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Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy

The value of combined L-(methyl-[(11)C]) methionine positron-emitting tomography (MET-PET) and magnetic resonance imaging (MRI) with regard to tumor extent, entity prediction, and therapy effects in clinical routine in patients with suspicion of a brain tumor was investigated. In n = 65 patients wit...

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Autores principales: Laukamp, Kai R., Lindemann, Florian, Weckesser, Matthias, Hesselmann, Volker, Ligges, Sandra, Wölfer, Johannes, Jeibmann, Astrid, Zinnhardt, Bastian, Viel, Thomas, Schäfers, Michael, Paulus, Werner, Stummer, Walter, Schober, Otmar, Jacobs, Andreas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470145/
https://www.ncbi.nlm.nih.gov/pubmed/28654379
http://dx.doi.org/10.1177/1536012116687651
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author Laukamp, Kai R.
Lindemann, Florian
Weckesser, Matthias
Hesselmann, Volker
Ligges, Sandra
Wölfer, Johannes
Jeibmann, Astrid
Zinnhardt, Bastian
Viel, Thomas
Schäfers, Michael
Paulus, Werner
Stummer, Walter
Schober, Otmar
Jacobs, Andreas H.
author_facet Laukamp, Kai R.
Lindemann, Florian
Weckesser, Matthias
Hesselmann, Volker
Ligges, Sandra
Wölfer, Johannes
Jeibmann, Astrid
Zinnhardt, Bastian
Viel, Thomas
Schäfers, Michael
Paulus, Werner
Stummer, Walter
Schober, Otmar
Jacobs, Andreas H.
author_sort Laukamp, Kai R.
collection PubMed
description The value of combined L-(methyl-[(11)C]) methionine positron-emitting tomography (MET-PET) and magnetic resonance imaging (MRI) with regard to tumor extent, entity prediction, and therapy effects in clinical routine in patients with suspicion of a brain tumor was investigated. In n = 65 patients with histologically verified brain lesions n = 70 MET-PET and MRI (T1-weighted gadolinium-enhanced [T1w-Gd] and fluid-attenuated inversion recovery or T2-weighted [FLAIR/T2w]) examinations were performed. The computer software “visualization and analysis framework volume rendering engine (Voreen)” was used for analysis of extent and intersection of tumor compartments. Binary logistic regression models were developed to differentiate between World Health Organization (WHO) tumor types/grades. Tumor sizes as defined by thresholding based on tumor-to-background ratios were significantly different as determined by MET-PET (21.6 ± 36.8 cm(3)), T1w-Gd-MRI (3.9 ± 7.8 cm(3)), and FLAIR/T2-MRI (64.8 ± 60.4 cm(3); P < .001). The MET-PET visualized tumor activity where MRI parameters were negative: PET positive tumor volume without Gd enhancement was 19.8 ± 35.0 cm(3) and without changes in FLAIR/T2 10.3 ± 25.7 cm(3). FLAIR/T2-MRI visualized greatest tumor extent with differences to MET-PET being greater in posttherapy (64.6 ± 62.7 cm(3)) than in newly diagnosed patients (20.5 ± 52.6 cm(3)). The binary logistic regression model differentiated between WHO tumor types (fibrillary astrocytoma II n = 10 from other gliomas n = 16) with an accuracy of 80.8% in patients at primary diagnosis. Combined PET and MRI improve the evaluation of tumor activity, extent, type/grade prediction, and therapy-induced changes in patients with glioma and serve information highly relevant for diagnosis and management.
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spelling pubmed-54701452017-06-22 Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy Laukamp, Kai R. Lindemann, Florian Weckesser, Matthias Hesselmann, Volker Ligges, Sandra Wölfer, Johannes Jeibmann, Astrid Zinnhardt, Bastian Viel, Thomas Schäfers, Michael Paulus, Werner Stummer, Walter Schober, Otmar Jacobs, Andreas H. Mol Imaging Research Article The value of combined L-(methyl-[(11)C]) methionine positron-emitting tomography (MET-PET) and magnetic resonance imaging (MRI) with regard to tumor extent, entity prediction, and therapy effects in clinical routine in patients with suspicion of a brain tumor was investigated. In n = 65 patients with histologically verified brain lesions n = 70 MET-PET and MRI (T1-weighted gadolinium-enhanced [T1w-Gd] and fluid-attenuated inversion recovery or T2-weighted [FLAIR/T2w]) examinations were performed. The computer software “visualization and analysis framework volume rendering engine (Voreen)” was used for analysis of extent and intersection of tumor compartments. Binary logistic regression models were developed to differentiate between World Health Organization (WHO) tumor types/grades. Tumor sizes as defined by thresholding based on tumor-to-background ratios were significantly different as determined by MET-PET (21.6 ± 36.8 cm(3)), T1w-Gd-MRI (3.9 ± 7.8 cm(3)), and FLAIR/T2-MRI (64.8 ± 60.4 cm(3); P < .001). The MET-PET visualized tumor activity where MRI parameters were negative: PET positive tumor volume without Gd enhancement was 19.8 ± 35.0 cm(3) and without changes in FLAIR/T2 10.3 ± 25.7 cm(3). FLAIR/T2-MRI visualized greatest tumor extent with differences to MET-PET being greater in posttherapy (64.6 ± 62.7 cm(3)) than in newly diagnosed patients (20.5 ± 52.6 cm(3)). The binary logistic regression model differentiated between WHO tumor types (fibrillary astrocytoma II n = 10 from other gliomas n = 16) with an accuracy of 80.8% in patients at primary diagnosis. Combined PET and MRI improve the evaluation of tumor activity, extent, type/grade prediction, and therapy-induced changes in patients with glioma and serve information highly relevant for diagnosis and management. SAGE Publications 2017-01-24 /pmc/articles/PMC5470145/ /pubmed/28654379 http://dx.doi.org/10.1177/1536012116687651 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Article
Laukamp, Kai R.
Lindemann, Florian
Weckesser, Matthias
Hesselmann, Volker
Ligges, Sandra
Wölfer, Johannes
Jeibmann, Astrid
Zinnhardt, Bastian
Viel, Thomas
Schäfers, Michael
Paulus, Werner
Stummer, Walter
Schober, Otmar
Jacobs, Andreas H.
Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy
title Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy
title_full Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy
title_fullStr Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy
title_full_unstemmed Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy
title_short Multimodal Imaging of Patients With Gliomas Confirms (11)C-MET PET as a Complementary Marker to MRI for Noninvasive Tumor Grading and Intraindividual Follow-Up After Therapy
title_sort multimodal imaging of patients with gliomas confirms (11)c-met pet as a complementary marker to mri for noninvasive tumor grading and intraindividual follow-up after therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470145/
https://www.ncbi.nlm.nih.gov/pubmed/28654379
http://dx.doi.org/10.1177/1536012116687651
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