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Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs)

BACKGROUND: The clinical validation of the EARL harmonization program for standardised uptake value (SUV) metrics is well documented; however, its potential for defining metabolic active tumour volume (MATV) has not yet been investigated. We aimed to compare delineation of MATV on images reconstruct...

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Autores principales: Lasnon, Charline, Enilorac, Blandine, Popotte, Hosni, Aide, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374086/
https://www.ncbi.nlm.nih.gov/pubmed/28361349
http://dx.doi.org/10.1186/s13550-017-0279-y
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author Lasnon, Charline
Enilorac, Blandine
Popotte, Hosni
Aide, Nicolas
author_facet Lasnon, Charline
Enilorac, Blandine
Popotte, Hosni
Aide, Nicolas
author_sort Lasnon, Charline
collection PubMed
description BACKGROUND: The clinical validation of the EARL harmonization program for standardised uptake value (SUV) metrics is well documented; however, its potential for defining metabolic active tumour volume (MATV) has not yet been investigated. We aimed to compare delineation of MATV on images reconstructed using conventional ordered subset expectation maximisation (OSEM) with those reconstructed using point spread function modelling (PSF-reconstructed images), and either optimised for diagnostic potential (PSF) or filtered to meet the EANM/EARL harmonising standards (PSF(7)). METHODS: Images from 18 stage IIIA-IIIB lung cancer patients were reconstructed using all the three methods. MATVs were then delineated using both a 40% isocontour and a gradient-based method. MATVs were compared by means of Bland–Altman analyses, and Dice coefficients and concordance indices based on the unions and intersections between each pair of reconstructions (PSF vs OSEM, PSF(7) vs PSF and PSF(7) vs OSEM). RESULTS: Using the 40% isocontour method and taking the MATVs delineated on OSEM images as a reference standard, the use of PSF(7) images led to significantly higher Dice coefficients (median value = 0.96 vs 0.77; P < 0.0001) and concordance indices (median value = 0.92 vs 0.64; P < 0.0001) than those obtained using PSF images. The gradient-based methodology was less sensitive to reconstruction variability than the 40% isocontour method; Dice coefficients and concordance indices were superior to 0.8 for both PSF reconstruction methods. However, the use of PSF(7) images led to narrower interquartile ranges and significantly higher Dice coefficients (median value = 0.96 vs 0.94; P = 0.01) and concordance indices (median value = 0.89 vs 0.85; P = 0.003) than those obtained with PSF images. CONCLUSION: This study demonstrates that automatic contouring of lung tumours on EARL-compliant PSF images using the widely adopted automatic isocontour methodology is an accurate means of overcoming reconstruction variability in MATV delineation. Although gradient-based methodology appears to be less sensitive to reconstruction variability, the use of EARL-compliant PSF images significantly improved the Dice coefficients and concordance indices, demonstrating the importance of harmonised-images, even when more advanced contouring algorithms are used. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13550-017-0279-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-53740862017-04-12 Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs) Lasnon, Charline Enilorac, Blandine Popotte, Hosni Aide, Nicolas EJNMMI Res Short Communication BACKGROUND: The clinical validation of the EARL harmonization program for standardised uptake value (SUV) metrics is well documented; however, its potential for defining metabolic active tumour volume (MATV) has not yet been investigated. We aimed to compare delineation of MATV on images reconstructed using conventional ordered subset expectation maximisation (OSEM) with those reconstructed using point spread function modelling (PSF-reconstructed images), and either optimised for diagnostic potential (PSF) or filtered to meet the EANM/EARL harmonising standards (PSF(7)). METHODS: Images from 18 stage IIIA-IIIB lung cancer patients were reconstructed using all the three methods. MATVs were then delineated using both a 40% isocontour and a gradient-based method. MATVs were compared by means of Bland–Altman analyses, and Dice coefficients and concordance indices based on the unions and intersections between each pair of reconstructions (PSF vs OSEM, PSF(7) vs PSF and PSF(7) vs OSEM). RESULTS: Using the 40% isocontour method and taking the MATVs delineated on OSEM images as a reference standard, the use of PSF(7) images led to significantly higher Dice coefficients (median value = 0.96 vs 0.77; P < 0.0001) and concordance indices (median value = 0.92 vs 0.64; P < 0.0001) than those obtained using PSF images. The gradient-based methodology was less sensitive to reconstruction variability than the 40% isocontour method; Dice coefficients and concordance indices were superior to 0.8 for both PSF reconstruction methods. However, the use of PSF(7) images led to narrower interquartile ranges and significantly higher Dice coefficients (median value = 0.96 vs 0.94; P = 0.01) and concordance indices (median value = 0.89 vs 0.85; P = 0.003) than those obtained with PSF images. CONCLUSION: This study demonstrates that automatic contouring of lung tumours on EARL-compliant PSF images using the widely adopted automatic isocontour methodology is an accurate means of overcoming reconstruction variability in MATV delineation. Although gradient-based methodology appears to be less sensitive to reconstruction variability, the use of EARL-compliant PSF images significantly improved the Dice coefficients and concordance indices, demonstrating the importance of harmonised-images, even when more advanced contouring algorithms are used. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13550-017-0279-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-03-31 /pmc/articles/PMC5374086/ /pubmed/28361349 http://dx.doi.org/10.1186/s13550-017-0279-y Text en © The Author(s). 2017 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 Short Communication
Lasnon, Charline
Enilorac, Blandine
Popotte, Hosni
Aide, Nicolas
Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs)
title Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs)
title_full Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs)
title_fullStr Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs)
title_full_unstemmed Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs)
title_short Impact of the EARL harmonization program on automatic delineation of metabolic active tumour volumes (MATVs)
title_sort impact of the earl harmonization program on automatic delineation of metabolic active tumour volumes (matvs)
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374086/
https://www.ncbi.nlm.nih.gov/pubmed/28361349
http://dx.doi.org/10.1186/s13550-017-0279-y
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