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Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic
Programmed death-1 (PD-1) and programmed death ligand 1 (PD-L1) inhibitors target the important molecular interplay between PD-1 and PD-L1, a key pathway contributing to immune evasion in the tumor microenvironment (TME). Long-term clinical benefit has been observed in patients receiving PD-(L)1 inh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8420047/ https://www.ncbi.nlm.nih.gov/pubmed/34497758 http://dx.doi.org/10.3389/fonc.2021.698425 |
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author | Leung, David Bonacorsi, Samuel Smith, Ralph Adam Weber, Wolfgang Hayes, Wendy |
author_facet | Leung, David Bonacorsi, Samuel Smith, Ralph Adam Weber, Wolfgang Hayes, Wendy |
author_sort | Leung, David |
collection | PubMed |
description | Programmed death-1 (PD-1) and programmed death ligand 1 (PD-L1) inhibitors target the important molecular interplay between PD-1 and PD-L1, a key pathway contributing to immune evasion in the tumor microenvironment (TME). Long-term clinical benefit has been observed in patients receiving PD-(L)1 inhibitors, alone and in combination with other treatments, across multiple tumor types. PD-L1 expression has been associated with response to immune checkpoint inhibitors, and treatment strategies are often guided by immunohistochemistry-based diagnostic tests assessing expression of PD-L1. However, challenges related to the implementation, interpretation, and clinical utility of PD-L1 diagnostic tests have led to an increasing number of preclinical and clinical studies exploring interrogation of the TME by real-time imaging of PD-(L)1 expression by positron emission tomography (PET). PET imaging utilizes radiolabeled molecules to non-invasively assess PD-(L)1 expression spatially and temporally. Several PD-(L)1 PET tracers have been tested in preclinical and clinical studies, with clinical trials in progress to assess their use in a number of cancer types. This review will showcase the development of PD-(L)1 PET tracers from preclinical studies through to clinical use, and will explore the opportunities in drug development and possible future clinical implementation. |
format | Online Article Text |
id | pubmed-8420047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84200472021-09-07 Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic Leung, David Bonacorsi, Samuel Smith, Ralph Adam Weber, Wolfgang Hayes, Wendy Front Oncol Oncology Programmed death-1 (PD-1) and programmed death ligand 1 (PD-L1) inhibitors target the important molecular interplay between PD-1 and PD-L1, a key pathway contributing to immune evasion in the tumor microenvironment (TME). Long-term clinical benefit has been observed in patients receiving PD-(L)1 inhibitors, alone and in combination with other treatments, across multiple tumor types. PD-L1 expression has been associated with response to immune checkpoint inhibitors, and treatment strategies are often guided by immunohistochemistry-based diagnostic tests assessing expression of PD-L1. However, challenges related to the implementation, interpretation, and clinical utility of PD-L1 diagnostic tests have led to an increasing number of preclinical and clinical studies exploring interrogation of the TME by real-time imaging of PD-(L)1 expression by positron emission tomography (PET). PET imaging utilizes radiolabeled molecules to non-invasively assess PD-(L)1 expression spatially and temporally. Several PD-(L)1 PET tracers have been tested in preclinical and clinical studies, with clinical trials in progress to assess their use in a number of cancer types. This review will showcase the development of PD-(L)1 PET tracers from preclinical studies through to clinical use, and will explore the opportunities in drug development and possible future clinical implementation. Frontiers Media S.A. 2021-08-23 /pmc/articles/PMC8420047/ /pubmed/34497758 http://dx.doi.org/10.3389/fonc.2021.698425 Text en Copyright © 2021 Leung, Bonacorsi, Smith, Weber and Hayes https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Leung, David Bonacorsi, Samuel Smith, Ralph Adam Weber, Wolfgang Hayes, Wendy Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic |
title | Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic |
title_full | Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic |
title_fullStr | Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic |
title_full_unstemmed | Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic |
title_short | Molecular Imaging and the PD-L1 Pathway: From Bench to Clinic |
title_sort | molecular imaging and the pd-l1 pathway: from bench to clinic |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8420047/ https://www.ncbi.nlm.nih.gov/pubmed/34497758 http://dx.doi.org/10.3389/fonc.2021.698425 |
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