rash/desquamation (Rash/Desquamation)
CL Item
Dyspnea (Dyspnea (shortness of breath))
C2998 (NCI Thesaurus)
C0013404 (UMLS 2011AA)
Item
Category Code*
text
CL.17
Code List
Category Code*
CL Item
Gastrointestinal (GASTROINTESTINAL)
C13359 (NCI Thesaurus)
C0521362 (UMLS 2011AA)
CL Item
Pain (Pain)
C3303 (NCI Thesaurus)
C0030193 (UMLS 2011AA)
CL Item
Infection (Infection)
C0021311 (NCI Metathesaurus)
CL Item
Pulmonary (PULMONARY)
C13304 (NCI Thesaurus)
C2709248 (UMLS 2011AA)
CL Item
Constitutional Symptoms (Constitutional Symptoms)
CL Item
Dermatology/skin (Dermatology/Skin)
NCICCTGuseonlyToxCode
Item
NCIC CTG use only Tox Code
text
CTCAdverseEventGrade
Item
Worst Severity/Grade* (0=None NA=Not Assessed * Code/grade according to Common Toxicity Criteria, Version 2.0)
text
Item
Relation to Protocol Therapy
text
CL.18
Code List
Relation to Protocol Therapy
CL Item
Unrelated (1=unrelated)
C25328 (NCI Thesaurus)
C0445356 (UMLS 2011AA)
CL Item
Unlikely (2=unlikely)
CL Item
Possibly (3=possible)
CL Item
Probably (4=probable)
CL Item
Definitely (5=definite)
Comments
Item
COMMENTS
text
Item Group
7. Comments
Item Group
8. Have You Attached Copies Of
Item
8. HAVE YOU ATTACHED COPIES OF (please _)
text
CL.19
Code List
8. HAVE YOU ATTACHED COPIES OF (please _)
CL Item
Autopsy Report (if applicable) (Autopsy Report (if applicable))
CL Item
Supporting documentation (if applicable) (Supporting documentation (if applicable))
Item Group
9. Investigator Signature
InvestigatorSignature
Item
Signature of Responsible Investigator
text
C25678 (NCI Thesaurus Property)
C1519316 (UMLS 2011AA Property)
C17089 (NCI Thesaurus ObjectClass)
C0035173 (UMLS 2011AA ObjectClass)
PersonCompletingForm,LastName
Item
Name of Clinical Research Associate
text
FormCompletionDate,Original
Item
Date
date
Item Group
Ccrr Module For Form 6 - Final Report
PersonCompletingForm,FirstName
Item
Person Completing Form, First Name
text
C25190 (NCI Thesaurus ObjectClass)
C0027361 (UMLS 2011AA ObjectClass)
C25364 (NCI Thesaurus Property)
C0600091 (UMLS 2011AA Property)
CTCAdverseEventTerm,Other
Item
CTC Adverse Event Term, Other
text
Non-ProtocolEpidermalGrowthFactorReceptorTyrosineKinaseInhibitorAdministeredInd-3
Item
Non-Protocol EGFR Inhibitor Ind
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
C25590 (NCI Thesaurus ObjectClass)
C1518384 (UMLS 2011AA ObjectClass)
C2167 (NCI Thesaurus ObjectClass-2)
C1443775 (UMLS 2011AA ObjectClass-2)
C25382 (NCI Thesaurus Property)
C1521801 (UMLS 2011AA Property)
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