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Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation
BACKGROUND: To compare the apparent diffusion coefficient (ADC) on diffusion-weighted imaging (DWI) with the standardized uptake values (SUV) measured by(18)F-FDG-PET/CT in naïve hepatocellular carcinoma (HCC) nodules, and to determine whether these markers are associated with tumours at high-risk o...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756529/ https://www.ncbi.nlm.nih.gov/pubmed/26883745 http://dx.doi.org/10.1186/s40644-016-0062-8 |
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author | Boussouar, Samia Itti, Emmanuel Lin, Shih-Jui Decaens, Thomas Evangelista, Eva Chiaradia, Melanie Chalaye, Julia Baranes, Laurence Calderaro, Julien Laurent, Alexis Pigneur, Frederic Duvoux, Christophe Azoulay, Daniel Costentin, Charlotte Rahmouni, Alain Luciani, Alain |
author_facet | Boussouar, Samia Itti, Emmanuel Lin, Shih-Jui Decaens, Thomas Evangelista, Eva Chiaradia, Melanie Chalaye, Julia Baranes, Laurence Calderaro, Julien Laurent, Alexis Pigneur, Frederic Duvoux, Christophe Azoulay, Daniel Costentin, Charlotte Rahmouni, Alain Luciani, Alain |
author_sort | Boussouar, Samia |
collection | PubMed |
description | BACKGROUND: To compare the apparent diffusion coefficient (ADC) on diffusion-weighted imaging (DWI) with the standardized uptake values (SUV) measured by(18)F-FDG-PET/CT in naïve hepatocellular carcinoma (HCC) nodules, and to determine whether these markers are associated with tumours at high-risk of aggressiveness. METHODS: From 2007 to 2010, all patients with HCC on the waiting list for liver transplantation and who underwent both FDG-PET/CT and 1.5-T DWI-MRI (b values: 0, 200, 400, and 800 s/mm(2)) were included in this institutional review board-approved retrospective study. Tumour size, tumour ADC, tumour-to-liver ADC ratio (ADC(T/L)), maximal tumour SUV and tumour-to-liver SUV ratio (SUV(T/L)) were measured and compared to serum alpha-fetoprotein (AFP) levels, tumour size and differentiation grade on explanted specimens. RESULTS: A total of 37 HCC nodules in 28 patients were available for correlation between MRI and PET/CT, 7 of which (in 7 patients) showed a SUV(T/L) > 1.15. We did not find any correlation between tumour ADC or ADC(T/L) and tumour SUV or SUV(T/L). To note, SUV(T/L) was positively correlated with AFP levels (R = 0.95, P ≤ 0.0001), while ADC(T/L) was not (P = 0.73). Twenty-four patients (with 32 nodules) underwent liver transplantation. In this subgroup, an increased SUV(T/L) ratio was associated with larger tumours (average size, 32 ± 14 mm; range, 18–60 mm; P < 0.0001) and with poor differentiation on pathology (grades 3 and 4; P = 0.04), while ADC(T/L) was neither associated with tumour size or differentiation grade. CONCLUSIONS: ADC and SUV measures in HCC nodules are not correlated. SUV(T/L) ratio correlates with AFP levels, tumour size and poor differentiation, and should probably be integrated as a co-variable in a predictive outcome model of patients on the waiting-list for liver transplantation. |
format | Online Article Text |
id | pubmed-4756529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47565292016-02-18 Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation Boussouar, Samia Itti, Emmanuel Lin, Shih-Jui Decaens, Thomas Evangelista, Eva Chiaradia, Melanie Chalaye, Julia Baranes, Laurence Calderaro, Julien Laurent, Alexis Pigneur, Frederic Duvoux, Christophe Azoulay, Daniel Costentin, Charlotte Rahmouni, Alain Luciani, Alain Cancer Imaging Research Article BACKGROUND: To compare the apparent diffusion coefficient (ADC) on diffusion-weighted imaging (DWI) with the standardized uptake values (SUV) measured by(18)F-FDG-PET/CT in naïve hepatocellular carcinoma (HCC) nodules, and to determine whether these markers are associated with tumours at high-risk of aggressiveness. METHODS: From 2007 to 2010, all patients with HCC on the waiting list for liver transplantation and who underwent both FDG-PET/CT and 1.5-T DWI-MRI (b values: 0, 200, 400, and 800 s/mm(2)) were included in this institutional review board-approved retrospective study. Tumour size, tumour ADC, tumour-to-liver ADC ratio (ADC(T/L)), maximal tumour SUV and tumour-to-liver SUV ratio (SUV(T/L)) were measured and compared to serum alpha-fetoprotein (AFP) levels, tumour size and differentiation grade on explanted specimens. RESULTS: A total of 37 HCC nodules in 28 patients were available for correlation between MRI and PET/CT, 7 of which (in 7 patients) showed a SUV(T/L) > 1.15. We did not find any correlation between tumour ADC or ADC(T/L) and tumour SUV or SUV(T/L). To note, SUV(T/L) was positively correlated with AFP levels (R = 0.95, P ≤ 0.0001), while ADC(T/L) was not (P = 0.73). Twenty-four patients (with 32 nodules) underwent liver transplantation. In this subgroup, an increased SUV(T/L) ratio was associated with larger tumours (average size, 32 ± 14 mm; range, 18–60 mm; P < 0.0001) and with poor differentiation on pathology (grades 3 and 4; P = 0.04), while ADC(T/L) was neither associated with tumour size or differentiation grade. CONCLUSIONS: ADC and SUV measures in HCC nodules are not correlated. SUV(T/L) ratio correlates with AFP levels, tumour size and poor differentiation, and should probably be integrated as a co-variable in a predictive outcome model of patients on the waiting-list for liver transplantation. BioMed Central 2016-02-16 /pmc/articles/PMC4756529/ /pubmed/26883745 http://dx.doi.org/10.1186/s40644-016-0062-8 Text en © Boussouar et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Boussouar, Samia Itti, Emmanuel Lin, Shih-Jui Decaens, Thomas Evangelista, Eva Chiaradia, Melanie Chalaye, Julia Baranes, Laurence Calderaro, Julien Laurent, Alexis Pigneur, Frederic Duvoux, Christophe Azoulay, Daniel Costentin, Charlotte Rahmouni, Alain Luciani, Alain Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation |
title | Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation |
title_full | Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation |
title_fullStr | Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation |
title_full_unstemmed | Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation |
title_short | Functional imaging of hepatocellular carcinoma using diffusion-weighted MRI and (18)F-FDG PET/CT in patients on waiting-list for liver transplantation |
title_sort | functional imaging of hepatocellular carcinoma using diffusion-weighted mri and (18)f-fdg pet/ct in patients on waiting-list for liver transplantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756529/ https://www.ncbi.nlm.nih.gov/pubmed/26883745 http://dx.doi.org/10.1186/s40644-016-0062-8 |
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