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Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography

BACKGROUND: After the diagnosis Non-Small-Cell Lung Carcinoma (NSCLC) has been established, consideration must turn toward the stage of disease, because this will impact directly on management and prognosis. Staging is used to predict survival and to guide the patient toward the most appropriate tre...

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Autores principales: Harders, Stefan Walbom, Madsen, Hans Henrik, Hjorthaug, Karin, Arveschoug, Anne Kirstine, Rasmussen, Torben Riis, Meldgaard, Peter, Hoejbjerg, Johanne Andersen, Pilegaard, Hans Kristian, Hager, Henrik, Rehling, Michael, Rasmussen, Finn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331828/
https://www.ncbi.nlm.nih.gov/pubmed/25608616
http://dx.doi.org/10.1186/1470-7330-14-23
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author Harders, Stefan Walbom
Madsen, Hans Henrik
Hjorthaug, Karin
Arveschoug, Anne Kirstine
Rasmussen, Torben Riis
Meldgaard, Peter
Hoejbjerg, Johanne Andersen
Pilegaard, Hans Kristian
Hager, Henrik
Rehling, Michael
Rasmussen, Finn
author_facet Harders, Stefan Walbom
Madsen, Hans Henrik
Hjorthaug, Karin
Arveschoug, Anne Kirstine
Rasmussen, Torben Riis
Meldgaard, Peter
Hoejbjerg, Johanne Andersen
Pilegaard, Hans Kristian
Hager, Henrik
Rehling, Michael
Rasmussen, Finn
author_sort Harders, Stefan Walbom
collection PubMed
description BACKGROUND: After the diagnosis Non-Small-Cell Lung Carcinoma (NSCLC) has been established, consideration must turn toward the stage of disease, because this will impact directly on management and prognosis. Staging is used to predict survival and to guide the patient toward the most appropriate treatment regimen or clinical trial. Distinguishing malignant involvement of the mediastinal lymph nodes (N2 or N3) from the hilar lymph nodes, or no lymph nodes (N0 or N1) is critical, because malignant involvement of N2 or N3 lymph nodes usually indicates non–surgically resectable disease. The purpose of this study was to examine and compare CT versus integrated F18-FDG PET/low dose CT (FDG PET/CT) for mediastinal staging in NSCLC, and the desire was to safely distinguish between malignant and benign lesions without the need for invasive procedures. All results were controlled for reproducibility. METHODS: 114 participants with NSCLC were included in a prospective cohort study. Blinded CT and FDG PET/CT images were reviewed. The participants’ mediastinums were staged based on lymph node sizes (CT), or on FDG uptake (FDG PET/CT). Reference standard was tissue sampling. RESULTS: We found that there was no measureable difference between CT and FDG PET/CT mediastinal staging results; overall two-thirds of the participants in the study were correctly staged, and almost one-third of the participants were falsely staged. CONCLUSION: Neither CT nor FDG PET/CT could obviate the need for further invasive staging prior to thoracotomy in patients with NSCLC; for that purpose, the results of both modalities were too meagre. Therefore, these patients still depend on invasive staging methods. In our study, invasive staging was accomplished by mediastinoscopy. However, today this is increasingly replaced by EBUS or EUS.
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spelling pubmed-43318282015-02-19 Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography Harders, Stefan Walbom Madsen, Hans Henrik Hjorthaug, Karin Arveschoug, Anne Kirstine Rasmussen, Torben Riis Meldgaard, Peter Hoejbjerg, Johanne Andersen Pilegaard, Hans Kristian Hager, Henrik Rehling, Michael Rasmussen, Finn Cancer Imaging Research Article BACKGROUND: After the diagnosis Non-Small-Cell Lung Carcinoma (NSCLC) has been established, consideration must turn toward the stage of disease, because this will impact directly on management and prognosis. Staging is used to predict survival and to guide the patient toward the most appropriate treatment regimen or clinical trial. Distinguishing malignant involvement of the mediastinal lymph nodes (N2 or N3) from the hilar lymph nodes, or no lymph nodes (N0 or N1) is critical, because malignant involvement of N2 or N3 lymph nodes usually indicates non–surgically resectable disease. The purpose of this study was to examine and compare CT versus integrated F18-FDG PET/low dose CT (FDG PET/CT) for mediastinal staging in NSCLC, and the desire was to safely distinguish between malignant and benign lesions without the need for invasive procedures. All results were controlled for reproducibility. METHODS: 114 participants with NSCLC were included in a prospective cohort study. Blinded CT and FDG PET/CT images were reviewed. The participants’ mediastinums were staged based on lymph node sizes (CT), or on FDG uptake (FDG PET/CT). Reference standard was tissue sampling. RESULTS: We found that there was no measureable difference between CT and FDG PET/CT mediastinal staging results; overall two-thirds of the participants in the study were correctly staged, and almost one-third of the participants were falsely staged. CONCLUSION: Neither CT nor FDG PET/CT could obviate the need for further invasive staging prior to thoracotomy in patients with NSCLC; for that purpose, the results of both modalities were too meagre. Therefore, these patients still depend on invasive staging methods. In our study, invasive staging was accomplished by mediastinoscopy. However, today this is increasingly replaced by EBUS or EUS. BioMed Central 2014-06-03 /pmc/articles/PMC4331828/ /pubmed/25608616 http://dx.doi.org/10.1186/1470-7330-14-23 Text en Copyright © 2014 Harders et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Harders, Stefan Walbom
Madsen, Hans Henrik
Hjorthaug, Karin
Arveschoug, Anne Kirstine
Rasmussen, Torben Riis
Meldgaard, Peter
Hoejbjerg, Johanne Andersen
Pilegaard, Hans Kristian
Hager, Henrik
Rehling, Michael
Rasmussen, Finn
Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography
title Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography
title_full Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography
title_fullStr Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography
title_full_unstemmed Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography
title_short Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography
title_sort mediastinal staging in non-small-cell lung carcinoma: computed tomography versus f-18-fluorodeoxyglucose positron-emission tomography and computed tomography
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331828/
https://www.ncbi.nlm.nih.gov/pubmed/25608616
http://dx.doi.org/10.1186/1470-7330-14-23
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