Cargando…
Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody
We report a case of a 38-year-old woman who was diagnosed with stage IV lung adenocarcinoma, harboring an epidermal growth factor receptor (EGFR) L858R mutation on exon 21 and a T790 M mutation on exon 20. The patient was treated with osimertinib, a third-generation EGFR tyrosine kinase inhibitor (E...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5306260/ https://www.ncbi.nlm.nih.gov/pubmed/27599705 http://dx.doi.org/10.1007/s10637-016-0389-9 |
_version_ | 1782507163596357632 |
---|---|
author | Mamesaya, Nobuaki Kenmotsu, Hirotsugu Katsumata, Mineo Nakajima, Takashi Endo, Masahiro Takahashi, Toshiaki |
author_facet | Mamesaya, Nobuaki Kenmotsu, Hirotsugu Katsumata, Mineo Nakajima, Takashi Endo, Masahiro Takahashi, Toshiaki |
author_sort | Mamesaya, Nobuaki |
collection | PubMed |
description | We report a case of a 38-year-old woman who was diagnosed with stage IV lung adenocarcinoma, harboring an epidermal growth factor receptor (EGFR) L858R mutation on exon 21 and a T790 M mutation on exon 20. The patient was treated with osimertinib, a third-generation EGFR tyrosine kinase inhibitor (EGFR-TKI) following treatment with nivolumab, an anti-Programmed Cell Death 1 (anti-PD1) antibody. After initiating osimertinib treatment, the patient began to complain of low-grade fever and shortness of breath without hypoxemia, and her chest radiograph and a CT scan revealed a remarkable antitumor response, although faint infiltrations were observed in the bilateral lung field. Bronchoalveolar lavage fluid mainly contained lymphocytes (CD4+/CD8+ ratio of 0.3), and a transbronchial lung biopsy specimen showed lymphocytic alveolitis with partial organization in several alveolar spaces. Therefore we diagnosed the patient with osimertinib-induced interstitial lung disease (ILD) after treatment with anti-PD1 antibody. We considered anti-PD1 therapies may be the risk factor of EGFR-TKI-induced ILD. |
format | Online Article Text |
id | pubmed-5306260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-53062602017-02-27 Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody Mamesaya, Nobuaki Kenmotsu, Hirotsugu Katsumata, Mineo Nakajima, Takashi Endo, Masahiro Takahashi, Toshiaki Invest New Drugs Short Report We report a case of a 38-year-old woman who was diagnosed with stage IV lung adenocarcinoma, harboring an epidermal growth factor receptor (EGFR) L858R mutation on exon 21 and a T790 M mutation on exon 20. The patient was treated with osimertinib, a third-generation EGFR tyrosine kinase inhibitor (EGFR-TKI) following treatment with nivolumab, an anti-Programmed Cell Death 1 (anti-PD1) antibody. After initiating osimertinib treatment, the patient began to complain of low-grade fever and shortness of breath without hypoxemia, and her chest radiograph and a CT scan revealed a remarkable antitumor response, although faint infiltrations were observed in the bilateral lung field. Bronchoalveolar lavage fluid mainly contained lymphocytes (CD4+/CD8+ ratio of 0.3), and a transbronchial lung biopsy specimen showed lymphocytic alveolitis with partial organization in several alveolar spaces. Therefore we diagnosed the patient with osimertinib-induced interstitial lung disease (ILD) after treatment with anti-PD1 antibody. We considered anti-PD1 therapies may be the risk factor of EGFR-TKI-induced ILD. Springer US 2016-09-06 2017 /pmc/articles/PMC5306260/ /pubmed/27599705 http://dx.doi.org/10.1007/s10637-016-0389-9 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Short Report Mamesaya, Nobuaki Kenmotsu, Hirotsugu Katsumata, Mineo Nakajima, Takashi Endo, Masahiro Takahashi, Toshiaki Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody |
title | Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody |
title_full | Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody |
title_fullStr | Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody |
title_full_unstemmed | Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody |
title_short | Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody |
title_sort | osimertinib-induced interstitial lung disease after treatment with anti-pd1 antibody |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5306260/ https://www.ncbi.nlm.nih.gov/pubmed/27599705 http://dx.doi.org/10.1007/s10637-016-0389-9 |
work_keys_str_mv | AT mamesayanobuaki osimertinibinducedinterstitiallungdiseaseaftertreatmentwithantipd1antibody AT kenmotsuhirotsugu osimertinibinducedinterstitiallungdiseaseaftertreatmentwithantipd1antibody AT katsumatamineo osimertinibinducedinterstitiallungdiseaseaftertreatmentwithantipd1antibody AT nakajimatakashi osimertinibinducedinterstitiallungdiseaseaftertreatmentwithantipd1antibody AT endomasahiro osimertinibinducedinterstitiallungdiseaseaftertreatmentwithantipd1antibody AT takahashitoshiaki osimertinibinducedinterstitiallungdiseaseaftertreatmentwithantipd1antibody |