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Itemgroups: Header module,Vital Signs,Comments
Itemgroups: Subject Visit,Assessment of Disease Progression,Vital Signs,BPI-SF,ECOG Performance Status,Hematology (with DBC),General Chemistry - Serum,Skeletal Related Events
Itemgroups: CRF Header,AML: Form Administration,AML: Disease Description,Comments
Itemgroups: CRF Header,AML/MDS: Form Administration,AML/MDS: Disease Description,Comments
Itemgroups: CALGB Form,Patient Description,Organ Involvement,Current Symptoms,Lab data at Study Entry,CCRR MODULE
Itemgroups: MODULE 1,PRE-TREATMENT CHACTERISTICS,LYMPH NODE ASSESSMENT
Itemgroup: Repeat Telemetry Abnormalities
Itemgroup: Holter ECG Results
Itemgroups: RTOG clinical trial administrative data,Patient status,Tumor Involvement,pStage I, II breast cancer AND at least one of the following (see below and code all),Tumor Information,Study Cancer,Baseline Labs,Examinations/Consultations,General Conditions,Footer Module
Itemgroups: Header Module,Eligibility Screening Form,Randomization,Informed Consent,Header,Vital signs and physical measurements,ECG,LVEF,HER2/neu status (local lab),Central Laboratory,Hormonal receptor status,History of primary breast cancer,Hematology and Biochemistry,History of primary cancer (continued),Sentinel nodes sampling,Primary breast cancer surgery,Axillary node dissection,Prior neo-/adjuvant chemotherapy for primary breast cancer,Previous or current cardiovascular disease,Previous or current diseases other than primary breast and cardiovascular diseases,Radiological examination,Translational Research (Appendix 5)
Itemgroups: Header,PRE-TREATMENT CHACTERISTICS,LYMPH NODE ASSESSMENT,Comments
Itemgroups: Header,Patient demographics,Data amendment,Pre-Registration Evaluation,Prior Treatment for this Disease,Disease Description,Footer Module