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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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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 |
Sumario: | 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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