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Clinical applications of PD-L1 bioassays for cancer immunotherapy
Programmed death ligand 1 (PD-L1) has emerged as a biomarker that can help to predict responses to immunotherapies targeted against PD-L1 and its receptor (PD-1). Companion tests for evaluating PD-L1 expression as a biomarker of response have been developed for many cancer immunotherapy agents. Thes...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436438/ https://www.ncbi.nlm.nih.gov/pubmed/28514966 http://dx.doi.org/10.1186/s13045-017-0479-y |
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author | Liu, Delong Wang, Shuhang Bindeman, Wendy |
author_facet | Liu, Delong Wang, Shuhang Bindeman, Wendy |
author_sort | Liu, Delong |
collection | PubMed |
description | Programmed death ligand 1 (PD-L1) has emerged as a biomarker that can help to predict responses to immunotherapies targeted against PD-L1 and its receptor (PD-1). Companion tests for evaluating PD-L1 expression as a biomarker of response have been developed for many cancer immunotherapy agents. These assays use a variety of detection platforms at different levels (protein, mRNA), employ diverse biopsy and surgical samples, and have disparate positivity cutoff points and scoring systems, all of which complicate the standardization of clinical decision-making. This review summarizes the current understanding and ongoing investigations regarding PD-L1 expression as a potential biomarker for clinical outcomes of anti-PD-1/PD-L1 immunotherapy. |
format | Online Article Text |
id | pubmed-5436438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54364382017-05-19 Clinical applications of PD-L1 bioassays for cancer immunotherapy Liu, Delong Wang, Shuhang Bindeman, Wendy J Hematol Oncol Review Programmed death ligand 1 (PD-L1) has emerged as a biomarker that can help to predict responses to immunotherapies targeted against PD-L1 and its receptor (PD-1). Companion tests for evaluating PD-L1 expression as a biomarker of response have been developed for many cancer immunotherapy agents. These assays use a variety of detection platforms at different levels (protein, mRNA), employ diverse biopsy and surgical samples, and have disparate positivity cutoff points and scoring systems, all of which complicate the standardization of clinical decision-making. This review summarizes the current understanding and ongoing investigations regarding PD-L1 expression as a potential biomarker for clinical outcomes of anti-PD-1/PD-L1 immunotherapy. BioMed Central 2017-05-17 /pmc/articles/PMC5436438/ /pubmed/28514966 http://dx.doi.org/10.1186/s13045-017-0479-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Review Liu, Delong Wang, Shuhang Bindeman, Wendy Clinical applications of PD-L1 bioassays for cancer immunotherapy |
title | Clinical applications of PD-L1 bioassays for cancer immunotherapy |
title_full | Clinical applications of PD-L1 bioassays for cancer immunotherapy |
title_fullStr | Clinical applications of PD-L1 bioassays for cancer immunotherapy |
title_full_unstemmed | Clinical applications of PD-L1 bioassays for cancer immunotherapy |
title_short | Clinical applications of PD-L1 bioassays for cancer immunotherapy |
title_sort | clinical applications of pd-l1 bioassays for cancer immunotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436438/ https://www.ncbi.nlm.nih.gov/pubmed/28514966 http://dx.doi.org/10.1186/s13045-017-0479-y |
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