Comparison of the performance of tracer kinetic model-driven registration for dynamic contrast enhanced MRI using different models of contrast enhancement
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Buonaccorsi, Giovanni A.
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
Buonaccorsi, Giovanni A.
Roberts, Caleb
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
Roberts, Caleb
Cheung, Sue
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
Cheung, Sue
Watson, Yvonne
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
Watson, Yvonne
O'Connor, James P. B.
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
O'Connor, James P. B.
Davies, Karen
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
Davies, Karen
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Jackson, Alan
Jayson, Gordon C.
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
Jayson, Gordon C.
Parker, Geoff J. M.
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机构:Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
Parker, Geoff J. M.
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[1] Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
[2] Christie Hosp NHS Trust, Dept Med Oncol, Canc Res UK, Manchester M20 4BX, Lancs, England
Rationale and Objectives. The quantitative analysis of dynamic contrast-enhanced (DCE) magnetic resonance imaging (MRI) data is subject to model fitting errors caused by motion during the time-series data acquisition. However, the time-varying features that occur as a result of contrast enhancement can confound motion correction techniques based on conventional registration similarity measures. We have therefore developed a heuristic, locally controlled tracer kinetic model-driven registration procedure, in which the model accounts for contrast enhancement, and applied it to the registration of abdominal DCE-MRI data at high temporal resolution. Materials and Methods. Using severely motion-corrupted data sets that had been excluded from analysis in a clinical trial of an antiangiogenic agent, we compared the results obtained when using different models to drive the tracer kinetic model-driven registration with those obtained when using a conventional registration against the time series mean image volume. Results. Using tracer kinetic model-driven registration, it was possible to improve model fitting by reducing the sum of squared errors but the improvement was only realized when using a model that adequately described the features of the time series data. The registration against the time series mean significantly distorted the time series data, as did tracer kinetic model-driven registration using a simpler model of contrast enhancement. Conclusion. When an appropriate model is used, tracer kinetic model-driven registration influences motion-corrupted model fit parameter estimates and provides significant improvements in localization in three-dimensional parameter maps. This has positive implications for the use of quantitative DCE-MRl for example in clinical trials of antiangiogenic or antivascular agents.