No Instruction available.

  1. StudyEvent: ADVL0212: Reporting Period Worksheet (Leukemia)
    1. No Instruction available.
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Header
Protocol ID COG
Item
COG Study Number
text
C25337 (NCI Thesaurus ValueDomain)
C3274381 (UMLS CUI-1)
C25320 (NCI Thesaurus ObjectClass)
C1516477 (UMLS CUI-2)
C25364 (NCI Thesaurus Property)
Institution Name
Item
Institution Name
text
C25191 (NCI Thesaurus ValueDomain)
C1301943 (UMLS CUI-1)
C21541 (NCI Thesaurus ObjectClass)
C21541 (NCI Thesaurus ValueDomain-2)
C25364 (NCI Thesaurus Property)
Patient ID COG
Item
COG Patient ID
text
C25337 (NCI Thesaurus ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C25364 (NCI Thesaurus Property)
C39353 (NCI Thesaurus Property-2)
C2348585 (UMLS CUI-1)
Patient Initials
Item
Patient's Initials
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
Reporting Period Number
Item
Reporting Period Number
text
C25337 (NCI Thesaurus ValueDomain)
C25616 (NCI Thesaurus Property)
C15368 (NCI Thesaurus ObjectClass)
C25651 (NCI Thesaurus Property-2)
C0237753 (UMLS CUI-1)
C1948053 (UMLS CUI-2)
C0700287 (UMLS CUI-3)
Reporting Period Start Date
Item
Reporting Period start date
date
C15368 (NCI Thesaurus ObjectClass)
C25616 (NCI Thesaurus Property)
C2361257 (UMLS CUI-1)
C25651 (NCI Thesaurus Property-2)
C25164 (NCI Thesaurus ValueDomain)
C25431 (NCI Thesaurus ValueDomain-2)
Reporting Period End Date
Item
Reporting Period End date
date
C25164 (NCI Thesaurus ValueDomain)
C2361259 (UMLS CUI-1)
C25616 (NCI Thesaurus Property)
C15368 (NCI Thesaurus ObjectClass)
C25651 (NCI Thesaurus Property-2)
Research Comments
Item
Comments
text
C25704 (NCI Thesaurus ValueDomain)
C0947611 (UMLS CUI-1)
C15319 (NCI Thesaurus ObjectClass)
C25393 (NCI Thesaurus Property)
Item Group
Patient characteristics
C0815172 (UMLS CUI-1)
Patient Height
Item
Height
float
C25209 (NCI Thesaurus ValueDomain)
C0489786 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25347 (NCI Thesaurus Property)
Patient Weight
Item
Weight
float
C25209 (NCI Thesaurus ValueDomain)
C0005910 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25208 (NCI Thesaurus Property)
Bone marrow
Item
Was patient's bone marrow status evaluated during this reporting interval?
boolean
C38148 (NCI Thesaurus ValueDomain)
C25214 (NCI Thesaurus Property)
C12431 (NCI Thesaurus ObjectClass)
C0005953 (UMLS CUI-1)
Bone marrow date
Item
what was the date of exam?
date
C25164 (NCI Thesaurus ValueDomain)
C25214 (NCI Thesaurus Property)
C12431 (NCI Thesaurus ObjectClass)
C0005953 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
Bone Marrow Involvement
Item
does patient have bone marrow involvement?
boolean
C38148 (NCI Thesaurus ValueDomain)
C12431 (NCI Thesaurus ObjectClass)
C25548 (NCI Thesaurus Property)
C0005953 (UMLS CUI-1)
C1314939 (UMLS CUI-2)
EF
Item
Was patients shortening fraction determined by echocardiogram?
boolean
C38147 (NCI Thesaurus ValueDomain)
C25217 (NCI Thesaurus Property)
C0232174 (UMLS CUI-1)
EF
Item
what is the percentage?
float
C20200 (NCI Thesaurus Property)
C38020 (NCI Thesaurus ObjectClass)
C0232174 (UMLS CUI-1)
off protocoll therapy
Item
Is patient off protocol therapy at the end of this reporting period?
boolean
C38148 (NCI Thesaurus ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C25601 (NCI Thesaurus Property)
C1518544 (UMLS CUI-1)
Date Last Dose
Item
date of last dose for this reporting period
date
C25164 (NCI Thesaurus ValueDomain)
C1762893 (UMLS CUI-1)
C15368 (NCI Thesaurus ObjectClass)
C25509 (NCI Thesaurus Property)
C25256 (NCI Thesaurus Property-2)
Item
reason treatment ended
text
C25601 (NCI Thesaurus ObjectClass)
C25365 (NCI Thesaurus Property)
C1518544 (UMLS CUI-1)
Code List
reason treatment ended
CL Item
Progressive disease (1)
CL Item
Irreversible dose-limiting toxicity (2)
CL Item
Patient withdrawal from protocol (3)
CL Item
Off Study (4)
CL Item
Alternative Therapy (5)
CL Item
Lost To Follow-up (6)
CL Item
Death On Study (7)
CL Item
Cytogenetic Resistance (8)
CL Item
Disease Progression, Relapse During Active Treatment (9)
CL Item
Disease Progression Before Active Treatment (10)
CL Item
Other (11)
CL Item
Patient Off-treatment For Other Complicating Disease (12)
CL Item
Patient Withdrawal Or Refusal After Beginning Protocol Therapy (13)
CL Item
Patient Withdrawal Or Refusal Before Beginning Protocol Therapy (14)
CL Item
Treatment Completed Per Protocol Criteria (15)
RestingHeartRate
Item
Did resting heart rate increase by 35%?
boolean
CTCAdverseEventArrhythmiaAtrialGrade
Item
Did patient experience any of the following: SVT, atrial fibrillation, or atrial flutter?
float
C41331 (NCI Thesaurus ObjectClass)
C0877248 (UMLS 2011AA ObjectClass)
C25365 (NCI Thesaurus Property)
C0678257 (UMLS 2011AA Property)
Item
check all that apply
text
C41331 (NCI Thesaurus ObjectClass)
C25365 (NCI Thesaurus Property)
C0877248 (UMLS CUI-1)
C0678257 (UMLS CUI-2)
Code List
check all that apply
CL Item
SVT (SVT)
CL Item
Atrial fibrillation (Atrial fibrillation)
CL Item
Atrial flutter (Atrial flutter)
CTCAdverseEventIntervalGrade
Item
Did patient experience prolonged QTc compared to baseline?
float
C41331 (NCI Thesaurus ObjectClass)
C0877248 (UMLS 2011AA ObjectClass)
C25365 (NCI Thesaurus Property)
C0678257 (UMLS 2011AA Property)
Item
check all that apply
integer
C25284 (NCI Thesaurus ValueDomain)
C0003811 (UMLS CUI-1)
C0683312 (UMLS CUI-2)
Code List
check all that apply
CL Item
To greater than or equal to 480 msec (1)
CL Item
Increase of greater than or equal to 50 msec (2)
CL Item
Increase by 15 % (3)
TWaveInversionInd
Item
Was there a T wave inversion in leads II, III, AVF (inferior leads) or V4, V5, and V6 (lateral leads)?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
STSegmentInd-2
Item
Was ST segment at the J-point greater than or equal to 2 mm below baseline in leads II, II AVF (inferior leads), V4, V5, V6 (lateral leads)?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
CTC AE Arrhythmia Ventricular Grade
Item
Did patient experience ventricular arrhythmia?
integer
C41331 (NCI Thesaurus ObjectClass)
C25365 (NCI Thesaurus Property)
C0877248 (UMLS CUI-1)
C0678257 (UMLS CUI-2)
CTCAdverseEventTroponinIGrade
Item
Was there a change in Troponin I?
float
C41331 (NCI Thesaurus ObjectClass)
C0877248 (UMLS 2011AA ObjectClass)
C25365 (NCI Thesaurus Property)
C0678257 (UMLS 2011AA Property)
Item
Was there a change to LVEF?
integer
C2061502 (UMLS CUI-1)
Code List
Was there a change to LVEF?
CL Item
Yes, decrease to less than or equal to 40% (2)
CL Item
Yes, decrease by greater than or equal to 25%, but not below 40% (1)
CL Item
No (0)
Blasts, Bone Marrow
Item
What was the patient's bone marrow status at the end of this reporting period?
float
C25294 (NCI Thesaurus ObjectClass)
C1982687 (UMLS CUI-1)
C12431 (NCI Thesaurus Property)
C20200 (NCI Thesaurus Property-2)
C12918 (NCI Thesaurus Property-3)
C25613 (NCI Thesaurus ValueDomain)
C25712 (NCI Thesaurus ValueDomain-2)
Item Group
Treatment
C0087111 (UMLS CUI-1)
Agent name
Item
Agent name
text
C25364 (NCI Thesaurus Property)
C1708 (NCI Thesaurus ObjectClass)
C1708 (NCI Thesaurus ValueDomain)
C42614 (NCI Thesaurus ValueDomain-2)
C1521826 (UMLS CUI-1)
Agent Total Dose
Item
Total mg dose of Depsipeptide received during this reporting period
float
C25304 (NCI Thesaurus ValueDomain)
C2986497 (UMLS CUI-1)
C25379 (NCI Thesaurus Property)
C25488 (NCI Thesaurus ValueDomain-2)
C1708 (NCI Thesaurus ObjectClass)
Dose Interruption
Item
Were any of the infusions of Depsipeptide interrupted for any reason?
boolean
C38148 (NCI Thesaurus ValueDomain)
C25488 (NCI Thesaurus ObjectClass)
C25542 (NCI Thesaurus Property)
C0178602 (UMLS CUI-1)
C1512900 (UMLS CUI-2)
TreatmentInterruptionDayDuration
Item
please state the time point of the interruption
float
C25301 (NCI Thesaurus ValueDomain)
C0439228 (UMLS 2011AA ValueDomain)
C15368 (NCI Thesaurus ObjectClass)
C25330 (NCI Thesaurus ValueDomain-2)
C0449238 (UMLS 2011AA ValueDomain-2)
C25542 (NCI Thesaurus Property)
C1512900 (UMLS 2011AA Property)
Item
Was there a deviation from protocol therapy?
integer
C25180 (NCI Thesaurus ValueDomain)
C25256 (NCI Thesaurus ObjectClass)
C25572 (NCI Thesaurus Property)
C25572 (NCI Thesaurus ValueDomain-2)
C1707811 (UMLS CUI-1)
Code List
Was there a deviation from protocol therapy?
CL Item
Yes, protocol specified modification for toxicity (1)
CL Item
Yes non-protocol specified modification for toxicity (2)
CL Item
Yes, other reason for deviation (3)
CL Item
No (0)
CL Item
Unknown (-1)
CL Item
Yes, Planned (i.e., The Treatment Was Changed According To Protocol Guidelines) (4)
CL Item
Yes, Unplanned (i.e., The Treatment Change Was Not Part Of Protocol Guidelines) (5)
RTTreatmentInd-3
Item
Did the patient receive radiation therapy during this reporting period?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
C15313 (NCI Thesaurus ObjectClass)
C1522449 (UMLS 2011AA ObjectClass)
C15368 (NCI Thesaurus Property)
Radiation Therapy Body Site
Item
Specify sites
text
C25191 (NCI Thesaurus ValueDomain)
C1997599 (UMLS CUI-1)
C25341 (NCI Thesaurus Property)
C15313 (NCI Thesaurus ObjectClass)
TissueBiologicalSourceSurgicalInd-2
Item
Was tumor tissue surgically obtained for biology studies (e.g. biopsy, resection, fine needle aspiration)?
boolean
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
C12801 (NCI Thesaurus ObjectClass)
C0040300 (UMLS 2011AA ObjectClass)
C25683 (NCI Thesaurus Property)
C0449416 (UMLS 2011AA Property)
DoseModificationText
Item
please describe.
text
C25704 (NCI Thesaurus ValueDomain)
C1527021 (UMLS 2011AA ValueDomain)
C25256 (NCI Thesaurus ObjectClass)
C1265611 (UMLS 2011AA ObjectClass)
C25572 (NCI Thesaurus Property)
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
Concomitant Medication
Item
Did patient receive concomitant medications while on protocol therapy?
boolean
C38147 (NCI Thesaurus ValueDomain)
C459 (NCI Thesaurus ObjectClass)
C25639 (NCI Thesaurus Property)
C2347852 (UMLS CUI-1)
Item
Type
text
C25284 (NCI Thesaurus ValueDomain)
C459 (NCI Thesaurus ObjectClass)
C25639 (NCI Thesaurus Property)
C0332307 (UMLS CUI-1)
C0013227 (UMLS CUI-2)
Code List
Type
CL Item
Corticosteroid (Corticosteroid)
C2322 (NCI Thesaurus)
C0001617 (UMLS CUI-1)
CL Item
Anti-convulsant (Anti-Convulsant)
C0003286 (UMLS CUI-1)
CL Item
Anti-fungal (Anti-Fungal)
C0718566 (NCI Metathesaurus)
C0003308 (UMLS CUI-1)
CL Item
Growth Factor (Growth factor)
C20424 (NCI Thesaurus)
C0018284 (UMLS CUI-1)
CL Item
Other Specify (Other, specify)
C3844311 (UMLS CUI-1)
ConcomitantMedicationUseSpecify
Item
please list type
text
C25685 (NCI Thesaurus ValueDomain)
C1521902 (UMLS 2011AA ValueDomain)
C459 (NCI Thesaurus ObjectClass)
C0013227 (UMLS 2011AA ObjectClass)
C25730 (NCI Thesaurus ObjectClass-2)
C0521115 (UMLS 2011AA ObjectClass-2)
C25340 (NCI Thesaurus Property)
C0457083 (UMLS 2011AA Property)
Treatment Begin Date
Item
Start Date
date
C15368 (NCI Thesaurus ObjectClass)
C25431 (NCI Thesaurus Property)
C3173309 (UMLS CUI-1)
C25275 (NCI Thesaurus Property-2)
C25164 (NCI Thesaurus ValueDomain)
C25431 (NCI Thesaurus ValueDomain-2)
Treatment End Date
Item
End Date
date
C25164 (NCI Thesaurus ValueDomain)
C1531784 (UMLS CUI-1)
C15368 (NCI Thesaurus ObjectClass)
C25275 (NCI Thesaurus Property)
ConcomitantMedicationReceivedText
Item
Description
text
C459 (NCI Thesaurus ObjectClass)
C0013227 (UMLS 2011AA ObjectClass)
C25639 (NCI Thesaurus Property)
C1514756 (UMLS 2011AA Property)
Concomitant Medication Use Indication
Item
Reason for Administration
text
C459 (NCI Thesaurus ObjectClass)
C2826696 (UMLS CUI-1)
C25730 (NCI Thesaurus ObjectClass-2)
C25382 (NCI Thesaurus Property)
C25704 (NCI Thesaurus ValueDomain)
C25638 (NCI Thesaurus ValueDomain-2)
Item Group
New Cancer
NewCancerDiagnosisInd-3
Item
Has a new primary cancer of MDS been diagnosed that has not been previously reported?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
C25586 (NCI Thesaurus ObjectClass)
C0205314 (UMLS 2011AA ObjectClass)
C9305 (NCI Thesaurus ObjectClass-2)
C0006826 (UMLS 2011AA ObjectClass-2)
C15220 (NCI Thesaurus Property)
C0011900 (UMLS 2011AA Property)
NewCancerDiagnosisDate
Item
New Cancer Diagnosis Date
date
C25586 (NCI Thesaurus ObjectClass)
C0205314 (UMLS 2011AA ObjectClass)
C9305 (NCI Thesaurus ObjectClass-2)
C0006826 (UMLS 2011AA ObjectClass-2)
C15220 (NCI Thesaurus Property)
C0011900 (UMLS 2011AA Property)
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C25367 (NCI Thesaurus ValueDomain-2)
Item Group
Follow-Up
C1522577 (UMLS CUI-1)
Item
Vital Status
text
C16960 (NCI Thesaurus ObjectClass)
C18003 (NCI Thesaurus ValueDomain)
C25688 (NCI Thesaurus ValueDomain-2)
C25365 (NCI Thesaurus Property)
C3846084 (UMLS CUI-1)
Code List
Vital Status
CL Item
Alive (Alive)
C2584946 (UMLS CUI-1)
CL Item
Dead (Dead)
C0011065 (UMLS CUI-1)
PatientLostFollow-upInd-2
Item
Was the patient unable to be contacted for current scheduled follow-up?
boolean
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25560 (NCI Thesaurus Property)
C0745777 (UMLS 2011AA Property)
C16033 (NCI Thesaurus Property-2)
C1522577 (UMLS 2011AA Property-2)
PatientOtherEnrollmentInd-2
Item
Was patient enrolled on another COG therapeutic study at the end of this reporting period?
boolean
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C25171 (NCI Thesaurus Property)
C0013893 (UMLS 2011AA Property)
PatientWithdrawFollow-upConsentInd-2
Item
Was patient's consent withdrawn?
boolean
C16960 (NCI Thesaurus ObjectClass)
C0030705 (UMLS 2011AA ObjectClass)
C16033 (NCI Thesaurus Property)
C1522577 (UMLS 2011AA Property)
C25460 (NCI Thesaurus Property-2)
C1511481 (UMLS 2011AA Property-2)
C38061 (NCI Thesaurus Property-3)
C2349954 (UMLS 2011AA Property-3)
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
DiseaseProgressionInd-3
Item
Did patient relapse or experience disease progression during this reporting period?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
C25331 (NCI Thesaurus Property)
C2991 (NCI Thesaurus ObjectClass)
C0012634 (UMLS 2011AA ObjectClass)
DiseaseProgressionDate
Item
date of relapse or progression
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C25367 (NCI Thesaurus ValueDomain-2)
C25331 (NCI Thesaurus Property)
C2991 (NCI Thesaurus ObjectClass)
C0012634 (UMLS 2011AA ObjectClass)
Item Group
Adverse event
C0877248 (UMLS CUI-1)
Item
Category
text
C41331 (NCI Thesaurus ObjectClass)
C25161 (NCI Thesaurus Property)
C0877248 (UMLS CUI-1)
C0008902 (UMLS CUI-2)
Code List
Category
CL Item
Gastrointestinal (Gastrointestinal)
C13359 (NCI Thesaurus)
C0521362 (UMLS 2011AA)
CL Item
Infection Febrile Neutropenia (Infection/Febrile Neutropenia)
CL Item
Blood/bone Marrow (Blood/Bone Marrow)
CL324677 (NCI Metathesaurus)
CL Item
Hepatic (Hepatic)
C13308 (NCI Thesaurus)
C0205054 (UMLS 2011AA)
CL Item
Renal/genitourinary (Renal/Genitourinary)
CL328688 (NCI Metathesaurus)
CL Item
Cardiovascular (arrhythmia) (Cardiovascular (Arrhythmia))
CL Item
Constitutional Symptoms (Constitutional Symptoms)
CL Item
Metabolic/laboratory (Metabolic/Laboratory)
CL Item
Other, specify [unnamed category] (Other)
CTC Adverse Event Reported Term
Item
Other, specify [unnamed category]
text
C25685 (NCI Thesaurus ValueDomain)
C1516728 (UMLS CUI-1)
C49704 (NCI Thesaurus ObjectClass)
C2699044 (UMLS CUI-2)
C25161 (NCI Thesaurus Property)
Item
Type
text
C41331 (NCI Thesaurus ObjectClass)
C25703 (NCI Thesaurus Property)
C1516728 (UMLS CUI-1)
C2826934 (UMLS CUI-2)
Code List
Type
CL Item
Nausea (0)
C0027497 (UMLS CUI-1)
CL Item
Vomiting Nos (1)
C1963281 (UMLS CUI-1)
CL Item
Febrile Neutropenia (2)
C0746883 (UMLS CUI-1)
CL Item
Neutropenia (3)
C0027947 (UMLS CUI-1)
CL Item
Aspartate Aminotransferase Increased (4)
C0151904 (UMLS CUI-1)
CL Item
Alanine Aminotransferase Increased (5)
C0151905 (UMLS CUI-1)
CL Item
Blood Creatinine Increased (6)
C1561535 (UMLS CUI-1)
CL Item
Platelet Count Decreased (7)
C1963076 (UMLS CUI-1)
CL Item
Ventricular Arrhythmia Nos (8)
C0085612 (UMLS CUI-1)
CL Item
Fatigue (9)
C0015672 (UMLS CUI-1)
CL Item
Blood Creatine Phosphokinase Increased (10)
C0151576 (UMLS CUI-1)
CL Item
Other, specify [unnamed type] (11)
C0205394 (UMLS CUI-1)
CTCAdverseEventTermSpecify
Item
Other, specify [unnamed type]
text
C25685 (NCI Thesaurus ValueDomain)
C1521902 (UMLS 2011AA ValueDomain)
C41331 (NCI Thesaurus ObjectClass)
C0877248 (UMLS 2011AA ObjectClass)
C25703 (NCI Thesaurus Property)
C1515273 (UMLS 2011AA Property)
Item
Code
text
C49704 (NCI Thesaurus ObjectClass)
C45559 (NCI Thesaurus Property)
C1516728 (UMLS CUI-1)
Code List
Code
CL Item
Nausea (408)
C3258 (NCI Thesaurus)
C0027497 (UMLS CUI-1)
CL Item
Vomiting (426)
C3442 (NCI Thesaurus)
C0042963 (UMLS CUI-1)
CL Item
Febrile Neutropenia (494)
C0746883 (NCI Metathesaurus)
C0746883 (UMLS CUI-1)
CL Item
Neutrophils/granulocytes (anc/agc) (146)
CL Item
Sgot (ast) (481)
C0201899 (UMLS CUI-1)
CL Item
Sgpt (alt) (482)
C0201836 (UMLS CUI-1)
CL Item
Creatinine (784)
C0201976 (UMLS CUI-1)
CL Item
Platelets (148)
C0005821 (UMLS CUI-1)
CL Item
Ventricular Arrhythmia Nos (181)
CL Item
Fatigue (262)
C3036 (NCI Thesaurus)
C0015672 (UMLS CUI-1)
CL Item
Creatinine Phosphokinase (cpk) (532)
CL Item
Other, Specify (Other)
CTC Adverse Event COG Code
Item
Other, specify [unnamed code]
text
C25364 (NCI Thesaurus Property)
C41331 (NCI Thesaurus ObjectClass)
C0600091 (UMLS CUI-1)
C0877248 (UMLS CUI-2)
CTCAdverseEventGrade2
Item
Grade
integer
C41331 (NCI Thesaurus ObjectClass)
C25365 (NCI Thesaurus Property)
C0877248 (UMLS CUI-1)
C0678257 (UMLS CUI-2)
Item
Attribution
text
C25664 (NCI Thesaurus ValueDomain)
C49704 (NCI Thesaurus ObjectClass)
C25358 (NCI Thesaurus Property)
C1706735 (UMLS CUI-1)
Code List
Attribution
CL Item
Unrelated (1)
C0445356 (UMLS CUI-1)
CL Item
Unlikely (2)
C0750558 (UMLS CUI-1)
CL Item
Possible (3)
C0332149 (UMLS CUI-1)
CL Item
Probable (4)
C1709683 (UMLS CUI-1)
CL Item
Definite (5)
C1704787 (UMLS CUI-1)
ADRFiledInd-3
Item
Adverse Drug Experience?
boolean
C38148 (NCI Thesaurus ValueDomain)
C1512699 (UMLS 2011AA ValueDomain)
C25410 (NCI Thesaurus ObjectClass)
C1521800 (UMLS 2011AA ObjectClass)
C25175 (NCI Thesaurus Property)
C1522646 (UMLS 2011AA Property)
ToxicityReportInd-2
Item
Dose Limiting Toxicity?
boolean
C38147 (NCI Thesaurus ValueDomain)
C1512698 (UMLS 2011AA ValueDomain)
C27990 (NCI Thesaurus ObjectClass)
C0600688 (UMLS 2011AA ObjectClass)
C25375 (NCI Thesaurus Property)
C0684224 (UMLS 2011AA Property)
Adverse Event Onset Date
Item
Date Onset
date
C41331 (NCI Thesaurus ObjectClass)
C2985916 (UMLS CUI-1)
C25279 (NCI Thesaurus Property)
Adverse Event Resolution Date
Item
Date of test or evaluation showing toxicity resolved to eligibility requirements or baseline
date
C25164 (NCI Thesaurus ValueDomain)
C2985918 (UMLS CUI-1)
C25367 (NCI Thesaurus ValueDomain-2)
C49704 (NCI Thesaurus ObjectClass)
C25655 (NCI Thesaurus Property)
Item
check box if not resolved [toxicity]
text
C25180 (NCI Thesaurus ValueDomain)
C49704 (NCI Thesaurus ObjectClass)
C25655 (NCI Thesaurus Property)
C1516728 (UMLS CUI-1)
C1514893 (UMLS CUI-2)
Code List
check box if not resolved [toxicity]
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
Yes (Yes)
C49488 (NCI Thesaurus)
C1705108 (UMLS 2011AA)
CL Item
Not Applicable (Not applicable)
C48660 (NCI Thesaurus)
C1272460 (UMLS 2011AA)

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial