ID

9208

Descrizione

Form 1 - Eligibility Checklist and Initial Evaluation 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=A7422C05-78BD-5678-E034-0003BA0B1A09

collegamento

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=A7422C05-78BD-5678-E034-0003BA0B1A09

Keywords

  1. 19/09/12 19/09/12 -
  2. 09/01/15 09/01/15 - Martin Dugas
  3. 22/03/15 22/03/15 - Martin Dugas
  4. 20/09/21 20/09/21 -
Caricato su

9 gennaio 2015

DOI

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Licenza

Creative Commons BY-NC 3.0 Legacy

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Lung Cancer NCT00049543 On-Study - Form 1 - Eligibility Checklist and Initial Evaluation - 2055363v3.0

No Instruction available.

  1. StudyEvent: Form 1 - Eligibility Checklist and Initial Evaluation
    1. No Instruction available.
Patient Information
Descrizione

Patient Information

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Gender
Descrizione

PatientGender

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25372
UMLS 2011AA ValueDomain
C0683312
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C17357
UMLS 2011AA Property
C0079399
Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Patient Medical Record Number
Descrizione

PatientMedicalRecordNumber

Tipo di dati

text

Institution Name
Descrizione

InstitutionName

Tipo di dati

text

Registered Investigator (NCI Investigator #)
Descrizione

RegisteredInvestigator

Tipo di dati

text

Patient's Date of Birth (yyyy mmm dd)
Descrizione

PatientBirthDate

Tipo di dati

date

Alias
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C25275
UMLS 2011AA Property
C2745955
Patient Race (check _ all that apply)
Descrizione

PatientRace

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C17049
UMLS 2011AA Property
C0034510
Patient Ethnicity (check _ one only)
Descrizione

PatientEthnicity

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C17049
UMLS 2011AA Property
C0034510
Payment Method (check _ one USA only)
Descrizione

PaymentMethod

Tipo di dati

text

IRB/REB Approval Date (yyyy mmm dd)
Descrizione

IRBApprovalDate

Tipo di dati

date

Alias
NCI Thesaurus ObjectClass
C25320
UMLS 2011AA ObjectClass
C1507394
NCI Thesaurus Property
C25425
UMLS 2011AA Property
C0205540
Projected Start Date of Treatment (yyyy mmm dd)
Descrizione

ProjectedTreatmentBeginDate

Tipo di dati

date

Ncic Ctg Use Only
Descrizione

Ncic Ctg Use Only

Logged
Descrizione

LoggedEntryInitials

Tipo di dati

text

Unnamed (Logged Date)
Descrizione

LoggedEntryDate

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
RA
Descrizione

RegulatoryAffairsReviewInitials

Tipo di dati

text

Unnamed (RA Date)
Descrizione

RegulatoryAffairsReviewDate

Tipo di dati

date

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

CoordinatorReviewInitials

Tipo di dati

text

Unnamed (Coord Date)
Descrizione

CoordinatorReviewDate

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
Phy
Descrizione

PhysicianReviewInitials

Tipo di dati

text

Data Ent'd
Descrizione

DataEntryInitials

Tipo di dati

text

Verified
Descrizione

DataVerificationInitials

Tipo di dati

text

Header
Descrizione

Header

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Eligibility Checklist
Descrizione

Eligibility Checklist

Patient has histological proof of a primary non-small cell lung cancer (bronchoalveolar carcinomas presenting as a discrete radiological mass or node are eligible. Please specify)
Descrizione

LungCancerProofInd

Tipo di dati

text

Histologic Type
Descrizione

HistologicType

Tipo di dati

text

Post operatively the patient had a pathological stage of
Descrizione

PathologicStagePostoperativeInd

Tipo di dati

text

Stage
Descrizione

StageGrouping

Tipo di dati

text

Adequate Lymph Node sampling was performed (see section 5.1.1.4 of the protocol)
Descrizione

LymphNodeAdequateSamplingInd

Tipo di dati

text

Please specify the extent of lymph node sampling (check _ one only)
Descrizione

LymphNodeSamplingExtent

Tipo di dati

text

Nodes >= 1.5 cm were sampled (specify)
Descrizione

LymphNodeSamplingExtentLargeSite

Tipo di dati

text

Other (specify)
Descrizione

LymphNodeSamplingOtherExtent

Tipo di dati

text

Surgery consisted of lobectomy, sleeve resection, bilobectomy or pneumonectomy. (segmentectomy or wedge resection only is not eligible)
Descrizione

LungCarcinomaSurgicalProcedureTherapyInd-3

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
NCI Thesaurus Property
C15329
UMLS 2011AA Property
C0543467
NCI Thesaurus ObjectClass
C4878
UMLS 2011AA ObjectClass
C0684249
Patient has had all gross disease surgically removed.
Descrizione

GrossDiseaseRemovedInd

Tipo di dati

text

All surgical margins of resection are negative for tumour.
Descrizione

SurgicalResectionNegativeMarginIndicator

Tipo di dati

text

No more than 16 weeks may have elapsed between surgical resection and randomization.
Descrizione

MaximumTimePostSurgeryIndicator

Tipo di dati

text

Surgery Date (yyyy mmm dd)
Descrizione

SurgeryDate

Tipo di dati

date

A representative formalin fixed paraffin block of tumour tissue must be submitted at the request of the central tumour bank in order that specific EGFR correlative marker assays may be conducted.
Descrizione

TumorBlocksSentIndicator

Tipo di dati

text

Performance Status is <= 2. (see protocol appendix II)
Descrizione

MinimumPerformanceStatusIndicator

Tipo di dati

text

Required hematologic and biochemistry investigations done within 14 days prior to randomization, including:
Descrizione

RequiredHematology14DaysIndicator

Tipo di dati

text

Date Hematology (Blood) Sample Obtained (yyyy mmm dd)
Descrizione

Lab,Hematology,SampleCollectionDate

Tipo di dati

date

Peripheral WBC Count (1000/uL or x 10 9/L)
Descrizione

Lab,Hematology,WBC

Tipo di dati

float

Peripheral neutrophil count (>= 1.5 x 10 9/L or >= 1500/uL; Value)
Descrizione

Lab,Hematology,NeutrophilCount

Tipo di dati

float

Peripheral Platelet Count (1000/uL or x 10 9/L)
Descrizione

Lab,Hematology,Platelets

Tipo di dati

float

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Ncic Ctg Use Only
Descrizione

Ncic Ctg Use Only

Patient Gender
Descrizione

PatientGender

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25372
UMLS 2011AA ValueDomain
C0683312
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C17357
UMLS 2011AA Property
C0079399
Histologic Type
Descrizione

HistologicType

Tipo di dati

text

Stage
Descrizione

StageGrouping

Tipo di dati

text

Unnamed2
Descrizione

Unnamed2

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Eligibility Checklist Continued
Descrizione

Eligibility Checklist Continued

Specimen Collection Date (Biochemistry, yyyy mmm dd)
Descrizione

SpecimenCollectionDate

Tipo di dati

date

Required biochemistry investigations done within 14 days prior to randomization, and greater than 8 days following surgical resection, including
Descrizione

RequiredBiochemistry14DaysIndicator

Tipo di dati

text

Bilirubin (uL or 10 9/L)
Descrizione

Lab,Hepatic,Bilirubin

Tipo di dati

float

Bilirubin ULN
Descrizione

HepaticBilirubinLabUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C305
UMLS 2011AA Property-2
C0005437
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Date Adjuvant Radiation Therapy Ended (yyyy mmm dd)
Descrizione

AdjuvantRTEndDate

Tipo di dati

date

SGOT (AST) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
Descrizione

Lab,Hepatic,SGOT

Tipo di dati

float

SGOT (AST) ULN
Descrizione

SGOTLabUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
SGPT (ALT) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
Descrizione

Lab,Hepatic,SGPT

Tipo di dati

float

SGPT (ALT) ULN
Descrizione

SGPTLabUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Alkaline Phosphatase (U/L; * If alkaline phosphatase is greater than ULN but <= 2.5 X ULN, ultrasound or CT scan of abdomen and bone scan MUST be done prior to randomization)
Descrizione

Lab,Hepatic,AlkalinePhosphatase

Tipo di dati

float

Alkaline Phosphatase ULN
Descrizione

Alkaline Phosphatase ULN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS CUI-1
C0151420
NCI Thesaurus Property
C20200
NCI Thesaurus Property-2
C16276
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain-2
C25706
Creatinine (mg/dl or umol/L)
Descrizione

Lab,Renal,Creatinine

Tipo di dati

float

Creatinine ULN
Descrizione

Creatinine, serum ULN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS CUI-1
C0201976
NCI Thesaurus Property
C20200
UMLS CUI-2
C1519815
NCI Thesaurus Property-2
C399
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain-2
C25706
Patient's age is >= 18 years (lower age limit subject to local policy regarding age at which patient may sign own consent)
Descrizione

PatientAge18YearsIndicator

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38147
UMLS 2011AA ValueDomain
C1512698
Patient has had a chest x-ray within 14 days of randomization.
Descrizione

PrestudyChestX-RayIndicator

Tipo di dati

text

Date of chest x-ray (yyyy mmm dd)
Descrizione

ChestX-RayAssessmentDate

Tipo di dati

date

Patient has had a CT or MRI scan of the chest within 42 days prior to surgery.
Descrizione

PrestudyChestCTIndicator

Tipo di dati

text

Date of CT or MRI of chest (yyyy mmm dd)
Descrizione

ChestComputedTomographyMagneticResonanceImagingDiagnosticImagingPerformedDate

Tipo di dati

date

Alias
NCI Thesaurus ObjectClass
C16502
UMLS 2011AA ObjectClass
C0011923
NCI Thesaurus ObjectClass-2
C17204
UMLS 2011AA ObjectClass-2
C0040405
NCI Thesaurus ObjectClass-3
C25389
UMLS 2011AA ObjectClass-3
C0817096
NCI Thesaurus ObjectClass-4
C16809
UMLS 2011AA ObjectClass-4
C0024485
NCI Thesaurus Property
C38000
UMLS 2011AA Property
C0884358
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
Patient has had an EKG within 14 days prior to randomization.
Descrizione

PrestudyEKGIndicator

Tipo di dati

text

Date of EKG (yyyy mmm dd)
Descrizione

DiagnosticElectrocardiogramPerformedDate

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
NCI Thesaurus Property
C38000
UMLS 2011AA Property
C0884358
NCI Thesaurus ObjectClass
C25482
UMLS 2011AA ObjectClass
C0348026
NCI Metathesaurus ObjectClass
C0013798
Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Men and women of childbearing age will use adequate contraception.
Descrizione

EligibilityContraceptionIndicator

Tipo di dati

text

Patient has received post-operative radiation. (If patient has received post-operative radiation therapy)
Descrizione

PrestudyPostoperativeRadiationTherapyIndicator

Tipo di dati

boolean

Radiation therapy has been completed at least three weeks prior to randomization
Descrizione

PrestudyRadiationTherapyCompleteIndicator

Tipo di dati

text

The patient has recovered from all radiation therapy related toxicity
Descrizione

RadiationTherapyToxicityRecoveryIndicator

Tipo di dati

text

Informed consent has been signed and dated by patient.
Descrizione

PatientConsentSignedIndicator

Tipo di dati

text

Date informed consent signed (yyyy mmm dd)
Descrizione

InformedConsentDateSigned

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
Patient accessible for treatment and follow-up.
Descrizione

PatientTherapeuticProcedureFollow-upEligibilityDeterminationInd-2

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C16033
UMLS 2011AA Property
C1522577
NCI Thesaurus Property-2
C49236
UMLS 2011AA Property-2
C0087111
NCI Thesaurus Property-3
C25171
UMLS 2011AA Property-3
C0013893
NCI Thesaurus ValueDomain
C38147
UMLS 2011AA ValueDomain
C1512698
Initiation of protocol therapy will begin within 10 working days of randomization.
Descrizione

TreatmentRequirementBeginIndicator

Tipo di dati

text

Ncic Ctg Use Only2
Descrizione

Ncic Ctg Use Only2

Post-operative radiotherapy
Descrizione

PostoperativeRadiotherapyStatus

Tipo di dati

text

Unnamed3
Descrizione

Unnamed3

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Eligibility Checklist Continued2
Descrizione

Eligibility Checklist Continued2

No other prior or concurrent malignancies within the last 5 years, except as specified in protocol section 5.2.1.
Descrizione

NoOtherMalignancyIndicator

Tipo di dati

text

No combination of small cell and non-small cell carcinomas or a pulmonary carcinoid tumour.
Descrizione

NoCombinationLungCancerIndicator

Tipo di dati

text

No more than one discrete area of apparent primary cancer (even if within same lobe, T4, IIIB are ineligible)
Descrizione

OneDiscretePrimaryCancerIndicator

Tipo di dati

text

No clinically significant or untreated ophthalmologic or gastrointestinal conditions.
Descrizione

NoOphthalmologicGastrointestinalDiseaseIndicator

Tipo di dati

text

No active pathological condition that would render the protocol treatment dangerous. (see protocol section 5.2.5 )
Descrizione

NoPathologicRiskConditionIndicator

Tipo di dati

text

No history of psychiatric or neurological disorder that would make the obtainment of informed consent problematic, or that would limit compliance with study requirements.
Descrizione

NoPsychiatricImpairmentHistoryIndicator

Tipo di dati

text

Patient, if female, is not pregnant or breast feeding.
Descrizione

FemalePatientNotPregnantIndicator

Tipo di dati

text

No prior adjuvant or neoadjuvant chemotherapy or immunotherapy for NSCLC. (limited low dose preoperative radiation therapy or endobronchial brachytherapy or laser therapy for short term control of hemoptysis or lobar obstruction is permitted, however full dose, pre-operative radiotherapy of curative intent is cause for exclusion )
Descrizione

NoPriorLungChemotherapyIndicator

Tipo di dati

text

No history of allergic reactions to compounds of similar chemical or biologic composition to IRESSA.
Descrizione

NoAgentAllergyHistoryIndicator

Tipo di dati

text

Patient does not take drugs which induce CYP3A4 enzymes, e.g., phenytoin, carbamazepine, barbiturates, rifampicin or St John's Wort.
Descrizione

NoCYP3A4EnzymeMedicationsIndicator

Tipo di dati

text

Adequate healing from previous oncologic or other major surgery has occurred.
Descrizione

AdequateSurgicalHealingIndicator

Tipo di dati

text

Randomization
Descrizione

Randomization

Randomization Date (yyyy mmm dd)
Descrizione

RandomizationDate

Tipo di dati

date

Investigator Signature
Descrizione

InvestigatorSignature

Tipo di dati

text

Alias
NCI Thesaurus Property
C25678
UMLS 2011AA Property
C1519316
NCI Thesaurus ObjectClass
C17089
UMLS 2011AA ObjectClass
C0035173
Person Completing Form, Last Name
Descrizione

PersonCompletingForm,LastName

Tipo di dati

text

Date of Investigator Signature (yyyy mmm dd)
Descrizione

InvestigatorSignatureDate

Tipo di dati

date

Person Completing Form, First Name
Descrizione

PersonCompletingForm,FirstName

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C25190
UMLS 2011AA ObjectClass
C0027361
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
Form Completion Date, Original (yyyy mmm dd)
Descrizione

FormCompletionDate,Original

Tipo di dati

date

Unnamed4
Descrizione

Unnamed4

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
History And Physical Exam
Descrizione

History And Physical Exam

Is patient currently smoking?
Descrizione

PatientCurrentSmokerIndicator

Tipo di dati

text

Date of evaluation (yyyy mmm dd)
Descrizione

AssessmentDate

Tipo di dati

date

Has previously been a smoker?
Descrizione

PatientPreviousSmokerIndicator

Tipo di dati

text

Performance Status (check _ one)
Descrizione

PerformanceStatus

Tipo di dati

text

Patient Height (cm)
Descrizione

PatientHeight

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C25347
UMLS 2011AA Property
C0489786
Patient Weight (kg)
Descrizione

PatientWeight

Tipo di dati

float

Investigations
Descrizione

Investigations

Imaging Site
Descrizione

DiagnosticImagingAnatomicSite

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C13717
UMLS 2011AA ValueDomain
C1515974
NCI Thesaurus Property
C25341
UMLS 2011AA Property
C0450429
NCI Thesaurus ObjectClass
C16502
UMLS 2011AA ObjectClass
C0011923
NCI Thesaurus Property-2
C25421
UMLS 2011AA Property-2
C0002808
Method of Evaluation
Descrizione

AssessmentType

Tipo di dati

text

Date of evaluation (yyyy mmm dd)
Descrizione

AssessmentDate

Tipo di dati

date

Pregnancy test
Descrizione

PregnancyTestResult

Tipo di dati

text

Unnamed5
Descrizione

Unnamed5

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Baseline Hematology/biochemistry Values
Descrizione

Baseline Hematology/biochemistry Values

Hemoglobin (g/dl or g/L)
Descrizione

Lab,Hematology,Hemoglobin

Tipo di dati

float

Peripheral Neutrophils (%)
Descrizione

Lab,Hematology,Neutrophils,CellPercentage

Tipo di dati

float

Date Hematology (Blood) Sample Obtained (yyyy mmm dd)
Descrizione

Lab,Hematology,SampleCollectionDate

Tipo di dati

date

Peripheral WBC Count (1000/uL or x 10 9/L)
Descrizione

Lab,Hematology,WBC

Tipo di dati

float

Peripheral Platelet Count (1000/uL or x 10 9/L)
Descrizione

Lab,Hematology,Platelets

Tipo di dati

float

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Biochemistry
Descrizione

Biochemistry

Specimen Collection Date (Biochemistry, yyyy mmm dd)
Descrizione

SpecimenCollectionDate

Tipo di dati

date

Bilirubin (uL or 10 9/L)
Descrizione

Lab,Hepatic,Bilirubin

Tipo di dati

float

Bilirubin ULN
Descrizione

HepaticBilirubinLabUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C305
UMLS 2011AA Property-2
C0005437
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
SGOT (AST) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
Descrizione

Lab,Hepatic,SGOT

Tipo di dati

float

SGOT (AST) ULN
Descrizione

SGOTLabUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
SGPT (ALT) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
Descrizione

Lab,Hepatic,SGPT

Tipo di dati

float

SGPT (ALT) ULN
Descrizione

SGPTLabUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Alkaline Phosphatase (U/L; * If alkaline phosphatase is greater than ULN but <= 2.5 X ULN, ultrasound or CT scan of abdomen and bone scan MUST be done prior to randomization)
Descrizione

Lab,Hepatic,AlkalinePhosphatase

Tipo di dati

float

Alkaline Phosphatase ULN
Descrizione

Alkaline Phosphatase ULN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS CUI-1
C0151420
NCI Thesaurus Property
C20200
NCI Thesaurus Property-2
C16276
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain-2
C25706
Lactate Dehydrogenase (LDH) (U/L)
Descrizione

Lab,Chemistry,LactateDehydrogenase

Tipo di dati

float

Lactate Dehydrogenase ULN
Descrizione

Lab,Chemistry,LactateDehydrogenase,ULN

Tipo di dati

float

Creatinine (mg/dl or umol/L)
Descrizione

Lab,Renal,Creatinine

Tipo di dati

float

Creatinine ULN
Descrizione

Creatinine, serum ULN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS CUI-1
C0201976
NCI Thesaurus Property
C20200
UMLS CUI-2
C1519815
NCI Thesaurus Property-2
C399
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain-2
C25706
BUN (mg/dl or umol/L)
Descrizione

Lab,Renal,BUN

Tipo di dati

float

BUN ULN
Descrizione

LaboratoryProcedureBloodUreaNitrogenResultUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C61019
UMLS 2011AA Property-2
C0005845
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Potassium (K) (mEq/L)
Descrizione

Lab,Electrolytes,Potassium

Tipo di dati

float

Potassium LLN
Descrizione

LaboratoryProcedurePotassiumElectrolytesOutcomeLowerLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C464
UMLS 2011AA Property-2
C0013832
NCI Thesaurus Property-3
C765
UMLS 2011AA Property-3
C0032821
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25555
UMLS 2011AA ValueDomain-2
C1518030
Potassium ULN
Descrizione

LaboratoryProcedurePotassiumElectrolytesOutcomeUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C464
UMLS 2011AA Property-2
C0013832
NCI Thesaurus Property-3
C765
UMLS 2011AA Property-3
C0032821
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Sodium (Na) (mmol/L)
Descrizione

Lab,Electrolytes,Sodium

Tipo di dati

float

Sodium LLN
Descrizione

LaboratoryProcedureSodiumElectrolytesOutcomeLowerLimitofNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C830
UMLS 2011AA Property-2
C0037473
NCI Thesaurus Property-3
C464
UMLS 2011AA Property-3
C0013832
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25555
UMLS 2011AA ValueDomain-2
C1518030
Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Sodium ULN
Descrizione

LaboratoryProcedureSodiumElectrolytesOutcomeUpperLimitofNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C830
UMLS 2011AA Property-2
C0037473
NCI Thesaurus Property-3
C464
UMLS 2011AA Property-3
C0013832
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Chloride (Cl) (mEq/L)
Descrizione

Lab,Electrolytes,Chloride

Tipo di dati

float

Chloride LLN
Descrizione

LaboratoryProcedureChlorideIonElectrolytesOutcomeLowerLimitofNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C464
UMLS 2011AA Property-2
C0013832
NCI Thesaurus Property-3
C1741
UMLS 2011AA Property-3
C0596019
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25555
UMLS 2011AA ValueDomain-2
C1518030
Chloride ULN
Descrizione

LaboratoryProcedureChlorideIonElectrolytesOutcomeUpperLimitofNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C464
UMLS 2011AA Property-2
C0013832
NCI Thesaurus Property-3
C1741
UMLS 2011AA Property-3
C0596019
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Calcium (Ca) (mg/dL or umol/L)
Descrizione

Lab,Electrolytes,Calcium

Tipo di dati

float

Calcium LLN
Descrizione

LaboratoryProcedureCalciumElectrolytesOutcomeLowerLimitofNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C331
UMLS 2011AA Property
C0006675
NCI Thesaurus Property-2
C20200
UMLS 2011AA Property-2
C1274040
NCI Thesaurus Property-3
C464
UMLS 2011AA Property-3
C0013832
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25555
UMLS 2011AA ValueDomain-2
C1518030
Calcium ULN
Descrizione

LaboratoryProcedureCalciumElectrolytesOutcomeUpperLimitofNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C331
UMLS 2011AA Property
C0006675
NCI Thesaurus Property-2
C20200
UMLS 2011AA Property-2
C1274040
NCI Thesaurus Property-3
C464
UMLS 2011AA Property-3
C0013832
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Albumin (g/dl or g/L)
Descrizione

Chemistry,BloodAlbumin

Tipo di dati

float

Albumin LLN
Descrizione

LaboratoryProcedureAlbuminResultLowerLimitofNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C214
UMLS 2011AA Property-2
C0001924
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25555
UMLS 2011AA ValueDomain-2
C1518030
Albumin ULN
Descrizione

LaboratoryProcedureAlbuminResultUpperLimitNormalValue

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
UMLS 2011AA ObjectClass
C0022885
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
NCI Thesaurus Property-2
C214
UMLS 2011AA Property-2
C0001924
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain-2
C25706
UMLS 2011AA ValueDomain-2
C1519815
Unnamed6
Descrizione

Unnamed6

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Disease History/prior Treatment
Descrizione

Disease History/prior Treatment

Primary Surgery Date (yyyy mmm dd)
Descrizione

PrimarySurgeryDate

Tipo di dati

date

N Stage, Pathologic (check _ one)
Descrizione

NStage,Pathologic

Tipo di dati

text

Histologic Type
Descrizione

HistologicType

Tipo di dati

text

T Stage, Pathologic (check _ one)
Descrizione

TStage,Pathologic

Tipo di dati

text

Stage Grouping, Pathologic
Descrizione

StageGrouping,Pathologic

Tipo di dati

text

Specify other histologic type
Descrizione

HistologicType,OtherName

Tipo di dati

text

Histologic Grade (WHO)
Descrizione

HistologicGrade

Tipo di dati

text

Is there vascular invasion?
Descrizione

VascularInvasionInd

Tipo di dati

text

Is the parietal pleural margin involved?
Descrizione

ParietalPleuralMarginInvolvedInd

Tipo di dati

text

Was lymph node sampling done?
Descrizione

LymphNodeSamplingInd

Tipo di dati

text

Number of Lymph Nodes Examined (If yes,)
Descrizione

LymphNode(s)ExaminedNumber

Tipo di dati

float

Alias
NCI Thesaurus Property
C25500
UMLS 2011AA Property
C0332128
NCI Thesaurus ObjectClass
C12745
UMLS 2011AA ObjectClass
C0024204
Number of Positive Lymph Nodes
Descrizione

LymphNode(s)PositiveNumber

Tipo di dati

float

Alias
NCI Thesaurus Property
C25246
UMLS 2011AA Property
C1446409
NCI Thesaurus ObjectClass
C12745
UMLS 2011AA ObjectClass
C0024204
Lymph Nodes Type (Station)
Descrizione

LymphNodesType

Tipo di dati

text

Lymph Node Involvement (* Indicate Node Involvement: 0= not evaluated; 3= pathologically positive; 4= pathologically negative; 5= equivocal; 6= unknown)
Descrizione

LymphNodeInvolvement

Tipo di dati

text

Unnamed7
Descrizione

Unnamed7

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Disease History/prior Treatment Continued
Descrizione

Disease History/prior Treatment Continued

Type of Procedure
Descrizione

SurgicalProcedureType

Tipo di dati

text

Tumour Size, Maximum Diameter (cm Record longest or largest diameter of tumour.)
Descrizione

TumorSize,MaximumDiameter

Tipo di dati

float

Tumour Location, Side
Descrizione

TumorLocation,Side

Tipo di dati

text

Tumour Location, Area (check _ all that apply)
Descrizione

TumorLocation,Area

Tipo di dati

text

Other, specify
Descrizione

TumorLocation,AreaOther

Tipo di dati

text

Tumour Location, Zone (check _ all that apply)
Descrizione

TumorLocation,Zone

Tipo di dati

text

Does the tumour involve the pleura?
Descrizione

PleuraInvolvedInd

Tipo di dati

text

Is the tumour at the surgical margin?
Descrizione

TumorMarginInd

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C3262
UMLS 2011AA ObjectClass
C0027651
NCI Thesaurus Property
C25563
UMLS 2011AA Property
C0205284
Tumour Extension (check _ all that apply)
Descrizione

TumorExtension

Tipo di dati

text

Other, specify
Descrizione

TumorExtension,OtherStructures

Tipo di dati

text

Prior Treatment
Descrizione

Prior Treatment

Prior adjuvant RT? (If yes, record below)
Descrizione

PriorAdjuvantRTInd

Tipo di dati

text

Date Adjuvant Radiation Therapy Started (yyyy mmm dd)
Descrizione

AdjuvantRTBeginDate

Tipo di dati

date

Date Adjuvant Radiation Therapy Ended (yyyy mmm dd)
Descrizione

AdjuvantRTEndDate

Tipo di dati

date

Total dose of Radiation Therapy (cGy)
Descrizione

RTTotalDose

Tipo di dati

float

Prior Adjuvant Chemotherapy?
Descrizione

PriorAdjuvantChemotherapyInd

Tipo di dati

text

Unnamed8
Descrizione

Unnamed8

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Baseline Symptoms/"toxicity" Status
Descrizione

Baseline Symptoms/"toxicity" Status

COMMENTS
Descrizione

Comments

Tipo di dati

text

CTC Adverse Event Term (* Code/grade according to NCI Common Toxicity Criteria, version 2.0; Include all symptoms/findings including disease related symptoms present at baseline. All symptoms listed here must be reported on subsequent forms.)
Descrizione

CTCAdverseEventTerm

Tipo di dati

text

CTC Adverse Event Term, Other
Descrizione

CTCAdverseEventTerm,Other

Tipo di dati

text

CTG Adverse Event Category (* Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
Descrizione

CTCAdverseEventCategory

Tipo di dati

text

CTC Adverse Event Grade (0=None NA=Not Assessed; * Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
Descrizione

CTCAdverseEventGrade

Tipo di dati

text

Concomitant Medications
Descrizione

Concomitant Medications

Agent Name (generic or trade name)
Descrizione

AgentName

Tipo di dati

text

Unnamed9
Descrizione

Unnamed9

Patient Study ID, Coordinating Group
Descrizione

PatientStudyID,CoordinatingGroup

Tipo di dati

text

Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Other Major Medical Problems
Descrizione

Other Major Medical Problems

Date Documented (yyyy mmm dd)
Descrizione

PatientMedicalConditionDate

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C25261
UMLS 2011AA Property
C0205476
NCI Thesaurus Property-2
C25457
UMLS 2011AA Property-2
C0348080
Condition (e.g. diabetes)
Descrizione

PatientMedicalConditionText

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25704
UMLS 2011AA ValueDomain
C1527021
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C25261
UMLS 2011AA Property
C0205476
NCI Thesaurus Property-2
C25457
UMLS 2011AA Property-2
C0348080
Other Relevant Details (e.g. insulin treatment)
Descrizione

PatientHistoryText

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25704
UMLS 2011AA ValueDomain
C1527021
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C18772
UMLS 2011AA Property
C0262926
Comments
Descrizione

Comments

COMMENTS
Descrizione

Comments

Tipo di dati

text

Investigator Signature
Descrizione

Investigator Signature

Investigator Signature
Descrizione

InvestigatorSignature

Tipo di dati

text

Alias
NCI Thesaurus Property
C25678
UMLS 2011AA Property
C1519316
NCI Thesaurus ObjectClass
C17089
UMLS 2011AA ObjectClass
C0035173
Person Completing Form, Last Name
Descrizione

PersonCompletingForm,LastName

Tipo di dati

text

Person Completing Form, First Name
Descrizione

PersonCompletingForm,FirstName

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C25190
UMLS 2011AA ObjectClass
C0027361
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
Form Completion Date, Original (yyyy mmm dd)
Descrizione

FormCompletionDate,Original

Tipo di dati

date

Ccrr Module For Form 1 - Eligibility Checklist And Initial Evaluation
Descrizione

Ccrr Module For Form 1 - Eligibility Checklist And Initial Evaluation

Similar models

No Instruction available.

  1. StudyEvent: Form 1 - Eligibility Checklist and Initial Evaluation
    1. No Instruction available.
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Patient Information
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Item
Patient Gender
text
C25372 (NCI Thesaurus ValueDomain)
C0683312 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C17357 (NCI Thesaurus Property)
C0079399 (UMLS 2011AA Property)
Code List
Patient Gender
CL Item
Male (Male)
C46109 (NCI Thesaurus)
C1706180 (UMLS 2011AA)
CL Item
Female (Female)
C46110 (NCI Thesaurus)
C0015780 (UMLS 2011AA)
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
PatientMedicalRecordNumber
Item
Patient Medical Record Number
text
InstitutionName
Item
Institution Name
text
RegisteredInvestigator
Item
Registered Investigator (NCI Investigator #)
text
PatientBirthDate
Item
Patient's Date of Birth (yyyy mmm dd)
date
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25275 (NCI Thesaurus Property)
C2745955 (UMLS 2011AA Property)
Item
Patient Race (check _ all that apply)
text
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C17049 (NCI Thesaurus Property)
C0034510 (UMLS 2011AA Property)
Code List
Patient Race (check _ all that apply)
CL Item
White_cdus (White)
CL Item
Black_cdus (Black or African American)
CL Item
Pacific_islander_cdus (Native Hawaiian or other Pacific Islander)
CL Item
Asian_cdus (Asian)
CL Item
Native_american_cdus (American Indian or Alaska Native)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Patient Ethnicity (check _ one only)
text
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C17049 (NCI Thesaurus Property)
C0034510 (UMLS 2011AA Property)
Code List
Patient Ethnicity (check _ one only)
CL Item
Hispanic_or_latino (Hispanic or Latino)
CL Item
Non_hispanic (Non-Hispanic)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Payment Method (check _ one USA only)
text
Code List
Payment Method (check _ one USA only)
CL Item
Private Insurance (Private Insurance)
CL Item
Medicare (Medicare)
C16665 (NCI Thesaurus)
C0018717 (UMLS 2011AA)
CL Item
Medicare And Private Insurance (Medicare/Private Insurance)
CL Item
Medicaid (Medicaid)
C0025071 (NCI Metathesaurus)
CL Item
Medicaid And Medicare (Medicaid & Medicare)
CL Item
Military Or Veterans Sponsored Nos (Military or Veterans Sponsored NOS)
CL Item
Military Sponsored (including Champus & Tricare) (Military Sponsored (including CHAMPUS and TRICARE))
CL Item
Veterans Sponsored (Veterans Sponsored)
CL Item
Self Pay (no Insurance) (Self pay (no insurance))
CL Item
No Means Of Payment (no Insurance) (No means of payment (no insurance))
CL Item
Other (Other)
C17649 (NCI Thesaurus)
C0205394 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
IRBApprovalDate
Item
IRB/REB Approval Date (yyyy mmm dd)
date
C25320 (NCI Thesaurus ObjectClass)
C1507394 (UMLS 2011AA ObjectClass)
C25425 (NCI Thesaurus Property)
C0205540 (UMLS 2011AA Property)
ProjectedTreatmentBeginDate
Item
Projected Start Date of Treatment (yyyy mmm dd)
date
Item Group
Ncic Ctg Use Only
LoggedEntryInitials
Item
Logged
text
LoggedEntryDate
Item
Unnamed (Logged Date)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
RegulatoryAffairsReviewInitials
Item
RA
text
RegulatoryAffairsReviewDate
Item
Unnamed (RA Date)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
CoordinatorReviewInitials
Item
Study Coord
text
CoordinatorReviewDate
Item
Unnamed (Coord Date)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
PhysicianReviewInitials
Item
Phy
text
DataEntryInitials
Item
Data Ent'd
text
DataVerificationInitials
Item
Verified
text
Item Group
Header
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Eligibility Checklist
LungCancerProofInd
Item
Patient has histological proof of a primary non-small cell lung cancer (bronchoalveolar carcinomas presenting as a discrete radiological mass or node are eligible. Please specify)
text
Item
Histologic Type
text
Code List
Histologic Type
CL Item
Squamous Cell Carcinoma (Squamous cell carcinoma)
C2929 (NCI Thesaurus)
C0007137 (UMLS 2011AA)
CL Item
Adenocarcinoma (Adenocarcinoma)
C2852 (NCI Thesaurus)
C0001418 (UMLS 2011AA)
CL Item
Adenosquamous Carcinoma (Adenosquamous carcinoma)
CL Item
Large Cell Undifferentiated (Large cell undifferentiated)
CL Item
Other, Specify (Other)
PathologicStagePostoperativeInd
Item
Post operatively the patient had a pathological stage of
text
Item
Stage
text
Code List
Stage
CL Item
Refer To Figo Staging For Specific Gynecologic Cancer (IB)
CL Item
Refer To Figo Staging For Specific Gynecologic Cancer (II)
CL Item
Refer To Figo Staging For Specific Gynecologic Cancer (IIIA)
LymphNodeAdequateSamplingInd
Item
Adequate Lymph Node sampling was performed (see section 5.1.1.4 of the protocol)
text
Item
Please specify the extent of lymph node sampling (check _ one only)
text
Code List
Please specify the extent of lymph node sampling (check _ one only)
CL Item
Complete Mediastinal Resection (Complete mediastinal resection)
CL Item
Partial Mediastinal Resection (Partial mediastinal resection)
CL Item
Nodes >= 1.5 Cm Were Sampled (Nodes >= 1.5 cm were sampled)
CL Item
No Enlarged Lymph Nodes On Ct Chest, No Mediastinal Sampling Done (No enlarged lymph nodes on CT chest, no mediastinal sampling done)
CL Item
Other (Other)
C17649 (NCI Thesaurus)
C0205394 (UMLS 2011AA)
LymphNodeSamplingExtentLargeSite
Item
Nodes >= 1.5 cm were sampled (specify)
text
LymphNodeSamplingOtherExtent
Item
Other (specify)
text
LungCarcinomaSurgicalProcedureTherapyInd-3
Item
Surgery consisted of lobectomy, sleeve resection, bilobectomy or pneumonectomy. (segmentectomy or wedge resection only is not eligible)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
C15329 (NCI Thesaurus Property)
C0543467 (UMLS 2011AA Property)
C4878 (NCI Thesaurus ObjectClass)
C0684249 (UMLS 2011AA ObjectClass)
GrossDiseaseRemovedInd
Item
Patient has had all gross disease surgically removed.
text
SurgicalResectionNegativeMarginIndicator
Item
All surgical margins of resection are negative for tumour.
text
MaximumTimePostSurgeryIndicator
Item
No more than 16 weeks may have elapsed between surgical resection and randomization.
text
SurgeryDate
Item
Surgery Date (yyyy mmm dd)
date
TumorBlocksSentIndicator
Item
A representative formalin fixed paraffin block of tumour tissue must be submitted at the request of the central tumour bank in order that specific EGFR correlative marker assays may be conducted.
text
MinimumPerformanceStatusIndicator
Item
Performance Status is <= 2. (see protocol appendix II)
text
RequiredHematology14DaysIndicator
Item
Required hematologic and biochemistry investigations done within 14 days prior to randomization, including:
text
Lab,Hematology,SampleCollectionDate
Item
Date Hematology (Blood) Sample Obtained (yyyy mmm dd)
date
Lab,Hematology,WBC
Item
Peripheral WBC Count (1000/uL or x 10 9/L)
float
Lab,Hematology,NeutrophilCount
Item
Peripheral neutrophil count (>= 1.5 x 10 9/L or >= 1500/uL; Value)
float
Lab,Hematology,Platelets
Item
Peripheral Platelet Count (1000/uL or x 10 9/L)
float
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Ul (uL)
CL Item
X10^9/l (10 9/L)
CL Item
U/l (U/L)
CL Item
Mg/dl (mg/dl)
CL Item
Umol/l (umol/L)
CL Item
Meq/l (mEq/L)
CL Item
Mmol/l (mmol/L)
CL Item
G/dl (g/dL)
CL Item
G/l (g/L)
Item Group
Ncic Ctg Use Only
Item
Patient Gender
text
C25372 (NCI Thesaurus ValueDomain)
C0683312 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C17357 (NCI Thesaurus Property)
C0079399 (UMLS 2011AA Property)
Code List
Patient Gender
CL Item
Male (Male)
C46109 (NCI Thesaurus)
C1706180 (UMLS 2011AA)
CL Item
Female (Female)
C46110 (NCI Thesaurus)
C0015780 (UMLS 2011AA)
Item
Histologic Type
text
Code List
Histologic Type
CL Item
Squamous Cell Carcinoma (Squamous cell carcinoma)
C2929 (NCI Thesaurus)
C0007137 (UMLS 2011AA)
CL Item
Adenocarcinoma (Adenocarcinoma)
C2852 (NCI Thesaurus)
C0001418 (UMLS 2011AA)
CL Item
Adenosquamous Carcinoma (Adenosquamous carcinoma)
CL Item
Large Cell Undifferentiated (Large cell undifferentiated)
CL Item
Other, Specify (Other)
Item
Stage
text
Code List
Stage
CL Item
Refer To Figo Staging For Specific Gynecologic Cancer (IB)
CL Item
Refer To Figo Staging For Specific Gynecologic Cancer (II)
CL Item
Refer To Figo Staging For Specific Gynecologic Cancer (IIIA)
Item Group
Unnamed2
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Eligibility Checklist Continued
SpecimenCollectionDate
Item
Specimen Collection Date (Biochemistry, yyyy mmm dd)
date
RequiredBiochemistry14DaysIndicator
Item
Required biochemistry investigations done within 14 days prior to randomization, and greater than 8 days following surgical resection, including
text
Lab,Hepatic,Bilirubin
Item
Bilirubin (uL or 10 9/L)
float
HepaticBilirubinLabUpperLimitNormalValue
Item
Bilirubin ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C305 (NCI Thesaurus Property-2)
C0005437 (UMLS 2011AA Property-2)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
AdjuvantRTEndDate
Item
Date Adjuvant Radiation Therapy Ended (yyyy mmm dd)
date
Lab,Hepatic,SGOT
Item
SGOT (AST) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
float
SGOTLabUpperLimitNormalValue
Item
SGOT (AST) ULN
float
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Hepatic,SGPT
Item
SGPT (ALT) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
float
SGPTLabUpperLimitNormalValue
Item
SGPT (ALT) ULN
float
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Hepatic,AlkalinePhosphatase
Item
Alkaline Phosphatase (U/L; * If alkaline phosphatase is greater than ULN but <= 2.5 X ULN, ultrasound or CT scan of abdomen and bone scan MUST be done prior to randomization)
float
Alkaline Phosphatase ULN
Item
Alkaline Phosphatase ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0151420 (UMLS CUI-1)
C20200 (NCI Thesaurus Property)
C16276 (NCI Thesaurus Property-2)
C25712 (NCI Thesaurus ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
Lab,Renal,Creatinine
Item
Creatinine (mg/dl or umol/L)
float
Creatinine, serum ULN
Item
Creatinine ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0201976 (UMLS CUI-1)
C20200 (NCI Thesaurus Property)
C1519815 (UMLS CUI-2)
C399 (NCI Thesaurus Property-2)
C25712 (NCI Thesaurus ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
PatientAge18YearsIndicator
Item
Patient's age is >= 18 years (lower age limit subject to local policy regarding age at which patient may sign own consent)
text
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
PrestudyChestX-RayIndicator
Item
Patient has had a chest x-ray within 14 days of randomization.
text
ChestX-RayAssessmentDate
Item
Date of chest x-ray (yyyy mmm dd)
date
PrestudyChestCTIndicator
Item
Patient has had a CT or MRI scan of the chest within 42 days prior to surgery.
text
ChestComputedTomographyMagneticResonanceImagingDiagnosticImagingPerformedDate
Item
Date of CT or MRI of chest (yyyy mmm dd)
date
C16502 (NCI Thesaurus ObjectClass)
C0011923 (UMLS 2011AA ObjectClass)
C17204 (NCI Thesaurus ObjectClass-2)
C0040405 (UMLS 2011AA ObjectClass-2)
C25389 (NCI Thesaurus ObjectClass-3)
C0817096 (UMLS 2011AA ObjectClass-3)
C16809 (NCI Thesaurus ObjectClass-4)
C0024485 (UMLS 2011AA ObjectClass-4)
C38000 (NCI Thesaurus Property)
C0884358 (UMLS 2011AA Property)
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
PrestudyEKGIndicator
Item
Patient has had an EKG within 14 days prior to randomization.
text
DiagnosticElectrocardiogramPerformedDate
Item
Date of EKG (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C38000 (NCI Thesaurus Property)
C0884358 (UMLS 2011AA Property)
C25482 (NCI Thesaurus ObjectClass)
C0348026 (UMLS 2011AA ObjectClass)
C0013798 (NCI Metathesaurus ObjectClass)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Ul (uL)
CL Item
X10^9/l (10 9/L)
CL Item
U/l (U/L)
CL Item
Mg/dl (mg/dl)
CL Item
Umol/l (umol/L)
CL Item
Meq/l (mEq/L)
CL Item
Mmol/l (mmol/L)
CL Item
G/dl (g/dL)
CL Item
G/l (g/L)
EligibilityContraceptionIndicator
Item
Men and women of childbearing age will use adequate contraception.
text
PrestudyPostoperativeRadiationTherapyIndicator
Item
Patient has received post-operative radiation. (If patient has received post-operative radiation therapy)
boolean
PrestudyRadiationTherapyCompleteIndicator
Item
Radiation therapy has been completed at least three weeks prior to randomization
text
RadiationTherapyToxicityRecoveryIndicator
Item
The patient has recovered from all radiation therapy related toxicity
text
PatientConsentSignedIndicator
Item
Informed consent has been signed and dated by patient.
text
InformedConsentDateSigned
Item
Date informed consent signed (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
PatientTherapeuticProcedureFollow-upEligibilityDeterminationInd-2
Item
Patient accessible for treatment and follow-up.
text
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C16033 (NCI Thesaurus Property)
C1522577 (UMLS 2011AA Property)
C49236 (NCI Thesaurus Property-2)
C0087111 (UMLS 2011AA Property-2)
C25171 (NCI Thesaurus Property-3)
C0013893 (UMLS 2011AA Property-3)
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
TreatmentRequirementBeginIndicator
Item
Initiation of protocol therapy will begin within 10 working days of randomization.
text
Item Group
Ncic Ctg Use Only2
Item
Post-operative radiotherapy
text
Code List
Post-operative radiotherapy
CL Item
Given (Given)
CL Item
Not Given (Not given)
Item Group
Unnamed3
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Eligibility Checklist Continued2
NoOtherMalignancyIndicator
Item
No other prior or concurrent malignancies within the last 5 years, except as specified in protocol section 5.2.1.
text
NoCombinationLungCancerIndicator
Item
No combination of small cell and non-small cell carcinomas or a pulmonary carcinoid tumour.
text
OneDiscretePrimaryCancerIndicator
Item
No more than one discrete area of apparent primary cancer (even if within same lobe, T4, IIIB are ineligible)
text
NoOphthalmologicGastrointestinalDiseaseIndicator
Item
No clinically significant or untreated ophthalmologic or gastrointestinal conditions.
text
NoPathologicRiskConditionIndicator
Item
No active pathological condition that would render the protocol treatment dangerous. (see protocol section 5.2.5 )
text
NoPsychiatricImpairmentHistoryIndicator
Item
No history of psychiatric or neurological disorder that would make the obtainment of informed consent problematic, or that would limit compliance with study requirements.
text
Item
Patient, if female, is not pregnant or breast feeding.
text
Code List
Patient, if female, is not pregnant or breast feeding.
CL Item
Na (NA)
NoPriorLungChemotherapyIndicator
Item
No prior adjuvant or neoadjuvant chemotherapy or immunotherapy for NSCLC. (limited low dose preoperative radiation therapy or endobronchial brachytherapy or laser therapy for short term control of hemoptysis or lobar obstruction is permitted, however full dose, pre-operative radiotherapy of curative intent is cause for exclusion )
text
NoAgentAllergyHistoryIndicator
Item
No history of allergic reactions to compounds of similar chemical or biologic composition to IRESSA.
text
NoCYP3A4EnzymeMedicationsIndicator
Item
Patient does not take drugs which induce CYP3A4 enzymes, e.g., phenytoin, carbamazepine, barbiturates, rifampicin or St John's Wort.
text
AdequateSurgicalHealingIndicator
Item
Adequate healing from previous oncologic or other major surgery has occurred.
text
Item Group
Randomization
RandomizationDate
Item
Randomization Date (yyyy mmm dd)
date
InvestigatorSignature
Item
Investigator Signature
text
C25678 (NCI Thesaurus Property)
C1519316 (UMLS 2011AA Property)
C17089 (NCI Thesaurus ObjectClass)
C0035173 (UMLS 2011AA ObjectClass)
PersonCompletingForm,LastName
Item
Person Completing Form, Last Name
text
InvestigatorSignatureDate
Item
Date of Investigator Signature (yyyy mmm dd)
date
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)
FormCompletionDate,Original
Item
Form Completion Date, Original (yyyy mmm dd)
date
Item Group
Unnamed4
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
History And Physical Exam
Item
Is patient currently smoking?
text
Code List
Is patient currently smoking?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
AssessmentDate
Item
Date of evaluation (yyyy mmm dd)
date
Item
Has previously been a smoker?
text
Code List
Has previously been a smoker?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Performance Status (check _ one)
text
Code List
Performance Status (check _ one)
CL Item
0 (0 = Fully active, able to carry on all pre-disease performance without restriction (Karnofsky 90-100))
C0919414 (NCI Metathesaurus)
CL Item
1 (1 = Restricted in physically strenuous activity but ambulatory (K 70-80))
CL Item
2 (2 = Ambulatory and capable of all self-care but unable to carry out any work activities (K 50-60))
C66833 (NCI Thesaurus)
C0205448 (UMLS 2011AA)
CL Item
3 (3 = Capable of only limited self-care, confined to bed or chair more than 50% of waking hours (K 30-40))
CL Item
4 (4 = Completely disabled, cannot carry on any self-care. Totally confined to bed or chair (K 10-20))
PatientHeight
Item
Patient Height (cm)
float
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25347 (NCI Thesaurus Property)
C0489786 (UMLS 2011AA Property)
PatientWeight
Item
Patient Weight (kg)
float
Item Group
Investigations
Item
Imaging Site
text
C13717 (NCI Thesaurus ValueDomain)
C1515974 (UMLS 2011AA ValueDomain)
C25341 (NCI Thesaurus Property)
C0450429 (UMLS 2011AA Property)
C16502 (NCI Thesaurus ObjectClass)
C0011923 (UMLS 2011AA ObjectClass)
C25421 (NCI Thesaurus Property-2)
C0002808 (UMLS 2011AA Property-2)
Code List
Imaging Site
CL Item
Chest (Chest)
C25389 (NCI Thesaurus)
C0817096 (UMLS 2011AA)
CL Item
Brain (Brain)
C12439 (NCI Thesaurus)
C0006104 (UMLS 2011AA)
CL Item
Abdomen (Abdomen)
C12664 (NCI Thesaurus)
C0230168 (UMLS 2011AA)
CL Item
Bone (Bone)
C12366 (NCI Thesaurus)
C0262950 (UMLS 2011AA)
CL Item
Cardiac (Cardiac)
C13306 (NCI Thesaurus)
C1522601 (UMLS 2011AA)
Item
Method of Evaluation
text
Code List
Method of Evaluation
CL Item
Chest X-ray (Chest x-ray)
CL Item
Ct Scan (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
Ekg (EKG)
CL Item
Not Evaluated (Not evaluated)
AssessmentDate
Item
Date of evaluation (yyyy mmm dd)
date
Item
Pregnancy test
text
Code List
Pregnancy test
CL Item
Positive (Positive)
C25246 (NCI Thesaurus)
C1446409 (UMLS 2011AA)
CL Item
Negative (Negative)
C25247 (NCI Thesaurus)
C0205160 (UMLS 2011AA)
CL Item
Not Evaluated (Not evaluated)
Item Group
Unnamed5
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Baseline Hematology/biochemistry Values
Lab,Hematology,Hemoglobin
Item
Hemoglobin (g/dl or g/L)
float
Lab,Hematology,Neutrophils,CellPercentage
Item
Peripheral Neutrophils (%)
float
Lab,Hematology,SampleCollectionDate
Item
Date Hematology (Blood) Sample Obtained (yyyy mmm dd)
date
Lab,Hematology,WBC
Item
Peripheral WBC Count (1000/uL or x 10 9/L)
float
Lab,Hematology,Platelets
Item
Peripheral Platelet Count (1000/uL or x 10 9/L)
float
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Ul (uL)
CL Item
X10^9/l (10 9/L)
CL Item
U/l (U/L)
CL Item
Mg/dl (mg/dl)
CL Item
Umol/l (umol/L)
CL Item
Meq/l (mEq/L)
CL Item
Mmol/l (mmol/L)
CL Item
G/dl (g/dL)
CL Item
G/l (g/L)
Item Group
Biochemistry
SpecimenCollectionDate
Item
Specimen Collection Date (Biochemistry, yyyy mmm dd)
date
Lab,Hepatic,Bilirubin
Item
Bilirubin (uL or 10 9/L)
float
HepaticBilirubinLabUpperLimitNormalValue
Item
Bilirubin ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C305 (NCI Thesaurus Property-2)
C0005437 (UMLS 2011AA Property-2)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Hepatic,SGOT
Item
SGOT (AST) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
float
SGOTLabUpperLimitNormalValue
Item
SGOT (AST) ULN
float
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Hepatic,SGPT
Item
SGPT (ALT) (U/L; ** If AST SGOT or ALT SGPT is greater than ULN but <= 2.5 X ULN, ultrasound, CT or MRI of abdomen MUST be done prior to randomization)
float
SGPTLabUpperLimitNormalValue
Item
SGPT (ALT) ULN
float
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Hepatic,AlkalinePhosphatase
Item
Alkaline Phosphatase (U/L; * If alkaline phosphatase is greater than ULN but <= 2.5 X ULN, ultrasound or CT scan of abdomen and bone scan MUST be done prior to randomization)
float
Alkaline Phosphatase ULN
Item
Alkaline Phosphatase ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0151420 (UMLS CUI-1)
C20200 (NCI Thesaurus Property)
C16276 (NCI Thesaurus Property-2)
C25712 (NCI Thesaurus ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
Lab,Chemistry,LactateDehydrogenase
Item
Lactate Dehydrogenase (LDH) (U/L)
float
Lab,Chemistry,LactateDehydrogenase,ULN
Item
Lactate Dehydrogenase ULN
float
Lab,Renal,Creatinine
Item
Creatinine (mg/dl or umol/L)
float
Creatinine, serum ULN
Item
Creatinine ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0201976 (UMLS CUI-1)
C20200 (NCI Thesaurus Property)
C1519815 (UMLS CUI-2)
C399 (NCI Thesaurus Property-2)
C25712 (NCI Thesaurus ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
Lab,Renal,BUN
Item
BUN (mg/dl or umol/L)
float
LaboratoryProcedureBloodUreaNitrogenResultUpperLimitNormalValue
Item
BUN ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C61019 (NCI Thesaurus Property-2)
C0005845 (UMLS 2011AA Property-2)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Electrolytes,Potassium
Item
Potassium (K) (mEq/L)
float
LaboratoryProcedurePotassiumElectrolytesOutcomeLowerLimitNormalValue
Item
Potassium LLN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C464 (NCI Thesaurus Property-2)
C0013832 (UMLS 2011AA Property-2)
C765 (NCI Thesaurus Property-3)
C0032821 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25555 (NCI Thesaurus ValueDomain-2)
C1518030 (UMLS 2011AA ValueDomain-2)
LaboratoryProcedurePotassiumElectrolytesOutcomeUpperLimitNormalValue
Item
Potassium ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C464 (NCI Thesaurus Property-2)
C0013832 (UMLS 2011AA Property-2)
C765 (NCI Thesaurus Property-3)
C0032821 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Electrolytes,Sodium
Item
Sodium (Na) (mmol/L)
float
LaboratoryProcedureSodiumElectrolytesOutcomeLowerLimitofNormalValue
Item
Sodium LLN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C830 (NCI Thesaurus Property-2)
C0037473 (UMLS 2011AA Property-2)
C464 (NCI Thesaurus Property-3)
C0013832 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25555 (NCI Thesaurus ValueDomain-2)
C1518030 (UMLS 2011AA ValueDomain-2)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Ul (uL)
CL Item
X10^9/l (10 9/L)
CL Item
U/l (U/L)
CL Item
Mg/dl (mg/dl)
CL Item
Umol/l (umol/L)
CL Item
Meq/l (mEq/L)
CL Item
Mmol/l (mmol/L)
CL Item
G/dl (g/dL)
CL Item
G/l (g/L)
LaboratoryProcedureSodiumElectrolytesOutcomeUpperLimitofNormalValue
Item
Sodium ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C830 (NCI Thesaurus Property-2)
C0037473 (UMLS 2011AA Property-2)
C464 (NCI Thesaurus Property-3)
C0013832 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Electrolytes,Chloride
Item
Chloride (Cl) (mEq/L)
float
LaboratoryProcedureChlorideIonElectrolytesOutcomeLowerLimitofNormalValue
Item
Chloride LLN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C464 (NCI Thesaurus Property-2)
C0013832 (UMLS 2011AA Property-2)
C1741 (NCI Thesaurus Property-3)
C0596019 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25555 (NCI Thesaurus ValueDomain-2)
C1518030 (UMLS 2011AA ValueDomain-2)
LaboratoryProcedureChlorideIonElectrolytesOutcomeUpperLimitofNormalValue
Item
Chloride ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C464 (NCI Thesaurus Property-2)
C0013832 (UMLS 2011AA Property-2)
C1741 (NCI Thesaurus Property-3)
C0596019 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Lab,Electrolytes,Calcium
Item
Calcium (Ca) (mg/dL or umol/L)
float
LaboratoryProcedureCalciumElectrolytesOutcomeLowerLimitofNormalValue
Item
Calcium LLN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C331 (NCI Thesaurus Property)
C0006675 (UMLS 2011AA Property)
C20200 (NCI Thesaurus Property-2)
C1274040 (UMLS 2011AA Property-2)
C464 (NCI Thesaurus Property-3)
C0013832 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25555 (NCI Thesaurus ValueDomain-2)
C1518030 (UMLS 2011AA ValueDomain-2)
LaboratoryProcedureCalciumElectrolytesOutcomeUpperLimitofNormalValue
Item
Calcium ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C331 (NCI Thesaurus Property)
C0006675 (UMLS 2011AA Property)
C20200 (NCI Thesaurus Property-2)
C1274040 (UMLS 2011AA Property-2)
C464 (NCI Thesaurus Property-3)
C0013832 (UMLS 2011AA Property-3)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Chemistry,BloodAlbumin
Item
Albumin (g/dl or g/L)
float
LaboratoryProcedureAlbuminResultLowerLimitofNormalValue
Item
Albumin LLN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C214 (NCI Thesaurus Property-2)
C0001924 (UMLS 2011AA Property-2)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25555 (NCI Thesaurus ValueDomain-2)
C1518030 (UMLS 2011AA ValueDomain-2)
LaboratoryProcedureAlbuminResultUpperLimitNormalValue
Item
Albumin ULN
float
C25294 (NCI Thesaurus ObjectClass)
C0022885 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
C214 (NCI Thesaurus Property-2)
C0001924 (UMLS 2011AA Property-2)
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain-2)
C1519815 (UMLS 2011AA ValueDomain-2)
Item Group
Unnamed6
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Disease History/prior Treatment
PrimarySurgeryDate
Item
Primary Surgery Date (yyyy mmm dd)
date
Item
N Stage, Pathologic (check _ one)
text
Code List
N Stage, Pathologic (check _ one)
CL Item
N0, According To Ajcc Criteria (N0)
CL Item
N1, According To Ajcc Criteria (N1)
CL Item
N2, According To Ajcc Criteria (N2)
CL Item
N3, According To Ajcc Criteria (N3)
CL Item
Nx, According To Ajcc Criteria (Nx)
Item
Histologic Type
text
Code List
Histologic Type
CL Item
Squamous Cell Carcinoma (Squamous cell carcinoma)
C2929 (NCI Thesaurus)
C0007137 (UMLS 2011AA)
CL Item
Adenocarcinoma (Adenocarcinoma)
C2852 (NCI Thesaurus)
C0001418 (UMLS 2011AA)
CL Item
Adenosquamous Carcinoma (Adenosquamous carcinoma)
CL Item
Large Cell Undifferentiated (Large cell undifferentiated)
CL Item
Other, Specify (Other)
Item
T Stage, Pathologic (check _ one)
text
Code List
T Stage, Pathologic (check _ one)
CL Item
Tumor 2 Cm Or Less In Greatest Dimension (T1)
CL Item
Tumor More Than 2 Cm But Not More Than 5 Cm In Greatest Dimension (T2)
CL Item
Tumor More Than 5 Cm In Greatest Dimension (T3)
CL Item
Tumor Of Any Size With Direct (T4)
Item
Stage Grouping, Pathologic
text
Code List
Stage Grouping, Pathologic
CL Item
Ib, According To Current Ajcc Guidelines (IB)
CL Item
Iia, According To Current Ajcc Guidelines (IIA)
CL Item
Iib, According To Current Ajcc Guidelines (IIB)
CL Item
Iiia, According To Current Ajcc Guidelines (IIIA)
HistologicType,OtherName
Item
Specify other histologic type
text
Item
Histologic Grade (WHO)
text
Code List
Histologic Grade (WHO)
CL Item
Well Differentiated (Grade I)
C14171 (NCI Thesaurus)
C0205615 (UMLS 2011AA)
CL Item
Moderate (Grade II)
CL Item
Poor (Grade III)
Item
Is there vascular invasion?
text
Code List
Is there vascular invasion?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Is the parietal pleural margin involved?
text
Code List
Is the parietal pleural margin involved?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Was lymph node sampling done?
text
Code List
Was lymph node sampling done?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
LymphNode(s)ExaminedNumber
Item
Number of Lymph Nodes Examined (If yes,)
float
C25500 (NCI Thesaurus Property)
C0332128 (UMLS 2011AA Property)
C12745 (NCI Thesaurus ObjectClass)
C0024204 (UMLS 2011AA ObjectClass)
LymphNode(s)PositiveNumber
Item
Number of Positive Lymph Nodes
float
C25246 (NCI Thesaurus Property)
C1446409 (UMLS 2011AA Property)
C12745 (NCI Thesaurus ObjectClass)
C0024204 (UMLS 2011AA ObjectClass)
Item
Lymph Nodes Type (Station)
text
Code List
Lymph Nodes Type (Station)
CL Item
Highest Mediastinal Node (Highest mediastinal (1))
CL Item
Right Upper Paratracheal Node (Right upper paratracheal (2R))
CL Item
Left Upper Paratracheal Node (Left upper paratracheal (2L))
CL Item
Pre- And Retro Paratracheal Node (Pre- and retro paratracheal (3))
CL Item
Right Lower Paratracheal Node (Right lower paratracheal (4R))
CL Item
Left Lower Paratracheal Node (Left lower paratracheal (4L))
CL Item
Subaortic Node (Subaortic (5))
CL Item
Para-aortic Node (Para-aortic (6))
CL Item
Subcarinal Node (Subcarinal (7))
CL Item
Paraesophageal (Paraesophageal (8))
C25344 (NCI Thesaurus)
C0475302 (UMLS 2011AA)
CL Item
Pulmonary Ligament (Pulmonary ligament (9))
C0225794 (NCI Metathesaurus)
CL Item
Right Hilar Node (Right hilar (10R))
CL Item
Left Hilar Node (Left hilar (10L))
CL Item
Interlobar Node (Interlobar (11))
CL Item
Right Lobar Node (Right lobar (12R))
CL Item
Left Lobar Node (Left lobar (12L))
CL Item
Right Segmental Node (Right segmental (13R))
CL Item
Left Segmental Node (Left segmental (13L))
CL Item
Right Subsegmental Node (Right subsegmental (14R))
CL Item
Left Subsegmental Node (Left subsegmental (14L))
Item
Lymph Node Involvement (* Indicate Node Involvement: 0= not evaluated; 3= pathologically positive; 4= pathologically negative; 5= equivocal; 6= unknown)
text
Code List
Lymph Node Involvement (* Indicate Node Involvement: 0= not evaluated; 3= pathologically positive; 4= pathologically negative; 5= equivocal; 6= unknown)
CL Item
Not Evaluated (not evaluated)
CL Item
The Node Is Considered To Be Positive Based Upon Histological Evaluation. (pathologically positive)
CL Item
The Node Is Considered To Be Negative Based Upon Histological Evaluation. (pathologically negative)
CL Item
Equivocal (equivocal)
C86071 (NCI Thesaurus)
C0332241 (UMLS 2011AA)
CL Item
Unknown (unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item Group
Unnamed7
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Disease History/prior Treatment Continued
Item
Type of Procedure
text
Code List
Type of Procedure
CL Item
Lobectomy (Lobectomy)
C15272 (NCI Thesaurus)
C0023928 (UMLS 2011AA)
CL Item
Pneumonectomy (Pneumonectomy)
C15305 (NCI Thesaurus)
C0032284 (UMLS 2011AA)
CL Item
Bilobectomy (Bilobectomy)
CL Item
Bronchial Sleeve Resection (Bronchial sleeve resection)
TumorSize,MaximumDiameter
Item
Tumour Size, Maximum Diameter (cm Record longest or largest diameter of tumour.)
float
Item
Tumour Location, Side
text
Code List
Tumour Location, Side
CL Item
Left (Left)
C25229 (NCI Thesaurus)
C0205091 (UMLS 2011AA)
CL Item
Right (Right)
C25228 (NCI Thesaurus)
C0205090 (UMLS 2011AA)
Item
Tumour Location, Area (check _ all that apply)
text
Code List
Tumour Location, Area (check _ all that apply)
CL Item
Upper Lobe (Upper lobe)
CL Item
Middle Lobe (Middle lobe)
CL Item
Lower Lobe (Lower lobe)
CL Item
Mainstem Bronchus (Mainstem bronchus)
CL Item
Carina (Carina)
C25264 (NCI Thesaurus)
C0225594 (UMLS 2011AA)
CL Item
Other, Specify (Other, specify)
TumorLocation,AreaOther
Item
Other, specify
text
Item
Tumour Location, Zone (check _ all that apply)
text
Code List
Tumour Location, Zone (check _ all that apply)
CL Item
Predominantly Central (Predominantly central)
CL Item
Predominantly Peripheral (Predominantly peripheral)
CL Item
Indeterminate (Indeterminate)
C48658 (NCI Thesaurus)
C0205258 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Does the tumour involve the pleura?
text
Code List
Does the tumour involve the pleura?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Is the tumour at the surgical margin?
text
C3262 (NCI Thesaurus ObjectClass)
C0027651 (UMLS 2011AA ObjectClass)
C25563 (NCI Thesaurus Property)
C0205284 (UMLS 2011AA Property)
Code List
Is the tumour at the surgical margin?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item
Tumour Extension (check _ all that apply)
text
Code List
Tumour Extension (check _ all that apply)
CL Item
Chest Wall (Chest Wall)
CL035093 (NCI Metathesaurus)
C62484 (NCI Thesaurus)
C0205076 (UMLS 2011AA)
CL Item
Pericardium (Pericardium)
C13005 (NCI Thesaurus)
C0031050 (UMLS 2011AA)
CL Item
Mediastinum (Mediastinum)
C12748 (NCI Thesaurus)
C0025066 (UMLS 2011AA)
CL Item
Diaphragm (Diaphragm)
C12702 (NCI Thesaurus)
C0011980 (UMLS 2011AA)
CL Item
Esophagus (Esophagus)
C12389 (NCI Thesaurus)
C0014876 (UMLS 2011AA)
CL Item
Other, Specify (Other, specify)
TumorExtension,OtherStructures
Item
Other, specify
text
Item Group
Prior Treatment
Item
Prior adjuvant RT? (If yes, record below)
text
Code List
Prior adjuvant RT? (If yes, record below)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
AdjuvantRTBeginDate
Item
Date Adjuvant Radiation Therapy Started (yyyy mmm dd)
date
AdjuvantRTEndDate
Item
Date Adjuvant Radiation Therapy Ended (yyyy mmm dd)
date
RTTotalDose
Item
Total dose of Radiation Therapy (cGy)
float
Item
Prior Adjuvant Chemotherapy?
text
Code List
Prior Adjuvant Chemotherapy?
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
Item Group
Unnamed8
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Baseline Symptoms/"toxicity" Status
Comments
Item
COMMENTS
text
Item
CTC Adverse Event Term (* Code/grade according to NCI Common Toxicity Criteria, version 2.0; Include all symptoms/findings including disease related symptoms present at baseline. All symptoms listed here must be reported on subsequent forms.)
text
Code List
CTC Adverse Event Term (* Code/grade according to NCI Common Toxicity Criteria, version 2.0; Include all symptoms/findings including disease related symptoms present at baseline. All symptoms listed here must be reported on subsequent forms.)
CL Item
Anorexia (anorexia)
CL Item
Chest Pain (chest pain (non-cardiac and non-pleuritic))
CL Item
Constipation (constipation)
CL Item
Diarrhea For Patients Without Colostomy (diarrhea (patients without colostomy))
CL Item
Dry Skin (dry skin)
CL Item
Dyspnea (dyspnea (shortness of breath))
CL Item
Fatigue (fatigue (lethargy, malaise, asthenia))
CL Item
Infection Without Neutropenia (infection (without neutropenia))
CL Item
Nausea (nausea)
CL Item
Pruritus (pruritus)
CL Item
Rash/desquamation (rash / desquamation)
CL Item
Vomiting (vomiting)
CTCAdverseEventTerm,Other
Item
CTC Adverse Event Term, Other
text
Item
CTG Adverse Event Category (* Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
text
Code List
CTG Adverse Event Category (* Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
CL Item
Gastrointestinal (Gastrointestinal)
CL Item
Pain (Pain)
CL Item
Dermatology/skin (Dermatology/Skin)
CL Item
Pulmonary (Pulmonary)
CL Item
Constitutional Symptoms (Constitutional Symptoms)
CL Item
Infection (Infection)
CTCAdverseEventGrade
Item
CTC Adverse Event Grade (0=None NA=Not Assessed; * Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
text
Item Group
Concomitant Medications
AgentName
Item
Agent Name (generic or trade name)
text
Item Group
Unnamed9
PatientStudyID,CoordinatingGroup
Item
Patient Study ID, Coordinating Group
text
Patient Initials
Item
Patient Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Item Group
Other Major Medical Problems
PatientMedicalConditionDate
Item
Date Documented (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25261 (NCI Thesaurus Property)
C0205476 (UMLS 2011AA Property)
C25457 (NCI Thesaurus Property-2)
C0348080 (UMLS 2011AA Property-2)
PatientMedicalConditionText
Item
Condition (e.g. diabetes)
text
C25704 (NCI Thesaurus ValueDomain)
C1527021 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25261 (NCI Thesaurus Property)
C0205476 (UMLS 2011AA Property)
C25457 (NCI Thesaurus Property-2)
C0348080 (UMLS 2011AA Property-2)
PatientHistoryText
Item
Other Relevant Details (e.g. insulin treatment)
text
C25704 (NCI Thesaurus ValueDomain)
C1527021 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C18772 (NCI Thesaurus Property)
C0262926 (UMLS 2011AA Property)
Item Group
Comments
Comments
Item
COMMENTS
text
Item Group
Investigator Signature
InvestigatorSignature
Item
Investigator Signature
text
C25678 (NCI Thesaurus Property)
C1519316 (UMLS 2011AA Property)
C17089 (NCI Thesaurus ObjectClass)
C0035173 (UMLS 2011AA ObjectClass)
PersonCompletingForm,LastName
Item
Person Completing Form, Last Name
text
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)
FormCompletionDate,Original
Item
Form Completion Date, Original (yyyy mmm dd)
date
Item Group
Ccrr Module For Form 1 - Eligibility Checklist And Initial Evaluation

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