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Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy
BACKGROUND: Immune-related adverse events (irAEs) may complicate the immune checkpoint inhibition (ICI) therapy. The effect of age on these irAEs is not elucidated. The aim of the study was to compare the occurrence of irAEs in different age groups. METHODS: Patients with lung cancer receiving anti-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155669/ https://www.ncbi.nlm.nih.gov/pubmed/34055598 http://dx.doi.org/10.3389/fonc.2021.619385 |
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author | Huang, Xinyi Tian, Tiantian Zhang, Yan Zhou, Shengjian Hu, Pingping Zhang, Jiandong |
author_facet | Huang, Xinyi Tian, Tiantian Zhang, Yan Zhou, Shengjian Hu, Pingping Zhang, Jiandong |
author_sort | Huang, Xinyi |
collection | PubMed |
description | BACKGROUND: Immune-related adverse events (irAEs) may complicate the immune checkpoint inhibition (ICI) therapy. The effect of age on these irAEs is not elucidated. The aim of the study was to compare the occurrence of irAEs in different age groups. METHODS: Patients with lung cancer receiving anti-programmed death- (ligand)1 (PD-(L)1) were selected from the US Food and Drug Administration Adverse Event Reporting System (FAERS) database. Immune cell infiltration data set was obtained from TIMER 2.0 web server. The patients were stratified for age as follows: <65 year-old (young patients, YP), 65 to 75 year-old (middle aged patients, MP), ≥75 year-old (old patients, OP). The severity of irAEs was compared using logistic binary regression model. The distribution differences of immune cell infiltration were estimated using non-parametric tests. RESULTS: Of all the 17,006 patients treated by anti-PD-(L)1, 7,355 were <65 (YP), 6,706 were 65–75 (MP), and 2,945 were ≥75 (OP). In general, we analyzed a total of 16 irAEs in this article and found that pulmonary toxicity was more frequent in OP (OP vs. YP: OR = 1.45, 95% CI: 1.28–1.64) and MP (MP vs. YP: OR = 1.38, 95% CI: 1.24–1.52), but hepatitis was less frequent in OP (OP vs. YP: OR = 0.56, 95% CI: 0.32–0.97) and MP (MP vs. YP: OR = 0.57, 95%CI: 0.38–0.85). Further analysis demonstrated that older patients showed less B cell, CD8(+) T cell and myeloid dendritic cell infiltration than younger patients. CONCLUSIONS: Elderly patients exhibited higher incidences of pulmonary toxicity, while hepatitis was found at low incidence. Therefore, clinicians should carefully monitor comorbidities in elderly patients. |
format | Online Article Text |
id | pubmed-8155669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81556692021-05-28 Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy Huang, Xinyi Tian, Tiantian Zhang, Yan Zhou, Shengjian Hu, Pingping Zhang, Jiandong Front Oncol Oncology BACKGROUND: Immune-related adverse events (irAEs) may complicate the immune checkpoint inhibition (ICI) therapy. The effect of age on these irAEs is not elucidated. The aim of the study was to compare the occurrence of irAEs in different age groups. METHODS: Patients with lung cancer receiving anti-programmed death- (ligand)1 (PD-(L)1) were selected from the US Food and Drug Administration Adverse Event Reporting System (FAERS) database. Immune cell infiltration data set was obtained from TIMER 2.0 web server. The patients were stratified for age as follows: <65 year-old (young patients, YP), 65 to 75 year-old (middle aged patients, MP), ≥75 year-old (old patients, OP). The severity of irAEs was compared using logistic binary regression model. The distribution differences of immune cell infiltration were estimated using non-parametric tests. RESULTS: Of all the 17,006 patients treated by anti-PD-(L)1, 7,355 were <65 (YP), 6,706 were 65–75 (MP), and 2,945 were ≥75 (OP). In general, we analyzed a total of 16 irAEs in this article and found that pulmonary toxicity was more frequent in OP (OP vs. YP: OR = 1.45, 95% CI: 1.28–1.64) and MP (MP vs. YP: OR = 1.38, 95% CI: 1.24–1.52), but hepatitis was less frequent in OP (OP vs. YP: OR = 0.56, 95% CI: 0.32–0.97) and MP (MP vs. YP: OR = 0.57, 95%CI: 0.38–0.85). Further analysis demonstrated that older patients showed less B cell, CD8(+) T cell and myeloid dendritic cell infiltration than younger patients. CONCLUSIONS: Elderly patients exhibited higher incidences of pulmonary toxicity, while hepatitis was found at low incidence. Therefore, clinicians should carefully monitor comorbidities in elderly patients. Frontiers Media S.A. 2021-05-13 /pmc/articles/PMC8155669/ /pubmed/34055598 http://dx.doi.org/10.3389/fonc.2021.619385 Text en Copyright © 2021 Huang, Tian, Zhang, Zhou, Hu and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Huang, Xinyi Tian, Tiantian Zhang, Yan Zhou, Shengjian Hu, Pingping Zhang, Jiandong Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy |
title | Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy |
title_full | Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy |
title_fullStr | Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy |
title_full_unstemmed | Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy |
title_short | Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy |
title_sort | age-associated changes in adverse events arising from anti-pd-(l)1 therapy |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155669/ https://www.ncbi.nlm.nih.gov/pubmed/34055598 http://dx.doi.org/10.3389/fonc.2021.619385 |
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