Cargando…

Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers

OBJECTIVES: To propose a novel robust radiogenomics approach to the identification of epidermal growth factor receptor (EGFR) mutations among patients with non-small cell lung cancer (NSCLC) using Betti numbers (BNs). MATERIALS AND METHODS: Contrast enhanced computed tomography (CT) images of 194 mu...

Descripción completa

Detalles Bibliográficos
Autores principales: Ninomiya, Kenta, Arimura, Hidetaka, Chan, Wai Yee, Tanaka, Kentaro, Mizuno, Shinichi, Muhammad Gowdh, Nadia Fareeda, Yaakup, Nur Adura, Liam, Chong-Kin, Chai, Chee-Shee, Ng, Kwan Hoong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7799813/
https://www.ncbi.nlm.nih.gov/pubmed/33428651
http://dx.doi.org/10.1371/journal.pone.0244354
_version_ 1783635212931956736
author Ninomiya, Kenta
Arimura, Hidetaka
Chan, Wai Yee
Tanaka, Kentaro
Mizuno, Shinichi
Muhammad Gowdh, Nadia Fareeda
Yaakup, Nur Adura
Liam, Chong-Kin
Chai, Chee-Shee
Ng, Kwan Hoong
author_facet Ninomiya, Kenta
Arimura, Hidetaka
Chan, Wai Yee
Tanaka, Kentaro
Mizuno, Shinichi
Muhammad Gowdh, Nadia Fareeda
Yaakup, Nur Adura
Liam, Chong-Kin
Chai, Chee-Shee
Ng, Kwan Hoong
author_sort Ninomiya, Kenta
collection PubMed
description OBJECTIVES: To propose a novel robust radiogenomics approach to the identification of epidermal growth factor receptor (EGFR) mutations among patients with non-small cell lung cancer (NSCLC) using Betti numbers (BNs). MATERIALS AND METHODS: Contrast enhanced computed tomography (CT) images of 194 multi-racial NSCLC patients (79 EGFR mutants and 115 wildtypes) were collected from three different countries using 5 manufacturers’ scanners with a variety of scanning parameters. Ninety-nine cases obtained from the University of Malaya Medical Centre (UMMC) in Malaysia were used for training and validation procedures. Forty-one cases collected from the Kyushu University Hospital (KUH) in Japan and fifty-four cases obtained from The Cancer Imaging Archive (TCIA) in America were used for a test procedure. Radiomic features were obtained from BN maps, which represent topologically invariant heterogeneous characteristics of lung cancer on CT images, by applying histogram- and texture-based feature computations. A BN-based signature was determined using support vector machine (SVM) models with the best combination of features that maximized a robustness index (RI) which defined a higher total area under receiver operating characteristics curves (AUCs) and lower difference of AUCs between the training and the validation. The SVM model was built using the signature and optimized in a five-fold cross validation. The BN-based model was compared to conventional original image (OI)- and wavelet-decomposition (WD)-based models with respect to the RI between the validation and the test. RESULTS: The BN-based model showed a higher RI of 1.51 compared with the models based on the OI (RI: 1.33) and the WD (RI: 1.29). CONCLUSION: The proposed model showed higher robustness than the conventional models in the identification of EGFR mutations among NSCLC patients. The results suggested the robustness of the BN-based approach against variations in image scanner/scanning parameters.
format Online
Article
Text
id pubmed-7799813
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-77998132021-01-22 Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers Ninomiya, Kenta Arimura, Hidetaka Chan, Wai Yee Tanaka, Kentaro Mizuno, Shinichi Muhammad Gowdh, Nadia Fareeda Yaakup, Nur Adura Liam, Chong-Kin Chai, Chee-Shee Ng, Kwan Hoong PLoS One Research Article OBJECTIVES: To propose a novel robust radiogenomics approach to the identification of epidermal growth factor receptor (EGFR) mutations among patients with non-small cell lung cancer (NSCLC) using Betti numbers (BNs). MATERIALS AND METHODS: Contrast enhanced computed tomography (CT) images of 194 multi-racial NSCLC patients (79 EGFR mutants and 115 wildtypes) were collected from three different countries using 5 manufacturers’ scanners with a variety of scanning parameters. Ninety-nine cases obtained from the University of Malaya Medical Centre (UMMC) in Malaysia were used for training and validation procedures. Forty-one cases collected from the Kyushu University Hospital (KUH) in Japan and fifty-four cases obtained from The Cancer Imaging Archive (TCIA) in America were used for a test procedure. Radiomic features were obtained from BN maps, which represent topologically invariant heterogeneous characteristics of lung cancer on CT images, by applying histogram- and texture-based feature computations. A BN-based signature was determined using support vector machine (SVM) models with the best combination of features that maximized a robustness index (RI) which defined a higher total area under receiver operating characteristics curves (AUCs) and lower difference of AUCs between the training and the validation. The SVM model was built using the signature and optimized in a five-fold cross validation. The BN-based model was compared to conventional original image (OI)- and wavelet-decomposition (WD)-based models with respect to the RI between the validation and the test. RESULTS: The BN-based model showed a higher RI of 1.51 compared with the models based on the OI (RI: 1.33) and the WD (RI: 1.29). CONCLUSION: The proposed model showed higher robustness than the conventional models in the identification of EGFR mutations among NSCLC patients. The results suggested the robustness of the BN-based approach against variations in image scanner/scanning parameters. Public Library of Science 2021-01-11 /pmc/articles/PMC7799813/ /pubmed/33428651 http://dx.doi.org/10.1371/journal.pone.0244354 Text en © 2021 Ninomiya et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ninomiya, Kenta
Arimura, Hidetaka
Chan, Wai Yee
Tanaka, Kentaro
Mizuno, Shinichi
Muhammad Gowdh, Nadia Fareeda
Yaakup, Nur Adura
Liam, Chong-Kin
Chai, Chee-Shee
Ng, Kwan Hoong
Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers
title Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers
title_full Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers
title_fullStr Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers
title_full_unstemmed Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers
title_short Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers
title_sort robust radiogenomics approach to the identification of egfr mutations among patients with nsclc from three different countries using topologically invariant betti numbers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7799813/
https://www.ncbi.nlm.nih.gov/pubmed/33428651
http://dx.doi.org/10.1371/journal.pone.0244354
work_keys_str_mv AT ninomiyakenta robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT arimurahidetaka robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT chanwaiyee robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT tanakakentaro robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT mizunoshinichi robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT muhammadgowdhnadiafareeda robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT yaakupnuradura robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT liamchongkin robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT chaicheeshee robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers
AT ngkwanhoong robustradiogenomicsapproachtotheidentificationofegfrmutationsamongpatientswithnsclcfromthreedifferentcountriesusingtopologicallyinvariantbettinumbers