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Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems
Background. Innovative drugs targeting the PD1/PD-L1 axis have opened promising scenarios in modern cancer therapy. Plenty of assays and scoring systems have been developed for the evaluation of PD-L1 immunohistochemical expression, so far considered the most reliable therapeutic predictive marker....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321150/ https://www.ncbi.nlm.nih.gov/pubmed/35887569 http://dx.doi.org/10.3390/jpm12071073 |
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author | Marletta, Stefano Fusco, Nicola Munari, Enrico Luchini, Claudio Cimadamore, Alessia Brunelli, Matteo Querzoli, Giulia Martini, Maurizio Vigliar, Elena Colombari, Romano Girolami, Ilaria Pagni, Fabio Eccher, Albino |
author_facet | Marletta, Stefano Fusco, Nicola Munari, Enrico Luchini, Claudio Cimadamore, Alessia Brunelli, Matteo Querzoli, Giulia Martini, Maurizio Vigliar, Elena Colombari, Romano Girolami, Ilaria Pagni, Fabio Eccher, Albino |
author_sort | Marletta, Stefano |
collection | PubMed |
description | Background. Innovative drugs targeting the PD1/PD-L1 axis have opened promising scenarios in modern cancer therapy. Plenty of assays and scoring systems have been developed for the evaluation of PD-L1 immunohistochemical expression, so far considered the most reliable therapeutic predictive marker. Methods. By gathering the opinion of acknowledged experts in dedicated fields of pathology, we sought to update the currently available evidence on PD-L1 assessment in various types of tumors. Results. Robust data were progressively collected for several anatomic districts and leading international agencies to approve specific protocols: among these, TPS with 22C3, SP142 and SP263 clones in lung cancer; IC with SP142 antibody in breast, lung and urothelial tumors; and CPS with 22C3/SP263 assays in head and neck and urothelial carcinomas. On the other hand, for other malignancies, such as gastroenteric neoplasms, immunotherapy has been only recently introduced, often for particular histotypes, so specific guidelines are still lacking. Conclusions. PD-L1 immunohistochemical scoring is currently the basis for allowing many cancer patients to receive properly targeted therapies. While protocols supported by proven data are already available for many tumors, dedicated studies and clinical trials focusing on harmonization of the topic in other still only partially explored fields are surely yet advisable. |
format | Online Article Text |
id | pubmed-9321150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93211502022-07-27 Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems Marletta, Stefano Fusco, Nicola Munari, Enrico Luchini, Claudio Cimadamore, Alessia Brunelli, Matteo Querzoli, Giulia Martini, Maurizio Vigliar, Elena Colombari, Romano Girolami, Ilaria Pagni, Fabio Eccher, Albino J Pers Med Review Background. Innovative drugs targeting the PD1/PD-L1 axis have opened promising scenarios in modern cancer therapy. Plenty of assays and scoring systems have been developed for the evaluation of PD-L1 immunohistochemical expression, so far considered the most reliable therapeutic predictive marker. Methods. By gathering the opinion of acknowledged experts in dedicated fields of pathology, we sought to update the currently available evidence on PD-L1 assessment in various types of tumors. Results. Robust data were progressively collected for several anatomic districts and leading international agencies to approve specific protocols: among these, TPS with 22C3, SP142 and SP263 clones in lung cancer; IC with SP142 antibody in breast, lung and urothelial tumors; and CPS with 22C3/SP263 assays in head and neck and urothelial carcinomas. On the other hand, for other malignancies, such as gastroenteric neoplasms, immunotherapy has been only recently introduced, often for particular histotypes, so specific guidelines are still lacking. Conclusions. PD-L1 immunohistochemical scoring is currently the basis for allowing many cancer patients to receive properly targeted therapies. While protocols supported by proven data are already available for many tumors, dedicated studies and clinical trials focusing on harmonization of the topic in other still only partially explored fields are surely yet advisable. MDPI 2022-06-29 /pmc/articles/PMC9321150/ /pubmed/35887569 http://dx.doi.org/10.3390/jpm12071073 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Marletta, Stefano Fusco, Nicola Munari, Enrico Luchini, Claudio Cimadamore, Alessia Brunelli, Matteo Querzoli, Giulia Martini, Maurizio Vigliar, Elena Colombari, Romano Girolami, Ilaria Pagni, Fabio Eccher, Albino Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems |
title | Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems |
title_full | Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems |
title_fullStr | Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems |
title_full_unstemmed | Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems |
title_short | Atlas of PD-L1 for Pathologists: Indications, Scores, Diagnostic Platforms and Reporting Systems |
title_sort | atlas of pd-l1 for pathologists: indications, scores, diagnostic platforms and reporting systems |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321150/ https://www.ncbi.nlm.nih.gov/pubmed/35887569 http://dx.doi.org/10.3390/jpm12071073 |
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