Cargando…
CXCR4-targeted theranostics in oncology
A growing body of literature reports on the upregulation of C-X-C motif chemokine receptor 4 (CXCR4) in a variety of cancer entities, rendering this receptor as suitable target for molecular imaging and endoradiotherapy in a theranostic setting. For instance, the CXCR4-targeting positron emission to...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525349/ https://www.ncbi.nlm.nih.gov/pubmed/35674738 http://dx.doi.org/10.1007/s00259-022-05849-y |
_version_ | 1784800686787002368 |
---|---|
author | Buck, Andreas K. Serfling, Sebastian E. Lindner, Thomas Hänscheid, Heribert Schirbel, Andreas Hahner, Stefanie Fassnacht, Martin Einsele, Hermann Werner, Rudolf A. |
author_facet | Buck, Andreas K. Serfling, Sebastian E. Lindner, Thomas Hänscheid, Heribert Schirbel, Andreas Hahner, Stefanie Fassnacht, Martin Einsele, Hermann Werner, Rudolf A. |
author_sort | Buck, Andreas K. |
collection | PubMed |
description | A growing body of literature reports on the upregulation of C-X-C motif chemokine receptor 4 (CXCR4) in a variety of cancer entities, rendering this receptor as suitable target for molecular imaging and endoradiotherapy in a theranostic setting. For instance, the CXCR4-targeting positron emission tomography (PET) agent [(68) Ga]PentixaFor has been proven useful for a comprehensive assessment of the current status quo of solid tumors, including adrenocortical carcinoma or small-cell lung cancer. In addition, [(68) Ga]PentixaFor has also provided an excellent readout for hematological malignancies, such as multiple myeloma, marginal zone lymphoma, or mantle cell lymphoma. PET-based quantification of the CXCR4 capacities in vivo allows for selecting candidates that would be suitable for treatment using the theranostic equivalent [(177)Lu]/[(90)Y]PentixaTher. This CXCR4-directed theranostic concept has been used as a conditioning regimen prior to hematopoietic stem cell transplantation and to achieve sufficient anti-lymphoma/-tumor activity in particular for malignant tissues that are highly sensitive to radiation, such as the hematological system. Increasing the safety margin, pretherapeutic dosimetry is routinely performed to determine the optimal activity to enhance therapeutic efficacy and to reduce off-target adverse events. The present review will provide an overview of current applications for CXCR4-directed molecular imaging and will introduce the CXCR4-targeted theranostic concept for advanced hematological malignancies. |
format | Online Article Text |
id | pubmed-9525349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-95253492022-10-02 CXCR4-targeted theranostics in oncology Buck, Andreas K. Serfling, Sebastian E. Lindner, Thomas Hänscheid, Heribert Schirbel, Andreas Hahner, Stefanie Fassnacht, Martin Einsele, Hermann Werner, Rudolf A. Eur J Nucl Med Mol Imaging Review Article A growing body of literature reports on the upregulation of C-X-C motif chemokine receptor 4 (CXCR4) in a variety of cancer entities, rendering this receptor as suitable target for molecular imaging and endoradiotherapy in a theranostic setting. For instance, the CXCR4-targeting positron emission tomography (PET) agent [(68) Ga]PentixaFor has been proven useful for a comprehensive assessment of the current status quo of solid tumors, including adrenocortical carcinoma or small-cell lung cancer. In addition, [(68) Ga]PentixaFor has also provided an excellent readout for hematological malignancies, such as multiple myeloma, marginal zone lymphoma, or mantle cell lymphoma. PET-based quantification of the CXCR4 capacities in vivo allows for selecting candidates that would be suitable for treatment using the theranostic equivalent [(177)Lu]/[(90)Y]PentixaTher. This CXCR4-directed theranostic concept has been used as a conditioning regimen prior to hematopoietic stem cell transplantation and to achieve sufficient anti-lymphoma/-tumor activity in particular for malignant tissues that are highly sensitive to radiation, such as the hematological system. Increasing the safety margin, pretherapeutic dosimetry is routinely performed to determine the optimal activity to enhance therapeutic efficacy and to reduce off-target adverse events. The present review will provide an overview of current applications for CXCR4-directed molecular imaging and will introduce the CXCR4-targeted theranostic concept for advanced hematological malignancies. Springer Berlin Heidelberg 2022-06-08 2022 /pmc/articles/PMC9525349/ /pubmed/35674738 http://dx.doi.org/10.1007/s00259-022-05849-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Buck, Andreas K. Serfling, Sebastian E. Lindner, Thomas Hänscheid, Heribert Schirbel, Andreas Hahner, Stefanie Fassnacht, Martin Einsele, Hermann Werner, Rudolf A. CXCR4-targeted theranostics in oncology |
title | CXCR4-targeted theranostics in oncology |
title_full | CXCR4-targeted theranostics in oncology |
title_fullStr | CXCR4-targeted theranostics in oncology |
title_full_unstemmed | CXCR4-targeted theranostics in oncology |
title_short | CXCR4-targeted theranostics in oncology |
title_sort | cxcr4-targeted theranostics in oncology |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525349/ https://www.ncbi.nlm.nih.gov/pubmed/35674738 http://dx.doi.org/10.1007/s00259-022-05849-y |
work_keys_str_mv | AT buckandreask cxcr4targetedtheranosticsinoncology AT serflingsebastiane cxcr4targetedtheranosticsinoncology AT lindnerthomas cxcr4targetedtheranosticsinoncology AT hanscheidheribert cxcr4targetedtheranosticsinoncology AT schirbelandreas cxcr4targetedtheranosticsinoncology AT hahnerstefanie cxcr4targetedtheranosticsinoncology AT fassnachtmartin cxcr4targetedtheranosticsinoncology AT einselehermann cxcr4targetedtheranosticsinoncology AT wernerrudolfa cxcr4targetedtheranosticsinoncology |