Similarity clustering-based atlas selection for pelvic CT image segmentation.


Journal

Medical physics
ISSN: 2473-4209
Titre abrégé: Med Phys
Pays: United States
ID NLM: 0425746

Informations de publication

Date de publication:
May 2019
Historique:
received: 29 08 2018
revised: 29 01 2019
accepted: 02 03 2019
pubmed: 20 3 2019
medline: 3 9 2019
entrez: 20 3 2019
Statut: ppublish

Résumé

To demonstrate selection of a small representative subset of images from a pool of images comprising a potential atlas (PA) pelvic CT set to be used for autosegmentation of a separate target image set. The aim is to balance the need for the atlas set to represent anatomical diversity with the need to minimize resources required to create a high quality atlas set (such as multiobserver delineation), while retaining access to additional information available for the PA image set. Preprocessing was performed for image standardization, followed by image registration. Clustering was used to select the subset that provided the best coverage of a target dataset as measured by postregistration image intensity similarities. Tests for clustering robustness were performed including repeated clustering runs using different starting seeds and clustering repeatedly using 90% of the target dataset chosen randomly. Comparisons of coverage of a target set (comprising 711 pelvic CT images) were made for atlas sets of five images (chosen from a PA set of 39 pelvic CT and MR images) (a) at random (averaged over 50 random atlas selections), (b) based solely on image similarities within the PA set (representing prospective atlas development), (c) based on similarities within the PA set and between the PA and target dataset (representing retrospective atlas development). Comparisons were also made to coverage provided by the entire PA set of 39 images. Exemplar selection was highly robust with exemplar selection results being unaffected by choice of starting seed with very occasional change to one of the exemplar choices when the target set was reduced. Coverage of the target set, as measured by best normalized cross-correlation similarity of target images to any exemplar image, provided by five well-selected atlas images (mean = 0.6497) was more similar to coverage provided by the entire PA set (mean = 0.6658) than randomly chosen atlas subsets (mean = 0.5977). This was true both of the mean values and the shape of the distributions. Retrospective selection of atlases (mean = 0.6497) provided a very small improvement over prospective atlas selection (mean = 0.6431). All differences were significant (P < 1.0E-10). Selection of a small representative image set from one dataset can be utilized to develop an atlas set for either retrospective or prospective autosegmentation of a different target dataset. The coverage provided by such a judiciously selected subset has the potential to facilitate propagation of numerous retrospectively defined structures, utilizing additional information available with multimodal imaging in the atlas set, without the need to create large atlas image sets.

Identifiants

pubmed: 30887526
doi: 10.1002/mp.13494
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2243-2250

Subventions

Organisme : National Health and Medical Research Council
ID : 1077788

Informations de copyright

© 2019 Commonwealth of Australia. Medical Physics © 2019 American Association of Physicists in Medicine.

Auteurs

Angel Kennedy (A)

Radiation Oncology, Sir Charles Gairdner Hospital, Nedlands, WA, 6009, Australia.

Jason Dowling (J)

Australian e-Health Research Centre, CSIRO, Royal Brisbane and Women's Hospital, Herston, QLD, 4029, Australia.
School of Mathematical and Physical Sciences, University of Newcastle, Newcastle, NSW, 2308, Australia.
South Western Sydney Clinical School, University of New South Wales, Sydney, NSW, 2052, Australia.
Centre for Medical Radiation Physics, University of Wollongong, Wollongong, NSW, 2522, Australia.

Peter B Greer (PB)

Calvary Mater Newcastle Hospital, Newcastle, NSW, 2298, Australia.
School of Mathematical and Physical Sciences, University of Newcastle, Newcastle, NSW, 2308, Australia.

Lois Holloway (L)

Ingham Institute for Applied Medical Research, Sydney, NSW, 2170, Australia.
Liverpool Cancer Therapy Centre, Liverpool Hospital, Sydney, NSW, 2170, Australia.
South Western Sydney Clinical School, University of New South Wales, Sydney, NSW, 2052, Australia.
Centre for Medical Radiation Physics, University of Wollongong, Wollongong, NSW, 2522, Australia.

Michael G Jameson (MG)

Ingham Institute for Applied Medical Research, Sydney, NSW, 2170, Australia.
Liverpool Cancer Therapy Centre, Liverpool Hospital, Sydney, NSW, 2170, Australia.
South Western Sydney Clinical School, University of New South Wales, Sydney, NSW, 2052, Australia.

Dale Roach (D)

Liverpool Cancer Therapy Centre, Liverpool Hospital, Sydney, NSW, 2170, Australia.
South Western Sydney Clinical School, University of New South Wales, Sydney, NSW, 2052, Australia.

Soumya Ghose (S)

Department of Biomedical Engineering, Case Western University, Cleveland, OH, 44106, USA.

David Rivest-Hénault (D)

Australian e-Health Research Centre, CSIRO, Royal Brisbane and Women's Hospital, Herston, QLD, 4029, Australia.

Marco Marcello (M)

School of Physics and Astrophysics, University of Western Australia, Crawley, WA, 6009, Australia.

Martin A Ebert (MA)

Radiation Oncology, Sir Charles Gairdner Hospital, Nedlands, WA, 6009, Australia.
Centre for Medical Radiation Physics, University of Wollongong, Wollongong, NSW, 2522, Australia.
School of Physics and Astrophysics, University of Western Australia, Crawley, WA, 6009, Australia.
5D Clinics, Claremont, WA, 6010, Australia.

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