ID

42137

Descrizione

FORM 1 - ELIGIBILITY CHECK LIST AND INITIAL EVALUATION MA.27 Quality Of Life Companion Study For JMA27 (NCIC-MA.27): A Randomized Phase III Trial Of Exemestane Versus Anastrozole With Or Without Celecoxib In Postmenopausal Women With Receptor Positive Primary Breast Cancer Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=ABF84340-BD14-67AC-E034-0003BA12F5E7

collegamento

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=ABF84340-BD14-67AC-E034-0003BA12F5E7

Keywords

  1. 26/08/12 26/08/12 -
  2. 12/12/14 12/12/14 - Martin Dugas
  3. 13/04/21 13/04/21 - Dr. rer. medic Philipp Neuhaus
Caricato su

13 aprile 2021

DOI

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Licenza

Creative Commons BY-NC 3.0 Legacy

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Breast Cancer NCT00090974 On-Study - FORM 1 - ELIGIBILITY CHECK LIST AND INITIAL EVALUATION MA.27 - 2067101v3.0

A RANDOMIZED PHASE III TRIAL OF EXEMESTANE VERSUS ANASTROZOLE WITH OR WITHOUT CELECOXIB IN POSTMENOPAUSAL WOMEN WITH RECEPTOR POSITIVE PRIMARY BREAST CANCER-MA.27

Patient Information
Descrizione

Patient Information

Patient Medical Record Number
Descrizione

PatientMedicalRecordNumber

Tipo di dati

text

Investigator Name
Descrizione

InvestigatorName

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

Patient's Date of Birth (yyyy mmm dd)

Tipo di dati

date

Alias
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25275
UMLS CUI-1
C0421451
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 Race (check all that apply Patient is encouraged to self designate: Race Categories and Definitions definitions given with each value)
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 Ethnicity Categories and Definitions definition given with value value)
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 ([initial approval or annual renewal] 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 ([within 10 working days of randomization] yyyy mmm dd)
Descrizione

ProjectedTreatmentBeginDate

Tipo di dati

date

Eligibility Checklist
Descrizione

Eligibility Checklist

Patient has completely resected and histologically confirmed invasive breast carcinoma.
Descrizione

Patient has completely resected and histologically confirmed invasive breast carcinoma.

Tipo di dati

boolean

Date Prior Adjuvant Chemotherapy Ended (yyyy-mmm-dd)
Descrizione

PriorAdjuvantChemotherapyEndDate

Tipo di dati

date

Pathological TNM classification is (M stage)
Descrizione

TNMClassificationScheme

Tipo di dati

text

Pathological TNM classification is (M stage)
Descrizione

TNMClassificationScheme

Tipo di dati

text

Pathological TNM classification is (M stage)
Descrizione

TNMClassificationScheme

Tipo di dati

text

Primary tumour is receptor positive i.e. ER and/or PgR positive (defined as receptor content of >= 10fmol/mg protein or receptor positive by ERICA or PgRICA).
Descrizione

Primary tumour is receptor positive i.e. ER and/or PgR positive (defined as receptor content of >= 10fmol/mg protein or receptor positive by ERICA or PgRICA).

Tipo di dati

boolean

If patient has bilateral breast cancer, both were diagnosed at the same time and at least one of the bilateral cancers is receptor positive (as defined above)
Descrizione

If patient has bilateral breast cancer, both were diagnosed at the same time and at least one of the bilateral cancers is receptor positive (as defined above)

Tipo di dati

boolean

Patient is post-menopausal according to one of these three criteria
Descrizione

VerificationofPostmenopausalStatus

Tipo di dati

text

Alias
NCI Thesaurus Property
C38008
UMLS 2011AA Property
C0687676
NCI Thesaurus Property
C3231
UMLS 2011AA Property
C0025320
NCI Thesaurus ObjectClass
C25171
UMLS 2011AA ObjectClass
C0013893
FSH value
Descrizione

FSHvalue

Tipo di dati

text

Date (FSH value) (yyyy mmm dd)
Descrizione

Date (FSH value) (yyyy mmm dd)

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
NCI Thesaurus Property
C20200
NCI Thesaurus ObjectClass
C25294
NCI Thesaurus Property
C2286
UMLS CUI-1
C0011008
UMLS CUI-2
C1274040
UMLS CUI-3
C0022885
UMLS CUI-4
C0733758
Radiologic investigations have been completed within 4 weeks prior to surgical resection of primary tumour and are negative for metastases
Descrizione

Radiologic investigations have been completed within 4 weeks prior to surgical resection of primary tumour and are negative for metastases

Tipo di dati

boolean

Radiologic investigations have been completed (To specify investigations)
Descrizione

Radiologic investigations have been completed (To specify investigations)

Tipo di dati

integer

bone scan (required only if alkaline phosphatase is >= 2 x UNL and/or there are symptoms of metastatic disease a confirmatory x-ray or other imaging study such as CT or MRI is required if the results from the bone scan are questionable)
Descrizione

bonescan

Tipo di dati

text

abdominal ultrasound or CT abdomen (required only if the AST/ALT or alkaline phosphatase is > 2 x UNL unless the elevation is in the bone fraction)
Descrizione

abdominalultrasoundorCTabdomen

Tipo di dati

text

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

ChestX-RayAssessmentDate

Tipo di dati

date

Patient has had a bilateral mammogram within 10 months prior to randomization.
Descrizione

Patient has had a bilateral mammogram within 10 months prior to randomization.

Tipo di dati

boolean

Alias
NCI Thesaurus ObjectClass
C20178
NCI Thesaurus ObjectClass
C13332
NCI Thesaurus Property
C25171
NCI Metathesaurus Property
CL158135
UMLS CUI-1
C0024671
UMLS CUI-2
C0238767
UMLS CUI-3
C0013893
Date of bilateral mammogram (yyyy mmm dd)
Descrizione

Dateofbilateralmammogram

Tipo di dati

text

If patient has received prior adjuvant chemotherapy, no less than 3 weeks and no more than 3 months have elapsed since completion of chemotherapy (planned radiotherapy may be given concurrently with protocol therapy).
Descrizione

If patient has received prior adjuvant chemotherapy, no less than 3 weeks and no more than 3 months have elapsed since completion of chemotherapy (planned radiotherapy may be given concurrently with protocol therapy).

Tipo di dati

boolean

Patient has a minimum life expectancy of 5 years.
Descrizione

Patient has a minimum life expectancy of 5 years.

Tipo di dati

boolean

Performance Status (ECOG) is (circle one see Appendix II)
Descrizione

PerformanceStatus

Tipo di dati

text

Patient is able to swallow the study medication and have adequate unassisted oral intake to maintain a reasonable state of nutrition.
Descrizione

Patient is able to swallow the study medication and have adequate unassisted oral intake to maintain a reasonable state of nutrition.

Tipo di dati

boolean

Patient is able and willing to comply with scheduled study visits at the participating centre.
Descrizione

Patient is able and willing to comply with scheduled study visits at the participating centre.

Tipo di dati

boolean

Informed consent has been signed and dated by patient.
Descrizione

Informed consent has been signed and dated by patient.

Tipo di dati

boolean

Alias
UMLS CUI-1
C0021430
Date informed consent signed (yyyy mmm dd)
Descrizione

InformedConsentDateSigned

Tipo di dati

date

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

Stratification

Axillary Nodes
Descrizione

AxillaryNodes

Tipo di dati

text

Prior adjuvant chemotherapy?
Descrizione

PriorAdjuvantChemotherapyInd

Tipo di dati

text

Chronic low dose prophylactic aspirin use
Descrizione

Chroniclowdoseprophylacticaspirinuse

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Eligibility Checklist Continued
Descrizione

Eligibility Checklist Continued

Required hematologic investigations done within 4 weeks prior to randomization and are within the required parameters for eligibility.
Descrizione

Required hematologic investigations done within 4 weeks prior to randomization and are within the required parameters for eligibility.

Tipo di dati

boolean

Required biochemistry investigations done within 4 weeks prior to randomization and are within the required parameters for eligibility unless imaging examinations have ruled out metastatic disease.
Descrizione

Required biochemistry investigations done within 4 weeks prior to randomization and are within the required parameters for eligibility unless imaging examinations have ruled out metastatic disease.

Tipo di dati

boolean

Initiation of protocol therapy will begin within 10 working days of randomization.
Descrizione

TreatmentRequirementBeginIndicator

Tipo di dati

text

Patient has no history of other malignancies except adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix or other solid tumours curatively treated with no evidence of disease for >= 5 years from randomization.
Descrizione

Patient has no history of other malignancies except adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix or other solid tumours curatively treated with no evidence of disease for >= 5 years from randomization.

Tipo di dati

boolean

Patient is not receiving concurrent hormonal therapy with estrogens, progesterones, androgens or any selective estrogen receptor modulator (SERM). (previous use of Raloxifene, specifically, is permitted provided this is discontinued at least 3 weeks prior to randomization; intermittent use, i.e. maximum of 2 x per week, of vaginal estrogens is permitted on protocol if other local [trunc. see form])
Descrizione

Patient is not receiving concurrent hormonal therapy with estrogens, progesterones, androgens or any selective estrogen receptor modulator (SERM). (previous use of Raloxifene, specifically, is permitted provided this is discontinued at least 3 weeks prior to randomization; intermittent use, i.e. maximum of 2 x per week, of vaginal estrogens is permitted on protocol if other local [trunc. see form])

Tipo di dati

boolean

No prior treatment with a recognized aromatase inhibitor.
Descrizione

No prior treatment with a recognized aromatase inhibitor.

Tipo di dati

boolean

No known or incompletely treated peptic ulcer disease.
Descrizione

No known or incompletely treated peptic ulcer disease.

Tipo di dati

boolean

Patient is not receiving concurrent NSAID therapy or Cox-2 Inhibitor therapy e.g. Vioxx. (chronic low dose, i.e. <= 81 mg/day, prophylactic aspirin will be allowed)
Descrizione

Patient is not receiving concurrent NSAID therapy or Cox-2 Inhibitor therapy e.g. Vioxx. (chronic low dose, i.e. <= 81 mg/day, prophylactic aspirin will be allowed)

Tipo di dati

boolean

No known allergy to sulphonamides.
Descrizione

Noknownallergytosulphonamides.

Tipo di dati

text

No history of asthma, urticaria or allergic type reactions after taking aspirin or other NSAIDs.
Descrizione

No history of asthma, urticaria or allergic type reactions after taking aspirin or other NSAIDs.

Tipo di dati

boolean

No co-existing medical or psychiatric condition that is likely to interfere with study procedures or results.
Descrizione

No co-existing medical or psychiatric condition that is likely to interfere with study procedures or results.

Tipo di dati

boolean

If patient has participated in another trial for breast cancer (e.g. adjuvant chemotherapeutic trial), permission has been obtained, from the sponsors of that trial for the patients to participate in MA.27.
Descrizione

If patient has participated in another trial for breast cancer (e.g. adjuvant chemotherapeutic trial), permission has been obtained, from the sponsors of that trial for the patients to participate in MA.27.

Tipo di dati

boolean

Randomization Date (yyyy mmm dd)
Descrizione

RandomizationDate

Tipo di dati

date

Certificate Of Eligibility
Descrizione

Certificate Of Eligibility

In the opinion of the investigator is the patient eligible?
Descrizione

PatientEligibilityInd

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25180
UMLS 2011AA ValueDomain
C1522602
NCI Thesaurus ObjectClass
C16960
UMLS 2011AA ObjectClass
C0030705
NCI Thesaurus Property
C25171
UMLS 2011AA Property
C0013893
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
Date of Investigator Signature (yyyy mmm dd)
Descrizione

InvestigatorSignatureDate

Tipo di dati

date

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

History And Physical Exam
Descrizione

History And Physical Exam

Date of Evaluation (yyyy-mmm-dd)
Descrizione

AssessmentDate

Tipo di dati

date

Performance Status (check one see protocol Appendix II)
Descrizione

PerformanceStatus

Tipo di dati

text

Patient Height (cm)
Descrizione

PatientHeight

Tipo di dati

double

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

double

Patient is post-menopausal according to one of these three criteria
Descrizione

VerificationofPostmenopausalStatus

Tipo di dati

text

Alias
NCI Thesaurus Property
C38008
UMLS 2011AA Property
C0687676
NCI Thesaurus Property
C3231
UMLS 2011AA Property
C0025320
NCI Thesaurus ObjectClass
C25171
UMLS 2011AA ObjectClass
C0013893
FSH value
Descrizione

FSHvalue

Tipo di dati

text

Date (FSH value) (yyyy mmm dd)
Descrizione

Date (FSH value) (yyyy mmm dd)

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
NCI Thesaurus Property
C20200
NCI Thesaurus ObjectClass
C25294
NCI Thesaurus Property
C2286
UMLS CUI-1
C0011008
UMLS CUI-2
C1274040
UMLS CUI-3
C0022885
UMLS CUI-4
C0733758
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
C25421
UMLS 2011AA Property
C0002808
Date of Evaluation (yyyy-mmm-dd)
Descrizione

AssessmentDate

Tipo di dati

date

Method of Evaluation
Descrizione

AssessmentType

Tipo di dati

text

Investigations Continued Baseline Hematology/biochemistry Values
Descrizione

Investigations Continued Baseline Hematology/biochemistry Values

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

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

Tipo di dati

date

Hemoglobin (Value)
Descrizione

Hemoglobin (Value)

Tipo di dati

float

Alias
UMLS CUI-1
C0019046
Peripheral Platelet Count (Value)
Descrizione

Lab,Hematology,Platelets

Tipo di dati

double

Peripheral WBC Count (Value)
Descrizione

Lab,Hematology,WBC

Tipo di dati

double

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Lab Unit of Measure (circle unit used)
Descrizione

Lab,UnitsofMeasure

Tipo di dati

text

Peripheral Neutrophils (granulocytes) (Value)
Descrizione

Lab,Hematology,NeutrophilCount

Tipo di dati

double

Specimen Collection Date (Biochemistry yyyy mmm dd)
Descrizione

SpecimenCollectionDate

Tipo di dati

date

SGOT (AST) (Value; Must be < 2 x ULN unless imaging examinations have ruled out metastatic disease.)
Descrizione

Lab,Hepatic,SGOT

Tipo di dati

double

SGOT (AST) ULN
Descrizione

SGOTLabUpperLimitNormalValue

Tipo di dati

double

Alias
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain
C25706
UMLS 2011AA ValueDomain
C1519815
SGPT (ALT) (Value; Must be < 2 x ULN unless imaging examinations have ruled out metastatic disease.)
Descrizione

Lab,Hepatic,SGPT

Tipo di dati

double

SGPT (ALT) ULN
Descrizione

SGPTLabUpperLimitNormalValue

Tipo di dati

double

Alias
NCI Thesaurus ValueDomain
C25712
UMLS 2011AA ValueDomain
C1522609
NCI Thesaurus ValueDomain
C25706
UMLS 2011AA ValueDomain
C1519815
Alkaline Phosphatase (Value; Must be < 2 x ULN unless imaging examinations have ruled out metastatic disease.)
Descrizione

Lab,Hepatic,AlkalinePhosphatase

Tipo di dati

double

Alkaline Phosphatase ULN
Descrizione

Alkaline Phosphatase ULN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
NCI Thesaurus Property
C20200
NCI Thesaurus Property
C16276
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain
C25706
UMLS CUI-1
C0022885
UMLS CUI-2
C1274040
UMLS CUI-3
C0002059
UMLS CUI-4
C1522609
UMLS CUI-5
C1519815
Creatinine (Value)
Descrizione

Lab,Renal,Creatinine

Tipo di dati

double

Creatinine ULN
Descrizione

Creatinine ULN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
NCI Thesaurus Property
C20200
NCI Thesaurus Property
C399
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain
C25706
UMLS CUI-1
C0022885
UMLS CUI-2
C1274040
UMLS CUI-3
C0010294
UMLS CUI-4
C1522609
UMLS CUI-5
C1519815
Calcium (Ca) (Value)
Descrizione

Calcium(Ca)

Tipo di dati

double

Calcium LLN
Descrizione

Calcium LLN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
NCI Thesaurus Property
C331
NCI Thesaurus Property
C20200
NCI Thesaurus Property
C464
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain
C25555
UMLS CUI-1
C0022885
UMLS CUI-2
C0006675
UMLS CUI-3
C1274040
UMLS CUI-4
C0013832
UMLS CUI-5
C1522609
UMLS CUI-6
C1518030
Calcium ULN
Descrizione

Calcium ULN

Tipo di dati

float

Alias
NCI Thesaurus ObjectClass
C25294
NCI Thesaurus Property
C331
NCI Thesaurus Property
C20200
NCI Thesaurus Property
C464
NCI Thesaurus ValueDomain
C25712
NCI Thesaurus ValueDomain
C25706
UMLS CUI-1
C0022885
UMLS CUI-2
C0006675
UMLS CUI-3
C1274040
UMLS CUI-4
C0013832
UMLS CUI-5
C1522609
UMLS CUI-6
C1519815
Follicle Stimulating Hormone (FSH) (Value; ** Required only if necessary to confirm postmenopausal status.)
Descrizione

FollicleStimulatingHormone(FSH)

Tipo di dati

double

Postmenopausal LLN
Descrizione

PostmenopausalLLN

Tipo di dati

double

Postmenopausal ULN
Descrizione

Postmenopausal ULN

Tipo di dati

float

Disease History/prior Treatment/adverse Events
Descrizione

Disease History/prior Treatment/adverse Events

First Positive Biopsy Date (date of initial pathologic diagnosis yyyy mmm dd)
Descrizione

FirstPositiveBiopsyDate

Tipo di dati

date

Most Extensive Primary Surgery Date (if required, use last re-excision date yyyy mmm dd)
Descrizione

PrimarySurgeryDate

Tipo di dati

date

Most extensive primary surgery
Descrizione

PrimarySurgeryType

Tipo di dati

text

Was axillary dissection performed?
Descrizione

AxillaryDissectionInd

Tipo di dati

text

Axillary Dissection Date (yyyy mmm dd)
Descrizione

AxillaryDissectionDate

Tipo di dati

date

Number of lymph nodes examined
Descrizione

LymphNode(s)ExaminedNumber

Tipo di dati

double

Alias
NCI Thesaurus Property
C25500
UMLS 2011AA Property
C0332128
NCI Thesaurus ObjectClass
C12745
UMLS 2011AA ObjectClass
C0024204
Number of positive lymph nodes examined
Descrizione

LymphNode(s)PositiveNumber

Tipo di dati

double

Alias
NCI Thesaurus Property
C25246
UMLS 2011AA Property
C1446409
NCI Thesaurus ObjectClass
C12745
UMLS 2011AA ObjectClass
C0024204
Disease History... Continued
Descrizione

Disease History... Continued

Tumour Laterality (check one)
Descrizione

PrimaryTumorLaterality

Tipo di dati

text

Receptor Status, ER (If measure in fmols/mg, cytosl protein >= 10 is postive. If other measures are used, apply institutional standards; borderline results should be reported as positive)
Descrizione

ERStatus

Tipo di dati

text

Receptor Status, PgR (If measure in fmols/mg, cytosl protein >= 10 is postive. If other measures are used, apply institutional standards; borderline results should be reported as positive)
Descrizione

PgRStatus

Tipo di dati

text

T Stage, Pathologic (check one)
Descrizione

TStage,Pathologic

Tipo di dati

text

N Stage, Pathologic (check one)
Descrizione

NStage,Pathologic

Tipo di dati

text

M Stage, Pathologic (check one)
Descrizione

MStage,Pathologic

Tipo di dati

text

Prior Treatment For Cancer
Descrizione

Prior Treatment For Cancer

Prior adjuvant chemotherapy?
Descrizione

PriorAdjuvantChemotherapyInd

Tipo di dati

text

Other (specify) (agent name)
Descrizione

AgentName

Tipo di dati

text

Date Prior Adjuvant Chemotherapy Ended (yyyy-mmm-dd)
Descrizione

PriorAdjuvantChemotherapyEndDate

Tipo di dati

date

Total Number of Cycles Given
Descrizione

TotalCourseNumber

Tipo di dati

double

Prior raloxifene therapy?
Descrizione

Prior raloxifene therapy?

Tipo di dati

boolean

Alias
NCI Thesaurus ObjectClass
C15445
NCI Thesaurus Property
C1518
NCI Thesaurus Property
C25629
NCI Thesaurus Property
C25639
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C0279025
UMLS CUI-2
C0244404
UMLS CUI-3
C0332152
UMLS CUI-4
C1514756
UMLS CUI-5
C1512699
Date Prior Raloxifene Therapy Ended (yyyy mmm dd)
Descrizione

AgentEndDate

Tipo di dati

date

Prior adjuvant RT?
Descrizione

PriorAdjuvantRTInd

Tipo di dati

text

Date Adjuvant Radiation Therapy Started (yyyy mmm dd)
Descrizione

AdjuvantRTBeginDate

Tipo di dati

date

Total dose of Radiation Therapy (cGy)
Descrizione

RTTotalDose

Tipo di dati

double

Date Adjuvant Radiation Therapy Ended (yyyy mmm dd)
Descrizione

AdjuvantRTEndDate

Tipo di dati

date

Is concurrent RT planned for this patient?
Descrizione

IsconcurrentRTplannedforthispatient?

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Planned Concurrent RT Start Date (yyyy mmm dd)
Descrizione

PlannedConcurrentRTStartDate

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
Disease History... Continued; Bone Fractures
Descrizione

Disease History... Continued; Bone Fractures

Has the patient experienced a bone fracture in the last 10 years?
Descrizione

Has the patient experienced a bone fracture in the last 10 years?

Tipo di dati

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C1512699
Bone Fracture Site, Spinal (Check)
Descrizione

BoneFractureSite,Spinal

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Bone Fracture Site, Wrist (Check)
Descrizione

BoneFractureSite,Wrist

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Bone Fracture Site, Pelvis (Check)
Descrizione

BoneFractureSite,Pelvis

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Bone Fracture Site, Hip (Check)
Descrizione

BoneFractureSite,Hip

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Bone Fracture Site, Femur (Check)
Descrizione

BoneFractureSite,Femur

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Bone Fracture Site, Tibia (Check)
Descrizione

BoneFractureSite,Tibia

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Bone Fracture Site, Ankle (Check)
Descrizione

BoneFractureSite,Ankle

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Bone Fracture Site, Other (specify) (Check)
Descrizione

BoneFractureSite,Other(specify)

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
If sites other than specified, indicated site (bone fracture site)
Descrizione

indicatesite(bonefracturesite)

Tipo di dati

text

Date of Bone Fracture (yyyy-mmm-dd)
Descrizione

BoneFractureDate

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
NCI Thesaurus ObjectClass
C12366
UMLS 2011AA ObjectClass
C0262950
NCI Thesaurus Property
C3046
UMLS 2011AA Property
C0016658
Osteoporosis
Descrizione

Osteoporosis

Has the patient had a diagnosis of osteoporosis?
Descrizione

Has the patient had a diagnosis of osteoporosis?

Tipo di dati

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C0029456
Date of diagnosis of osteoporosis (yyyy mmm dd)
Descrizione

DiseaseOsteoporosisDiagnosisDate

Tipo di dati

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
NCI Thesaurus Property
C3298
UMLS 2011AA Property
C0029456
NCI Thesaurus ObjectClass
C2991
UMLS 2011AA ObjectClass
C0012634
NCI Thesaurus Property
C15220
UMLS 2011AA Property
C0011900
Cardiovascular Morbidity
Descrizione

Cardiovascular Morbidity

Has the patient suffered cardiovascular disease?
Descrizione

CardiovascularDiseasePresentInd-2

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38147
UMLS 2011AA ValueDomain
C1512698
NCI Thesaurus Property
C25626
UMLS 2011AA Property
C0150312
NCI Thesaurus ObjectClass
C25292
UMLS 2011AA ObjectClass
C0007226
NCI Thesaurus ObjectClass
C2991
UMLS 2011AA ObjectClass
C0012634
Cardiovascular Event
Descrizione

Cardiovascular Event

Myocardial infarction
Descrizione

Myocardial infarction

Tipo di dati

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C0027051
Stroke/transient ischemic attack (TIA)
Descrizione

Stroke/transient ischemic attack (TIA)

Tipo di dati

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C1512699
On-going angina (no surgical intervention)
Descrizione

CardiovascularEvent,On-goingangina(nosurgicalintervention)

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Angina requiring percutaneous transluminal coronary angioplasty (PTCA)
Descrizione

Angina requiring percutaneous transluminal coronary angioplasty (PTCA)

Tipo di dati

boolean

Alias
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus ObjectClass
C12727
NCI Thesaurus Property
C51221
NCI Thesaurus Property
C38078
NCI Thesaurus Property
C18772
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C0002962
UMLS CUI-2
C0002997
Thromboembolic event
Descrizione

Thromboembolic event

Tipo di dati

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C1512699
Other (specify), Cardiovascular Event
Descrizione

CardiovascularEvent,Other(specify)

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
please describe event (cardiovascular event) (If other specified,)
Descrizione

please describe event (cardiovascular event) (If other specified,)

Tipo di dati

text

Baseline Symptoms - Toxicity Status
Descrizione

Baseline Symptoms - Toxicity Status

CTC Adverse Event Term (Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
Descrizione

CTCAdverseEventTerm

Tipo di dati

text

CTC Adverse Event Term, Other (specify; other CTC adverse event term)
Descrizione

CTCAdverseEventTerm,Other

Tipo di dati

text

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

CTCAdverseEventCategory

Tipo di dati

text

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

CTCAdverseEventGrade

Tipo di dati

text

COMMENTS
Descrizione

Comments

Tipo di dati

text

Concomitant Medications
Descrizione

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Is the patient taking any medication?
Descrizione

Isthepatienttakinganymedication?

Tipo di dati

boolean

Alias
NCI Thesaurus ValueDomain
C38148
UMLS CUI-1
C1512699
Agent Name (generic or trade name)
Descrizione

AgentName

Tipo di dati

text

Alias
NCI Metathesaurus ValueDomain
C0027365
Other (specify) (agent name)
Descrizione

AgentName

Tipo di dati

text

Indication (chronic low dose, prophylactic)
Descrizione

AgentAdministeredReason

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25638
UMLS 2011AA ValueDomain
C0392360
NCI Thesaurus ObjectClass
C1708
UMLS 2011AA ObjectClass
C0450442
NCI Thesaurus Property
C25382
UMLS 2011AA Property
C1521801
Continuing
Descrizione

Continuing

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C38148
UMLS 2011AA ValueDomain
C1512699
Other Major Medical Problems
Descrizione

Other Major Medical Problems

Have there been any major medical problems?
Descrizione

Have there been any major medical problems?

Tipo di dati

boolean

Major Medical Problem (e.g. hypertension, diabetes, previous cancers)
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
C25457
UMLS 2011AA Property
C0348080
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

Similar models

A RANDOMIZED PHASE III TRIAL OF EXEMESTANE VERSUS ANASTROZOLE WITH OR WITHOUT CELECOXIB IN POSTMENOPAUSAL WOMEN WITH RECEPTOR POSITIVE PRIMARY BREAST CANCER-MA.27

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Patient Information
PatientMedicalRecordNumber
Item
Patient Medical Record Number
text
InvestigatorName
Item
Investigator Name
text
InstitutionName
Item
Institution Name
text
RegisteredInvestigator
Item
Registered Investigator (NCI Investigator #)
text
Patient birth date
Item
Patient's Date of Birth (yyyy mmm dd)
date
C16960 (NCI Thesaurus ObjectClass)
C25275 (NCI Thesaurus Property)
C0421451 (UMLS CUI-1)
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)
CL Item
Female (Female)
Item
Patient Race (check all that apply Patient is encouraged to self designate: Race Categories and Definitions definitions given with each value)
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 Patient is encouraged to self designate: Race Categories and Definitions definitions given with each value)
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 Ethnicity Categories and Definitions definition given with value value)
text
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C17049 (NCI Thesaurus Property)
C0034510 (UMLS 2011AA Property)
Code List
Patient Ethnicity (check one only Ethnicity Categories and Definitions definition given with value value)
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 and Private Insurance)
CL Item
Medicaid (Medicaid)
C0025071 (NCI Metathesaurus)
CL Item
Medicaid And Medicare (Medicaid and 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
Unknown (Unknown)
C17998 (NCI Thesaurus)
C0439673 (UMLS 2011AA)
CL Item
Other (Other)
C17649 (NCI Thesaurus)
C0205394 (UMLS 2011AA)
IRBApprovalDate
Item
IRB/REB Approval Date ([initial approval or annual renewal] 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 ([within 10 working days of randomization] yyyy mmm dd)
date
Item Group
Eligibility Checklist
Completely resected and histologically confirmed invasive breast carcinoma
Item
Patient has completely resected and histologically confirmed invasive breast carcinoma.
boolean
PriorAdjuvantChemotherapyEndDate
Item
Date Prior Adjuvant Chemotherapy Ended (yyyy-mmm-dd)
date
Item
Pathological TNM classification is (M stage)
text
Code List
Pathological TNM classification is (M stage)
CL Item
M0 (M0)
Item
Pathological TNM classification is (M stage)
text
Code List
Pathological TNM classification is (M stage)
CL Item
M0 (M0)
Item
Pathological TNM classification is (M stage)
text
Code List
Pathological TNM classification is (M stage)
CL Item
M0 (M0)
Primary tumour receptorpositive
Item
Primary tumour is receptor positive i.e. ER and/or PgR positive (defined as receptor content of >= 10fmol/mg protein or receptor positive by ERICA or PgRICA).
boolean
If bilateral breast cancer then diagnosed simultaneously and receptor positive
Item
If patient has bilateral breast cancer, both were diagnosed at the same time and at least one of the bilateral cancers is receptor positive (as defined above)
boolean
Item
Patient is post-menopausal according to one of these three criteria
text
C38008 (NCI Thesaurus Property)
C0687676 (UMLS 2011AA Property)
C3231 (NCI Thesaurus Property)
C0025320 (UMLS 2011AA Property)
C25171 (NCI Thesaurus ObjectClass)
C0013893 (UMLS 2011AA ObjectClass)
Code List
Patient is post-menopausal according to one of these three criteria
CL Item
greater than (>) 55 years of age with no spontaneous menses for at least 12 months; (greater than (>) 55 years of age with no spontaneous menses for at least 12 months;)
CL Item
less or equal to (<=) 55 years of age with no spontaneous menses within the past 12 months (i.e. spontaneous cessation or secondary to hysterectomy) AND with and FSH level in the postmenopausal range according to institutional/laboratory standards (less or equal to (<=) 55 years of age with no spontaneous menses within the past 12 months (i.e. spontaneous cessation or secondary to hysterectomy) AND with and FSH level in the postmenopausal range according to institutional/laboratory standards)
CL Item
Bilateral Oophorectomy (bilateral oophorectomy)
FSHvalue
Item
FSH value
text
FSH date
Item
Date (FSH value) (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C20200 (NCI Thesaurus Property)
C25294 (NCI Thesaurus ObjectClass)
C2286 (NCI Thesaurus Property)
C0011008 (UMLS CUI-1)
C1274040 (UMLS CUI-2)
C0022885 (UMLS CUI-3)
C0733758 (UMLS CUI-4)
No Metastases in radiologic investigations within 4 weeks prior to surgical resection
Item
Radiologic investigations have been completed within 4 weeks prior to surgical resection of primary tumour and are negative for metastases
boolean
Item
Radiologic investigations have been completed (To specify investigations)
integer
Code List
Radiologic investigations have been completed (To specify investigations)
CL Item
Bone Scan (1)
CL Item
Abdominal Ultrasound Or Ct Abdomen (2)
CL Item
Chest X-ray (3)
Item
bone scan (required only if alkaline phosphatase is >= 2 x UNL and/or there are symptoms of metastatic disease a confirmatory x-ray or other imaging study such as CT or MRI is required if the results from the bone scan are questionable)
text
Code List
bone scan (required only if alkaline phosphatase is >= 2 x UNL and/or there are symptoms of metastatic disease a confirmatory x-ray or other imaging study such as CT or MRI is required if the results from the bone scan are questionable)
CL Item
Not Applicable (Not Applicable)
C48660 (NCI Thesaurus)
C1272460 (UMLS 2011AA)
Item
abdominal ultrasound or CT abdomen (required only if the AST/ALT or alkaline phosphatase is > 2 x UNL unless the elevation is in the bone fraction)
text
Code List
abdominal ultrasound or CT abdomen (required only if the AST/ALT or alkaline phosphatase is > 2 x UNL unless the elevation is in the bone fraction)
CL Item
Not Applicable (Not Applicable)
C48660 (NCI Thesaurus)
C1272460 (UMLS 2011AA)
ChestX-RayAssessmentDate
Item
Date of chest x-ray (yyyy mmm dd)
date
Bilateral Mammogram within 10 months
Item
Patient has had a bilateral mammogram within 10 months prior to randomization.
boolean
C20178 (NCI Thesaurus ObjectClass)
C13332 (NCI Thesaurus ObjectClass)
C25171 (NCI Thesaurus Property)
CL158135 (NCI Metathesaurus Property)
C0024671 (UMLS CUI-1)
C0238767 (UMLS CUI-2)
C0013893 (UMLS CUI-3)
Dateofbilateralmammogram
Item
Date of bilateral mammogram (yyyy mmm dd)
text
If adjuvant chemotherapy then within 3 weeks to 3 months
Item
If patient has received prior adjuvant chemotherapy, no less than 3 weeks and no more than 3 months have elapsed since completion of chemotherapy (planned radiotherapy may be given concurrently with protocol therapy).
boolean
Minimum life expectancy of 5 years
Item
Patient has a minimum life expectancy of 5 years.
boolean
Item
Performance Status (ECOG) is (circle one see Appendix II)
text
Code List
Performance Status (ECOG) is (circle one see Appendix II)
CL Item
0 (0)
C0919414 (NCI Metathesaurus)
CL Item
1 (1)
CL Item
2 (2)
C66833 (NCI Thesaurus)
C0205448 (UMLS 2011AA)
Patientis able to swallow study medication and adequate unassisted oral intake
Item
Patient is able to swallow the study medication and have adequate unassisted oral intake to maintain a reasonable state of nutrition.
boolean
Compliance with study visits
Item
Patient is able and willing to comply with scheduled study visits at the participating centre.
boolean
Informed consent
Item
Informed consent has been signed and dated by patient.
boolean
C0021430 (UMLS CUI-1)
InformedConsentDateSigned
Item
Date informed consent signed (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
Item Group
Stratification
Item
Axillary Nodes
text
Code List
Axillary Nodes
CL Item
Regional Lymph Nodes Cannot Be Assessed (e.g., Previously Removed) (NX)
CL Item
No Regional Lymph Node Metastasis (N0)
CL Item
Metastasis To Movable Ipsilateral Axillary Lymph Node(s) (N1)
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
Chronic low dose prophylactic aspirin use
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Chronic low dose prophylactic aspirin use
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
Item Group
Eligibility Checklist Continued
Hematologic investigations matching eligibility criteria within 4 weeks prior to randomization
Item
Required hematologic investigations done within 4 weeks prior to randomization and are within the required parameters for eligibility.
boolean
Biochemistry investigations within 4 weeks match eligibility criteria
Item
Required biochemistry investigations done within 4 weeks prior to randomization and are within the required parameters for eligibility unless imaging examinations have ruled out metastatic disease.
boolean
TreatmentRequirementBeginIndicator
Item
Initiation of protocol therapy will begin within 10 working days of randomization.
text
No history of other non-curated malignancies within past 5 years
Item
Patient has no history of other malignancies except adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix or other solid tumours curatively treated with no evidence of disease for >= 5 years from randomization.
boolean
No concurrent hormonal therapy
Item
Patient is not receiving concurrent hormonal therapy with estrogens, progesterones, androgens or any selective estrogen receptor modulator (SERM). (previous use of Raloxifene, specifically, is permitted provided this is discontinued at least 3 weeks prior to randomization; intermittent use, i.e. maximum of 2 x per week, of vaginal estrogens is permitted on protocol if other local [trunc. see form])
boolean
No prior treatment with aromataseinhibitor
Item
No prior treatment with a recognized aromatase inhibitor.
boolean
No peptic ulcer disease
Item
No known or incompletely treated peptic ulcer disease.
boolean
No concurrent NSAID or Cox-2 Inhibitor therapy
Item
Patient is not receiving concurrent NSAID therapy or Cox-2 Inhibitor therapy e.g. Vioxx. (chronic low dose, i.e. <= 81 mg/day, prophylactic aspirin will be allowed)
boolean
Noknownallergytosulphonamides.
Item
No known allergy to sulphonamides.
text
No allergic reaction to NSAIDs
Item
No history of asthma, urticaria or allergic type reactions after taking aspirin or other NSAIDs.
boolean
No co-existing interfering medical or psychiatric conditions
Item
No co-existing medical or psychiatric condition that is likely to interfere with study procedures or results.
boolean
Permission from sponsor of other trial
Item
If patient has participated in another trial for breast cancer (e.g. adjuvant chemotherapeutic trial), permission has been obtained, from the sponsors of that trial for the patients to participate in MA.27.
boolean
RandomizationDate
Item
Randomization Date (yyyy mmm dd)
date
Item Group
Certificate Of Eligibility
Item
In the opinion of the investigator is the patient eligible?
text
C25180 (NCI Thesaurus ValueDomain)
C1522602 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25171 (NCI Thesaurus Property)
C0013893 (UMLS 2011AA Property)
Code List
In the opinion of the investigator is the patient eligible?
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
InvestigatorSignature
Item
Investigator Signature
text
C25678 (NCI Thesaurus Property)
C1519316 (UMLS 2011AA Property)
C17089 (NCI Thesaurus ObjectClass)
C0035173 (UMLS 2011AA ObjectClass)
InvestigatorSignatureDate
Item
Date of Investigator Signature (yyyy mmm dd)
date
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
History And Physical Exam
AssessmentDate
Item
Date of Evaluation (yyyy-mmm-dd)
date
Item
Performance Status (check one see protocol Appendix II)
text
Code List
Performance Status (check one see protocol Appendix II)
CL Item
0 (Fully active, able to carry on all pre-disease performance without restriction (Karnofsky 90 - 100))
C0919414 (NCI Metathesaurus)
CL Item
1 (Restricted in physically strenuous activity but ambulatory (K 70 - 80))
CL Item
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 (Capable of only limited self-care, confined to bed or chair more than 50% of waking hours (K 30-40))
CL Item
4 (Completely disabled. Cannot carry on any self-care. Totally confined to bed or chair (K 10-20))
PatientHeight
Item
Patient Height (cm)
double
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25347 (NCI Thesaurus Property)
C0489786 (UMLS 2011AA Property)
PatientWeight
Item
Patient Weight (kg)
double
Item
Patient is post-menopausal according to one of these three criteria
text
C38008 (NCI Thesaurus Property)
C0687676 (UMLS 2011AA Property)
C3231 (NCI Thesaurus Property)
C0025320 (UMLS 2011AA Property)
C25171 (NCI Thesaurus ObjectClass)
C0013893 (UMLS 2011AA ObjectClass)
Code List
Patient is post-menopausal according to one of these three criteria
CL Item
greater than (>) 55 years of age with no spontaneous menses for at least 12 months; (greater than (>) 55 years of age with no spontaneous menses for at least 12 months;)
CL Item
less or equal to (<=) 55 years of age with no spontaneous menses within the past 12 months (i.e. spontaneous cessation or secondary to hysterectomy) AND with and FSH level in the postmenopausal range according to institutional/laboratory standards (less or equal to (<=) 55 years of age with no spontaneous menses within the past 12 months (i.e. spontaneous cessation or secondary to hysterectomy) AND with and FSH level in the postmenopausal range according to institutional/laboratory standards)
CL Item
Bilateral Oophorectomy (bilateral oophorectomy)
FSHvalue
Item
FSH value
text
FSH date
Item
Date (FSH value) (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C20200 (NCI Thesaurus Property)
C25294 (NCI Thesaurus ObjectClass)
C2286 (NCI Thesaurus Property)
C0011008 (UMLS CUI-1)
C1274040 (UMLS CUI-2)
C0022885 (UMLS CUI-3)
C0733758 (UMLS CUI-4)
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)
C0002808 (UMLS 2011AA Property)
Code List
Imaging Site
CL Item
Chest (Chest)
C25389 (NCI Thesaurus)
C0817096 (UMLS 2011AA)
CL Item
Abdomen (Abdomen)
C12664 (NCI Thesaurus)
C0230168 (UMLS 2011AA)
CL Item
Bone (Bone)
C12366 (NCI Thesaurus)
C0262950 (UMLS 2011AA)
AssessmentDate
Item
Date of Evaluation (yyyy-mmm-dd)
date
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
Bilateral Mammogram (Bilateral Mammogram)
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)
Item Group
Investigations Continued Baseline Hematology/biochemistry Values
Hematology lab date
Item
Date Hematology (Blood) Sample Obtained (yyyy mmm dd)
date
Hemoglobin
Item
Hemoglobin (Value)
float
C0019046 (UMLS CUI-1)
Lab,Hematology,Platelets
Item
Peripheral Platelet Count (Value)
double
Lab,Hematology,WBC
Item
Peripheral WBC Count (Value)
double
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Item
Lab Unit of Measure (circle unit used)
text
Code List
Lab Unit of Measure (circle unit used)
CL Item
Iu/l (IU/L)
Lab,Hematology,NeutrophilCount
Item
Peripheral Neutrophils (granulocytes) (Value)
double
SpecimenCollectionDate
Item
Specimen Collection Date (Biochemistry yyyy mmm dd)
date
Lab,Hepatic,SGOT
Item
SGOT (AST) (Value; Must be < 2 x ULN unless imaging examinations have ruled out metastatic disease.)
double
SGOTLabUpperLimitNormalValue
Item
SGOT (AST) ULN
double
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain)
C1519815 (UMLS 2011AA ValueDomain)
Lab,Hepatic,SGPT
Item
SGPT (ALT) (Value; Must be < 2 x ULN unless imaging examinations have ruled out metastatic disease.)
double
SGPTLabUpperLimitNormalValue
Item
SGPT (ALT) ULN
double
C25712 (NCI Thesaurus ValueDomain)
C1522609 (UMLS 2011AA ValueDomain)
C25706 (NCI Thesaurus ValueDomain)
C1519815 (UMLS 2011AA ValueDomain)
Lab,Hepatic,AlkalinePhosphatase
Item
Alkaline Phosphatase (Value; Must be < 2 x ULN unless imaging examinations have ruled out metastatic disease.)
double
Alkaline Phosphatase Upper Limit Normal value
Item
Alkaline Phosphatase ULN
float
C25294 (NCI Thesaurus ObjectClass)
C20200 (NCI Thesaurus Property)
C16276 (NCI Thesaurus Property)
C25712 (NCI Thesaurus ValueDomain)
C25706 (NCI Thesaurus ValueDomain)
C0022885 (UMLS CUI-1)
C1274040 (UMLS CUI-2)
C0002059 (UMLS CUI-3)
C1522609 (UMLS CUI-4)
C1519815 (UMLS CUI-5)
Lab,Renal,Creatinine
Item
Creatinine (Value)
double
Creatinine Upper Limit Normal value
Item
Creatinine ULN
float
C25294 (NCI Thesaurus ObjectClass)
C20200 (NCI Thesaurus Property)
C399 (NCI Thesaurus Property)
C25712 (NCI Thesaurus ValueDomain)
C25706 (NCI Thesaurus ValueDomain)
C0022885 (UMLS CUI-1)
C1274040 (UMLS CUI-2)
C0010294 (UMLS CUI-3)
C1522609 (UMLS CUI-4)
C1519815 (UMLS CUI-5)
Calcium(Ca)
Item
Calcium (Ca) (Value)
double
Calcium Electrolytes Lower Limit of Normal Value
Item
Calcium LLN
float
C25294 (NCI Thesaurus ObjectClass)
C331 (NCI Thesaurus Property)
C20200 (NCI Thesaurus Property)
C464 (NCI Thesaurus Property)
C25712 (NCI Thesaurus ValueDomain)
C25555 (NCI Thesaurus ValueDomain)
C0022885 (UMLS CUI-1)
C0006675 (UMLS CUI-2)
C1274040 (UMLS CUI-3)
C0013832 (UMLS CUI-4)
C1522609 (UMLS CUI-5)
C1518030 (UMLS CUI-6)
Calcium Electrolytes Upper Limit of Normal Value
Item
Calcium ULN
float
C25294 (NCI Thesaurus ObjectClass)
C331 (NCI Thesaurus Property)
C20200 (NCI Thesaurus Property)
C464 (NCI Thesaurus Property)
C25712 (NCI Thesaurus ValueDomain)
C25706 (NCI Thesaurus ValueDomain)
C0022885 (UMLS CUI-1)
C0006675 (UMLS CUI-2)
C1274040 (UMLS CUI-3)
C0013832 (UMLS CUI-4)
C1522609 (UMLS CUI-5)
C1519815 (UMLS CUI-6)
FollicleStimulatingHormone(FSH)
Item
Follicle Stimulating Hormone (FSH) (Value; ** Required only if necessary to confirm postmenopausal status.)
double
PostmenopausalLLN
Item
Postmenopausal LLN
double
Postmenopausal ULN
Item
Postmenopausal ULN
float
Item Group
Disease History/prior Treatment/adverse Events
FirstPositiveBiopsyDate
Item
First Positive Biopsy Date (date of initial pathologic diagnosis yyyy mmm dd)
date
PrimarySurgeryDate
Item
Most Extensive Primary Surgery Date (if required, use last re-excision date yyyy mmm dd)
date
Item
Most extensive primary surgery
text
Code List
Most extensive primary surgery
CL Item
Partial Mastectomy/lumpectomy/excisional Biopsy (partial mastectomy/lumpectomy/excisional biopsy)
CL Item
Mastectomy, Nos (mastectomy, NOS)
Item
Was axillary dissection performed?
text
Code List
Was axillary dissection performed?
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
AxillaryDissectionDate
Item
Axillary Dissection Date (yyyy mmm dd)
date
LymphNode(s)ExaminedNumber
Item
Number of lymph nodes examined
double
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 examined
double
C25246 (NCI Thesaurus Property)
C1446409 (UMLS 2011AA Property)
C12745 (NCI Thesaurus ObjectClass)
C0024204 (UMLS 2011AA ObjectClass)
Item Group
Disease History... Continued
Item
Tumour Laterality (check one)
text
Code List
Tumour Laterality (check one)
CL Item
Left (Left)
C25229 (NCI Thesaurus)
C0205091 (UMLS 2011AA)
CL Item
Right (Right)
C25228 (NCI Thesaurus)
C0205090 (UMLS 2011AA)
CL Item
Bilateral (Bilateral)
Item
Receptor Status, ER (If measure in fmols/mg, cytosl protein >= 10 is postive. If other measures are used, apply institutional standards; borderline results should be reported as positive)
text
Code List
Receptor Status, ER (If measure in fmols/mg, cytosl protein >= 10 is postive. If other measures are used, apply institutional standards; borderline results should be reported as positive)
CL Item
Positive (Positive)
C25246 (NCI Thesaurus)
C1446409 (UMLS 2011AA)
CL Item
Negative (Negative)
C25247 (NCI Thesaurus)
C0205160 (UMLS 2011AA)
Item
Receptor Status, PgR (If measure in fmols/mg, cytosl protein >= 10 is postive. If other measures are used, apply institutional standards; borderline results should be reported as positive)
text
Code List
Receptor Status, PgR (If measure in fmols/mg, cytosl protein >= 10 is postive. If other measures are used, apply institutional standards; borderline results should be reported as positive)
CL Item
Positive (Positive)
C25246 (NCI Thesaurus)
C1446409 (UMLS 2011AA)
CL Item
Negative (Negative)
C25247 (NCI Thesaurus)
C0205160 (UMLS 2011AA)
Item
T Stage, Pathologic (check one)
text
Code List
T Stage, Pathologic (check one)
CL Item
Refer To Figo And/or Ajcc Staging Guidelines Per Protocol (TX)
CL Item
Refer To Figo And/or Ajcc Staging Guidelines Per Protocol (T1)
CL Item
Refer To Figo And/or Ajcc Staging Guidelines Per Protocol (T2)
CL Item
Refer To Figo And/or Ajcc Staging Guidelines Per Protocol (T3)
Item
N Stage, Pathologic (check one)
text
Code List
N Stage, Pathologic (check one)
CL Item
Nx, According To Ajcc Criteria (NX)
CL Item
N0, According To Ajcc Criteria (N0)
CL Item
N1, According To Ajcc Criteria (N1)
Item
M Stage, Pathologic (check one)
text
Code List
M Stage, Pathologic (check one)
CL Item
No Distant Metastasis (M0)
Item Group
Prior Treatment For Cancer
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)
AgentName
Item
Other (specify) (agent name)
text
PriorAdjuvantChemotherapyEndDate
Item
Date Prior Adjuvant Chemotherapy Ended (yyyy-mmm-dd)
date
TotalCourseNumber
Item
Total Number of Cycles Given
double
Prior Raloxifene therapy
Item
Prior raloxifene therapy?
boolean
C15445 (NCI Thesaurus ObjectClass)
C1518 (NCI Thesaurus Property)
C25629 (NCI Thesaurus Property)
C25639 (NCI Thesaurus Property)
C38148 (NCI Thesaurus ValueDomain)
C0279025 (UMLS CUI-1)
C0244404 (UMLS CUI-2)
C0332152 (UMLS CUI-3)
C1514756 (UMLS CUI-4)
C1512699 (UMLS CUI-5)
AgentEndDate
Item
Date Prior Raloxifene Therapy Ended (yyyy mmm dd)
date
Item
Prior adjuvant RT?
text
Code List
Prior adjuvant RT?
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
RTTotalDose
Item
Total dose of Radiation Therapy (cGy)
double
AdjuvantRTEndDate
Item
Date Adjuvant Radiation Therapy Ended (yyyy mmm dd)
date
Item
Is concurrent RT planned for this patient?
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Is concurrent RT planned for this patient?
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
PlannedConcurrentRTStartDate
Item
Planned Concurrent RT Start Date (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
Item Group
Disease History... Continued; Bone Fractures
Bone fracture within past 10 years
Item
Has the patient experienced a bone fracture in the last 10 years?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS CUI-1)
Item
Bone Fracture Site, Spinal (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Spinal (Check)
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
Bone Fracture Site, Wrist (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Wrist (Check)
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
Bone Fracture Site, Pelvis (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Pelvis (Check)
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
Bone Fracture Site, Hip (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Hip (Check)
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
Bone Fracture Site, Femur (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Femur (Check)
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
Bone Fracture Site, Tibia (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Tibia (Check)
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
Bone Fracture Site, Ankle (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Ankle (Check)
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
Bone Fracture Site, Other (specify) (Check)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Bone Fracture Site, Other (specify) (Check)
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)
indicatesite(bonefracturesite)
Item
If sites other than specified, indicated site (bone fracture site)
text
BoneFractureDate
Item
Date of Bone Fracture (yyyy-mmm-dd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C12366 (NCI Thesaurus ObjectClass)
C0262950 (UMLS 2011AA ObjectClass)
C3046 (NCI Thesaurus Property)
C0016658 (UMLS 2011AA Property)
Item Group
Osteoporosis
Osteoporosis
Item
Has the patient had a diagnosis of osteoporosis?
boolean
C38148 (NCI Thesaurus ValueDomain)
C0029456 (UMLS CUI-1)
DiseaseOsteoporosisDiagnosisDate
Item
Date of diagnosis of osteoporosis (yyyy mmm dd)
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C3298 (NCI Thesaurus Property)
C0029456 (UMLS 2011AA Property)
C2991 (NCI Thesaurus ObjectClass)
C0012634 (UMLS 2011AA ObjectClass)
C15220 (NCI Thesaurus Property)
C0011900 (UMLS 2011AA Property)
Item Group
Cardiovascular Morbidity
Item
Has the patient suffered cardiovascular disease?
text
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
C25626 (NCI Thesaurus Property)
C0150312 (UMLS 2011AA Property)
C25292 (NCI Thesaurus ObjectClass)
C0007226 (UMLS 2011AA ObjectClass)
C2991 (NCI Thesaurus ObjectClass)
C0012634 (UMLS 2011AA ObjectClass)
Code List
Has the patient suffered cardiovascular disease?
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
Item Group
Cardiovascular Event
Myocardial infarction
Item
Myocardial infarction
boolean
C38148 (NCI Thesaurus ValueDomain)
C0027051 (UMLS CUI-1)
Stroke or TIA
Item
Stroke/transient ischemic attack (TIA)
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS CUI-1)
Item
On-going angina (no surgical intervention)
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
On-going angina (no surgical intervention)
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)
Angina pectoris with PTCA
Item
Angina requiring percutaneous transluminal coronary angioplasty (PTCA)
boolean
C16960 (NCI Thesaurus ObjectClass)
C12727 (NCI Thesaurus ObjectClass)
C51221 (NCI Thesaurus Property)
C38078 (NCI Thesaurus Property)
C18772 (NCI Thesaurus Property)
C38148 (NCI Thesaurus ValueDomain)
C0002962 (UMLS CUI-1)
C0002997 (UMLS CUI-2)
Thromboembolic event
Item
Thromboembolic event
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS CUI-1)
Item
Other (specify), Cardiovascular Event
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Other (specify), Cardiovascular Event
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)
Event description
Item
please describe event (cardiovascular event) (If other specified,)
text
Item Group
Baseline Symptoms - Toxicity Status
Item
CTC Adverse Event Term (Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
text
Code List
CTC Adverse Event Term (Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
CL Item
edema (edema)
CL Item
fatigue (lethary/malaise/asthenia) (fatigue (lethary/malaise/asthenia))
CL Item
sweating (diaphoresis) (sweating (diaphoresis))
CL Item
rash/desquamation (rash/desquamation)
CL Item
hot flashes/flushes (hot flashes/flushes)
CL Item
anorexia (anorexia)
CL Item
constipation (constipation)
CL Item
diarrhea (patients without colostomy) (diarrhea (patients without colostomy))
CL Item
dyspepsia/heartburn (dyspepsia/heartburn)
CL Item
flatulence (flatulence)
CL Item
nausea (nausea)
CL Item
vomiting (vomiting)
CL Item
vaginal bleeding (vaginal bleeding)
CL Item
infection (without neutropenia) (infection (without neutropenia))
CL Item
hypercholesterolemia (hypercholesterolemia)
CL Item
dizziness/lightheadedness (dizziness/lightheadedness)
CL Item
abdominal pain or cramping (abdominal pain or cramping)
CL Item
arthralgia (joint pain) (arthralgia (joint pain))
CL Item
headache (headache)
CL Item
cough (cough)
CL Item
dyspnea (shortness of breath) (dyspnea (shortness of breath))
CL Item
other (other)
CTCAdverseEventTerm,Other
Item
CTC Adverse Event Term, Other (specify; other CTC adverse event term)
text
Item
CTC Adverse Event Category (Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
text
Code List
CTC Adverse Event Category (Code/grade according to NCI Common Toxicity Criteria, Version 2.0)
CL Item
cardiovascular (cardiovascular)
CL Item
constitutional symptoms (constitutional symptoms)
CL Item
dermatology/skin (dermatology/skin)
CL Item
endocrine (endocrine)
CL Item
gastrointestinal (gastrointestinal)
CL Item
hemorrhage (hemorrhage)
CL Item
infection (infection)
CL Item
metabolic (metabolic)
CL Item
neurology (neurology)
CL Item
pain (pain)
CL Item
pulmonary (pulmonary)
CTCAdverseEventGrade
Item
CTC Adverse Event Grade (Code/grade according to NCI Common Toxicity Criteria, Version 2.0 0=None NA=Not Assessed)
text
Comments
Item
COMMENTS
text
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Isthepatienttakinganymedication?
Item
Is the patient taking any medication?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS CUI-1)
Item
Agent Name (generic or trade name)
text
C0027365 (NCI Metathesaurus ValueDomain)
Code List
Agent Name (generic or trade name)
CL Item
Aspirin (Aspirin)
CL Item
Bisphosphonate (Bisphosphonate)
CL Item
Calcium (Calcium)
C331 (NCI Thesaurus)
C0006675 (UMLS 2011AA)
CL Item
Lipid Lowering Drug (Lipid Lowering Drug)
CL Item
Cardiovascular Medication (Cardiovascular Medication)
CL Item
Other Specify (Other (specify))
AgentName
Item
Other (specify) (agent name)
text
AgentAdministeredReason
Item
Indication (chronic low dose, prophylactic)
text
C25638 (NCI Thesaurus ValueDomain)
C0392360 (UMLS 2011AA ValueDomain)
C1708 (NCI Thesaurus ObjectClass)
C0450442 (UMLS 2011AA ObjectClass)
C25382 (NCI Thesaurus Property)
C1521801 (UMLS 2011AA Property)
Item
Continuing
text
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
Code List
Continuing
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
Other Major Medical Problems
Major ongoing medical problem
Item
Have there been any major medical problems?
boolean
PatientMedicalConditionText
Item
Major Medical Problem (e.g. hypertension, diabetes, previous cancers)
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)
C0348080 (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

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