Longitudinal Image Analysis of Tumor/Brain Change in Contrast Uptake Induced by Radiation
2009
- 595Usage
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Usage595
- Abstract Views405
- Downloads190
Article Description
This work is motivated by a quantitative Magnetic Resonance Imaging study of the differential tumor/healthy tissue change in contrast uptake induced by radiation. The goal is to determine the time in which there is maximal contrast uptake, a surrogate for permeability, in the tumor relative to healthy tissue. A notable feature of the data is its spatial heterogeneity. Zhang, Johnson, Little, and Cao (2008a and 2008b) discuss two parallel approaches to “denoise” a single image of change in contrast uptake from baseline to a single follow-up visit of interest. In this work we explore the longitudinal profile of the tumor/healthy tissue change in contrast uptake. In addition to the spatial correlation, we account for temporal correlation by jointly modeling multiple images on the individual subjects over time. We fit a two-stage model. First, we propose a longitudinal image model for each subject. This model simultaneously accounts for the spatial and temporal correlation and denoises the observed images by borrowing strength both across neighboring pixels and over time. We propose to use the area under the receiver operating characteristics (ROC) curve (AUC) to summarize the differential contrast uptake between tumor and healthy tissue. In the second stage, we fit a population model on the AUC values and estimate when it achieves the maximum.
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