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Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib
Nintedanib has been shown to significantly reduce the annual rate of decline in the forced vital capacity (FVC) in patients with idiopathic pulmonary fibrosis (IPF) in previous randomized trials. A 71-year-old man developed exertional dyspnea and was diagnosed with IPF. Four months after treatment w...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522408/ https://www.ncbi.nlm.nih.gov/pubmed/30568147 http://dx.doi.org/10.2169/internalmedicine.1890-18 |
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author | Nakano, Akiko Ohkubo, Hirotsugu Fukumitsu, Kensuke Fukuda, Satoshi Kanemitsu, Yoshihiro Takemura, Masaya Maeno, Ken Ito, Yutaka Oguri, Tetsuya Niimi, Akio |
author_facet | Nakano, Akiko Ohkubo, Hirotsugu Fukumitsu, Kensuke Fukuda, Satoshi Kanemitsu, Yoshihiro Takemura, Masaya Maeno, Ken Ito, Yutaka Oguri, Tetsuya Niimi, Akio |
author_sort | Nakano, Akiko |
collection | PubMed |
description | Nintedanib has been shown to significantly reduce the annual rate of decline in the forced vital capacity (FVC) in patients with idiopathic pulmonary fibrosis (IPF) in previous randomized trials. A 71-year-old man developed exertional dyspnea and was diagnosed with IPF. Four months after treatment with nintedanib, high-resolution computed tomography findings revealed reduced areas of ground-glass opacity and consolidation; 13 months after treatment, the FVC showed improvement from 3.07 to 3.43 L, and the serum Krebs von den Lungen (KL)-6 concentration showed a decline to normal levels. We herein report a patient with IPF who was considered a super responder to nintedanib. |
format | Online Article Text |
id | pubmed-6522408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-65224082019-05-20 Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib Nakano, Akiko Ohkubo, Hirotsugu Fukumitsu, Kensuke Fukuda, Satoshi Kanemitsu, Yoshihiro Takemura, Masaya Maeno, Ken Ito, Yutaka Oguri, Tetsuya Niimi, Akio Intern Med Case Report Nintedanib has been shown to significantly reduce the annual rate of decline in the forced vital capacity (FVC) in patients with idiopathic pulmonary fibrosis (IPF) in previous randomized trials. A 71-year-old man developed exertional dyspnea and was diagnosed with IPF. Four months after treatment with nintedanib, high-resolution computed tomography findings revealed reduced areas of ground-glass opacity and consolidation; 13 months after treatment, the FVC showed improvement from 3.07 to 3.43 L, and the serum Krebs von den Lungen (KL)-6 concentration showed a decline to normal levels. We herein report a patient with IPF who was considered a super responder to nintedanib. The Japanese Society of Internal Medicine 2018-12-18 2019-04-15 /pmc/articles/PMC6522408/ /pubmed/30568147 http://dx.doi.org/10.2169/internalmedicine.1890-18 Text en Copyright © 2019 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Nakano, Akiko Ohkubo, Hirotsugu Fukumitsu, Kensuke Fukuda, Satoshi Kanemitsu, Yoshihiro Takemura, Masaya Maeno, Ken Ito, Yutaka Oguri, Tetsuya Niimi, Akio Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib |
title | Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib |
title_full | Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib |
title_fullStr | Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib |
title_full_unstemmed | Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib |
title_short | Remarkable Improvement in a Patient with Idiopathic Pulmonary Fibrosis after Treatment with Nintedanib |
title_sort | remarkable improvement in a patient with idiopathic pulmonary fibrosis after treatment with nintedanib |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522408/ https://www.ncbi.nlm.nih.gov/pubmed/30568147 http://dx.doi.org/10.2169/internalmedicine.1890-18 |
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