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Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study

Immune checkpoint blockade‐related pneumonitis is a rare but potentially life‐threatening adverse effect, but its risk factors are not completely understood. This case‐control study was conducted to identify pneumonitis risk factors in patients treated with anti‐PD1 monoclonal antibodies (mAbs), inc...

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Autores principales: Cui, Pengfei, Liu, Zhefeng, Wang, Guoqiang, Ma, Junxun, Qian, Yuanyu, Zhang, Fan, Han, Chun, Long, Yaping, Li, Ye, Zheng, Xuan, Sun, Danyang, Zhang, Jing, Cai, Shangli, Jiao, Shunchang, Hu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089164/
https://www.ncbi.nlm.nih.gov/pubmed/29797416
http://dx.doi.org/10.1002/cam4.1579
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author Cui, Pengfei
Liu, Zhefeng
Wang, Guoqiang
Ma, Junxun
Qian, Yuanyu
Zhang, Fan
Han, Chun
Long, Yaping
Li, Ye
Zheng, Xuan
Sun, Danyang
Zhang, Jing
Cai, Shangli
Jiao, Shunchang
Hu, Yi
author_facet Cui, Pengfei
Liu, Zhefeng
Wang, Guoqiang
Ma, Junxun
Qian, Yuanyu
Zhang, Fan
Han, Chun
Long, Yaping
Li, Ye
Zheng, Xuan
Sun, Danyang
Zhang, Jing
Cai, Shangli
Jiao, Shunchang
Hu, Yi
author_sort Cui, Pengfei
collection PubMed
description Immune checkpoint blockade‐related pneumonitis is a rare but potentially life‐threatening adverse effect, but its risk factors are not completely understood. This case‐control study was conducted to identify pneumonitis risk factors in patients treated with anti‐PD1 monoclonal antibodies (mAbs), including all the patients who developed pneumonitis after anti‐PD‐1 mAbs treatment in the Cancer Center of the Chinese People's Liberation Army from September 2015 to September 2017. Two controls per case were matched according to a propensity‐score matching algorithm to account for confounding effects caused by individual baseline variables. Demographic and clinical information was obtained from medical records. In total, 55 cases and 110 controls were included in the study. No association was observed between smoking status or primary lung cancer and risk of pneumonitis. Significant risk factors for pneumonitis related to anti‐PD‐1 mAbs were prior thoracic radiotherapy, prior lung disease and combination therapy with odds ratios of 3.34 (1.51‐7.39), 2.86 (1.45‐5.64) and 2.73 (1.40‐5.31), respectively. The associations remained significant in the multivariable logistic regression model. The risk of pneumonitis induced by anti‐PD‐1 mAbs is associated with prior thoracic radiotherapy, prior lung disease, and combination therapy. Clinicians should monitor these features in patients receiving anti‐PD‐1 therapy to optimize clinical safety and efficacy.
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spelling pubmed-60891642018-08-17 Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study Cui, Pengfei Liu, Zhefeng Wang, Guoqiang Ma, Junxun Qian, Yuanyu Zhang, Fan Han, Chun Long, Yaping Li, Ye Zheng, Xuan Sun, Danyang Zhang, Jing Cai, Shangli Jiao, Shunchang Hu, Yi Cancer Med Cancer Prevention Immune checkpoint blockade‐related pneumonitis is a rare but potentially life‐threatening adverse effect, but its risk factors are not completely understood. This case‐control study was conducted to identify pneumonitis risk factors in patients treated with anti‐PD1 monoclonal antibodies (mAbs), including all the patients who developed pneumonitis after anti‐PD‐1 mAbs treatment in the Cancer Center of the Chinese People's Liberation Army from September 2015 to September 2017. Two controls per case were matched according to a propensity‐score matching algorithm to account for confounding effects caused by individual baseline variables. Demographic and clinical information was obtained from medical records. In total, 55 cases and 110 controls were included in the study. No association was observed between smoking status or primary lung cancer and risk of pneumonitis. Significant risk factors for pneumonitis related to anti‐PD‐1 mAbs were prior thoracic radiotherapy, prior lung disease and combination therapy with odds ratios of 3.34 (1.51‐7.39), 2.86 (1.45‐5.64) and 2.73 (1.40‐5.31), respectively. The associations remained significant in the multivariable logistic regression model. The risk of pneumonitis induced by anti‐PD‐1 mAbs is associated with prior thoracic radiotherapy, prior lung disease, and combination therapy. Clinicians should monitor these features in patients receiving anti‐PD‐1 therapy to optimize clinical safety and efficacy. John Wiley and Sons Inc. 2018-05-23 /pmc/articles/PMC6089164/ /pubmed/29797416 http://dx.doi.org/10.1002/cam4.1579 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons 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 Cancer Prevention
Cui, Pengfei
Liu, Zhefeng
Wang, Guoqiang
Ma, Junxun
Qian, Yuanyu
Zhang, Fan
Han, Chun
Long, Yaping
Li, Ye
Zheng, Xuan
Sun, Danyang
Zhang, Jing
Cai, Shangli
Jiao, Shunchang
Hu, Yi
Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study
title Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study
title_full Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study
title_fullStr Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study
title_full_unstemmed Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study
title_short Risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: A case‐control study
title_sort risk factors for pneumonitis in patients treated with anti‐programmed death‐1 therapy: a case‐control study
topic Cancer Prevention
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089164/
https://www.ncbi.nlm.nih.gov/pubmed/29797416
http://dx.doi.org/10.1002/cam4.1579
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