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CTRF Leadership Meeting

Institutional Partners. CTRF Leadership Meeting. Cancer Genomics and Development. of Diagnostic Tools and Therapies. April 7, 2003. 3/3/03. Minutes. Corrections Approval.

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CTRF Leadership Meeting

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  1. Institutional Partners CTRF Leadership Meeting Cancer Genomics and Development of Diagnostic Tools and Therapies April 7, 2003

  2. 3/3/03 Minutes Corrections Approval

  3. Develop Infrastructure and Intellectual Property that Enhances the Competitiveness of the Partners for Clinical and Extramural Funds Principal Objective

  4. Evaluate gene expression (and genetic changes) in human brain, ovarian, breast and hematopoetic cancers and lung, colo-rectal, head and neck, and biliary tract cancers Link gene expression (and genetic changes) to clinical findings and clinical laboratory findings (including histopathological diagnoses) in a common database Evaluate linked data using bioinformatics Research Objective

  5. Funding for CTRF

  6. Year 1 Account Balances as of 4/3/03 (Old Accounts)

  7. YR 2 Account Balances as of 4/1/03

  8. Cost Sharing Report as of 4/1/03

  9. Cost Share Expenses • Cost share expenditures not paid from cost share linked accounts must be documented using ‘In Kind/3rd Party Cost Share form’ obtained from Margie Booker’s office. (http://www.vcu.edu/finance/ In-kind%20Cost%20Sharing%Certification.pdf)

  10. Cost Share Update • Cost Sharing will be taken out of Ledger 1 Accounts and PAFs will be used to document Salaries • Cost sharing will be updated on a quarterly span • Documentation of Cost Share at VCU to be forwarded to Michael Newsome (manewsom@vcu.edu)

  11. Reminder Cost Share Form (VCU)

  12. Website Update www.ctrf-cagenomics.vcu.edu • Website has been updated in some areas • Information is still needed regarding various focus group activities • The CTRF Website is best viewed in Internet Explorer 5.0v or better

  13. SPIN Research • Jo Ann Breaux receiving daily notices of grant opportunities • Compiling weekly document of relevant findings • Monthly SMART documents currently on the CTRF website • Training is available: http://www.InfoEd.org/default.stm

  14. Tissue Bank Clinical & Pathology Laboratory Data Database Design QA/QC Data Analysis Chip Fabrication Focus Groups

  15. Focus Group Leaders

  16. VCU Tissue Bank Tissue Type Specimen Count

  17. Breast – Diagnosis Distribution

  18. Ovary – Diagnosis Distribution

  19. Hematopoietic Neoplasia – Diagnosis Distribution

  20. INOVA – CTRF – Tissue Bank • Jean Donovan being transitioned to full time CTRF Cancer Research Coordinator • In-Service Meetings are schedule with Cancer Committee, Pathology Department, and Surgical Department to inform them about CTRF study • Computer for data entry have been acquired; awaiting dedicated phone line.

  21. INOVA Tissue Bank • INOVA has begun accessioning tissue samples and obtaining consents. Tissue Type Specimen Count Brain 4 Breast 4

  22. Tissue Acquisition Database • Access Database • VCU linked by LAN for several users • Computer at INOVA to be upgraded and VPN software to be installed

  23. Questions_FactG FactG_ID Consent_ID FactG_Date GP1 GP2 GP3 GP4 GP5 GP6 GP7 GS1 GS2 GS3 Patient Patient_ID Name_Last Name_First Name_Middle Name_Full_Formatted Name_Last_Center Name_First_Center Name_Middle_Center Street1 Street2 City State_ID Zip Code Country_ID Area Code Phone Number Birth_Dt_Tm Gender_ID Race_ID Social_Security_Number Interview Deceased Deceased_Date Interview_type Patient_Consent State_Abbrev Consent_ID Patient_ID Consent_Dt_Tm Tissue_type_ID State_ID Abbreviation State/Possession Disease_Tissue Disease Disease_ID Disease_Desc Disease_ID Tissue_type_ID Institution Country Abbrev Institution_ID Institution_Desc Tissue_Bank_Extraction Patient_Alias Extraction_ID Alias Tissue_Bank_Case_Num Sample_Num Subsample_Num Date SpectRatioAC SpectRatioAB SpectConc SpectYield FluoPctDNA BioanlyzRation BioanlyzConc BioanlyzPctrRNA RNA Template CRNA260_280 cRNAYieldmicrog cRNAYielDist cDNASizeDist Removed_Person Institution_ID Protocol Removed_Dt_Tm Extracted_Sample_Size Returned_Dt_Tm Percent_Tumor Background_Avg Noise_RawQ Scale_Factor TGT_Value GAPDH B_actin SrRNA18 SrRNA28 Country_ID Abbreviation Country Patient_ID Medical_Record_Nu Institution_ID Patient_Alias_ID Tissue_Bank_Case Tissue_Bank_Case_Num Patient_Alias_ID Surgeon_ID Surgery_Dt_Tm Incision_Dt_Tm Extirpation_Dt_Tm Transport_Meth_ID Tissue_type_ID HP_Initial_Diagnosis AP_Accession Path_Report_Control Diagnosis Start_Anesth_Dt_Tm Consent_Status AP_Accession_Unformatted ICD9_Code Verify Tissue_Available Surg_Path_Pers Comment Cut_in Tissue_Bank_Subsample Gender Tissue_Bank_Case_Num Sample_Num Subsample_Num Alias Dimension1 Dimension2 DimensionCalc CubicSize SectionsCount Process_type_ID Process_Dt PctTumor CharChange Institution_ID Storage_Loc_Freezer Storage_Loc_Box Storage_Loc_Slot Storage_Loc_Slide Extracted Tissue_Type Gender_ID Gender_Desc Histopath_Ovarian Tissue_type_ID Tissue_type_Desc Quest_Form_ID Histopath_Ovarian_ID Tissue_Bank_Case_Num Gross Position Size Histo_Category_ID Histo_Clasification_ID Histo_SubClassification_ID Grade Invasion WHO_Code Tumor Lymph_Node Metastasis Pathological_Stage Race Race_ID Race_Desc Tissue_Bank_Sample Tissue_Bank_Case_Num Sample_Num Original_Sample_Size Current_Sample_Size Process_type_ID Tumor_Loc_ID Institution Storage_Loc_Freezer Storage_Loc_Box Storage_Loc_Slot Frozen_Dt_Tm AP_Specimen_Num Diagnosis Exhausted Cut_in Inadequate_Tumor

  24. Total Tissue by Disease

  25. HistoPath Done

  26. Questionnaires Done

  27. Clinical Data Model (VCU) - Primary: Data Collection AFFY Study ID Tissue ID Sample ID Sub-sample ID TISSBK & 1oCLINICAL & Consent Study ID SSN CERNER REGISTRY CLAIMS PathShadw MRN SSN Path Accsn MRN SSN ACCSN SEQ MRN SSN PAN Reg Shadw SPOTTED Histopath Risk Factors Path Dx Clin Lab Study ID Lab ID Tissue ID Run ID Clinical Risk Factors Treatments Outcomes Secondary: Queries, Data Reduction GeneX CEL file data Spot data Experimental (Metadata) Clinical Data Repository Table: Consent Info Tables: Extract Info StorageInfo Usage Info etc Tables: Histopath parameters Path Dxs SNOMED Text Repts Tables: Demogrphs Risk Factrs Nutirtion Comorbidty etc Tables: Tumor info Treatment Follow-up etc Tables: Surg Tx Medical Tx Radiatin Tx other dxs Tertiary: Analysis & Hypothesis Testing Gene Expression Non-genetic predictors Treatments Outcomes Analysis Database

  28. GMU Informatics Update • Create or Identify existing databases into which expression microarray data can be stored in electronic format in real time at this juncture. • Identified GeneX as candidate microarray database. • Worked with GeneX developers and UVA to modify GeneX to accept both cDNA and Affymetrix gene expression data • Instantiated new version of GeneX • Defined new LIMS schema for data management • Create or Identify existing databases into which clinical, laboratory, tissue bank information, and expression microarray can be stored in electronic format in real time at this juncture. • Examined several available clinical databases and found none to be sufficient in terms of performance and flexibility. • Used CGO as starting basis to generate new clinical schema. • Currently implementing clinical databases. • Create ODBC links between separate databases containing clinical, laboratory, and tissue bank data. • In progress.

  29. CTRF CA GENOMICS TISSUE UTILIZATION - PLAN QA Program

  30. Results (I) • By using TRIZOL we obtained undegraded RNA (28S/18S >1.5) but the cDNA synthesis was inhibited (accumulation of short, ~50 bp, molecules). • By cleaning up the RNA isolated using TRIZOL with the RNeasy cleanup protocol, we obtained cDNA molecules of greater size, with a max. peak at ~1,500 bp.

  31. Results (II) • By usingthe RNeasy RNA isolation protocol from breast tissue sections, we obtained total RNA with 28S/18S ratios << 1.5, and the cDNA molecules were shorter than expected (max. peak at ~500 bp). • Therefore, we decided to isolate the RNA using TRIZOL followed by the RNeasy cleanup protocol, to ensure cDNA molecules of greater size, (max. peak at ~1,500 bp).

  32. Tissue Devitalization • Awaiting specimen of sufficient size to create multiple samples over time Dr. Nasim and Dr. Grant

  33. Gene Expression Data Analysis

  34. Gene Expression Data Analysis of Breast & Ovary Tumors

  35. Cases Processed for Participating Labs

  36. CTRF – Promoting Focus Group Activity • Establish Standing Weekly or Biweekly Meeting Dates and Times • Document Discussions and Progress Using Listservs Complete the Milestone Updates

  37. Communication Amongst Members and Focus Groups 8 - LISTSERVS • CG-TISBK: Tissue Bank • CG-CLNDT: Clinical and Pathology Data • CG-DBDSN: Database Design • CG-ANLDT: Analyze Data (Data Analysis) • CG-QAQC: QAQC • CG-LDRPI: Focus Group Leaders and PIs • CG-MEMBS: All Members • CG-FBCHP: Chip Fabrication

  38. CTRF - Specific Reportables • - Reminder - - • Intellectual property reporting - licenses, patents, etc • Publications • New applications • Federal money leveraged • Private research money leveraged • Advancement of technology and economic development in VA

  39. New Grant Applications • $200,000 - Genomic Classification of Primary Brain Tumors and Development of Diagnostic Biochips (Anthony Guiseppi-Elie, Sc.D) • 01/01/04-12/31/07 - $2,000,000 - Clinical and Molecular Measurements Predicting Optimal Breast Cancer Therapies – (Peter O’Connell, Ph.D)

  40. Old Business • New Business

  41. Next Leadership Meeting Will be held: Monday, May 5, 2003 at 9:30am

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