Unnamed2
Protocol Number ECOG
text
Patient Initials
text
Patient ID ECOG
text
Study Number Participating Group
text
Institution Name
text
Trial subject ID Participating Group
text
Unnamed3
Data amended
text
Data amended date
date
On Treatment
Cycle number
text
Cycle number
text
Chemotherapy cycle
text
Chemotherapy cycle
text
Off Treatment
PersonOff-TreatmentTimePeriodType
text
Unnamed4
AdverseEventCurrentAssessmentInd
text
Adverse Event Start Date
date
Adverse Event End Date
date
Blood?bone Marrow/metabolic/laboratory
AdverseEventCommonTerminologyforAdverseEventsVersion4TermName
text
AdverseEventSeverityGrade
text
CTC Adverse Event Attribution Category
text
Unnamed5
AdverseEventCommonTerminologyforAdverseEventsVersion4TermName
text
AdverseEventSeverityGrade
text
CTC Adverse Event Attribution Category
text
Ii. Infections
AdverseEventCommonTerminologyforAdverseEventsVersion4TermName
text
CTC Adverse Event Term
text
AdverseEventSeverityGrade
text
CTC Adverse Event Attribution Category
text
Ii. Infections
CommonToxicityCriteriaAdverseEventShortNameType
text
CTC Adverse Event Term
text
CTC Adverse Event Grade
float
CTC Adverse Event Attribution Category
text
Comments
Research Comments
text
Investigator Signature
text
Investigator Signature Date
date