Objectives and current status of QIBA (Quantitative Imaging Biomarkers...
Transcript of Objectives and current status of QIBA (Quantitative Imaging Biomarkers...
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Objectives and current status of QIBA (Quantitative Imaging Biomarkers Alliance)
Daniel C. SullivanDepartment of Radiology, Duke University Medical Center
Abstract A quantitative imaging biomarker (QIB) is an objectively measured characteristic derived from an in vivo image as an indicator of normal biological processes, pathogenic processes or response to a therapeutic intervention. In 2007 the Radiological Society of North America (RSNA) organized the Quantitative Imaging Biomarkers Alliance (QIBA) whose mission is to improve the value and practicality of quantitative imaging biomarkers by reducing variability across devices, patients and time. The QIBA initiative involves: (1) stakeholder collaboration to identify needs and solutions to develop consistent and reliable quantitative imaging results across imaging platforms, clinical sites, and time to achieve accurate and reproducible quantitative results from imaging methods. Since the process of acquiring a clinical imaging scan is complex, the goal requires much coordinated work among many stakeholders. There are several sources of variability in quantitative results from clinical images: (1) image acquisition hardware, software and procedures; (2) measurement methods; and (3) reader variability. QIBA employs a consensus-driven approach to produce a QIBA Profile that includes one of more QIBA Claims and specifications for the image acquisition necessary to achieve the QIBA Claim. QIBA Profiles are based on published data whenever such data are available and on expert consensus opinion where no data exist. Although based primarily in the USA, there are QIBA participants from North and South America, Europe and Asia. At the 2015 European Congress on Radiology, the European Society of Radiology (ESR) announced the formation of the European Imaging Biomarkers Alliance (EIBALL). In addition, leaders of the Japan Radiological Society (JRS) have met with the QIBA leaders to discuss future collaborations. Dr. Sullivan’s lecture at the Fall Meeting of the JRS in October 2015 will provide more details about QIBA activities.
Key wordsQuantitative Imaging Biomarkers Alliance (QIBA), Radiological Society of North America (RSNA), standardization, reproducibility, precision medicine
Rinsho Hyoka Clinical Evaluation
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1.Introduction
2.Problem of variation and wrong scan interpretation
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Fig. 1 Operating points of 108 radiologists reading same 100 mammograms
0.0 0.2 0.4 0.6 0.8 1.0FP
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ValueJudgments
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2.1 Premise of the problem
2.2 Computers cannot replace radiologists
3.Motivation for QIBA
3.1 Quantitative imaging in healthcare
3.2 Physician’s use of quantitative information
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Fig. 2 Motivation for QIBA
Treat
Wait
ClinicalDecision
QuantitativeBiomarker
Measure = 10 ±6
?!
8.5
3.3 Variability in imaging measurements
3.4 Variability in scanner measurements
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3.5 Poor reproducibility ‒ Clinical implications
4.Quantification ‒ Consumer expectations
4.1 Publications show need for more quantitative information
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4.2 Research on quantitative imaging is increasing
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4.3 Current commercially available MR QIB applications
5.Impediments in using quantitative imaging
5.1 Lung densitometry example
5.2 Toward quantitative imaging
Fig. 3 Toward quantitative imaging
Clinical Valueof QI Data
Data fromclinical trials
showingClinical Value
Accurate,reproducible QI
Data fromscanners
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6.Quantitative Imaging Biomarkers Alliance (QIBA)
6.1 QIBA organization chart
Fig. 4 QIBA organization chart
QIBA Steering CommitteeJackson (Chair)
Perlman (Vice-Chair)
CT Coordinating CmteGoldmacher, Schwartz, Lynch
CT VolumetryBiomarker CmteGoldmacher, Samei,
Siegelman
Volumetry AlgorithmChallenge TF
Athelogou
Small Lung Nodule TFGierada, Mulshine, Armato
QIBA/fNIH FDABiomarker
QualificationPartnership
Lung DensityBiomarker CmteLynch, Fain, Fuld
Airway MeasurementTF
Fain
NM Coordinating CmteWahl, Perlman, Mozley
FDG-PET BiomarkerCmte
Sunderland, Subramaniam,Wollenweber
Profile ConformanceTF
Turkington, Lodge,Boellaard
QIBA/fNIH FDABiomarker
QualificationPartnership
PET-AmyloidBiomarker Cmte
Smith, Minoshima, Perlman
SPECT Biomarker CmteSeibyl, Mozley, Dewaraja
Clinical LiteratureReview TF
Seibyl
ImageAcquisition &
Image Processingfor DaTscan TF
Dewaraja
Phantoms DROTF
Dickson, Zimmerman
Quantitative & ImageAnalysis TF
Miyaoka, Seibyl
MR Coordinating CmteGuimaraes, Zahlmann, Elsinger
PDF-MRI BiomarkerCmte
Rosen, Boss, Kirsch
DWI-MRI TFBoss, Chenevert
DCE-MRI TFLaue, Chung
DSC-MRI TFErickson, Wu
DTI TFProvenzale, Schneider
MRE Biomarker CmteEhman, Cole
MRE Profile-Writing TFEhman, Cole
Proton Density FatFraction Biomarker
CmteReeder, Sirlin
fMRI Biomarker CmtePetrella, DeYoe, Reuss
fMRI Bias TFVoyvodic
US Coordinating CmteHall, Garra
US SWS BiomarkerCmte
Hall, Garra, Milkowski
System Dependencies/Phantom Testing TF
Palmeri, Wear
Clinical ApplicationsTF
Samir, Cohen-Bacrie,Cosgrove
US Volume FlowBiomarker CmteFowlkes, Kripfgans(AIUM supported)
US CEUS BiomarkerCmte
Averkiou, Barr
Process CmteO’Donnell, Sullivan
QIDW Oversight CmteErickson
TF = Task Force
27-May-2016
Scientific Liaisons:CT: Andrew BucklerMR: Tom ChenevertNM: Paul KinahanUS: Paul Carson
External RelationsLiaison:Daniel Sullivan
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6.2 QIBA meeting at RSNA annual meeting
6.3 QIBA approach
6.4 QIBA profiles
6.5 Bias and precision
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Fig. 5 FDG-PET SUV example
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Poor Accuracy and Poor Precision
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Fig. 6 Bias and precision
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6.6 QIBA profile structure
6.6.1 Examples of QIBA claim statements
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6.6.2 Expected precision for alternate scenarios
6.6.3 CT volumetry example ‒ coefficients of variation
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6.6.4 QIBA profile: Actors, Activities, Requirements
6.6.5 Conformance to QIBA profile
7.MR variables
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8.QIBA funds
9.Dynamic contrast-enhanced MRI (DCE MRI)
Fig. 7 RSNA QIBA DCE-MRI Digital Reference Object (DRO)
(Barboriak)• Simulated T1 measurement data for range of S0 levels and added
noise levels• Simulated DCE measurement data for range of S0 levels• Simulated DCE measurement data for extended Tofts model
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10.Biomarker development
11.European Imaging Biomarkers Alliance (EIBALL)
12.QIBA-related activity in Japan
13.Importance of obtaining clinical precision data
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14.Conclusion
Standardization and software
Q
SullivanQ
Sullivan
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Commitment of industries
Q
Sullivan
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Importance of quantitative imaging for drug development
Q
Sullivan
In the era of big data and precision medicine
Q
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Sullivan
Reproducibility and standardization in early and late phases
Q
Sullivan
Visual radiologist
Q
Sullivan
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Q
Sullivan
Q
Sullivan
Relationship between UPICT and QIBA
Q
Sullivan
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Q