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Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease

OBJECTIVE: Pembrolizumab has benefited patients with advanced non-small-cell lung cancer (NSCLC) with a programmed death-ligand (PD-L)1 high expression, but little information is available regarding its safety for patients with interstitial lung disease (ILD). The aim of this study was to assess the...

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Autores principales: Fujita, Tetsuo, Kuroki, Tsuguko, Hayama, Nami, Shiraishi, Yuka, Amano, Hiroyuki, Nakamura, Makoto, Hirano, Satoshi, Tabeta, Hiroshi, Nakamura, Sukeyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492129/
https://www.ncbi.nlm.nih.gov/pubmed/32389949
http://dx.doi.org/10.2169/internalmedicine.4552-20
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author Fujita, Tetsuo
Kuroki, Tsuguko
Hayama, Nami
Shiraishi, Yuka
Amano, Hiroyuki
Nakamura, Makoto
Hirano, Satoshi
Tabeta, Hiroshi
Nakamura, Sukeyuki
author_facet Fujita, Tetsuo
Kuroki, Tsuguko
Hayama, Nami
Shiraishi, Yuka
Amano, Hiroyuki
Nakamura, Makoto
Hirano, Satoshi
Tabeta, Hiroshi
Nakamura, Sukeyuki
author_sort Fujita, Tetsuo
collection PubMed
description OBJECTIVE: Pembrolizumab has benefited patients with advanced non-small-cell lung cancer (NSCLC) with a programmed death-ligand (PD-L)1 high expression, but little information is available regarding its safety for patients with interstitial lung disease (ILD). The aim of this study was to assess the efficacy and tolerability of pembrolizumab for patients with advanced NSCLC and preexisting ILD. METHODS: We retrospectively reviewed the medical records of five patients with advanced NSCLC and preexisting ILD who received pembrolizumab monotherapy in a first-line setting. PATIENTS: All patients had mild ILD and pulmonary emphysema with a forced vital capacity within the normal range. Pembrolizumab was administered at a dose of 200 mg/body on day 1 every 3 weeks. RESULTS: The overall response rate was 60%. Four patients developed pembrolizumab-induced lung injury, which was improved in all cases by corticosteroid therapy. One patient received pembrolizumab for two years, did not experience lung injury and achieved a complete response. CONCLUSION: Pembrolizumab has a high risk of inducing lung injury in patients with preexisting ILD, although it may be very effective in NSCLC patients with a high PD-L1 expression, even concurrent with preexisting ILD. Further large-scale studies are needed to determine risk factors of pembrolizumab-induced lung injury in such patients.
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spelling pubmed-74921292020-09-23 Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease Fujita, Tetsuo Kuroki, Tsuguko Hayama, Nami Shiraishi, Yuka Amano, Hiroyuki Nakamura, Makoto Hirano, Satoshi Tabeta, Hiroshi Nakamura, Sukeyuki Intern Med Original Article OBJECTIVE: Pembrolizumab has benefited patients with advanced non-small-cell lung cancer (NSCLC) with a programmed death-ligand (PD-L)1 high expression, but little information is available regarding its safety for patients with interstitial lung disease (ILD). The aim of this study was to assess the efficacy and tolerability of pembrolizumab for patients with advanced NSCLC and preexisting ILD. METHODS: We retrospectively reviewed the medical records of five patients with advanced NSCLC and preexisting ILD who received pembrolizumab monotherapy in a first-line setting. PATIENTS: All patients had mild ILD and pulmonary emphysema with a forced vital capacity within the normal range. Pembrolizumab was administered at a dose of 200 mg/body on day 1 every 3 weeks. RESULTS: The overall response rate was 60%. Four patients developed pembrolizumab-induced lung injury, which was improved in all cases by corticosteroid therapy. One patient received pembrolizumab for two years, did not experience lung injury and achieved a complete response. CONCLUSION: Pembrolizumab has a high risk of inducing lung injury in patients with preexisting ILD, although it may be very effective in NSCLC patients with a high PD-L1 expression, even concurrent with preexisting ILD. Further large-scale studies are needed to determine risk factors of pembrolizumab-induced lung injury in such patients. The Japanese Society of Internal Medicine 2020-05-08 2020-08-15 /pmc/articles/PMC7492129/ /pubmed/32389949 http://dx.doi.org/10.2169/internalmedicine.4552-20 Text en Copyright © 2020 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 Original Article
Fujita, Tetsuo
Kuroki, Tsuguko
Hayama, Nami
Shiraishi, Yuka
Amano, Hiroyuki
Nakamura, Makoto
Hirano, Satoshi
Tabeta, Hiroshi
Nakamura, Sukeyuki
Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease
title Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease
title_full Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease
title_fullStr Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease
title_full_unstemmed Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease
title_short Pembrolizumab for Previously Untreated Patients with Advanced Non-small-cell Lung Cancer and Preexisting Interstitial Lung Disease
title_sort pembrolizumab for previously untreated patients with advanced non-small-cell lung cancer and preexisting interstitial lung disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492129/
https://www.ncbi.nlm.nih.gov/pubmed/32389949
http://dx.doi.org/10.2169/internalmedicine.4552-20
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