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Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer

Immune checkpoint blockade therapy by targeting the programmed death protein 1/programmed death ligand 1 (PD-L1) axis using antibodies has yielded promising clinical responses in patients with non-small cell lung cancer (NSCLC). However, owing to the dynamic expression of PD-L1, degree of mutational...

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Detalles Bibliográficos
Autores principales: Liu, Xiaoming, Cho, William C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5250626/
https://www.ncbi.nlm.nih.gov/pubmed/28108884
http://dx.doi.org/10.1186/s40169-017-0136-7
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author Liu, Xiaoming
Cho, William C.
author_facet Liu, Xiaoming
Cho, William C.
author_sort Liu, Xiaoming
collection PubMed
description Immune checkpoint blockade therapy by targeting the programmed death protein 1/programmed death ligand 1 (PD-L1) axis using antibodies has yielded promising clinical responses in patients with non-small cell lung cancer (NSCLC). However, owing to the dynamic expression of PD-L1, degree of mutational/neoantigen load, intratumoral heterogeneity, infiltrated immune cells of tumor microenvironment of NSCLC, the response rates to these agents are limited, despite several companion diagnostic assays by detecting PD-L1 in tumor cells have been introduced into clinical practice. Therefore, in this era of precision medicine, there is an urgent need for predictive biomarkers to identify NSCLC patients likely to benefit from this novel therapy.
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spelling pubmed-52506262017-01-25 Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer Liu, Xiaoming Cho, William C. Clin Transl Med Commentary Immune checkpoint blockade therapy by targeting the programmed death protein 1/programmed death ligand 1 (PD-L1) axis using antibodies has yielded promising clinical responses in patients with non-small cell lung cancer (NSCLC). However, owing to the dynamic expression of PD-L1, degree of mutational/neoantigen load, intratumoral heterogeneity, infiltrated immune cells of tumor microenvironment of NSCLC, the response rates to these agents are limited, despite several companion diagnostic assays by detecting PD-L1 in tumor cells have been introduced into clinical practice. Therefore, in this era of precision medicine, there is an urgent need for predictive biomarkers to identify NSCLC patients likely to benefit from this novel therapy. Springer Berlin Heidelberg 2017-01-20 /pmc/articles/PMC5250626/ /pubmed/28108884 http://dx.doi.org/10.1186/s40169-017-0136-7 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.
spellingShingle Commentary
Liu, Xiaoming
Cho, William C.
Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer
title Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer
title_full Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer
title_fullStr Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer
title_full_unstemmed Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer
title_short Precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer
title_sort precision medicine in immune checkpoint blockade therapy for non-small cell lung cancer
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5250626/
https://www.ncbi.nlm.nih.gov/pubmed/28108884
http://dx.doi.org/10.1186/s40169-017-0136-7
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