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Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis
Recent clinical trials have demonstrated that anti‐PD‐1 blocking antibodies showed remarkable clinical efficacy in a subset of non‐small cell lung cancer (NSCLC) patients. Clinical trials usually exclude patients with renal dysfunction who are receiving hemodialysis (HD). Therefore, it is unclear wh...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825915/ https://www.ncbi.nlm.nih.gov/pubmed/31520515 http://dx.doi.org/10.1111/1759-7714.13197 |
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author | Osa, Akio Uenami, Takeshi Naito, Yujiro Hirata, Haruhiko Koyama, Shohei Takimoto, Takayuki Shiroyama, Takayuki Futami, Shinji Nakatsubo, Saeko Sawa, Nobuhiko Yano, Yukihiro Nagatomo, Izumi Takeda, Yoshito Mori, Masahide Kida, Hiroshi Kumanogoh, Atsushi |
author_facet | Osa, Akio Uenami, Takeshi Naito, Yujiro Hirata, Haruhiko Koyama, Shohei Takimoto, Takayuki Shiroyama, Takayuki Futami, Shinji Nakatsubo, Saeko Sawa, Nobuhiko Yano, Yukihiro Nagatomo, Izumi Takeda, Yoshito Mori, Masahide Kida, Hiroshi Kumanogoh, Atsushi |
author_sort | Osa, Akio |
collection | PubMed |
description | Recent clinical trials have demonstrated that anti‐PD‐1 blocking antibodies showed remarkable clinical efficacy in a subset of non‐small cell lung cancer (NSCLC) patients. Clinical trials usually exclude patients with renal dysfunction who are receiving hemodialysis (HD). Therefore, it is unclear whether these patients can be safely and effectively treated with pembrolizumab. Here, we present a non‐small cell lung cancer patient on HD who achieved complete remission after one dose of pembrolizumab without severe adverse events. We assessed pembrolizumab binding to peripheral blood T cells in this patient using a method that we recently developed. This is the first report to visualize pembrolizumab binding to T cells in a patient on HD during and after pembrolizumab treatment. The pharmacokinetics of pembrolizumab in this case were similar to those in patients with normal renal function, suggesting that severe renal dysfunction has little influence on the metabolism of pembrolizumab, and is not a contraindication for anti‐PD‐1 treatment. Immune checkpoint inhibitors, including pembrolizumab, may be a vital therapeutic option for lung cancer patients on HD. |
format | Online Article Text |
id | pubmed-6825915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68259152019-11-07 Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis Osa, Akio Uenami, Takeshi Naito, Yujiro Hirata, Haruhiko Koyama, Shohei Takimoto, Takayuki Shiroyama, Takayuki Futami, Shinji Nakatsubo, Saeko Sawa, Nobuhiko Yano, Yukihiro Nagatomo, Izumi Takeda, Yoshito Mori, Masahide Kida, Hiroshi Kumanogoh, Atsushi Thorac Cancer Case Reports Recent clinical trials have demonstrated that anti‐PD‐1 blocking antibodies showed remarkable clinical efficacy in a subset of non‐small cell lung cancer (NSCLC) patients. Clinical trials usually exclude patients with renal dysfunction who are receiving hemodialysis (HD). Therefore, it is unclear whether these patients can be safely and effectively treated with pembrolizumab. Here, we present a non‐small cell lung cancer patient on HD who achieved complete remission after one dose of pembrolizumab without severe adverse events. We assessed pembrolizumab binding to peripheral blood T cells in this patient using a method that we recently developed. This is the first report to visualize pembrolizumab binding to T cells in a patient on HD during and after pembrolizumab treatment. The pharmacokinetics of pembrolizumab in this case were similar to those in patients with normal renal function, suggesting that severe renal dysfunction has little influence on the metabolism of pembrolizumab, and is not a contraindication for anti‐PD‐1 treatment. Immune checkpoint inhibitors, including pembrolizumab, may be a vital therapeutic option for lung cancer patients on HD. John Wiley & Sons Australia, Ltd 2019-09-14 2019-11 /pmc/articles/PMC6825915/ /pubmed/31520515 http://dx.doi.org/10.1111/1759-7714.13197 Text en © 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Osa, Akio Uenami, Takeshi Naito, Yujiro Hirata, Haruhiko Koyama, Shohei Takimoto, Takayuki Shiroyama, Takayuki Futami, Shinji Nakatsubo, Saeko Sawa, Nobuhiko Yano, Yukihiro Nagatomo, Izumi Takeda, Yoshito Mori, Masahide Kida, Hiroshi Kumanogoh, Atsushi Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis |
title | Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis |
title_full | Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis |
title_fullStr | Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis |
title_full_unstemmed | Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis |
title_short | Monitoring antibody binding to T cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis |
title_sort | monitoring antibody binding to t cells in a pembrolizumab‐treated patient with lung adenocarcinoma on hemodialysis |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825915/ https://www.ncbi.nlm.nih.gov/pubmed/31520515 http://dx.doi.org/10.1111/1759-7714.13197 |
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