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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2019
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.
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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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