Cargando…
Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging
SIMPLE SUMMARY: Pancreatic ductal adenocarcinoma (PDAC) remains a devastating disease. However, variations in tumor biology influence individual patient outcomes greatly. We previously showed a strong association between magnetic resonance imaging-based tumor cell estimates and patient survival. In...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123300/ https://www.ncbi.nlm.nih.gov/pubmed/33922981 http://dx.doi.org/10.3390/cancers13092069 |
_version_ | 1783692863529287680 |
---|---|
author | Jungmann, Friederike Kaissis, Georgios A. Ziegelmayer, Sebastian Harder, Felix Schilling, Clara Yen, Hsi-Yu Steiger, Katja Weichert, Wilko Schirren, Rebekka Demir, Ishan Ekin Friess, Helmut Makowski, Markus R. Braren, Rickmer F. Lohöfer, Fabian K. |
author_facet | Jungmann, Friederike Kaissis, Georgios A. Ziegelmayer, Sebastian Harder, Felix Schilling, Clara Yen, Hsi-Yu Steiger, Katja Weichert, Wilko Schirren, Rebekka Demir, Ishan Ekin Friess, Helmut Makowski, Markus R. Braren, Rickmer F. Lohöfer, Fabian K. |
author_sort | Jungmann, Friederike |
collection | PubMed |
description | SIMPLE SUMMARY: Pancreatic ductal adenocarcinoma (PDAC) remains a devastating disease. However, variations in tumor biology influence individual patient outcomes greatly. We previously showed a strong association between magnetic resonance imaging-based tumor cell estimates and patient survival. In this study we aimed to transfer this finding to more broadly applied computed tomography (CT) imaging for non-invasive risk stratification. We correlated in vivo CT imaging with histopathological analyses and could show a strong association between regional Hounsfield Units (HU) and tumor cellularity. In conclusion, our study suggests CT-based tumor cell estimates as a widely applicable way of non-invasive tumor cellularity characterization in PDAC. ABSTRACT: Background: PDAC remains a tumor entity with poor prognosis and a 5-year survival rate below 10%. Recent research has revealed invasive biomarkers, such as distinct molecular subtypes, predictive for therapy response and patient survival. Non-invasive prediction of individual patient outcome however remains an unresolved task. Methods: Discrete cellularity regions of PDAC resection specimen (n = 43) were analyzed by routine histopathological work up. Regional tumor cellularity and CT-derived Hounsfield Units (HU, n = 66) as well as iodine concentrations were regionally matched. One-way ANOVA and pairwise t-tests were performed to assess the relationship between different cellularity level in conventional, virtual monoenergetic 40 keV (monoE 40 keV) and iodine map reconstructions. Results: A statistically significant negative correlation between regional tumor cellularity in histopathology and CT-derived HU from corresponding image regions was identified. Radiological differentiation was best possible in monoE 40 keV CT images. However, HU values differed significantly in conventional reconstructions as well, indicating the possibility of a broad clinical application of this finding. Conclusion: In this study we establish a novel method for CT-based prediction of tumor cellularity for in-vivo tumor characterization in PDAC patients. |
format | Online Article Text |
id | pubmed-8123300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81233002021-05-16 Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging Jungmann, Friederike Kaissis, Georgios A. Ziegelmayer, Sebastian Harder, Felix Schilling, Clara Yen, Hsi-Yu Steiger, Katja Weichert, Wilko Schirren, Rebekka Demir, Ishan Ekin Friess, Helmut Makowski, Markus R. Braren, Rickmer F. Lohöfer, Fabian K. Cancers (Basel) Article SIMPLE SUMMARY: Pancreatic ductal adenocarcinoma (PDAC) remains a devastating disease. However, variations in tumor biology influence individual patient outcomes greatly. We previously showed a strong association between magnetic resonance imaging-based tumor cell estimates and patient survival. In this study we aimed to transfer this finding to more broadly applied computed tomography (CT) imaging for non-invasive risk stratification. We correlated in vivo CT imaging with histopathological analyses and could show a strong association between regional Hounsfield Units (HU) and tumor cellularity. In conclusion, our study suggests CT-based tumor cell estimates as a widely applicable way of non-invasive tumor cellularity characterization in PDAC. ABSTRACT: Background: PDAC remains a tumor entity with poor prognosis and a 5-year survival rate below 10%. Recent research has revealed invasive biomarkers, such as distinct molecular subtypes, predictive for therapy response and patient survival. Non-invasive prediction of individual patient outcome however remains an unresolved task. Methods: Discrete cellularity regions of PDAC resection specimen (n = 43) were analyzed by routine histopathological work up. Regional tumor cellularity and CT-derived Hounsfield Units (HU, n = 66) as well as iodine concentrations were regionally matched. One-way ANOVA and pairwise t-tests were performed to assess the relationship between different cellularity level in conventional, virtual monoenergetic 40 keV (monoE 40 keV) and iodine map reconstructions. Results: A statistically significant negative correlation between regional tumor cellularity in histopathology and CT-derived HU from corresponding image regions was identified. Radiological differentiation was best possible in monoE 40 keV CT images. However, HU values differed significantly in conventional reconstructions as well, indicating the possibility of a broad clinical application of this finding. Conclusion: In this study we establish a novel method for CT-based prediction of tumor cellularity for in-vivo tumor characterization in PDAC patients. MDPI 2021-04-25 /pmc/articles/PMC8123300/ /pubmed/33922981 http://dx.doi.org/10.3390/cancers13092069 Text en © 2021 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 Jungmann, Friederike Kaissis, Georgios A. Ziegelmayer, Sebastian Harder, Felix Schilling, Clara Yen, Hsi-Yu Steiger, Katja Weichert, Wilko Schirren, Rebekka Demir, Ishan Ekin Friess, Helmut Makowski, Markus R. Braren, Rickmer F. Lohöfer, Fabian K. Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging |
title | Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging |
title_full | Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging |
title_fullStr | Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging |
title_full_unstemmed | Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging |
title_short | Prediction of Tumor Cellularity in Resectable PDAC from Preoperative Computed Tomography Imaging |
title_sort | prediction of tumor cellularity in resectable pdac from preoperative computed tomography imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123300/ https://www.ncbi.nlm.nih.gov/pubmed/33922981 http://dx.doi.org/10.3390/cancers13092069 |
work_keys_str_mv | AT jungmannfriederike predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT kaissisgeorgiosa predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT ziegelmayersebastian predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT harderfelix predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT schillingclara predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT yenhsiyu predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT steigerkatja predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT weichertwilko predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT schirrenrebekka predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT demirishanekin predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT friesshelmut predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT makowskimarkusr predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT brarenrickmerf predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging AT lohoferfabiank predictionoftumorcellularityinresectablepdacfrompreoperativecomputedtomographyimaging |