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      Novel penalised likelihood reconstruction of PET in the assessment of histologically verified small pulmonary nodules

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          Abstract

          Objectives

          Investigate the effect of a novel Bayesian penalised likelihood (BPL) reconstruction algorithm on analysis of pulmonary nodules examined with 18F-FDG PET/CT, and to determine its effect on small, sub-10-mm nodules.

          Methods

          18F-FDG PET/CTs performed for nodule evaluation in 104 patients (121 nodules) were retrospectively reconstructed using the new algorithm, and compared to time-of-flight ordered subset expectation maximisation (OSEM) reconstruction. Nodule and background parameters were analysed semi-quantitatively and visually.

          Results

          BPL compared to OSEM resulted in statistically significant increases in nodule SUV max (mean 5.3 to 8.1, p < 0.00001), signal-to-background (mean 3.6 to 5.3, p < 0.00001) and signal-to-noise (mean 24 to 41, p < 0.00001). Mean percentage increase in SUV max (%ΔSUV max) was significantly higher in nodules ≤10 mm ( n = 31, mean 73 %) compared to >10 mm ( n = 90, mean 42 %) ( p = 0.025). Increase in signal-to-noise was higher in nodules ≤10 mm (224 %, mean 12 to 27) compared to >10 mm (165 %, mean 28 to 46). When applying optimum SUV max thresholds for detecting malignancy, the sensitivity and accuracy increased using BPL, with the greatest improvements in nodules ≤10 mm.

          Conclusion

          BPL results in a significant increase in signal-to-background and signal-to-noise compared to OSEM. When semi-quantitative analyses to diagnose malignancy are applied, higher SUV max thresholds may be warranted owing to the SUV max increase compared to OSEM.

          Key Points

          Novel Bayesian penalised likelihood PET reconstruction was applied for lung nodule evaluation.

          This was compared to current standard of care OSEM reconstruction.

          The novel reconstruction generated significant increases in lung nodule signal-to-background and signal-to-noise.

          These increases were highest in small, sub-10-mm pulmonary nodules.

          Higher SUV max thresholds may be warranted when using semi-quantitative analyses to diagnose malignancy.

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          Most cited references16

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          Positron emission tomography-computed tomography standardized uptake values in clinical practice and assessing response to therapy.

          The use of standardized uptake values (SUVs) is now common place in clinical 2-deoxy-2-[(18)F] fluoro-D-glucose (FDG) position emission tomography-computed tomography oncology imaging and has a specific role in assessing patient response to cancer therapy. Ideally, the use of SUVs removes variability introduced by differences in patient size and the amount of injected FDG. However, in practice there are several sources of bias and variance that are introduced in the measurement of FDG uptake in tumors and also in the conversion of the image count data to SUVs. In this article the overall imaging process is reviewed and estimates of the magnitude of errors, where known, are given. Recommendations are provided for best practices in improving SUV accuracy. Copyright © 2010 Elsevier Inc. All rights reserved.
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            Accuracy of positron emission tomography for diagnosis of pulmonary nodules and mass lesions: a meta-analysis.

            Focal pulmonary lesions are commonly encountered in clinical practice, and positron emission tomography (PET) with the glucose analog 18-fluorodeoxyglucose (FDG) may be an accurate test for identifying malignant lesions. To estimate the diagnostic accuracy of FDG-PET for malignant focal pulmonary lesions. Studies published between January 1966 and September 2000 in the MEDLINE and CANCERLIT databases; reference lists of identified studies; abstracts from recent conference proceedings; and direct contact with investigators. Studies that examined FDG-PET or FDG with a modified gamma camera in coincidence mode for diagnosis of focal pulmonary lesions; enrolled at least 10 participants with pulmonary nodules or masses, including at least 5 participants with malignant lesions; and presented sufficient data to permit calculation of sensitivity and specificity were included in the analysis. Two reviewers independently assessed study quality and abstracted data regarding prevalence of malignancy and sensitivity and specificity of the imaging test. Disagreements were resolved by discussion. We used a meta-analytic method to construct summary receiver operating characteristic curves. Forty studies met inclusion criteria. Study methodological quality was fair. Sample sizes were small and blinding was often incomplete. For 1474 focal pulmonary lesions of any size, the maximum joint sensitivity and specificity (the upper left point on the receiver operating characteristic curve at which sensitivity and specificity are equal) of FDG-PET was 91.2% (95% confidence interval, 89.1%-92.9%). In current practice, FDG-PET operates at a point on the summary receiver operating characteristic curve that corresponds approximately to a sensitivity and specificity of 96.8% and 77.8%, respectively. There was no difference in diagnostic accuracy for pulmonary nodules compared with lesions of any size (P =.43), for semiquantitative methods of image interpretation compared with qualitative methods (P =.52), or for FDG-PET compared with FDG imaging with a modified gamma camera in coincidence mode (P =.19). Positron emission tomography with 18-fluorodeoxyglucose is an accurate noninvasive imaging test for diagnosis of pulmonary nodules and larger mass lesions, although few data exist for nodules smaller than 1 cm in diameter. In current practice, FDG-PET has high sensitivity and intermediate specificity for malignancy.
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              Resolution modeling in PET imaging: theory, practice, benefits, and pitfalls.

              In this paper, the authors review the field of resolution modeling in positron emission tomography (PET) image reconstruction, also referred to as point-spread-function modeling. The review includes theoretical analysis of the resolution modeling framework as well as an overview of various approaches in the literature. It also discusses potential advantages gained via this approach, as discussed with reference to various metrics and tasks, including lesion detection observer studies. Furthermore, attention is paid to issues arising from this approach including the pervasive problem of edge artifacts, as well as explanation and potential remedies for this phenomenon. Furthermore, the authors emphasize limitations encountered in the context of quantitative PET imaging, wherein increased intervoxel correlations due to resolution modeling can lead to significant loss of precision (reproducibility) for small regions of interest, which can be a considerable pitfall depending on the task of interest.
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                Author and article information

                Contributors
                +441865235761 , eugene.teoh@oncology.ox.ac.uk
                Journal
                Eur Radiol
                Eur Radiol
                European Radiology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0938-7994
                1432-1084
                20 May 2015
                20 May 2015
                2016
                : 26
                : 576-584
                Affiliations
                [ ]Department of Radiology, Churchill Hospital, Oxford University Hospitals NHS Trust, Old Road, Headington, Oxford, OX3 7LE UK
                [ ]Department of Oncology, University of Oxford, Oxford, OX3 7DQ UK
                [ ]Radiation Physics and Protection, Churchill Hospital, Oxford University Hospitals NHS Trust, Old Road, Oxford, OX3 7LE UK
                [ ]Department of Thoracic Surgery, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Headley Way, Oxford, OX3 7DU UK
                Article
                3832
                10.1007/s00330-015-3832-y
                4551414
                25991490
                d4541658-680f-4e4f-9d33-303901d7a57b
                © The Author(s) 2015

                Open Access This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 23 December 2014
                : 20 April 2015
                : 28 April 2015
                Categories
                Nuclear Medicine
                Custom metadata
                © European Society of Radiology 2016

                Radiology & Imaging
                solitary pulmonary nodule,positron-emission tomography,image reconstruction,signal-to-noise ratio,image quality enhancement

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