A preliminary PET radiomics study of brain metastases using a fully automatic segmentation method.


Journal

BMC bioinformatics
ISSN: 1471-2105
Titre abrégé: BMC Bioinformatics
Pays: England
ID NLM: 100965194

Informations de publication

Date de publication:
16 Sep 2020
Historique:
received: 18 06 2020
accepted: 09 07 2020
entrez: 17 9 2020
pubmed: 18 9 2020
medline: 22 10 2020
Statut: epublish

Résumé

Positron Emission Tomography (PET) is increasingly utilized in radiomics studies for treatment evaluation purposes. Nevertheless, lesion volume identification in PET images is a critical and still challenging step in the process of radiomics, due to the low spatial resolution and high noise level of PET images. Currently, the biological target volume (BTV) is manually contoured by nuclear physicians, with a time expensive and operator-dependent procedure. This study aims to obtain BTVs from cerebral metastases in patients who underwent L-[ For predictive evaluation, 3 features (asphericity, low-intensity run emphasis, and complexity) were able to discriminate between responder and non-responder patients, after feature reduction and selection. Best performance in patient discrimination was obtained using the combination of the three selected features (sensitivity 81.23%, specificity 73.97%, and accuracy 78.27%) compared to the use of all features. Secondly, for follow-up evaluation, 8 features (SUV The proposed system is able i) to extract 108 features for each automatically segmented lesion and ii) to select a sub-panel of 11C-MET PET features (3 and 8 in the case of predictive and follow-up evaluation), with valuable association with patient outcome. We believe that our model can be useful to improve treatment response and prognosis evaluation, potentially allowing the personalization of cancer treatment plans.

Sections du résumé

BACKGROUND BACKGROUND
Positron Emission Tomography (PET) is increasingly utilized in radiomics studies for treatment evaluation purposes. Nevertheless, lesion volume identification in PET images is a critical and still challenging step in the process of radiomics, due to the low spatial resolution and high noise level of PET images. Currently, the biological target volume (BTV) is manually contoured by nuclear physicians, with a time expensive and operator-dependent procedure. This study aims to obtain BTVs from cerebral metastases in patients who underwent L-[
RESULTS RESULTS
For predictive evaluation, 3 features (asphericity, low-intensity run emphasis, and complexity) were able to discriminate between responder and non-responder patients, after feature reduction and selection. Best performance in patient discrimination was obtained using the combination of the three selected features (sensitivity 81.23%, specificity 73.97%, and accuracy 78.27%) compared to the use of all features. Secondly, for follow-up evaluation, 8 features (SUV
CONCLUSIONS CONCLUSIONS
The proposed system is able i) to extract 108 features for each automatically segmented lesion and ii) to select a sub-panel of 11C-MET PET features (3 and 8 in the case of predictive and follow-up evaluation), with valuable association with patient outcome. We believe that our model can be useful to improve treatment response and prognosis evaluation, potentially allowing the personalization of cancer treatment plans.

Identifiants

pubmed: 32938360
doi: 10.1186/s12859-020-03647-7
pii: 10.1186/s12859-020-03647-7
pmc: PMC7493376
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

325

Subventions

Organisme : Italian Ministry of Economic Development
ID : Grant No. F/090012/01-02/X36

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Auteurs

Alessandro Stefano (A)

Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Cefalù, Italy.

Albert Comelli (A)

Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Cefalù, Italy.
Ri.MED Foundation, Palermo, Italy.

Valentina Bravatà (V)

Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Cefalù, Italy. valentina.bravata@ibfm.cnr.it.

Stefano Barone (S)

University of Palermo, Palermo, Italy.

Igor Daskalovski (I)

Department of Physics and Astronomy, University of Catania, Catania, Italy.

Gaetano Savoca (G)

Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Cefalù, Italy.

Maria Gabriella Sabini (MG)

Medical Physics Unit, Cannizzaro Hospital, Catania, Italy.

Massimo Ippolito (M)

Nuclear Medicine Department, Cannizzaro Hospital, Catania, Italy.

Giorgio Russo (G)

Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Cefalù, Italy.
Medical Physics Unit, Cannizzaro Hospital, Catania, Italy.

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