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QIBA DCE-MRI Technical Committee

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QIBA DCE-MRI Technical Committee Jeffrey L. Evelhoch, PhD Executive Director, Medical Sciences Head, Imaging Sciences MEDICAL IMAGING CONTINUUM Path Forward for ... – PowerPoint PPT presentation

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Title: QIBA DCE-MRI Technical Committee


1
QIBA DCE-MRI Technical Committee
  • Jeffrey L. Evelhoch, PhD
  • Executive Director, Medical Sciences
  • Head, Imaging Sciences

MEDICAL IMAGING CONTINUUM Path Forward for
Advancing the Uses of Medical Imaging in the
Development of New Biopharmaceutical Products 2-3
October 2008 Bethesda, MD
2
Members
  • M. Buonocore (UC Davis)
  • E. Jackson (MDACC)
  • G. Karczmar (Chicago)
  • D. Barboriak (Duke)
  • M. Rosen (Penn)
  • M. Schnall (Penn)
  • M. Knopp (OSU)
  • G. Zahlmann (Siemens)
  • D. Purdy (Siemens)
  • S. Gupta (GE)
  • L. Hilaire (GE)
  • G. Slavin (Philips)
  • E. Ashton (VirtualScopics)
  • A. Schmid (Perceptive)

3
Motivation
  • Pre-treatment tumor vascularization and/or early
    changes in tumor vascularization in response to
    treatment could identify patients most likely to
    benefit from treatment, particularly
    vascular-directed therapy
  • Requires parameters characterizing tumor
    vasculature (Ktrans, IAUC) to be comparable
    between patients, scanners, institutions and over
    time

4
Plans
  • Define phantom for quantitative DCE-MRI
  • Define generic DCE-MRI acquisition protocols
  • Plan and conduct phantom study to evaluate
    comparability of protocols across sites/platforms
  • Define procedure for routine phantom use
  • Develop simulated data set for algorithm testing
  • Plan and conduct multi-site test-retest study
    using phantom and generic protocol

5
Progress (1)
  • Define phantom for quantitative DCE-MRI
  • Modified IRAT/ADNI phantom (July 2008)

6
Progress (2)
  • Define generic DCE-MRI acquisition protocols
  • Generic protocols for 1.5 T (July 2008)
  • Dynamic
  • T1
  • Ratio (RF sensitivity correction?)
  • Implemented on GE, Philips Siemens scanners
    (September 2008)

7
Progress (3)
  • Develop simulated data set for algorithm testing
  • Dynamic data (August 2008)
  • T1 data (October 2008)

8
Progress (4)
  • Plan and conduct phantom study to evaluate
    protocol comparability across sites/platforms
    (anticipate mid-October 2008 for plan, target
    December 2008 for study completion)
  • Define procedure for routine phantom use (target
    January 2009)
  • Plan and conduct multi-site test-retest study
    using phantom and generic protocol (target 1Q09
    for plan, 3Q09 for completion)
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