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Pericardial disease in patients treated with immune checkpoint inhibitors
BACKGROUND: There are limited data on the occurrence, associations and outcomes of pericardial effusions and pericarditis on or after treatment with immune checkpoint inhibitors (ICIs). METHODS: This was a retrospective study at a single academic center that compared 2842 consecutive patients who re...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215235/ https://www.ncbi.nlm.nih.gov/pubmed/34145031 http://dx.doi.org/10.1136/jitc-2021-002771 |
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author | Gong, Jingyi Drobni, Zsofia Dora Zafar, Amna Quinaglia, Thiago Hartmann, Sarah Gilman, Hannah K Raghu, Vineet K Gongora, Carlos Sise, Meghan E Alvi, Raza M Zubiri, Leyre Nohria, Anju Sullivan, Ryan Reynolds, Kerry L Zlotoff, Daniel Neilan, Tomas G |
author_facet | Gong, Jingyi Drobni, Zsofia Dora Zafar, Amna Quinaglia, Thiago Hartmann, Sarah Gilman, Hannah K Raghu, Vineet K Gongora, Carlos Sise, Meghan E Alvi, Raza M Zubiri, Leyre Nohria, Anju Sullivan, Ryan Reynolds, Kerry L Zlotoff, Daniel Neilan, Tomas G |
author_sort | Gong, Jingyi |
collection | PubMed |
description | BACKGROUND: There are limited data on the occurrence, associations and outcomes of pericardial effusions and pericarditis on or after treatment with immune checkpoint inhibitors (ICIs). METHODS: This was a retrospective study at a single academic center that compared 2842 consecutive patients who received ICIs with 2699 age- and cancer-type matched patients with metastatic disease who did not receive ICI. A pericardial event was defined as a composite outcome of pericarditis and new or worsening moderate or large pericardial effusion. The endpoints were obtained through chart review and were blindly adjudicated. To identify risk factors associated with a pericardial event, we compared patients who developed an event on an ICI with patients treated with an ICI who did not develop a pericardial event. Cox proportional-hazard model and logistical regression analysis were performed to study the association between ICI use and pericardial disease as well as pericardial disease and mortality. An additional 6-week landmark analysis was performed to account for lead-time bias. RESULTS: There were 42 pericardial events in the patients treated with ICI (n=2842) over 193 days (IQR: 64–411), yielding an incidence rate of 1.57 events per 100 person-years. There was a more than fourfold increase in risk of pericarditis or a pericardial effusion among patients on an ICI compared with controls not treated with ICI after adjusting for potential confounders (HR 4.37, 95% CI 2.09 to 9.14, p<0.001). Patients who developed pericardial disease while on an ICI had a trend for increased all-cause mortality compared with patients who did not develop a pericardial event (HR 1.53, 95% CI 0.99 to 2.36, p=0.05). When comparing those who developed pericardial disease after ICI treatment with those who did not, a higher dose of corticosteroid pre-ICI (>0.7 mg/kg prednisone) was associated with increased risk of pericardial disease (HR 2.56, 95% CI 1.00 to 6.57, p=0.049). CONCLUSIONS: ICI use was associated with an increased risk of development of pericardial disease among patients with cancer and a pericardial event on an ICI was associated with a trend towards increase in mortality. |
format | Online Article Text |
id | pubmed-8215235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-82152352021-07-01 Pericardial disease in patients treated with immune checkpoint inhibitors Gong, Jingyi Drobni, Zsofia Dora Zafar, Amna Quinaglia, Thiago Hartmann, Sarah Gilman, Hannah K Raghu, Vineet K Gongora, Carlos Sise, Meghan E Alvi, Raza M Zubiri, Leyre Nohria, Anju Sullivan, Ryan Reynolds, Kerry L Zlotoff, Daniel Neilan, Tomas G J Immunother Cancer Clinical/Translational Cancer Immunotherapy BACKGROUND: There are limited data on the occurrence, associations and outcomes of pericardial effusions and pericarditis on or after treatment with immune checkpoint inhibitors (ICIs). METHODS: This was a retrospective study at a single academic center that compared 2842 consecutive patients who received ICIs with 2699 age- and cancer-type matched patients with metastatic disease who did not receive ICI. A pericardial event was defined as a composite outcome of pericarditis and new or worsening moderate or large pericardial effusion. The endpoints were obtained through chart review and were blindly adjudicated. To identify risk factors associated with a pericardial event, we compared patients who developed an event on an ICI with patients treated with an ICI who did not develop a pericardial event. Cox proportional-hazard model and logistical regression analysis were performed to study the association between ICI use and pericardial disease as well as pericardial disease and mortality. An additional 6-week landmark analysis was performed to account for lead-time bias. RESULTS: There were 42 pericardial events in the patients treated with ICI (n=2842) over 193 days (IQR: 64–411), yielding an incidence rate of 1.57 events per 100 person-years. There was a more than fourfold increase in risk of pericarditis or a pericardial effusion among patients on an ICI compared with controls not treated with ICI after adjusting for potential confounders (HR 4.37, 95% CI 2.09 to 9.14, p<0.001). Patients who developed pericardial disease while on an ICI had a trend for increased all-cause mortality compared with patients who did not develop a pericardial event (HR 1.53, 95% CI 0.99 to 2.36, p=0.05). When comparing those who developed pericardial disease after ICI treatment with those who did not, a higher dose of corticosteroid pre-ICI (>0.7 mg/kg prednisone) was associated with increased risk of pericardial disease (HR 2.56, 95% CI 1.00 to 6.57, p=0.049). CONCLUSIONS: ICI use was associated with an increased risk of development of pericardial disease among patients with cancer and a pericardial event on an ICI was associated with a trend towards increase in mortality. BMJ Publishing Group 2021-06-18 /pmc/articles/PMC8215235/ /pubmed/34145031 http://dx.doi.org/10.1136/jitc-2021-002771 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Clinical/Translational Cancer Immunotherapy Gong, Jingyi Drobni, Zsofia Dora Zafar, Amna Quinaglia, Thiago Hartmann, Sarah Gilman, Hannah K Raghu, Vineet K Gongora, Carlos Sise, Meghan E Alvi, Raza M Zubiri, Leyre Nohria, Anju Sullivan, Ryan Reynolds, Kerry L Zlotoff, Daniel Neilan, Tomas G Pericardial disease in patients treated with immune checkpoint inhibitors |
title | Pericardial disease in patients treated with immune checkpoint inhibitors |
title_full | Pericardial disease in patients treated with immune checkpoint inhibitors |
title_fullStr | Pericardial disease in patients treated with immune checkpoint inhibitors |
title_full_unstemmed | Pericardial disease in patients treated with immune checkpoint inhibitors |
title_short | Pericardial disease in patients treated with immune checkpoint inhibitors |
title_sort | pericardial disease in patients treated with immune checkpoint inhibitors |
topic | Clinical/Translational Cancer Immunotherapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215235/ https://www.ncbi.nlm.nih.gov/pubmed/34145031 http://dx.doi.org/10.1136/jitc-2021-002771 |
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