ID

781

Beskrivning

CALGB: Follow-up Solid Tumor Evaluation Form Trastuzumab With or Without Tamoxifen in Treating Women With Progressive Stage IV Breast Cancer Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=A73D1896-B650-4751-E034-0003BA0B1A09

Länk

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=A73D1896-B650-4751-E034-0003BA0B1A09

Nyckelord

  1. 2012-08-26 2012-08-26 -
  2. 2015-07-08 2015-07-08 -
  3. 2015-07-08 2015-07-08 -
Uppladdad den

26 augusti 2012

DOI

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Licens

Creative Commons BY-NC 3.0 Legacy

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Breast Cancer NCT00053339 Response - CALGB: Follow-up Solid Tumor Evaluation Form - 2054391v3.0

INSTRUCTIONS: Complete and submit this form as required by the protocol. Information in the upper right box must be completed for this form to be accepted. Do not leave any entries blank. Enter -1 to indicate that an answer in unknown, unobtainable, not applicable, or not done. Retain a copy for your records and submit ORIGINAL to the CALGB Data Management Center.

Unnamed1
Beskrivning

Unnamed1

CALGB Form
Beskrivning

CALGBForm

Datatyp

text

CALGB Study No
Beskrivning

CALGBStudyNo

Datatyp

text

CALGB Patient ID
Beskrivning

CALGBPatientID

Datatyp

text

Amended data?
Beskrivning

AmendedDataInd

Datatyp

text

Alias
NCI Thesaurus ObjectClass
C25474
UMLS 2011AA ObjectClass
C1511726
NCI Thesaurus Property
C25416
UMLS 2011AA Property
C1691222
Unnamed2
Beskrivning

Unnamed2

Patient's Name
Beskrivning

Patient'sName

Datatyp

text

Participating Group
Beskrivning

ParticipatingGroup

Datatyp

text

Alias
NCI Thesaurus ObjectClass
C17005
UMLS 2011AA ObjectClass
C1257890
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
Patient Hospital Number
Beskrivning

PatientHospitalNumber

Datatyp

text

Participating Group Protocol No.
Beskrivning

ParticipatingGroupProtocolNo.

Datatyp

text

Main Member Institution/Adjunct
Beskrivning

AffiliateName

Datatyp

text

Participating Group Patient No.
Beskrivning

ParticipatingGroupPatientID

Datatyp

text

Reporting Period
Beskrivning

Reporting Period

From
Beskrivning

IntervalReportFromDate

Datatyp

date

To
Beskrivning

IntervalReportToDate

Datatyp

date

Target Lesion(s) Follow-up Evaluation
Beskrivning

Target Lesion(s) Follow-up Evaluation

Lesion Number (unnamed)
Beskrivning

Lesion,ReferenceNumber

Datatyp

double

Site
Beskrivning

Lesion,AnatomicSite,New

Datatyp

text

Date of Evaluation
Beskrivning

AssessmentDate

Datatyp

date

Method of Evaluation
Beskrivning

AssessmentType

Datatyp

text

If other, specify (method of evaluation)
Beskrivning

AssessmentType,Specify

Datatyp

text

Longest Diameter (cm)
Beskrivning

Lesion,TumorDiameter

Datatyp

double

Alias
NCI Thesaurus ValueDomain
C25209
UMLS 2011AA ValueDomain
C0242485
Sum of Longest Diameteres of All Target lesions (cm)
Beskrivning

Lesion,Diameter,LongestSum

Datatyp

double

Response Status at this assessment (Target Lesion)
Beskrivning

ResponseCriteria

Datatyp

text

Non-target Lesion(s) Follow-up Evaluation
Beskrivning

Non-target Lesion(s) Follow-up Evaluation

Are there any non-target lesions?
Beskrivning

NontargetLesionInd

Datatyp

text

Lesion Number (unnamed)
Beskrivning

Lesion,ReferenceNumber

Datatyp

double

Site
Beskrivning

Lesion,AnatomicSite,Nontarget

Datatyp

text

Date of Evaluation
Beskrivning

AssessmentDate

Datatyp

date

Method of Evaluation
Beskrivning

AssessmentType

Datatyp

text

If other, specify (method of evaluation)
Beskrivning

AssessmentType,Specify

Datatyp

text

Response Status at this assessment (Target Lesion)
Beskrivning

ResponseCriteria

Datatyp

text

New Lesion(s) At Follow-up Evaluation
Beskrivning

New Lesion(s) At Follow-up Evaluation

Was the appearance of any new lesions documented since the baseline evaluation?
Beskrivning

NewLesionInd

Datatyp

text

Lesion Number (unnamed)
Beskrivning

Lesion,ReferenceNumber

Datatyp

double

Site
Beskrivning

Lesion,AnatomicSite,New

Datatyp

text

Date of Evaluation
Beskrivning

AssessmentDate

Datatyp

date

Method of Evaluation
Beskrivning

AssessmentType

Datatyp

text

If other, specify (method of evaluation)
Beskrivning

AssessmentType,Specify

Datatyp

text

Completed by
Beskrivning

PersonCompletingForm,FirstName

Datatyp

text

Alias
NCI Thesaurus ObjectClass
C25190
UMLS 2011AA ObjectClass
C0027361
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
Date completed
Beskrivning

FormCompletionDate,Original

Datatyp

date

Ccrr Module For Calgb: Follow-up Solid Tumor Evaluation Form
Beskrivning

Ccrr Module For Calgb: Follow-up Solid Tumor Evaluation Form

Similar models

INSTRUCTIONS: Complete and submit this form as required by the protocol. Information in the upper right box must be completed for this form to be accepted. Do not leave any entries blank. Enter -1 to indicate that an answer in unknown, unobtainable, not applicable, or not done. Retain a copy for your records and submit ORIGINAL to the CALGB Data Management Center.

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Unnamed1
CALGBForm
Item
CALGB Form
text
CALGBStudyNo
Item
CALGB Study No
text
CALGBPatientID
Item
CALGB Patient ID
text
Item
Amended data?
text
C25474 (NCI Thesaurus ObjectClass)
C1511726 (UMLS 2011AA ObjectClass)
C25416 (NCI Thesaurus Property)
C1691222 (UMLS 2011AA Property)
Code List
Amended data?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
Item Group
Unnamed2
Patient'sName
Item
Patient's Name
text
ParticipatingGroup
Item
Participating Group
text
C17005 (NCI Thesaurus ObjectClass)
C1257890 (UMLS 2011AA ObjectClass)
C25364 (NCI Thesaurus Property)
C0600091 (UMLS 2011AA Property)
PatientHospitalNumber
Item
Patient Hospital Number
text
ParticipatingGroupProtocolNo.
Item
Participating Group Protocol No.
text
AffiliateName
Item
Main Member Institution/Adjunct
text
ParticipatingGroupPatientID
Item
Participating Group Patient No.
text
Item Group
Reporting Period
IntervalReportFromDate
Item
From
date
IntervalReportToDate
Item
To
date
Item Group
Target Lesion(s) Follow-up Evaluation
Lesion,ReferenceNumber
Item
Lesion Number (unnamed)
double
Lesion,AnatomicSite,New
Item
Site
text
AssessmentDate
Item
Date of Evaluation
date
Item
Method of Evaluation
text
Code List
Method of Evaluation
CL Item
Clinical Examination (clinical examination)
CL Item
Chest X-ray (chest x-ray)
CL Item
Ct Scan (CT scan)
CL Item
Spiral Ct Scan (Spiral CT scan)
CL Item
Mri (MRI (NMR))
CL Item
Ultrasound (Ultrasound)
C64384 (NCI Thesaurus)
C1456803 (UMLS 2011AA)
CL Item
Bone Scan (Bone scan)
C17646 (NCI Thesaurus)
C0203668 (UMLS 2011AA)
CL Item
Not Evaluated (not evaluated)
CL Item
Other (other)
C17649 (NCI Thesaurus)
C0205394 (UMLS 2011AA)
Item
If other, specify (method of evaluation)
text
Code List
If other, specify (method of evaluation)
CL Item
complete response (CR) (complete response (CR))
CL Item
partial response (PR) (partial response (PR))
CL Item
stable disease (SD) (stable disease (SD))
CL Item
progressive disease (PD) (progressive disease (PD))
CL Item
insufficient evaluation to determine response status (insufficient evaluation to determine response status)
Lesion,TumorDiameter
Item
Longest Diameter (cm)
double
C25209 (NCI Thesaurus ValueDomain)
C0242485 (UMLS 2011AA ValueDomain)
Lesion,Diameter,LongestSum
Item
Sum of Longest Diameteres of All Target lesions (cm)
double
Item
Response Status at this assessment (Target Lesion)
text
Code List
Response Status at this assessment (Target Lesion)
CL Item
Complete Response (complete response (CR))
CL Item
Partial Response (partial response (PR))
C18212 (NCI Thesaurus)
CL Item
Incomplete Response Or Stable Disesase (stable disease (SD))
CL Item
Partial Response; At Least A 30% Decrease In The Sum Of Ld Of Target Lesions Taking As Reference The Baseline Sum Ld (progressive disease (PD))
CL Item
Insufficient Evaluation (insufficient evaluation to determine response status)
Item Group
Non-target Lesion(s) Follow-up Evaluation
Item
Are there any non-target lesions?
text
Code List
Are there any non-target lesions?
CL Item
No (no)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
Lesion,ReferenceNumber
Item
Lesion Number (unnamed)
double
Lesion,AnatomicSite,Nontarget
Item
Site
text
AssessmentDate
Item
Date of Evaluation
date
Item
Method of Evaluation
text
Code List
Method of Evaluation
CL Item
Clinical Examination (clinical examination)
CL Item
Chest X-ray (chest x-ray)
CL Item
Ct Scan (CT scan)
CL Item
Spiral Ct Scan (Spiral CT scan)
CL Item
Mri (MRI (NMR))
CL Item
Ultrasound (Ultrasound)
C64384 (NCI Thesaurus)
C1456803 (UMLS 2011AA)
CL Item
Bone Scan (Bone scan)
C17646 (NCI Thesaurus)
C0203668 (UMLS 2011AA)
CL Item
Not Evaluated (not evaluated)
CL Item
Other (other)
C17649 (NCI Thesaurus)
C0205394 (UMLS 2011AA)
Item
If other, specify (method of evaluation)
text
Code List
If other, specify (method of evaluation)
CL Item
complete response (CR) (complete response (CR))
CL Item
partial response (PR) (partial response (PR))
CL Item
stable disease (SD) (stable disease (SD))
CL Item
progressive disease (PD) (progressive disease (PD))
CL Item
insufficient evaluation to determine response status (insufficient evaluation to determine response status)
Item
Response Status at this assessment (Target Lesion)
text
Code List
Response Status at this assessment (Target Lesion)
CL Item
Complete Response (complete response (CR))
CL Item
Partial Response (partial response (PR))
C18212 (NCI Thesaurus)
CL Item
Incomplete Response Or Stable Disesase (stable disease (SD))
CL Item
Partial Response; At Least A 30% Decrease In The Sum Of Ld Of Target Lesions Taking As Reference The Baseline Sum Ld (progressive disease (PD))
CL Item
Insufficient Evaluation (insufficient evaluation to determine response status)
Item Group
New Lesion(s) At Follow-up Evaluation
Item
Was the appearance of any new lesions documented since the baseline evaluation?
text
Code List
Was the appearance of any new lesions documented since the baseline evaluation?
CL Item
No (no)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
Lesion,ReferenceNumber
Item
Lesion Number (unnamed)
double
Lesion,AnatomicSite,New
Item
Site
text
AssessmentDate
Item
Date of Evaluation
date
Item
Method of Evaluation
text
Code List
Method of Evaluation
CL Item
Clinical Examination (clinical examination)
CL Item
Chest X-ray (chest x-ray)
CL Item
Ct Scan (CT scan)
CL Item
Spiral Ct Scan (Spiral CT scan)
CL Item
Mri (MRI (NMR))
CL Item
Ultrasound (Ultrasound)
C64384 (NCI Thesaurus)
C1456803 (UMLS 2011AA)
CL Item
Bone Scan (Bone scan)
C17646 (NCI Thesaurus)
C0203668 (UMLS 2011AA)
CL Item
Not Evaluated (not evaluated)
CL Item
Other (other)
C17649 (NCI Thesaurus)
C0205394 (UMLS 2011AA)
Item
If other, specify (method of evaluation)
text
Code List
If other, specify (method of evaluation)
CL Item
complete response (CR) (complete response (CR))
CL Item
partial response (PR) (partial response (PR))
CL Item
stable disease (SD) (stable disease (SD))
CL Item
progressive disease (PD) (progressive disease (PD))
CL Item
insufficient evaluation to determine response status (insufficient evaluation to determine response status)
PersonCompletingForm,FirstName
Item
Completed by
text
C25190 (NCI Thesaurus ObjectClass)
C0027361 (UMLS 2011AA ObjectClass)
C25364 (NCI Thesaurus Property)
C0600091 (UMLS 2011AA Property)
FormCompletionDate,Original
Item
Date completed
date
Item Group
Ccrr Module For Calgb: Follow-up Solid Tumor Evaluation Form

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