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Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China

BACKGROUND: Immune checkpoint inhibitors (ICIs) are the standard treatment for advanced lung cancer, but immune‐related adverse events (irAEs) remain poorly understood, especially in a real‐world setting. METHODS: A multicenter observational study was conducted. Medical records of lung cancer patien...

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Autores principales: Shi, Yuequan, Fang, Jian, Zhou, Chengzhi, Liu, Anwen, Wang, Yan, Meng, Qingwei, Ding, Cuimin, Ai, Bin, Gu, Yangchun, Yao, Yu, Sun, Hong, Guo, Hui, Zhang, Cuiying, Song, Xia, Li, Junling, Xu, Bei, Han, Zhiqiang, Song, Meijun, Tang, Tingyu, Chen, Peifeng, Lu, Hongmin, Shui, Yongjie, Lou, Guangyuan, Zhang, Dongming, Liu, Jia, Liu, Xiaoyan, Liu, Xiangning, Gao, Xiaoxing, Zhou, Qing, Chen, Minjiang, Zhao, Jing, Zhong, Wei, Xu, Yan, Wang, Mengzhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807338/
https://www.ncbi.nlm.nih.gov/pubmed/34935288
http://dx.doi.org/10.1111/1759-7714.14274
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author Shi, Yuequan
Fang, Jian
Zhou, Chengzhi
Liu, Anwen
Wang, Yan
Meng, Qingwei
Ding, Cuimin
Ai, Bin
Gu, Yangchun
Yao, Yu
Sun, Hong
Guo, Hui
Zhang, Cuiying
Song, Xia
Li, Junling
Xu, Bei
Han, Zhiqiang
Song, Meijun
Tang, Tingyu
Chen, Peifeng
Lu, Hongmin
Shui, Yongjie
Lou, Guangyuan
Zhang, Dongming
Liu, Jia
Liu, Xiaoyan
Liu, Xiangning
Gao, Xiaoxing
Zhou, Qing
Chen, Minjiang
Zhao, Jing
Zhong, Wei
Xu, Yan
Wang, Mengzhao
author_facet Shi, Yuequan
Fang, Jian
Zhou, Chengzhi
Liu, Anwen
Wang, Yan
Meng, Qingwei
Ding, Cuimin
Ai, Bin
Gu, Yangchun
Yao, Yu
Sun, Hong
Guo, Hui
Zhang, Cuiying
Song, Xia
Li, Junling
Xu, Bei
Han, Zhiqiang
Song, Meijun
Tang, Tingyu
Chen, Peifeng
Lu, Hongmin
Shui, Yongjie
Lou, Guangyuan
Zhang, Dongming
Liu, Jia
Liu, Xiaoyan
Liu, Xiangning
Gao, Xiaoxing
Zhou, Qing
Chen, Minjiang
Zhao, Jing
Zhong, Wei
Xu, Yan
Wang, Mengzhao
author_sort Shi, Yuequan
collection PubMed
description BACKGROUND: Immune checkpoint inhibitors (ICIs) are the standard treatment for advanced lung cancer, but immune‐related adverse events (irAEs) remain poorly understood, especially in a real‐world setting. METHODS: A multicenter observational study was conducted. Medical records of lung cancer patients treated with ICIs at 26 hospitals from January 1, 2015, to February 28, 2021, were retrieved. Types of ICIs included antiprogrammed cell death 1 or antiprogrammed cell death ligand 1 (PD‐L1) monotherapy, anticytotoxic T‐lymphocyte antigen‐4 monotherapy, or combination therapy. RESULTS: In total, 1905 patients with advanced lung cancer were evaluated. The median age was 63 (range 28–87) years, and the male/female ratio was 3.1:1 (1442/463). The primary histological subtype was adenocarcinoma (915). A total of 26.9% (512/1905) of the patients developed 671 irAEs, and 5.8% (110/1905) developed 120 grade 3–5 irAEs. Median duration from ICI initiation to irAEs onset was 56 (range 0–1160) days. The most common irAEs were thyroid dysfunction (7.2%, 138/1905), pneumonitis (6.5%, 124/1905), and dermatological toxicities (6.0%, 115/1905). A total of 162 irAEs were treated with steroids and 11 irAEs led to death. Patients with positive PD‐L1 expression (≥1%) and who received first‐line ICI treatment developed more irAEs. Patients who developed irAEs had a better disease control rate (DCR, 71.3% [365/512] vs. 56.0% [780/1145]; p < 0.001). CONCLUSIONS: The incidence rate of irAEs was 26.9% in a real‐world setting. IrAEs might be related to a better DCR, but clinicians should be more aware of irAE recognition and management in clinical practice.
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spelling pubmed-88073382022-02-04 Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China Shi, Yuequan Fang, Jian Zhou, Chengzhi Liu, Anwen Wang, Yan Meng, Qingwei Ding, Cuimin Ai, Bin Gu, Yangchun Yao, Yu Sun, Hong Guo, Hui Zhang, Cuiying Song, Xia Li, Junling Xu, Bei Han, Zhiqiang Song, Meijun Tang, Tingyu Chen, Peifeng Lu, Hongmin Shui, Yongjie Lou, Guangyuan Zhang, Dongming Liu, Jia Liu, Xiaoyan Liu, Xiangning Gao, Xiaoxing Zhou, Qing Chen, Minjiang Zhao, Jing Zhong, Wei Xu, Yan Wang, Mengzhao Thorac Cancer Original Articles BACKGROUND: Immune checkpoint inhibitors (ICIs) are the standard treatment for advanced lung cancer, but immune‐related adverse events (irAEs) remain poorly understood, especially in a real‐world setting. METHODS: A multicenter observational study was conducted. Medical records of lung cancer patients treated with ICIs at 26 hospitals from January 1, 2015, to February 28, 2021, were retrieved. Types of ICIs included antiprogrammed cell death 1 or antiprogrammed cell death ligand 1 (PD‐L1) monotherapy, anticytotoxic T‐lymphocyte antigen‐4 monotherapy, or combination therapy. RESULTS: In total, 1905 patients with advanced lung cancer were evaluated. The median age was 63 (range 28–87) years, and the male/female ratio was 3.1:1 (1442/463). The primary histological subtype was adenocarcinoma (915). A total of 26.9% (512/1905) of the patients developed 671 irAEs, and 5.8% (110/1905) developed 120 grade 3–5 irAEs. Median duration from ICI initiation to irAEs onset was 56 (range 0–1160) days. The most common irAEs were thyroid dysfunction (7.2%, 138/1905), pneumonitis (6.5%, 124/1905), and dermatological toxicities (6.0%, 115/1905). A total of 162 irAEs were treated with steroids and 11 irAEs led to death. Patients with positive PD‐L1 expression (≥1%) and who received first‐line ICI treatment developed more irAEs. Patients who developed irAEs had a better disease control rate (DCR, 71.3% [365/512] vs. 56.0% [780/1145]; p < 0.001). CONCLUSIONS: The incidence rate of irAEs was 26.9% in a real‐world setting. IrAEs might be related to a better DCR, but clinicians should be more aware of irAE recognition and management in clinical practice. John Wiley & Sons Australia, Ltd 2021-12-21 2022-02 /pmc/articles/PMC8807338/ /pubmed/34935288 http://dx.doi.org/10.1111/1759-7714.14274 Text en © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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
Shi, Yuequan
Fang, Jian
Zhou, Chengzhi
Liu, Anwen
Wang, Yan
Meng, Qingwei
Ding, Cuimin
Ai, Bin
Gu, Yangchun
Yao, Yu
Sun, Hong
Guo, Hui
Zhang, Cuiying
Song, Xia
Li, Junling
Xu, Bei
Han, Zhiqiang
Song, Meijun
Tang, Tingyu
Chen, Peifeng
Lu, Hongmin
Shui, Yongjie
Lou, Guangyuan
Zhang, Dongming
Liu, Jia
Liu, Xiaoyan
Liu, Xiangning
Gao, Xiaoxing
Zhou, Qing
Chen, Minjiang
Zhao, Jing
Zhong, Wei
Xu, Yan
Wang, Mengzhao
Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China
title Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China
title_full Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China
title_fullStr Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China
title_full_unstemmed Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China
title_short Immune checkpoint inhibitor‐related adverse events in lung cancer: Real‐world incidence and management practices of 1905 patients in China
title_sort immune checkpoint inhibitor‐related adverse events in lung cancer: real‐world incidence and management practices of 1905 patients in china
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807338/
https://www.ncbi.nlm.nih.gov/pubmed/34935288
http://dx.doi.org/10.1111/1759-7714.14274
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