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High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer
Pembrolizumab appears promising for patients with programmed cell death ligand-1 (PD-L1)-positive solid tumors. However, data on immunotherapy for biliary tract cancers (BTC) are limited. We aimed to investigate the predictive value of PD-L1 expression as an immunotherapeutic biomarker in BTC. Patie...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378166/ https://www.ncbi.nlm.nih.gov/pubmed/32704067 http://dx.doi.org/10.1038/s41598-020-69366-4 |
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author | Ahn, Soomin Lee, Jong-chan Shin, Dong Woo Kim, Jaihwan Hwang, Jin-Hyeok |
author_facet | Ahn, Soomin Lee, Jong-chan Shin, Dong Woo Kim, Jaihwan Hwang, Jin-Hyeok |
author_sort | Ahn, Soomin |
collection | PubMed |
description | Pembrolizumab appears promising for patients with programmed cell death ligand-1 (PD-L1)-positive solid tumors. However, data on immunotherapy for biliary tract cancers (BTC) are limited. We aimed to investigate the predictive value of PD-L1 expression as an immunotherapeutic biomarker in BTC. Patients with advanced BTC (n = 175) were screened for PD-L1 expression using PharmDx assay and microsatellite instability (MSI) status. Of the total of 175 patients, 125 (71%) showed tumoral PD-L1 positivity (≥ 1%) while only two (2/142, 1.4%) showed MSI-High. Among 175 patients, 26 patients were treated with pembrolizumab as a second-line therapy, and tumor response was evaluated. Separating these patients into two groups by PD-L1 expression (high [≥ 50%] vs. low [< 50%]), overall response rate was 23% (56% [5/9] in high PD-L1 group vs. 6% [1/17] in low PD-L1 group, P = 0.004). Disease control rate was also higher in high PD-L1 group (78% vs. 35%, P = 0.019). The six responders showed median progression-free survival of 5.8 months after starting pembrolizumab, and none of them was MSI-High. High PD-L1 expression was associated with a better response to pembrolizumab. PD-L1 expression can potentially serve as an alternative predictive biomarker for pembrolizumab therapy in advanced BTC. |
format | Online Article Text |
id | pubmed-7378166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73781662020-07-24 High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer Ahn, Soomin Lee, Jong-chan Shin, Dong Woo Kim, Jaihwan Hwang, Jin-Hyeok Sci Rep Article Pembrolizumab appears promising for patients with programmed cell death ligand-1 (PD-L1)-positive solid tumors. However, data on immunotherapy for biliary tract cancers (BTC) are limited. We aimed to investigate the predictive value of PD-L1 expression as an immunotherapeutic biomarker in BTC. Patients with advanced BTC (n = 175) were screened for PD-L1 expression using PharmDx assay and microsatellite instability (MSI) status. Of the total of 175 patients, 125 (71%) showed tumoral PD-L1 positivity (≥ 1%) while only two (2/142, 1.4%) showed MSI-High. Among 175 patients, 26 patients were treated with pembrolizumab as a second-line therapy, and tumor response was evaluated. Separating these patients into two groups by PD-L1 expression (high [≥ 50%] vs. low [< 50%]), overall response rate was 23% (56% [5/9] in high PD-L1 group vs. 6% [1/17] in low PD-L1 group, P = 0.004). Disease control rate was also higher in high PD-L1 group (78% vs. 35%, P = 0.019). The six responders showed median progression-free survival of 5.8 months after starting pembrolizumab, and none of them was MSI-High. High PD-L1 expression was associated with a better response to pembrolizumab. PD-L1 expression can potentially serve as an alternative predictive biomarker for pembrolizumab therapy in advanced BTC. Nature Publishing Group UK 2020-07-23 /pmc/articles/PMC7378166/ /pubmed/32704067 http://dx.doi.org/10.1038/s41598-020-69366-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ahn, Soomin Lee, Jong-chan Shin, Dong Woo Kim, Jaihwan Hwang, Jin-Hyeok High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer |
title | High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer |
title_full | High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer |
title_fullStr | High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer |
title_full_unstemmed | High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer |
title_short | High PD-L1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer |
title_sort | high pd-l1 expression is associated with therapeutic response to pembrolizumab in patients with advanced biliary tract cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378166/ https://www.ncbi.nlm.nih.gov/pubmed/32704067 http://dx.doi.org/10.1038/s41598-020-69366-4 |
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