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Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity

SIMPLE SUMMARY: Tumoral heterogeneity, which is a major challenge in therapy planning, is often characterized by genetic alterations. In this study, an image-based approach was used to identify metastases subtypes by radiomics features. Feature selection and reduction using Pearson correlation thres...

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Autores principales: Tharmaseelan, Hishan, Hertel, Alexander, Tollens, Fabian, Rink, Johann, Woźnicki, Piotr, Haselmann, Verena, Ayx, Isabelle, Nörenberg, Dominik, Schoenberg, Stefan O., Froelich, Matthias F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997087/
https://www.ncbi.nlm.nih.gov/pubmed/35406418
http://dx.doi.org/10.3390/cancers14071646
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author Tharmaseelan, Hishan
Hertel, Alexander
Tollens, Fabian
Rink, Johann
Woźnicki, Piotr
Haselmann, Verena
Ayx, Isabelle
Nörenberg, Dominik
Schoenberg, Stefan O.
Froelich, Matthias F.
author_facet Tharmaseelan, Hishan
Hertel, Alexander
Tollens, Fabian
Rink, Johann
Woźnicki, Piotr
Haselmann, Verena
Ayx, Isabelle
Nörenberg, Dominik
Schoenberg, Stefan O.
Froelich, Matthias F.
author_sort Tharmaseelan, Hishan
collection PubMed
description SIMPLE SUMMARY: Tumoral heterogeneity, which is a major challenge in therapy planning, is often characterized by genetic alterations. In this study, an image-based approach was used to identify metastases subtypes by radiomics features. Feature selection and reduction using Pearson correlation threshold and LASSO regression resulted in four final features. After unsupervised clustering and following visual assessment, five lesion clusters could be identified and defined, which had a significant (p < 0.01) correlation with sex, primary location, T- and N-status, and mutational status. ABSTRACT: (1) Background: Tumoral heterogeneity (TH) is a major challenge in the treatment of metastatic colorectal cancer (mCRC) and is associated with inferior response. Therefore, the identification of TH would be beneficial for treatment planning. TH can be assessed by identifying genetic alterations. In this work, a radiomics-based approach for assessment of TH in colorectal liver metastases (CRLM) in CT scans is demonstrated. (2) Methods: In this retrospective study, CRLM of mCRC were segmented and radiomics features extracted using pyradiomics. Unsupervised k-means clustering was applied to features and lesions. Feature redundancy was evaluated by principal component analysis and reduced by Pearson correlation coefficient cutoff. Feature selection was conducted by LASSO regression and visual analysis of the clusters by radiologists. (3) Results: A total of 47 patients’ (36% female, median age 64) CTs with 261 lesions were included. Five clusters were identified, and the categories small disseminated (n = 31), heterogeneous (n = 105), homogeneous (n = 64), mixed (n = 59), and very large type (n = 2) were assigned based on visual characteristics. Further statistical analysis showed correlation (p < 0.01) of clusters with sex, primary location, T- and N-status, and mutational status. Feature reduction and selection resulted in the identification of four features as a final set for cluster definition. (4) Conclusions: Radiomics features can characterize TH in liver metastases of mCRC in CT scans, and may be suitable for a better pretherapeutic classification of liver lesion phenotypes.
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spelling pubmed-89970872022-04-12 Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity Tharmaseelan, Hishan Hertel, Alexander Tollens, Fabian Rink, Johann Woźnicki, Piotr Haselmann, Verena Ayx, Isabelle Nörenberg, Dominik Schoenberg, Stefan O. Froelich, Matthias F. Cancers (Basel) Article SIMPLE SUMMARY: Tumoral heterogeneity, which is a major challenge in therapy planning, is often characterized by genetic alterations. In this study, an image-based approach was used to identify metastases subtypes by radiomics features. Feature selection and reduction using Pearson correlation threshold and LASSO regression resulted in four final features. After unsupervised clustering and following visual assessment, five lesion clusters could be identified and defined, which had a significant (p < 0.01) correlation with sex, primary location, T- and N-status, and mutational status. ABSTRACT: (1) Background: Tumoral heterogeneity (TH) is a major challenge in the treatment of metastatic colorectal cancer (mCRC) and is associated with inferior response. Therefore, the identification of TH would be beneficial for treatment planning. TH can be assessed by identifying genetic alterations. In this work, a radiomics-based approach for assessment of TH in colorectal liver metastases (CRLM) in CT scans is demonstrated. (2) Methods: In this retrospective study, CRLM of mCRC were segmented and radiomics features extracted using pyradiomics. Unsupervised k-means clustering was applied to features and lesions. Feature redundancy was evaluated by principal component analysis and reduced by Pearson correlation coefficient cutoff. Feature selection was conducted by LASSO regression and visual analysis of the clusters by radiologists. (3) Results: A total of 47 patients’ (36% female, median age 64) CTs with 261 lesions were included. Five clusters were identified, and the categories small disseminated (n = 31), heterogeneous (n = 105), homogeneous (n = 64), mixed (n = 59), and very large type (n = 2) were assigned based on visual characteristics. Further statistical analysis showed correlation (p < 0.01) of clusters with sex, primary location, T- and N-status, and mutational status. Feature reduction and selection resulted in the identification of four features as a final set for cluster definition. (4) Conclusions: Radiomics features can characterize TH in liver metastases of mCRC in CT scans, and may be suitable for a better pretherapeutic classification of liver lesion phenotypes. MDPI 2022-03-24 /pmc/articles/PMC8997087/ /pubmed/35406418 http://dx.doi.org/10.3390/cancers14071646 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tharmaseelan, Hishan
Hertel, Alexander
Tollens, Fabian
Rink, Johann
Woźnicki, Piotr
Haselmann, Verena
Ayx, Isabelle
Nörenberg, Dominik
Schoenberg, Stefan O.
Froelich, Matthias F.
Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity
title Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity
title_full Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity
title_fullStr Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity
title_full_unstemmed Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity
title_short Identification of CT Imaging Phenotypes of Colorectal Liver Metastases from Radiomics Signatures—Towards Assessment of Interlesional Tumor Heterogeneity
title_sort identification of ct imaging phenotypes of colorectal liver metastases from radiomics signatures—towards assessment of interlesional tumor heterogeneity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997087/
https://www.ncbi.nlm.nih.gov/pubmed/35406418
http://dx.doi.org/10.3390/cancers14071646
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