Cargando…

Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images

We introduce a novel computational framework to enable automated identification of texture and shape features of lesions on (18)F-FDG-PET images through a graph-based image segmentation method. The proposed framework predicts future morphological changes of lesions with high accuracy. The presented...

Descripción completa

Detalles Bibliográficos
Autores principales: Bagci, Ulas, Yao, Jianhua, Miller-Jaster, Kirsten, Chen, Xinjian, Mollura, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576352/
https://www.ncbi.nlm.nih.gov/pubmed/23431398
http://dx.doi.org/10.1371/journal.pone.0057105
_version_ 1782259846108676096
author Bagci, Ulas
Yao, Jianhua
Miller-Jaster, Kirsten
Chen, Xinjian
Mollura, Daniel J.
author_facet Bagci, Ulas
Yao, Jianhua
Miller-Jaster, Kirsten
Chen, Xinjian
Mollura, Daniel J.
author_sort Bagci, Ulas
collection PubMed
description We introduce a novel computational framework to enable automated identification of texture and shape features of lesions on (18)F-FDG-PET images through a graph-based image segmentation method. The proposed framework predicts future morphological changes of lesions with high accuracy. The presented methodology has several benefits over conventional qualitative and semi-quantitative methods, due to its fully quantitative nature and high accuracy in each step of (i) detection, (ii) segmentation, and (iii) feature extraction. To evaluate our proposed computational framework, thirty patients received 2 (18)F-FDG-PET scans (60 scans total), at two different time points. Metastatic papillary renal cell carcinoma, cerebellar hemongioblastoma, non-small cell lung cancer, neurofibroma, lymphomatoid granulomatosis, lung neoplasm, neuroendocrine tumor, soft tissue thoracic mass, nonnecrotizing granulomatous inflammation, renal cell carcinoma with papillary and cystic features, diffuse large B-cell lymphoma, metastatic alveolar soft part sarcoma, and small cell lung cancer were included in this analysis. The radiotracer accumulation in patients' scans was automatically detected and segmented by the proposed segmentation algorithm. Delineated regions were used to extract shape and textural features, with the proposed adaptive feature extraction framework, as well as standardized uptake values (SUV) of uptake regions, to conduct a broad quantitative analysis. Evaluation of segmentation results indicates that our proposed segmentation algorithm has a mean dice similarity coefficient of 85.75±1.75%. We found that 28 of 68 extracted imaging features were correlated well with SUV(max) (p<0.05), and some of the textural features (such as entropy and maximum probability) were superior in predicting morphological changes of radiotracer uptake regions longitudinally, compared to single intensity feature such as SUV(max). We also found that integrating textural features with SUV measurements significantly improves the prediction accuracy of morphological changes (Spearman correlation coefficient = 0.8715, p<2e-16).
format Online
Article
Text
id pubmed-3576352
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35763522013-02-21 Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images Bagci, Ulas Yao, Jianhua Miller-Jaster, Kirsten Chen, Xinjian Mollura, Daniel J. PLoS One Research Article We introduce a novel computational framework to enable automated identification of texture and shape features of lesions on (18)F-FDG-PET images through a graph-based image segmentation method. The proposed framework predicts future morphological changes of lesions with high accuracy. The presented methodology has several benefits over conventional qualitative and semi-quantitative methods, due to its fully quantitative nature and high accuracy in each step of (i) detection, (ii) segmentation, and (iii) feature extraction. To evaluate our proposed computational framework, thirty patients received 2 (18)F-FDG-PET scans (60 scans total), at two different time points. Metastatic papillary renal cell carcinoma, cerebellar hemongioblastoma, non-small cell lung cancer, neurofibroma, lymphomatoid granulomatosis, lung neoplasm, neuroendocrine tumor, soft tissue thoracic mass, nonnecrotizing granulomatous inflammation, renal cell carcinoma with papillary and cystic features, diffuse large B-cell lymphoma, metastatic alveolar soft part sarcoma, and small cell lung cancer were included in this analysis. The radiotracer accumulation in patients' scans was automatically detected and segmented by the proposed segmentation algorithm. Delineated regions were used to extract shape and textural features, with the proposed adaptive feature extraction framework, as well as standardized uptake values (SUV) of uptake regions, to conduct a broad quantitative analysis. Evaluation of segmentation results indicates that our proposed segmentation algorithm has a mean dice similarity coefficient of 85.75±1.75%. We found that 28 of 68 extracted imaging features were correlated well with SUV(max) (p<0.05), and some of the textural features (such as entropy and maximum probability) were superior in predicting morphological changes of radiotracer uptake regions longitudinally, compared to single intensity feature such as SUV(max). We also found that integrating textural features with SUV measurements significantly improves the prediction accuracy of morphological changes (Spearman correlation coefficient = 0.8715, p<2e-16). Public Library of Science 2013-02-19 /pmc/articles/PMC3576352/ /pubmed/23431398 http://dx.doi.org/10.1371/journal.pone.0057105 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Bagci, Ulas
Yao, Jianhua
Miller-Jaster, Kirsten
Chen, Xinjian
Mollura, Daniel J.
Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images
title Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images
title_full Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images
title_fullStr Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images
title_full_unstemmed Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images
title_short Predicting Future Morphological Changes of Lesions from Radiotracer Uptake in 18F-FDG-PET Images
title_sort predicting future morphological changes of lesions from radiotracer uptake in 18f-fdg-pet images
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576352/
https://www.ncbi.nlm.nih.gov/pubmed/23431398
http://dx.doi.org/10.1371/journal.pone.0057105
work_keys_str_mv AT bagciulas predictingfuturemorphologicalchangesoflesionsfromradiotraceruptakein18ffdgpetimages
AT yaojianhua predictingfuturemorphologicalchangesoflesionsfromradiotraceruptakein18ffdgpetimages
AT millerjasterkirsten predictingfuturemorphologicalchangesoflesionsfromradiotraceruptakein18ffdgpetimages
AT chenxinjian predictingfuturemorphologicalchangesoflesionsfromradiotraceruptakein18ffdgpetimages
AT molluradanielj predictingfuturemorphologicalchangesoflesionsfromradiotraceruptakein18ffdgpetimages