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      18 F-FDG PET standard uptake values of the normal pons in children: establishing a reference value for diffuse intrinsic pontine glioma

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          Abstract

          Background

          Positron emission tomography (PET) scanning with [ 18 F]fluorodeoxyglucose ( 18 F-FDG) is a useful diagnostic and prediction tool in brain tumors, but its value in childhood diffuse intrinsic pontine glioma (DIPG) is still unclear. For interpretation of 18 F-FDG PET results in DIPG, uptake values of the normal pons of children of increasing ages are mandatory. The aim of this study was to determine 18 F-FDG standard uptake value ratios (SUVr) of the normal pons and to compare these to those of DIPG.

          Methods

          We studied 36 subjects with a normal, non-affected pons (aged 5 to 23 years) and 6 patients with DIPG (aged 4 to 17 years) who underwent 18 F-FDG PET scanning. Magnetic resonance imaging (MRI) was co-registered to define the regions of interest. SUVr and SUVrmax for the pons/cerebellum (SUVr p/c) and the pons/occipital lobe (SUVr p/o) were calculated. Independent-samples t tests and Mann–Whitney U tests were used to compare the mean SUVr and Pearson’s test for correlations.

          Results

          For the normal pons, mean SUVr p/c and SUVr p/o were 0.65 (±0.054) and 0.51 (±0.056), respectively. No significant correlations were found between the SUVr of the normal pons and sex, age, nor pontine volume. A modest but statistically significant correlation was found between SUVr and post-injection time acquisition timing. For DIPG, mean SUVr p/c and SUVr p/o were 0.74 (±0.20) and 0.65 (±0.30), respectively, while mean SUVr p(max)/c and SUVr p(max)/o were 1.95 (±0.48) and 1.81 (±0.20), respectively.

          Conclusion

          The SUVr of the unaffected pons are strikingly constant between children, irrespective of sex and age, and can therefore be well used as a reference value for 18 F-FDG PET studies in DIPG.

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          Most cited references25

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          Need for standardization of 18F-FDG PET/CT for treatment response assessments.

          Many factors affect standardized uptake values (SUVs) in (18)F-FDG PET/CT. The use of the SUV from a single PET scan in multicenter studies requires the standardization of (18)F-FDG PET/CT procedures. In the context of treatment response assessments (repeated PET scans), many factors may seem to have minor effects on percentage changes in SUVs, provided that imaging procedures are executed in a consistent manner for each subject. However, the use of (18)F-FDG PET/CT in a nonstandardized manner will result in unknown biases and reproducibilities of SUVs and SUV-based response measures. This article provides an overview of the need for standardization in relation to the specific use of SUVs and SUV changes in studies of treatment response assessments.
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            Diffuse intrinsic pontine gliomas: a systematic update on clinical trials and biology.

            Patients with diffuse intrinsic pontine gliomas (DIPG) have a poor prognosis. Although DIPG constitute only 10-15% of all pediatric brain tumors, they are the main cause of death in this group. Despite 26 clinical trials in newly diagnosed DIPG in the past 5years (including several targeted agents), there is no clear improvement in prognosis. However, knowledge on DIPG biology is increasing, mainly due to the (re)introduction of biopsies and autopsies, the possibility of gene expression profiling, and the development of in vivo models. Translation of this knowledge into clinical trials in combination with improved drug distribution methods may eventually lead to more effective treatment of this devastating disease. 2011 Elsevier Ltd. All rights reserved.
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              Performance evaluation of a whole-body PET scanner using the NEMA protocol. National Electrical Manufacturers Association.

              This study evaluates the performance of the newly developed high-resolution whole-body PET scanner ECAT EXACT HR+. The scanner consists of four rings of 72 bismuth germanate block detectors each, covering an axial field of view of 15.5 cm with a patient port of 56.2 cm. A single block detector is divided into an 8 x 8 matrix, giving a total of 32 rings with 576 detectors each. The dimensions of a single detector element are 4.39 x 4.05 x 30 mm3. The scanner is equipped with extendable tungsten septa for two-dimensional two-dimensional measurements, as well as with three 68Ge line sources for transmission scans and daily quality control. The spatial resolution, scatter fraction, count rate, sensitivity, uniformity and accuracy of the implemented correction algorithms were evaluated after the National Electrical Manufacturers Association protocol using the standard acquisition parameters. The transaxial resolution in the two-dimensional mode is 4.3 mm (4.4 mm) in the center and increases to 4.7 mm (4.8 mm) tangential and to 8.3 mm (8.0 mm) radial at a distance of r = 20 cm from the center. The axial slice width measured in the two-dimensional mode varies between 4.2 and 6.6 mm FWHM over the transaxial field of view. In the three-dimensional mode the average axial resolution varies between 4.1 mm FWHM in the center and 7.8 mm at r = 20 cm. The scatter fraction is 17.1% (32.5%) for a lower energy discriminator level of 350 keV. The maximum true event count rate of 263 (345) kcps was measured at an activity concentration of 142 (26.9) kBq/ml. The total system sensitivity for true events is 5.7 (27.7) cps/Bq/ml. From the uniformity measurements, we obtained a volume variance of 3.9% (5.0%) and a system variance of 1.6% (1.7%). The implemented three-dimensional scatter correction algorithm reveals very favorable properties, whereas the three-dimensional attenuation correction yields slightly inaccurate results in low- and high-density regions. The ECAT EXACT HR+ has an excellent, nearly isotropic spatial resolution, which is advantageous for brain and small animal studies. While the relatively low slice sensitivity may hamper the capability for performing fast dynamic two-dimensional studies, the scanner offers a sufficient sensitivity and count rate capacity for fully three-dimensional whole-body imaging.
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                Author and article information

                Journal
                EJNMMI Res
                EJNMMI Res
                EJNMMI Research
                Springer
                2191-219X
                2014
                28 January 2014
                : 4
                : 8
                Affiliations
                [1 ]Division of Oncology and Hematology, Department of Pediatrics, VU University Medical Center, De Boelelaan 1118, Amsterdam 1007 MB, the Netherlands
                [2 ]Department of Radiology and Nuclear Medicine, VU University Medical Center, De Boelelaan 1117, Amsterdam 1081 HV, the Netherlands
                [3 ]Neuro-oncology Research Group, Cancer Center Amsterdam, De Boelelaan 1117, Amsterdam 1081 HV, the Netherlands
                [4 ]Department of Epidemiology and Biostatistics, VU University Medical Center, De Boelelaan 1118, Amsterdam 1081 HV, the Netherlands
                [5 ]Department of Nuclear Medicine, U.L.B.-Hôpital Erasme Brussels, 808 route de Lennik, Brussels 1070, Belgium
                [6 ]Neurosurgical Center Amsterdam, VU University Medical Center, De Boelelaan 1117, Amsterdam 1081 HV, the Netherlands
                Article
                2191-219X-4-8
                10.1186/2191-219X-4-8
                3910228
                24472395
                02c83d3e-6374-4890-9323-2def97e83636
                Copyright © 2014 Jansen et al.; licensee Springer.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 20 September 2013
                : 14 January 2014
                Categories
                Original Research

                Radiology & Imaging
                pontine glioma,[18 f]fluorodeoxyglucose,positron emission tomography,pons,reference values,brain neoplasms

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