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Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer
Programmed death-ligand 1 (PD-L1) expression has now been implicated in gastric cancer (GC). This study was conducted to determine the impact of clinicopathological characteristics on PD-L1 expression and its association with survival in GC patients receiving standard-of-care. In total, 268 GC patie...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160126/ https://www.ncbi.nlm.nih.gov/pubmed/37142693 http://dx.doi.org/10.1038/s41598-023-34434-y |
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author | Chitapanarux, Taned Gumrai, Pawut Kongkarnka, Sarawut Wannasai, Komson Lertprasertsuke, Nirush |
author_facet | Chitapanarux, Taned Gumrai, Pawut Kongkarnka, Sarawut Wannasai, Komson Lertprasertsuke, Nirush |
author_sort | Chitapanarux, Taned |
collection | PubMed |
description | Programmed death-ligand 1 (PD-L1) expression has now been implicated in gastric cancer (GC). This study was conducted to determine the impact of clinicopathological characteristics on PD-L1 expression and its association with survival in GC patients receiving standard-of-care. In total, 268 GC patients receiving upfront surgery were enrolled at Chiang Mai University Hospital. PD-L1 expression was assayed by immunohistochemistry staining using the Dako 22C3 pharmDx. The rates of PD-L1 positivity by combined positive score (CPS) at a cutoff value of 1 and 5 were 22% and 7%. PD-L1 positivity was significantly higher in patients younger than 55 than those older than 55 (32.6% vs. 16.5%, p = 0.003; 11.6% vs. 4.4%, p = 0.027). PD-L1 positivity was observed more frequently in GC with metastases than without (25.2% vs. 17.1%, p = 0.112; 7.2% vs. 6.7%, p = 0.673). Patients with PD-L1 positive had a significantly shorter median overall survival than those with PD-L1 negative (32.7 vs. 41.6 months, p = 0.042, 27.6 vs. 40.8 months, p = 0.038). In conclusion, PD-L1 expression has been associated with young age, short survival, and metastases, although unrelated to the tumor stage. For GC patients, PD-L1 testing is recommended, especially among young patients with metastases. |
format | Online Article Text |
id | pubmed-10160126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101601262023-05-06 Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer Chitapanarux, Taned Gumrai, Pawut Kongkarnka, Sarawut Wannasai, Komson Lertprasertsuke, Nirush Sci Rep Article Programmed death-ligand 1 (PD-L1) expression has now been implicated in gastric cancer (GC). This study was conducted to determine the impact of clinicopathological characteristics on PD-L1 expression and its association with survival in GC patients receiving standard-of-care. In total, 268 GC patients receiving upfront surgery were enrolled at Chiang Mai University Hospital. PD-L1 expression was assayed by immunohistochemistry staining using the Dako 22C3 pharmDx. The rates of PD-L1 positivity by combined positive score (CPS) at a cutoff value of 1 and 5 were 22% and 7%. PD-L1 positivity was significantly higher in patients younger than 55 than those older than 55 (32.6% vs. 16.5%, p = 0.003; 11.6% vs. 4.4%, p = 0.027). PD-L1 positivity was observed more frequently in GC with metastases than without (25.2% vs. 17.1%, p = 0.112; 7.2% vs. 6.7%, p = 0.673). Patients with PD-L1 positive had a significantly shorter median overall survival than those with PD-L1 negative (32.7 vs. 41.6 months, p = 0.042, 27.6 vs. 40.8 months, p = 0.038). In conclusion, PD-L1 expression has been associated with young age, short survival, and metastases, although unrelated to the tumor stage. For GC patients, PD-L1 testing is recommended, especially among young patients with metastases. Nature Publishing Group UK 2023-05-04 /pmc/articles/PMC10160126/ /pubmed/37142693 http://dx.doi.org/10.1038/s41598-023-34434-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chitapanarux, Taned Gumrai, Pawut Kongkarnka, Sarawut Wannasai, Komson Lertprasertsuke, Nirush Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer |
title | Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer |
title_full | Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer |
title_fullStr | Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer |
title_full_unstemmed | Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer |
title_short | Programmed death-ligand 1 expression and overall survival in Thai patients with gastric cancer |
title_sort | programmed death-ligand 1 expression and overall survival in thai patients with gastric cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160126/ https://www.ncbi.nlm.nih.gov/pubmed/37142693 http://dx.doi.org/10.1038/s41598-023-34434-y |
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