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Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach

BACKGROUND: Expression of CXCR4, a chemokine (C-X-C motif) receptor that plays a central role in tumor growth and metastasis of circulating tumor cells, has been described in a variety of solid tumors. A high expression of CXCR4 has a prognostic significance with regard to overall and progression-fr...

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Autores principales: Linde, Philipp, Baues, Christian, Wegen, Simone, Trommer, Maike, Quaas, Alexander, Rosenbrock, Johannes, Celik, Eren, Marnitz, Simone, Bruns, Christiane J., Fischer, Thomas, Schomaecker, Klaus, Wester, Hans-Juergen, Drzezga, Alexander, van Heek, Lutz, Kobe, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881561/
https://www.ncbi.nlm.nih.gov/pubmed/33579381
http://dx.doi.org/10.1186/s40644-021-00391-w
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author Linde, Philipp
Baues, Christian
Wegen, Simone
Trommer, Maike
Quaas, Alexander
Rosenbrock, Johannes
Celik, Eren
Marnitz, Simone
Bruns, Christiane J.
Fischer, Thomas
Schomaecker, Klaus
Wester, Hans-Juergen
Drzezga, Alexander
van Heek, Lutz
Kobe, Carsten
author_facet Linde, Philipp
Baues, Christian
Wegen, Simone
Trommer, Maike
Quaas, Alexander
Rosenbrock, Johannes
Celik, Eren
Marnitz, Simone
Bruns, Christiane J.
Fischer, Thomas
Schomaecker, Klaus
Wester, Hans-Juergen
Drzezga, Alexander
van Heek, Lutz
Kobe, Carsten
author_sort Linde, Philipp
collection PubMed
description BACKGROUND: Expression of CXCR4, a chemokine (C-X-C motif) receptor that plays a central role in tumor growth and metastasis of circulating tumor cells, has been described in a variety of solid tumors. A high expression of CXCR4 has a prognostic significance with regard to overall and progression-free survival and offers a starting point for targeted therapies. In this context, [68]Ga-Pentixafor-Positron Emission Tomography/Computer Tomography (PET/CT) offers promising possibility of imaging the CXCR4 expression profile. We set out to compare a [18F] fluorodeoxyglucose (FDG)-PET/CT and a [68Ga]Pentixafor-PET/CT in (re-)staging and radiation planning of patients with localized esophageal cancer. MATERIALS AND METHODS: In this retrospective analysis, ten patients, with adeno- or squamous cell carcinoma of the esophagus (n = 3 and n = 7, respectively), which were scheduled for radio (chemo) therapy, were imaged using both Pentixafor and FDG PET/CT examinations. All lesions were visually rated as Pentixafor and FDG positive or negative. For both tracers, SUVmax was measured all lesions and compared to background. Additionally, immunohistochemistry of CXCR4 was obtained in patients undergoing surgery. RESULTS: FDG-positive tumor-suspicious lesions were detected in all patients and a total of 26 lesions were counted. The lesion-based analysis brought equal status in 14 lesions which were positive for both tracers while five lesions were FDG positive and Pentixafor negative and seven lesions were FDG negative, but Pentixafor positive. Histopathologic correlation was available in seven patients. The CXCR4 expression of four non-pretreated tumour lesion samples was confirmed immunohistochemically. CONCLUSION: Our data shows that additional PET/CT imaging with Pentixafor for imaging the CXCR4 chemokine receptor is feasible but heterogeneous in both newly diagnosed and pretreated recurrent esophageal cancer. In addition, the Pentixafor PET/CT may serve as complementary tool for radiation field expansion in radiooncology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40644-021-00391-w.
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spelling pubmed-78815612021-02-17 Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach Linde, Philipp Baues, Christian Wegen, Simone Trommer, Maike Quaas, Alexander Rosenbrock, Johannes Celik, Eren Marnitz, Simone Bruns, Christiane J. Fischer, Thomas Schomaecker, Klaus Wester, Hans-Juergen Drzezga, Alexander van Heek, Lutz Kobe, Carsten Cancer Imaging Research Article BACKGROUND: Expression of CXCR4, a chemokine (C-X-C motif) receptor that plays a central role in tumor growth and metastasis of circulating tumor cells, has been described in a variety of solid tumors. A high expression of CXCR4 has a prognostic significance with regard to overall and progression-free survival and offers a starting point for targeted therapies. In this context, [68]Ga-Pentixafor-Positron Emission Tomography/Computer Tomography (PET/CT) offers promising possibility of imaging the CXCR4 expression profile. We set out to compare a [18F] fluorodeoxyglucose (FDG)-PET/CT and a [68Ga]Pentixafor-PET/CT in (re-)staging and radiation planning of patients with localized esophageal cancer. MATERIALS AND METHODS: In this retrospective analysis, ten patients, with adeno- or squamous cell carcinoma of the esophagus (n = 3 and n = 7, respectively), which were scheduled for radio (chemo) therapy, were imaged using both Pentixafor and FDG PET/CT examinations. All lesions were visually rated as Pentixafor and FDG positive or negative. For both tracers, SUVmax was measured all lesions and compared to background. Additionally, immunohistochemistry of CXCR4 was obtained in patients undergoing surgery. RESULTS: FDG-positive tumor-suspicious lesions were detected in all patients and a total of 26 lesions were counted. The lesion-based analysis brought equal status in 14 lesions which were positive for both tracers while five lesions were FDG positive and Pentixafor negative and seven lesions were FDG negative, but Pentixafor positive. Histopathologic correlation was available in seven patients. The CXCR4 expression of four non-pretreated tumour lesion samples was confirmed immunohistochemically. CONCLUSION: Our data shows that additional PET/CT imaging with Pentixafor for imaging the CXCR4 chemokine receptor is feasible but heterogeneous in both newly diagnosed and pretreated recurrent esophageal cancer. In addition, the Pentixafor PET/CT may serve as complementary tool for radiation field expansion in radiooncology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40644-021-00391-w. BioMed Central 2021-02-12 /pmc/articles/PMC7881561/ /pubmed/33579381 http://dx.doi.org/10.1186/s40644-021-00391-w Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Linde, Philipp
Baues, Christian
Wegen, Simone
Trommer, Maike
Quaas, Alexander
Rosenbrock, Johannes
Celik, Eren
Marnitz, Simone
Bruns, Christiane J.
Fischer, Thomas
Schomaecker, Klaus
Wester, Hans-Juergen
Drzezga, Alexander
van Heek, Lutz
Kobe, Carsten
Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach
title Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach
title_full Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach
title_fullStr Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach
title_full_unstemmed Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach
title_short Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach
title_sort pentixafor pet/ct for imaging of chemokine receptor 4 expression in esophageal cancer – a first clinical approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881561/
https://www.ncbi.nlm.nih.gov/pubmed/33579381
http://dx.doi.org/10.1186/s40644-021-00391-w
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