Localization of anatomical changes in patients during proton therapy with in-beam PET monitoring: A voxel-based morphometry approach exploiting Monte Carlo simulations.
in-beam PET monitoring
proton therapy
voxel-based morphometry
Journal
Medical physics
ISSN: 2473-4209
Titre abrégé: Med Phys
Pays: United States
ID NLM: 0425746
Informations de publication
Date de publication:
Jan 2022
Jan 2022
Historique:
revised:
30
06
2021
received:
06
03
2021
accepted:
11
10
2021
pubmed:
24
11
2021
medline:
18
1
2022
entrez:
23
11
2021
Statut:
ppublish
Résumé
In-beam positron emission tomography (PET) is one of the modalities that can be used for in vivo noninvasive treatment monitoring in proton therapy. Although PET monitoring has been frequently applied for this purpose, there is still no straightforward method to translate the information obtained from the PET images into easy-to-interpret information for clinical personnel. The purpose of this work is to propose a statistical method for analyzing in-beam PET monitoring images that can be used to locate, quantify, and visualize regions with possible morphological changes occurring over the course of treatment. We selected a patient treated for squamous cell carcinoma (SCC) with proton therapy, to perform multiple Monte Carlo (MC) simulations of the expected PET signal at the start of treatment, and to study how the PET signal may change along the treatment course due to morphological changes. We performed voxel-wise two-tailed statistical tests of the simulated PET images, resembling the voxel-based morphometry (VBM) method commonly used in neuroimaging data analysis, to locate regions with significant morphological changes and to quantify the change. The VBM resembling method has been successfully applied to the simulated in-beam PET images, despite the fact that such images suffer from image artifacts and limited statistics. Three dimensional probability maps were obtained, that allowed to identify interfractional morphological changes and to visualize them superimposed on the computed tomography (CT) scan. In particular, the characteristic color patterns resulting from the two-tailed statistical tests lend themselves to trigger alarms in case of morphological changes along the course of treatment. The statistical method presented in this work is a promising method to apply to PET monitoring data to reveal interfractional morphological changes in patients, occurring over the course of treatment. Based on simulated in-beam PET treatment monitoring images, we showed that with our method it was possible to correctly identify the regions that changed. Moreover we could quantify the changes, and visualize them superimposed on the CT scan. The proposed method can possibly help clinical personnel in the replanning procedure in adaptive proton therapy treatments.
Identifiants
pubmed: 34813083
doi: 10.1002/mp.15336
pmc: PMC9303286
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
23-40Subventions
Organisme : Italian Ministry of Education
ID : PRIN MIUR 2010P98A75 INSIDE
Organisme : Italian Institute of Nuclear Physics
ID : RDH
Organisme : Italian Institute of Nuclear Physics
ID : INFN-RT2 PETRA 172800
Organisme : Historical Museum of Physics and the Enrico Fermi Study and Research Center and the
Organisme : Tuscany Government
ID : POR FSE 2014-2020
Organisme : Tuscany Government
ID : INFN-RT2 PETRA 172800
Organisme : CNAO Foundation
ID : INSIDE2
Informations de copyright
© 2021 The Authors. Medical Physics published by Wiley Periodicals LLC on behalf of American Association of Physicists in Medicine.
Références
Phys Med. 2018 Jul;51:71-80
pubmed: 29747928
Semin Radiat Oncol. 2019 Jul;29(3):245-257
pubmed: 31027642
Phys Med Biol. 2013 Jun 7;58(11):3837-47
pubmed: 23681116
Phys Med Biol. 2014 Jan 6;59(1):43-60
pubmed: 24321855
Phys Med Biol. 2014 Oct 7;59(19):5903-19
pubmed: 25211629
Radiother Oncol. 2019 Feb;131:127-134
pubmed: 30773179
Radiat Oncol. 2016 Apr 30;11:64
pubmed: 27129305
Int J Radiat Oncol Biol Phys. 2010 Jan 1;76(1):277-86
pubmed: 20005459
Nat Rev Clin Oncol. 2013 Jul;10(7):411-24
pubmed: 23689752
Med Phys. 2022 Jan;49(1):23-40
pubmed: 34813083
Med Phys. 2015 Sep;42(9):5287-300
pubmed: 26328978
J Med Imaging (Bellingham). 2017 Jan;4(1):011005
pubmed: 27981069
Int J Radiat Oncol Biol Phys. 2013 Dec 1;87(5):888-96
pubmed: 24351409
Eur Psychiatry. 2020 Mar 16;63(1):e27
pubmed: 32172703
Cancers Head Neck. 2020 Jan 09;5:1
pubmed: 31938572
Neuroimage. 2000 Jun;11(6 Pt 1):805-21
pubmed: 10860804
Phys Med. 2019 Aug;64:261-272
pubmed: 31515029
Z Med Phys. 2015 Jun;25(2):146-55
pubmed: 25193358
Neuroimage. 2012 Jan 16;59(2):1013-22
pubmed: 21896334
Stat Appl Genet Mol Biol. 2010;9:Article39
pubmed: 21044043
Med Phys. 2018 Nov;45(11):e1036-e1050
pubmed: 30421803
Am J Hum Genet. 2002 Aug;71(2):439-41
pubmed: 12111669
Int J Radiat Oncol Biol Phys. 2017 Mar 1;97(3):616-623
pubmed: 28011049
Phys Med Biol. 2006 Apr 21;51(8):1991-2009
pubmed: 16585841
Phys Med Biol. 2009 Jun 7;54(11):N217-28
pubmed: 19436106
Clin Oncol (R Coll Radiol). 2018 May;30(5):293-298
pubmed: 29551567
Phys Med Biol. 2015 Sep 7;60(17):6865-80
pubmed: 26301623
Br J Radiol. 2020 Mar;93(1107):20190594
pubmed: 31647313
Med Phys. 2015 Jan;42(1):263-75
pubmed: 25563266
Phys Med Biol. 2018 Jul 17;63(14):145018
pubmed: 29873299
Int J Radiat Oncol Biol Phys. 2012 Jun 1;83(2):712-9
pubmed: 22099037
Phys Med. 2008 Jun;24(2):102-6
pubmed: 18411070
Front Oncol. 2015 Jul 07;5:150
pubmed: 26217586
Phys Med Biol. 2015 Dec 7;60(23):8923-47
pubmed: 26539812
Phys Med Biol. 2011 Dec 7;56(23):7601-19
pubmed: 22086216
Int J Radiat Oncol Biol Phys. 2013 May 1;86(1):183-9
pubmed: 23391817
Phys Med Biol. 2000 Feb;45(2):459-78
pubmed: 10701515
Sci Rep. 2018 Mar 6;8(1):4100
pubmed: 29511282
Phys Med Biol. 2008 Aug 7;53(15):4137-51
pubmed: 18635897
Int J Radiat Oncol Biol Phys. 2011 Jan 1;79(1):297-304
pubmed: 20646839
Phys Med Biol. 2013 Jun 7;58(11):3815-35
pubmed: 23681070
Phys Med Biol. 2013 Aug 7;58(15):R131-60
pubmed: 23863203
Front Oncol. 2016 May 11;6:116
pubmed: 27242956