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Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response

We have seen a notable increase in the application of PD-1/PD-L1 inhibitors for the treatment of several solid and hematogenous malignancies including metastatic melanoma, non-small-cell lung cancer and lymphoma to name a few. The need for biomarkers for identification of a suitable patient populati...

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Detalles Bibliográficos
Autores principales: Diggs, Laurence P., Hsueh, Eddy C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353958/
https://www.ncbi.nlm.nih.gov/pubmed/28331612
http://dx.doi.org/10.1186/s40364-017-0093-8
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author Diggs, Laurence P.
Hsueh, Eddy C.
author_facet Diggs, Laurence P.
Hsueh, Eddy C.
author_sort Diggs, Laurence P.
collection PubMed
description We have seen a notable increase in the application of PD-1/PD-L1 inhibitors for the treatment of several solid and hematogenous malignancies including metastatic melanoma, non-small-cell lung cancer and lymphoma to name a few. The need for biomarkers for identification of a suitable patient population for this type of therapy is now pressing. While specific biomarker assays have been developed for these checkpoint inhibitors based on their respective epitopes, the available studies suggested the clinical utility of these biomarker assays is for response stratification and not patient selection. Further improvement in assay development is needed to utilize this type of assay in identification of ideal patient population for this therapy.
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spelling pubmed-53539582017-03-22 Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response Diggs, Laurence P. Hsueh, Eddy C. Biomark Res Review We have seen a notable increase in the application of PD-1/PD-L1 inhibitors for the treatment of several solid and hematogenous malignancies including metastatic melanoma, non-small-cell lung cancer and lymphoma to name a few. The need for biomarkers for identification of a suitable patient population for this type of therapy is now pressing. While specific biomarker assays have been developed for these checkpoint inhibitors based on their respective epitopes, the available studies suggested the clinical utility of these biomarker assays is for response stratification and not patient selection. Further improvement in assay development is needed to utilize this type of assay in identification of ideal patient population for this therapy. BioMed Central 2017-03-15 /pmc/articles/PMC5353958/ /pubmed/28331612 http://dx.doi.org/10.1186/s40364-017-0093-8 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
Diggs, Laurence P.
Hsueh, Eddy C.
Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response
title Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response
title_full Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response
title_fullStr Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response
title_full_unstemmed Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response
title_short Utility of PD-L1 immunohistochemistry assays for predicting PD-1/PD-L1 inhibitor response
title_sort utility of pd-l1 immunohistochemistry assays for predicting pd-1/pd-l1 inhibitor response
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353958/
https://www.ncbi.nlm.nih.gov/pubmed/28331612
http://dx.doi.org/10.1186/s40364-017-0093-8
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