Cargando…

Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer

Conventional transarterial chemoembolization (cTACE) is a guideline-approved image-guided therapy option for liver cancer using the radiopaque drug-carrier and micro-embolic agent Lipiodol, which has been previously established as an imaging biomarker for tumor response. To establish automated quant...

Descripción completa

Detalles Bibliográficos
Autores principales: Stark, Sophie, Wang, Clinton, Savic, Lynn Jeanette, Letzen, Brian, Schobert, Isabel, Miszczuk, Milena, Murali, Nikitha, Oestmann, Paula, Gebauer, Bernhard, Lin, MingDe, Duncan, James, Schlachter, Todd, Chapiro, Julius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582153/
https://www.ncbi.nlm.nih.gov/pubmed/33093524
http://dx.doi.org/10.1038/s41598-020-75120-7
_version_ 1783599130124222464
author Stark, Sophie
Wang, Clinton
Savic, Lynn Jeanette
Letzen, Brian
Schobert, Isabel
Miszczuk, Milena
Murali, Nikitha
Oestmann, Paula
Gebauer, Bernhard
Lin, MingDe
Duncan, James
Schlachter, Todd
Chapiro, Julius
author_facet Stark, Sophie
Wang, Clinton
Savic, Lynn Jeanette
Letzen, Brian
Schobert, Isabel
Miszczuk, Milena
Murali, Nikitha
Oestmann, Paula
Gebauer, Bernhard
Lin, MingDe
Duncan, James
Schlachter, Todd
Chapiro, Julius
author_sort Stark, Sophie
collection PubMed
description Conventional transarterial chemoembolization (cTACE) is a guideline-approved image-guided therapy option for liver cancer using the radiopaque drug-carrier and micro-embolic agent Lipiodol, which has been previously established as an imaging biomarker for tumor response. To establish automated quantitative and pattern-based image analysis techniques of Lipiodol deposition on 24 h post-cTACE CT as biomarker for treatment response. The density of Lipiodol deposits in 65 liver lesions was automatically quantified using Hounsfield Unit thresholds. Lipiodol deposition within the tumor was automatically assessed for patterns including homogeneity, sparsity, rim, and peripheral deposition. Lipiodol deposition was correlated with enhancing tumor volume (ETV) on baseline and follow-up MRI. ETV on baseline MRI strongly correlated with Lipiodol deposition on 24 h CT (p < 0.0001), with 8.22% ± 14.59 more Lipiodol in viable than necrotic tumor areas. On follow-up, tumor regions with Lipiodol showed higher rates of ETV reduction than areas without Lipiodol (p = 0.0475) and increasing densities of Lipiodol enhanced this effect. Also, homogeneous (p = 0.0006), non-sparse (p < 0.0001), rim deposition within sparse tumors (p = 0.045), and peripheral deposition (p < 0.0001) of Lipiodol showed improved response. This technical innovation study showed that an automated threshold-based volumetric feature characterization of Lipiodol deposits is feasible and enables practical use of Lipiodol as imaging biomarker for therapeutic efficacy after cTACE.
format Online
Article
Text
id pubmed-7582153
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75821532020-10-23 Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer Stark, Sophie Wang, Clinton Savic, Lynn Jeanette Letzen, Brian Schobert, Isabel Miszczuk, Milena Murali, Nikitha Oestmann, Paula Gebauer, Bernhard Lin, MingDe Duncan, James Schlachter, Todd Chapiro, Julius Sci Rep Article Conventional transarterial chemoembolization (cTACE) is a guideline-approved image-guided therapy option for liver cancer using the radiopaque drug-carrier and micro-embolic agent Lipiodol, which has been previously established as an imaging biomarker for tumor response. To establish automated quantitative and pattern-based image analysis techniques of Lipiodol deposition on 24 h post-cTACE CT as biomarker for treatment response. The density of Lipiodol deposits in 65 liver lesions was automatically quantified using Hounsfield Unit thresholds. Lipiodol deposition within the tumor was automatically assessed for patterns including homogeneity, sparsity, rim, and peripheral deposition. Lipiodol deposition was correlated with enhancing tumor volume (ETV) on baseline and follow-up MRI. ETV on baseline MRI strongly correlated with Lipiodol deposition on 24 h CT (p < 0.0001), with 8.22% ± 14.59 more Lipiodol in viable than necrotic tumor areas. On follow-up, tumor regions with Lipiodol showed higher rates of ETV reduction than areas without Lipiodol (p = 0.0475) and increasing densities of Lipiodol enhanced this effect. Also, homogeneous (p = 0.0006), non-sparse (p < 0.0001), rim deposition within sparse tumors (p = 0.045), and peripheral deposition (p < 0.0001) of Lipiodol showed improved response. This technical innovation study showed that an automated threshold-based volumetric feature characterization of Lipiodol deposits is feasible and enables practical use of Lipiodol as imaging biomarker for therapeutic efficacy after cTACE. Nature Publishing Group UK 2020-10-22 /pmc/articles/PMC7582153/ /pubmed/33093524 http://dx.doi.org/10.1038/s41598-020-75120-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Stark, Sophie
Wang, Clinton
Savic, Lynn Jeanette
Letzen, Brian
Schobert, Isabel
Miszczuk, Milena
Murali, Nikitha
Oestmann, Paula
Gebauer, Bernhard
Lin, MingDe
Duncan, James
Schlachter, Todd
Chapiro, Julius
Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer
title Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer
title_full Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer
title_fullStr Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer
title_full_unstemmed Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer
title_short Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer
title_sort automated feature quantification of lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582153/
https://www.ncbi.nlm.nih.gov/pubmed/33093524
http://dx.doi.org/10.1038/s41598-020-75120-7
work_keys_str_mv AT starksophie automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT wangclinton automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT saviclynnjeanette automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT letzenbrian automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT schobertisabel automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT miszczukmilena automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT muralinikitha automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT oestmannpaula automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT gebauerbernhard automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT linmingde automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT duncanjames automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT schlachtertodd automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer
AT chapirojulius automatedfeaturequantificationoflipiodolasimagingbiomarkertopredicttherapeuticefficacyofconventionaltransarterialchemoembolizationoflivercancer