Prognostic value of texture analysis of the primary tumour in high-risk neuroblastoma: An <sup>18</sup> F-DOPA PET study.
Détails
ID Serval
serval:BIB_809748CD0AED
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Prognostic value of texture analysis of the primary tumour in high-risk neuroblastoma: An <sup>18</sup> F-DOPA PET study.
Périodique
Pediatric blood & cancer
ISSN
1545-5017 (Electronic)
ISSN-L
1545-5009
Statut éditorial
Publié
Date de publication
11/2022
Peer-reviewed
Oui
Volume
69
Numéro
11
Pages
e29910
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
To evaluate the prognostic value of texture analysis of the primary tumour with <sup>18</sup> fluorine-dihydroxyphenylalanine positron emission tomography/X-ray computed tomography ( <sup>18</sup> F-DOPA PET/CT) in patients affected by high-risk neuroblastoma (HR-NBL).
We retrospectively analysed 18 patients with HR-NBL, which had been prospectively enrolled in the course of a previous trial investigating the diagnostic role of <sup>18</sup> F-DOPA PET/CT at the time of the first onset. Texture analysis of the primary tumour was carried out on the PET images using LifeX. Conventional indices, histogram parameters, grey level co-occurrence (GLCM), run-length (GLRLM), neighbouring difference (NGLDM) and zone-length (GLZLM) matrices parameter were extracted; their values were compared with the overall metastatic load, expressed by means of whole-body metabolic burden (WBMB) score and the progression-free/overall survival (PFS and OS).
There was a direct correlation between WBMB and radiomics parameter describing uptake intensity (SUV <sub>mean</sub> : p = .004) and voxel heterogeneity (entropy: p = .026; GLCM_Contrast: p = .001). Conversely, texture indices of homogeneity showed an inverse correlation with WBMB (energy: p = .026; GLCM_Homogeneity: p = .006). On the multivariate model, WBMB (p < .01) and the first standardised uptake value (SUV) quartile (p < .001) predicted PFS; OS was predicted by WBMB and the N-myc proto-oncogene protein (MYCN) amplification (p < .05) for both.
Textural parameters describing heterogeneity and metabolic intensity of the primary HR-NBL are closely associated with its overall metastatic burden. In turn, the whole-body tumour load appears to be one of the most relevant predictors of progression-free and overall survival.
We retrospectively analysed 18 patients with HR-NBL, which had been prospectively enrolled in the course of a previous trial investigating the diagnostic role of <sup>18</sup> F-DOPA PET/CT at the time of the first onset. Texture analysis of the primary tumour was carried out on the PET images using LifeX. Conventional indices, histogram parameters, grey level co-occurrence (GLCM), run-length (GLRLM), neighbouring difference (NGLDM) and zone-length (GLZLM) matrices parameter were extracted; their values were compared with the overall metastatic load, expressed by means of whole-body metabolic burden (WBMB) score and the progression-free/overall survival (PFS and OS).
There was a direct correlation between WBMB and radiomics parameter describing uptake intensity (SUV <sub>mean</sub> : p = .004) and voxel heterogeneity (entropy: p = .026; GLCM_Contrast: p = .001). Conversely, texture indices of homogeneity showed an inverse correlation with WBMB (energy: p = .026; GLCM_Homogeneity: p = .006). On the multivariate model, WBMB (p < .01) and the first standardised uptake value (SUV) quartile (p < .001) predicted PFS; OS was predicted by WBMB and the N-myc proto-oncogene protein (MYCN) amplification (p < .05) for both.
Textural parameters describing heterogeneity and metabolic intensity of the primary HR-NBL are closely associated with its overall metastatic burden. In turn, the whole-body tumour load appears to be one of the most relevant predictors of progression-free and overall survival.
Mots-clé
Dihydroxyphenylalanine/analogs & derivatives, Fluorine, Fluorodeoxyglucose F18, Humans, N-Myc Proto-Oncogene Protein, Neuroblastoma/diagnostic imaging, Positron Emission Tomography Computed Tomography/methods, Prognosis, Retrospective Studies, 18F-DOPA, PET, neuroblastoma, prognosis, radiomics
Pubmed
Web of science
Création de la notice
15/08/2022 13:31
Dernière modification de la notice
14/06/2023 5:56