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      Evaluation of principal component analysis-based data-driven respiratory gating for positron emission tomography

      research-article
      , PhD 1 , , FRCR FRCP 2 , , DPhil 1 , 3
      The British journal of radiology

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          Abstract

          Objective

          Respiratory motion can degrade PET image quality and lead to inaccurate quantification of lesion uptake. Such motion can be mitigated via respiratory gating. Our objective was to evaluate a data-driven gating (DDG) technique that is being developed commercially for clinical PET/CT.

          Methods

          A data-driven respiratory gating algorithm based on principal component analysis (PCA) was applied to phantom and FDG patient data. An anthropomorphic phantom and a NEMA IEC Body phantom were filled with 18F, placed on a respiratory motion platform, and imaged using a PET/CT scanner. Motion waveforms were measured using an infrared camera [the Real-time Position Management™ system (RPM)] and also extracted from the PET data using the DDG algorithm. The waveforms were compared via calculation of Pearson’s correlation coefficients. PET data were reconstructed using quiescent period gating (QPG) and compared via measurement of recovery percentage and background variability.

          Results

          Data-driven gating had similar performance to the external gating system, with correlation coefficients in excess of 0.97. Phantom and patient images were visually clearer with improved contrast when QPG was applied as compared to no motion compensation. Recovery coefficients in the phantoms were not significantly different between DDG- and RPM-based QPG, but were significantly higher than those found for no motion compensation ( p < 0.05).

          Conclusion

          A PCA-based DDG algorithm was evaluated and found to provide a reliable respiratory gating signal in anthropomorphic phantom studies and in example patients.

          Advances in knowledge

          The prototype commercial DDG algorithm may enable reliable respiratory gating in routine clinical PET-CT.

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          Most cited references20

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          Phantom and Clinical Evaluation of the Bayesian Penalized Likelihood Reconstruction Algorithm Q.Clear on an LYSO PET/CT System.

          Q.Clear, a Bayesian penalized-likelihood reconstruction algorithm for PET, was recently introduced by GE Healthcare on their PET scanners to improve clinical image quality and quantification. In this work, we determined the optimum penalization factor (beta) for clinical use of Q.Clear and compared Q.Clear with standard PET reconstructions.
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            Respiration-induced movement of the upper abdominal organs: a pitfall for the three-dimensional conformal radiation treatment of pancreatic cancer.

            Respiration-induced movement of the upper abdominal organs (pancreas, liver and kidneys) was assessed in 12 subjects using dynamic magnetic resonance imaging. The movement of each organ in the cranio-caudal, the lateral and the anterior-posterior direction was deduced from the movement of the center of gravity on two-dimensional images. This center of gravity was computed from the volume delineated on sequential 8-mm slices of both sagittal and coronal dynamic series. The largest movements were noticed in the cranio-caudal direction for pancreas and liver (23.7+/-15.9 mm and 24.4+/-16.4 mm). The kidneys showed smaller movements in the cranio-caudal direction (left kidney 16.9+/-6.7 mm and right kidney 16.1+/-7.9 mm). The movements of the different organs in the anterior-posterior and lateral directions were less pronounced. It is of the greatest importance to be aware of these movements in the planning of a conformal radiation treatment for pancreatic cancer.
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              Effect of respiratory gating on quantifying PET images of lung cancer.

              We have developed a new technique to gate lung 18F-FDG PET images in synchronization with the respiratory motion to reduce smearing due to breathing and improve quantitation of 18F-FDG uptake in lung lesions. A camera-based respiratory gating system, the real-time position management (RPM), is used to monitor the respiratory cycle. The RPM provides a trigger to the PET scanner to initiate the gating cycle. Each respiratory cycle is divided into discrete bins triggered at a defined amplitude or phase within the patient's breathing motion, into which PET data are acquired. The acquired data within the time bins correspond to different lesion positions within the breathing cycle. The study includes 5 patients with lung cancer. Measurements of the lesions' volumes in the gated mode showed a reduction of up to 34% compared with that of the nongated measurement. This reduction in the lesion volume has been accompanied by an increase in the intensity in the 18F-FDG signal per voxel. This finding has resulted in an improvement in measurement of the maximum standardized uptake value (SUV(max)), which increased in 1 patient by as much as 159%. The total lesion glycolysis, defined as the product of the SUV(max) and the lesion volume, was also measured in gated and nongated modes and showed a consistency between the 2 measurements. We have shown that image smearing can be reduced by gating 18F-FDG PET images in synchronization with the respiratory motion. This technique allows a more accurate definition of the lesion volume and improves the quantitation specific activity of the tracer (in this case, 18F-FDG), which are distorted because of the breathing motion.
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                Author and article information

                Journal
                0373125
                1903
                Br J Radiol
                Br J Radiol
                The British journal of radiology
                0007-1285
                1748-880X
                21 March 2018
                15 March 2018
                May 2018
                01 May 2018
                : 91
                : 1085
                : 20170793
                Affiliations
                [1 ]Radiation Physics and Protection, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
                [2 ]Department of Radiology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
                [3 ]Department of Oncology, University of Oxford, Oxford, UK
                Author notes
                Address correspondence to: Dr Matthew D Walker, matthew.walker@ 123456ouh.nhs.uk
                Article
                EMS76794
                10.1259/bjr.20170793
                5911393
                29419327
                105e6502-27e0-4e8f-a8f5-85fdab00ba34

                This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 Unported License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.

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                Radiology & Imaging
                Radiology & Imaging

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