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Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis

BACKGROUND: Myocarditis is a rare but life-threatening adverse event of cancer treatments with immune checkpoint inhibitors (ICIs). Recent guidelines recommend the use of high doses of corticosteroids as a first-line treatment, followed by intensified immunosuppressive therapy (IIST) in the case of...

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Autores principales: Cautela, Jennifer, Zeriouh, Sarah, Gaubert, Melanie, Bonello, Laurent, Laine, Marc, Peyrol, Michael, Paganelli, Franck, Lalevee, Nathalie, Barlesi, Fabrice, Thuny, Franck
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725077/
https://www.ncbi.nlm.nih.gov/pubmed/33298621
http://dx.doi.org/10.1136/jitc-2020-001887
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author Cautela, Jennifer
Zeriouh, Sarah
Gaubert, Melanie
Bonello, Laurent
Laine, Marc
Peyrol, Michael
Paganelli, Franck
Lalevee, Nathalie
Barlesi, Fabrice
Thuny, Franck
author_facet Cautela, Jennifer
Zeriouh, Sarah
Gaubert, Melanie
Bonello, Laurent
Laine, Marc
Peyrol, Michael
Paganelli, Franck
Lalevee, Nathalie
Barlesi, Fabrice
Thuny, Franck
author_sort Cautela, Jennifer
collection PubMed
description BACKGROUND: Myocarditis is a rare but life-threatening adverse event of cancer treatments with immune checkpoint inhibitors (ICIs). Recent guidelines recommend the use of high doses of corticosteroids as a first-line treatment, followed by intensified immunosuppressive therapy (IIST) in the case of unfavorable evolution. However, this strategy is empirical, and no studies have specifically addressed this issue. Therefore, we aimed to investigate and compare the clinical course, management and outcome of ICI-induced myocarditis patients requiring or not requiring IIST. METHODS: This case–control study included all patients consecutively admitted to The Mediterranean University Center of Cardio-Oncology (Aix-Marseille University, France) for the diagnosis of ICI-induced myocarditis according to Bonaca’s criteria and treated with or without IIST. In addition, we searched PubMed and included patients from previously published case reports treated with IIST in the analysis. The clinical, biological, imaging, treatment, all-cause death and cardiovascular death data of patients who required IIST were compared with those of patients who did not. RESULTS: A total of 60 patients (69±12 years) were included (36 were treated with IIST and 24 were not). Patients requiring IIST were more likely to have received a combination of ICIs (39% vs 8%, p=0.01), and developed the first symptoms/signs of myocarditis earlier after the onset of ICI therapy (median, 18 days vs 60 days, p=0.002). They had a significantly higher prevalence of sustained ventricular arrhythmia, complete atrioventricular block, cardiogenic shock and troponin elevation. Moreover, they were more likely to have other immune-related adverse events simultaneously (p<0.0001), especially myositis (p=0.0002) and myasthenia gravis (p=0.009). Patients who required IIST were more likely to die from any cause (50% vs 21%, p=0.02). Among them, patients who received infliximab were more likely to die from cardiovascular causes (OR, 12.0; 95% CI 2.1 to 67.1; p=0.005). CONCLUSION: The need for IIST was more common in patients who developed myocarditis very early after the start of ICI therapy, as well as when hemodynamic/electrical instability or neuromuscular adverse events occurred. Treatment with infliximab might be associated with an increased risk of cardiovascular death.
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spelling pubmed-77250772020-12-17 Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis Cautela, Jennifer Zeriouh, Sarah Gaubert, Melanie Bonello, Laurent Laine, Marc Peyrol, Michael Paganelli, Franck Lalevee, Nathalie Barlesi, Fabrice Thuny, Franck J Immunother Cancer Clinical/Translational Cancer Immunotherapy BACKGROUND: Myocarditis is a rare but life-threatening adverse event of cancer treatments with immune checkpoint inhibitors (ICIs). Recent guidelines recommend the use of high doses of corticosteroids as a first-line treatment, followed by intensified immunosuppressive therapy (IIST) in the case of unfavorable evolution. However, this strategy is empirical, and no studies have specifically addressed this issue. Therefore, we aimed to investigate and compare the clinical course, management and outcome of ICI-induced myocarditis patients requiring or not requiring IIST. METHODS: This case–control study included all patients consecutively admitted to The Mediterranean University Center of Cardio-Oncology (Aix-Marseille University, France) for the diagnosis of ICI-induced myocarditis according to Bonaca’s criteria and treated with or without IIST. In addition, we searched PubMed and included patients from previously published case reports treated with IIST in the analysis. The clinical, biological, imaging, treatment, all-cause death and cardiovascular death data of patients who required IIST were compared with those of patients who did not. RESULTS: A total of 60 patients (69±12 years) were included (36 were treated with IIST and 24 were not). Patients requiring IIST were more likely to have received a combination of ICIs (39% vs 8%, p=0.01), and developed the first symptoms/signs of myocarditis earlier after the onset of ICI therapy (median, 18 days vs 60 days, p=0.002). They had a significantly higher prevalence of sustained ventricular arrhythmia, complete atrioventricular block, cardiogenic shock and troponin elevation. Moreover, they were more likely to have other immune-related adverse events simultaneously (p<0.0001), especially myositis (p=0.0002) and myasthenia gravis (p=0.009). Patients who required IIST were more likely to die from any cause (50% vs 21%, p=0.02). Among them, patients who received infliximab were more likely to die from cardiovascular causes (OR, 12.0; 95% CI 2.1 to 67.1; p=0.005). CONCLUSION: The need for IIST was more common in patients who developed myocarditis very early after the start of ICI therapy, as well as when hemodynamic/electrical instability or neuromuscular adverse events occurred. Treatment with infliximab might be associated with an increased risk of cardiovascular death. BMJ Publishing Group 2020-12-08 /pmc/articles/PMC7725077/ /pubmed/33298621 http://dx.doi.org/10.1136/jitc-2020-001887 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical/Translational Cancer Immunotherapy
Cautela, Jennifer
Zeriouh, Sarah
Gaubert, Melanie
Bonello, Laurent
Laine, Marc
Peyrol, Michael
Paganelli, Franck
Lalevee, Nathalie
Barlesi, Fabrice
Thuny, Franck
Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis
title Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis
title_full Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis
title_fullStr Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis
title_full_unstemmed Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis
title_short Intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis
title_sort intensified immunosuppressive therapy in patients with immune checkpoint inhibitor-induced myocarditis
topic Clinical/Translational Cancer Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725077/
https://www.ncbi.nlm.nih.gov/pubmed/33298621
http://dx.doi.org/10.1136/jitc-2020-001887
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