Cargando…

Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors

BACKGROUND: Non‐small cell lung cancer (NSCLC) patients with pre‐existing respiratory diseases have been excluded in clinical trials of immune checkpoint inhibitor (ICI) therapy, and it is unknown whether the same degree of response can be expected as that in patients without pre‐existing respirator...

Descripción completa

Detalles Bibliográficos
Autores principales: Isono, Taisuke, Kagiyama, Naho, Takano, Kenji, Hosoda, Chiaki, Nishida, Takashi, Kawate, Eriko, Kobayashi, Yoichi, Ishiguro, Takashi, Takaku, Youtaro, Kurashima, Kazuyoshi, Yanagisawa, Tsutomu, Takayanagi, Noboru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812074/
https://www.ncbi.nlm.nih.gov/pubmed/33201587
http://dx.doi.org/10.1111/1759-7714.13736
_version_ 1783637591436820480
author Isono, Taisuke
Kagiyama, Naho
Takano, Kenji
Hosoda, Chiaki
Nishida, Takashi
Kawate, Eriko
Kobayashi, Yoichi
Ishiguro, Takashi
Takaku, Youtaro
Kurashima, Kazuyoshi
Yanagisawa, Tsutomu
Takayanagi, Noboru
author_facet Isono, Taisuke
Kagiyama, Naho
Takano, Kenji
Hosoda, Chiaki
Nishida, Takashi
Kawate, Eriko
Kobayashi, Yoichi
Ishiguro, Takashi
Takaku, Youtaro
Kurashima, Kazuyoshi
Yanagisawa, Tsutomu
Takayanagi, Noboru
author_sort Isono, Taisuke
collection PubMed
description BACKGROUND: Non‐small cell lung cancer (NSCLC) patients with pre‐existing respiratory diseases have been excluded in clinical trials of immune checkpoint inhibitor (ICI) therapy, and it is unknown whether the same degree of response can be expected as that in patients without pre‐existing respiratory diseases and if they are associated with increased risk for various immune‐related adverse events (irAEs) and ICI pneumonitis. This study aimed to evaluate predictive factors of clinical response, prognostic factors, risk factors of irAEs, and ICI pneumonitis in NSCLC patients with or without pre‐existing respiratory diseases. METHODS: We conducted a retrospective study of 180 NSCLC patients who received ICI monotherapy of nivolumab, pembrolizumab, or atezolizumab from 1 January 2016 to 31 March 2019. RESULTS: A total of 119 patients had pre‐existing respiratory diseases, including 20 with pre‐existing idiopathic interstitial pneumonias (IIPs). A total of 85 patients experienced irAEs, of which ICI pneumonitis was the most frequent adverse event, occurring in 27 patients. Of the three patients who died from irAEs, all from ICI pneumonitis, two had pulmonary emphysema and one had pre‐existing IIP. In multivariate analyses, irAEs were associated with objective response rate (ORR) and favorable OS, and IIPs were associated with increased risk for ICI pneumonitis. However, IIPs were not associated with low ORR or poor OS. CONCLUSIONS: Pre‐existing IIPs were a risk factor for ICI pneumonitis. However, this study showed that ICI therapy can be offered to patients with pre‐existing respiratory diseases with the expectation of the same degree of response as that in patients without pre‐existing respiratory diseases. KEY POINTS: Significant findings of the study: Pre‐existing IIPs were a risk factor for ICI pneumonitis, but objective response rate and prognosis of patients with IIPs were similar to those of other patients. What this study adds: In patients with pre‐existing IIPs, ICI pneumonitis should be noted. However, ICI therapy can be offered to patients with pre‐existing respiratory diseases with the expectation of the same degree of response as that in patients without pre‐existing respiratory diseases
format Online
Article
Text
id pubmed-7812074
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley & Sons Australia, Ltd
record_format MEDLINE/PubMed
spelling pubmed-78120742021-01-22 Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors Isono, Taisuke Kagiyama, Naho Takano, Kenji Hosoda, Chiaki Nishida, Takashi Kawate, Eriko Kobayashi, Yoichi Ishiguro, Takashi Takaku, Youtaro Kurashima, Kazuyoshi Yanagisawa, Tsutomu Takayanagi, Noboru Thorac Cancer Original Articles BACKGROUND: Non‐small cell lung cancer (NSCLC) patients with pre‐existing respiratory diseases have been excluded in clinical trials of immune checkpoint inhibitor (ICI) therapy, and it is unknown whether the same degree of response can be expected as that in patients without pre‐existing respiratory diseases and if they are associated with increased risk for various immune‐related adverse events (irAEs) and ICI pneumonitis. This study aimed to evaluate predictive factors of clinical response, prognostic factors, risk factors of irAEs, and ICI pneumonitis in NSCLC patients with or without pre‐existing respiratory diseases. METHODS: We conducted a retrospective study of 180 NSCLC patients who received ICI monotherapy of nivolumab, pembrolizumab, or atezolizumab from 1 January 2016 to 31 March 2019. RESULTS: A total of 119 patients had pre‐existing respiratory diseases, including 20 with pre‐existing idiopathic interstitial pneumonias (IIPs). A total of 85 patients experienced irAEs, of which ICI pneumonitis was the most frequent adverse event, occurring in 27 patients. Of the three patients who died from irAEs, all from ICI pneumonitis, two had pulmonary emphysema and one had pre‐existing IIP. In multivariate analyses, irAEs were associated with objective response rate (ORR) and favorable OS, and IIPs were associated with increased risk for ICI pneumonitis. However, IIPs were not associated with low ORR or poor OS. CONCLUSIONS: Pre‐existing IIPs were a risk factor for ICI pneumonitis. However, this study showed that ICI therapy can be offered to patients with pre‐existing respiratory diseases with the expectation of the same degree of response as that in patients without pre‐existing respiratory diseases. KEY POINTS: Significant findings of the study: Pre‐existing IIPs were a risk factor for ICI pneumonitis, but objective response rate and prognosis of patients with IIPs were similar to those of other patients. What this study adds: In patients with pre‐existing IIPs, ICI pneumonitis should be noted. However, ICI therapy can be offered to patients with pre‐existing respiratory diseases with the expectation of the same degree of response as that in patients without pre‐existing respiratory diseases John Wiley & Sons Australia, Ltd 2020-11-17 2021-01 /pmc/articles/PMC7812074/ /pubmed/33201587 http://dx.doi.org/10.1111/1759-7714.13736 Text en © 2020 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Isono, Taisuke
Kagiyama, Naho
Takano, Kenji
Hosoda, Chiaki
Nishida, Takashi
Kawate, Eriko
Kobayashi, Yoichi
Ishiguro, Takashi
Takaku, Youtaro
Kurashima, Kazuyoshi
Yanagisawa, Tsutomu
Takayanagi, Noboru
Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors
title Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors
title_full Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors
title_fullStr Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors
title_full_unstemmed Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors
title_short Outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors
title_sort outcome and risk factor of immune‐related adverse events and pneumonitis in patients with advanced or postoperative recurrent non‐small cell lung cancer treated with immune checkpoint inhibitors
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812074/
https://www.ncbi.nlm.nih.gov/pubmed/33201587
http://dx.doi.org/10.1111/1759-7714.13736
work_keys_str_mv AT isonotaisuke outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT kagiyamanaho outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT takanokenji outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT hosodachiaki outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT nishidatakashi outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT kawateeriko outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT kobayashiyoichi outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT ishigurotakashi outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT takakuyoutaro outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT kurashimakazuyoshi outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT yanagisawatsutomu outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors
AT takayanaginoboru outcomeandriskfactorofimmunerelatedadverseeventsandpneumonitisinpatientswithadvancedorpostoperativerecurrentnonsmallcelllungcancertreatedwithimmunecheckpointinhibitors