Automated feature quantification of Lipiodol as imaging biomarker to predict therapeutic efficacy of conventional transarterial chemoembolization of liver cancer.
Biomarkers
/ analysis
Carcinoma, Hepatocellular
/ diagnostic imaging
Chemoembolization, Therapeutic
/ methods
Contrast Media
/ analysis
Ethiodized Oil
/ analysis
Female
Humans
Image Processing, Computer-Assisted
/ methods
Liver Neoplasms
/ diagnostic imaging
Male
Middle Aged
Prospective Studies
Tomography, X-Ray Computed
/ methods
Treatment Outcome
Tumor Burden
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
22 10 2020
22 10 2020
Historique:
received:
22
04
2020
accepted:
09
10
2020
entrez:
23
10
2020
pubmed:
24
10
2020
medline:
19
3
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 33093524
doi: 10.1038/s41598-020-75120-7
pii: 10.1038/s41598-020-75120-7
pmc: PMC7582153
doi:
Substances chimiques
Biomarkers
0
Contrast Media
0
Ethiodized Oil
8008-53-5
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
18026Subventions
Organisme : NCI NIH HHS
ID : R01 CA206180
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NIH HHS
ID : NIH/NCI R01 CA206180
Pays : United States
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