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Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series

Nivolumab is an anti‐PD‐1 blocking monoclonal antibody approved for the treatment of non‐small cell lung cancer (NSCLC). However, some patients on immunotherapy may experience rapid progression and worsening clinical status, known as hyperprogressive disease. We retrospectively reviewed the clinical...

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Autores principales: Kanazu, Masaki, Edahiro, Ryuya, Krebe, Hiroyuki, Nishida, Kohei, Ishijima, Mikako, Uenami, Takeshi, Akazawa, Yuki, Yano, Yukihiro, Yamaguchi, Toshihiko, Mori, Masahide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275832/
https://www.ncbi.nlm.nih.gov/pubmed/30328672
http://dx.doi.org/10.1111/1759-7714.12894
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author Kanazu, Masaki
Edahiro, Ryuya
Krebe, Hiroyuki
Nishida, Kohei
Ishijima, Mikako
Uenami, Takeshi
Akazawa, Yuki
Yano, Yukihiro
Yamaguchi, Toshihiko
Mori, Masahide
author_facet Kanazu, Masaki
Edahiro, Ryuya
Krebe, Hiroyuki
Nishida, Kohei
Ishijima, Mikako
Uenami, Takeshi
Akazawa, Yuki
Yano, Yukihiro
Yamaguchi, Toshihiko
Mori, Masahide
author_sort Kanazu, Masaki
collection PubMed
description Nivolumab is an anti‐PD‐1 blocking monoclonal antibody approved for the treatment of non‐small cell lung cancer (NSCLC). However, some patients on immunotherapy may experience rapid progression and worsening clinical status, known as hyperprogressive disease. We retrospectively reviewed the clinical records of patients with NSCLC administered nivolumab therapy at Toneyama National Hospital, Japan, from January 2016 to January 2018. Of the 87 patients administered nivolumab therapy, five experienced rapid progression during one cycle of nivolumab therapy. Four patients were treated with corticosteroids to overcome their symptomatic events. Nivolumab exhibited efficacy after temporal progression, so‐called “pseudoprogression”, in three patients, and their symptoms and laboratory results improved. In the other patient, pleural and pericardial effusions increased after nivolumab therapy, and drainage was required, with no subsequent recurrence. The clinical courses of our case series indicate that alternative treatment, namely high‐dose corticosteroids, antibiotics, and drainage, effectively treated the symptoms of rapid tumor progression. Of note, corticosteroids suppressed the temporary inflammatory reaction to nivolumab. Although hyperprogressive disease is thought to be associated with poor quality of life and survival, these treatment strategies may be useful in patients with expected responses to immunotherapy.
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spelling pubmed-62758322018-12-06 Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series Kanazu, Masaki Edahiro, Ryuya Krebe, Hiroyuki Nishida, Kohei Ishijima, Mikako Uenami, Takeshi Akazawa, Yuki Yano, Yukihiro Yamaguchi, Toshihiko Mori, Masahide Thorac Cancer Case Reports Nivolumab is an anti‐PD‐1 blocking monoclonal antibody approved for the treatment of non‐small cell lung cancer (NSCLC). However, some patients on immunotherapy may experience rapid progression and worsening clinical status, known as hyperprogressive disease. We retrospectively reviewed the clinical records of patients with NSCLC administered nivolumab therapy at Toneyama National Hospital, Japan, from January 2016 to January 2018. Of the 87 patients administered nivolumab therapy, five experienced rapid progression during one cycle of nivolumab therapy. Four patients were treated with corticosteroids to overcome their symptomatic events. Nivolumab exhibited efficacy after temporal progression, so‐called “pseudoprogression”, in three patients, and their symptoms and laboratory results improved. In the other patient, pleural and pericardial effusions increased after nivolumab therapy, and drainage was required, with no subsequent recurrence. The clinical courses of our case series indicate that alternative treatment, namely high‐dose corticosteroids, antibiotics, and drainage, effectively treated the symptoms of rapid tumor progression. Of note, corticosteroids suppressed the temporary inflammatory reaction to nivolumab. Although hyperprogressive disease is thought to be associated with poor quality of life and survival, these treatment strategies may be useful in patients with expected responses to immunotherapy. John Wiley & Sons Australia, Ltd 2018-10-17 2018-12 /pmc/articles/PMC6275832/ /pubmed/30328672 http://dx.doi.org/10.1111/1759-7714.12894 Text en © 2018 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
Kanazu, Masaki
Edahiro, Ryuya
Krebe, Hiroyuki
Nishida, Kohei
Ishijima, Mikako
Uenami, Takeshi
Akazawa, Yuki
Yano, Yukihiro
Yamaguchi, Toshihiko
Mori, Masahide
Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series
title Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series
title_full Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series
title_fullStr Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series
title_full_unstemmed Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series
title_short Hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: A case series
title_sort hyperprogressive disease in patients with non‐small cell lung cancer treated with nivolumab: a case series
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275832/
https://www.ncbi.nlm.nih.gov/pubmed/30328672
http://dx.doi.org/10.1111/1759-7714.12894
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