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SUV variability in EARL-accredited conventional and digital PET
BACKGROUND: A high SUV-reproducibility is crucial when different PET scanners are in use. We evaluated the SUV variability in whole-body FDG-PET scans of patients with suspected or proven cancer using an EARL-accredited conventional and digital PET scanner. In a head-to-head comparison we studied im...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904705/ https://www.ncbi.nlm.nih.gov/pubmed/31823097 http://dx.doi.org/10.1186/s13550-019-0569-7 |
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author | Koopman, Daniëlle Jager, Pieter L. Slump, Cornelis H. Knollema, Siert van Dalen, Jorn A. |
author_facet | Koopman, Daniëlle Jager, Pieter L. Slump, Cornelis H. Knollema, Siert van Dalen, Jorn A. |
author_sort | Koopman, Daniëlle |
collection | PubMed |
description | BACKGROUND: A high SUV-reproducibility is crucial when different PET scanners are in use. We evaluated the SUV variability in whole-body FDG-PET scans of patients with suspected or proven cancer using an EARL-accredited conventional and digital PET scanner. In a head-to-head comparison we studied images of 50 patients acquired on a conventional scanner (cPET, Ingenuity TF PET/CT, Philips) and compared them with images acquired on a digital scanner (dPET, Vereos PET/CT, Philips). The PET scanning order was randomised and EARL-compatible reconstructions were applied. We measured SUV(mean), SUV(peak), SUV(max) and lesion diameter in up to 5 FDG-positive lesions per patient. The relative difference ΔSUV between cPET and dPET was calculated for each SUV-parameter. Furthermore, we calculated repeatability coefficients, reflecting the 95% confidence interval of ΔSUV. RESULTS: We included 128 lesions with an average size of 19 ± 14 mm. Average ΔSUVs were 6-8% with dPET values being higher for all three SUV-parameters (p < 0.001). ΔSUV(max) was significantly higher than ΔSUV(mean) (8% vs. 6%, p = 0.002) and than ΔSUV(peak) (8% vs. 7%, p = 0.03). Repeatability coefficients across individual lesions were 27% (ΔSUV(mean) and ΔSUV(peak)) and 33% (ΔSUV(max)) (p < 0.001). CONCLUSIONS: With EARL-accredited conventional and digital PET, we found a limited SUV variability with average differences up to 8%. Furthermore, only a limited number of lesions showed a SUV difference of more than 30%. These findings indicate that EARL standardisation works. TRIAL REGISTRATION: This prospective study was registered on the 31th of October 2017 at ClinicalTrials.cov. URL: https://clinicaltrials.gov/ct2/show/NCT03457506?id=03457506&rank=1. |
format | Online Article Text |
id | pubmed-6904705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-69047052019-12-26 SUV variability in EARL-accredited conventional and digital PET Koopman, Daniëlle Jager, Pieter L. Slump, Cornelis H. Knollema, Siert van Dalen, Jorn A. EJNMMI Res Original Research BACKGROUND: A high SUV-reproducibility is crucial when different PET scanners are in use. We evaluated the SUV variability in whole-body FDG-PET scans of patients with suspected or proven cancer using an EARL-accredited conventional and digital PET scanner. In a head-to-head comparison we studied images of 50 patients acquired on a conventional scanner (cPET, Ingenuity TF PET/CT, Philips) and compared them with images acquired on a digital scanner (dPET, Vereos PET/CT, Philips). The PET scanning order was randomised and EARL-compatible reconstructions were applied. We measured SUV(mean), SUV(peak), SUV(max) and lesion diameter in up to 5 FDG-positive lesions per patient. The relative difference ΔSUV between cPET and dPET was calculated for each SUV-parameter. Furthermore, we calculated repeatability coefficients, reflecting the 95% confidence interval of ΔSUV. RESULTS: We included 128 lesions with an average size of 19 ± 14 mm. Average ΔSUVs were 6-8% with dPET values being higher for all three SUV-parameters (p < 0.001). ΔSUV(max) was significantly higher than ΔSUV(mean) (8% vs. 6%, p = 0.002) and than ΔSUV(peak) (8% vs. 7%, p = 0.03). Repeatability coefficients across individual lesions were 27% (ΔSUV(mean) and ΔSUV(peak)) and 33% (ΔSUV(max)) (p < 0.001). CONCLUSIONS: With EARL-accredited conventional and digital PET, we found a limited SUV variability with average differences up to 8%. Furthermore, only a limited number of lesions showed a SUV difference of more than 30%. These findings indicate that EARL standardisation works. TRIAL REGISTRATION: This prospective study was registered on the 31th of October 2017 at ClinicalTrials.cov. URL: https://clinicaltrials.gov/ct2/show/NCT03457506?id=03457506&rank=1. Springer Berlin Heidelberg 2019-12-10 /pmc/articles/PMC6904705/ /pubmed/31823097 http://dx.doi.org/10.1186/s13550-019-0569-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted 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. |
spellingShingle | Original Research Koopman, Daniëlle Jager, Pieter L. Slump, Cornelis H. Knollema, Siert van Dalen, Jorn A. SUV variability in EARL-accredited conventional and digital PET |
title | SUV variability in EARL-accredited conventional and digital PET |
title_full | SUV variability in EARL-accredited conventional and digital PET |
title_fullStr | SUV variability in EARL-accredited conventional and digital PET |
title_full_unstemmed | SUV variability in EARL-accredited conventional and digital PET |
title_short | SUV variability in EARL-accredited conventional and digital PET |
title_sort | suv variability in earl-accredited conventional and digital pet |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904705/ https://www.ncbi.nlm.nih.gov/pubmed/31823097 http://dx.doi.org/10.1186/s13550-019-0569-7 |
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