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Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression
Immuno-checkpoint inhibitors (ICI) have become an effective treatment option for non-small-cell lung cancer patients. However, ICI therapy was reported to be less effective in patients with epidermal growth factor receptor (EGFR) mutations than in those with wild-type EGFR. We report here that an no...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135433/ https://www.ncbi.nlm.nih.gov/pubmed/30237726 http://dx.doi.org/10.2147/OTT.S168598 |
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author | Tozuka, Takehiro Seike, Masahiro Minegishi, Yuji Kitagawa, Shingo Kato, Tomomi Takano, Natsuki Hisakane, Kakeru Takahashi, Satoshi Kobayashi, Kenichi Kashiwada, Takeru Sugano, Teppei Takeuchi, Susumu Kunugi, Shinobu Noro, Rintaro Saito, Yoshinobu Kubota, Kaoru Gemma, Akihiko |
author_facet | Tozuka, Takehiro Seike, Masahiro Minegishi, Yuji Kitagawa, Shingo Kato, Tomomi Takano, Natsuki Hisakane, Kakeru Takahashi, Satoshi Kobayashi, Kenichi Kashiwada, Takeru Sugano, Teppei Takeuchi, Susumu Kunugi, Shinobu Noro, Rintaro Saito, Yoshinobu Kubota, Kaoru Gemma, Akihiko |
author_sort | Tozuka, Takehiro |
collection | PubMed |
description | Immuno-checkpoint inhibitors (ICI) have become an effective treatment option for non-small-cell lung cancer patients. However, ICI therapy was reported to be less effective in patients with epidermal growth factor receptor (EGFR) mutations than in those with wild-type EGFR. We report here that an non-small-cell lung cancer patient with the EGFR mutant T790M showed a programmed cell death ligand 1 (PD-L1) expression level that increased from <25% to >90% after eighth-line osimertinib therapy. He was treated with pembrolizumab as a ninth-line treatment, and attained stable disease. After the pembrolizumab therapy, he was treated with gemcitabine, which produced a good response despite being the 10th-line treatment. We should consider administering ICI and chemotherapy even to EGFR mutant patients after failure of EGFR tyrosine kinase inhibitor, especially in cases with high PD-LI expression. |
format | Online Article Text |
id | pubmed-6135433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61354332018-09-20 Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression Tozuka, Takehiro Seike, Masahiro Minegishi, Yuji Kitagawa, Shingo Kato, Tomomi Takano, Natsuki Hisakane, Kakeru Takahashi, Satoshi Kobayashi, Kenichi Kashiwada, Takeru Sugano, Teppei Takeuchi, Susumu Kunugi, Shinobu Noro, Rintaro Saito, Yoshinobu Kubota, Kaoru Gemma, Akihiko Onco Targets Ther Case Report Immuno-checkpoint inhibitors (ICI) have become an effective treatment option for non-small-cell lung cancer patients. However, ICI therapy was reported to be less effective in patients with epidermal growth factor receptor (EGFR) mutations than in those with wild-type EGFR. We report here that an non-small-cell lung cancer patient with the EGFR mutant T790M showed a programmed cell death ligand 1 (PD-L1) expression level that increased from <25% to >90% after eighth-line osimertinib therapy. He was treated with pembrolizumab as a ninth-line treatment, and attained stable disease. After the pembrolizumab therapy, he was treated with gemcitabine, which produced a good response despite being the 10th-line treatment. We should consider administering ICI and chemotherapy even to EGFR mutant patients after failure of EGFR tyrosine kinase inhibitor, especially in cases with high PD-LI expression. Dove Medical Press 2018-09-07 /pmc/articles/PMC6135433/ /pubmed/30237726 http://dx.doi.org/10.2147/OTT.S168598 Text en © 2018 Tozuka et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Report Tozuka, Takehiro Seike, Masahiro Minegishi, Yuji Kitagawa, Shingo Kato, Tomomi Takano, Natsuki Hisakane, Kakeru Takahashi, Satoshi Kobayashi, Kenichi Kashiwada, Takeru Sugano, Teppei Takeuchi, Susumu Kunugi, Shinobu Noro, Rintaro Saito, Yoshinobu Kubota, Kaoru Gemma, Akihiko Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression |
title | Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression |
title_full | Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression |
title_fullStr | Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression |
title_full_unstemmed | Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression |
title_short | Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression |
title_sort | pembrolizumab and salvage chemotherapy in egfr t790m-positive non-small-cell lung cancer with high pd-l1 expression |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135433/ https://www.ncbi.nlm.nih.gov/pubmed/30237726 http://dx.doi.org/10.2147/OTT.S168598 |
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