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Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics

BACKGROUND: The aim of this study is to determine if the choice of the (18)F-FDG-PET protocol, especially matrix size and reconstruction algorithm, is of importance to discriminate between immunohistochemical subtypes (luminal versus non-luminal) in breast cancer with textural features (TFs). PROCED...

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Autores principales: Aide, Nicolas, Salomon, Thibault, Blanc-Fournier, Cécile, Grellard, Jean-Michel, Levy, Christelle, Lasnon, Charline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311169/
https://www.ncbi.nlm.nih.gov/pubmed/30594961
http://dx.doi.org/10.1186/s13550-018-0466-5
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author Aide, Nicolas
Salomon, Thibault
Blanc-Fournier, Cécile
Grellard, Jean-Michel
Levy, Christelle
Lasnon, Charline
author_facet Aide, Nicolas
Salomon, Thibault
Blanc-Fournier, Cécile
Grellard, Jean-Michel
Levy, Christelle
Lasnon, Charline
author_sort Aide, Nicolas
collection PubMed
description BACKGROUND: The aim of this study is to determine if the choice of the (18)F-FDG-PET protocol, especially matrix size and reconstruction algorithm, is of importance to discriminate between immunohistochemical subtypes (luminal versus non-luminal) in breast cancer with textural features (TFs). PROCEDURES: Forty-seven patients referred for breast cancer staging in the framework of a prospective study were reviewed as part of an ancillary study. In addition to standard PET imaging (PSF(WholeBody)), a high-resolution breast acquisition was performed and reconstructed with OSEM and PSF (OSEM(breast)/PSF(breast)). PET standard metrics and TFs were extracted. For each reconstruction protocol, a prediction model for tumour classification was built using a random forests method. Spearman coefficients were used to seek correlation between PET metrics. RESULTS: PSF(WholeBody) showed lower numbers of voxels within VOIs than OSEM(breast) and PSF(breast) with median (interquartile range) equal to 130 (43–271), 316 (167–1042), 367 (107–1221), respectively (p < 0.0001). Therefore, using LifeX software, 28 (59%), 46 (98%) and 42 (89%) patients were exploitable with PSF(WholeBody), OSEM(breast) and PSF(breast), respectively. On matched comparisons, PSF(breast) reconstruction presented better abilities than PSF(wholeBody) and OSEM(breast) for the classification of luminal versus non-luminal breast tumours with an accuracy reaching 85.7% as compared to 67.8% for PSF(wholeBody) and 73.8% for OSEM(breast). PSF(breast) accuracy, sensitivity, specificity, PPV and NPV were equal to 85.7%, 94.3%, 42.9%, 89.2%, 60.0%, respectively. Coarseness and ZLNU were found to be main variables of importance, appearing in all three prediction models. Coarseness was correlated with SUV(max) on PSF(wholeBody) images (ρ = − 0.526, p = 0.005), whereas it was not on OSEM(breast) (ρ = − 0.183, p = 0.244) and PSF(breast) (ρ = − 0.244, p = 0.119) images. Moreover, the range of its values was higher on PSF(breast) images as compared to OSEM(breast), especially in small lesions (MTV < 3 ml). CONCLUSIONS: High-resolution breast PET acquisitions, applying both small-voxel matrix and PSF modelling, appeared to improve the characterisation of breast tumours. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13550-018-0466-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-63111692019-01-11 Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics Aide, Nicolas Salomon, Thibault Blanc-Fournier, Cécile Grellard, Jean-Michel Levy, Christelle Lasnon, Charline EJNMMI Res Original Research BACKGROUND: The aim of this study is to determine if the choice of the (18)F-FDG-PET protocol, especially matrix size and reconstruction algorithm, is of importance to discriminate between immunohistochemical subtypes (luminal versus non-luminal) in breast cancer with textural features (TFs). PROCEDURES: Forty-seven patients referred for breast cancer staging in the framework of a prospective study were reviewed as part of an ancillary study. In addition to standard PET imaging (PSF(WholeBody)), a high-resolution breast acquisition was performed and reconstructed with OSEM and PSF (OSEM(breast)/PSF(breast)). PET standard metrics and TFs were extracted. For each reconstruction protocol, a prediction model for tumour classification was built using a random forests method. Spearman coefficients were used to seek correlation between PET metrics. RESULTS: PSF(WholeBody) showed lower numbers of voxels within VOIs than OSEM(breast) and PSF(breast) with median (interquartile range) equal to 130 (43–271), 316 (167–1042), 367 (107–1221), respectively (p < 0.0001). Therefore, using LifeX software, 28 (59%), 46 (98%) and 42 (89%) patients were exploitable with PSF(WholeBody), OSEM(breast) and PSF(breast), respectively. On matched comparisons, PSF(breast) reconstruction presented better abilities than PSF(wholeBody) and OSEM(breast) for the classification of luminal versus non-luminal breast tumours with an accuracy reaching 85.7% as compared to 67.8% for PSF(wholeBody) and 73.8% for OSEM(breast). PSF(breast) accuracy, sensitivity, specificity, PPV and NPV were equal to 85.7%, 94.3%, 42.9%, 89.2%, 60.0%, respectively. Coarseness and ZLNU were found to be main variables of importance, appearing in all three prediction models. Coarseness was correlated with SUV(max) on PSF(wholeBody) images (ρ = − 0.526, p = 0.005), whereas it was not on OSEM(breast) (ρ = − 0.183, p = 0.244) and PSF(breast) (ρ = − 0.244, p = 0.119) images. Moreover, the range of its values was higher on PSF(breast) images as compared to OSEM(breast), especially in small lesions (MTV < 3 ml). CONCLUSIONS: High-resolution breast PET acquisitions, applying both small-voxel matrix and PSF modelling, appeared to improve the characterisation of breast tumours. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13550-018-0466-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-12-29 /pmc/articles/PMC6311169/ /pubmed/30594961 http://dx.doi.org/10.1186/s13550-018-0466-5 Text en © The Author(s). 2018 Open Access This 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
Aide, Nicolas
Salomon, Thibault
Blanc-Fournier, Cécile
Grellard, Jean-Michel
Levy, Christelle
Lasnon, Charline
Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics
title Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics
title_full Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics
title_fullStr Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics
title_full_unstemmed Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics
title_short Implications of reconstruction protocol for histo-biological characterisation of breast cancers using FDG-PET radiomics
title_sort implications of reconstruction protocol for histo-biological characterisation of breast cancers using fdg-pet radiomics
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311169/
https://www.ncbi.nlm.nih.gov/pubmed/30594961
http://dx.doi.org/10.1186/s13550-018-0466-5
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