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ICU admission for solid cancer patients treated with immune checkpoint inhibitors

BACKGROUND: Immune checkpoint inhibitors (ICI) have revolutionized the management of cancer. They can induce immune-related adverse events (irAE) leading to intensive care unit (ICU) admission. We aimed to describe irAEs for ICU admissions in solid cancer patients treated with ICIs. METHODS: This pr...

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Autores principales: Toffart, Anne-Claire, Meert, Anne-Pascale, Wallet, Florent, Gibelin, Aude, Guisset, Olivier, Gonzalez, Frédéric, Seguin, Amélie, Kouatchet, Achille, Delaunay, Myriam, Debieuvre, Didier, Duchemann, Boris, Rousseau-Bussac, Gaëlle, Nyunga, Martine, Grimaldi, David, Levrat, Albrice, Azoulay, Elie, Lemiale, Virginie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113402/
https://www.ncbi.nlm.nih.gov/pubmed/37072645
http://dx.doi.org/10.1186/s13613-023-01122-z
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author Toffart, Anne-Claire
Meert, Anne-Pascale
Wallet, Florent
Gibelin, Aude
Guisset, Olivier
Gonzalez, Frédéric
Seguin, Amélie
Kouatchet, Achille
Delaunay, Myriam
Debieuvre, Didier
Duchemann, Boris
Rousseau-Bussac, Gaëlle
Nyunga, Martine
Grimaldi, David
Levrat, Albrice
Azoulay, Elie
Lemiale, Virginie
author_facet Toffart, Anne-Claire
Meert, Anne-Pascale
Wallet, Florent
Gibelin, Aude
Guisset, Olivier
Gonzalez, Frédéric
Seguin, Amélie
Kouatchet, Achille
Delaunay, Myriam
Debieuvre, Didier
Duchemann, Boris
Rousseau-Bussac, Gaëlle
Nyunga, Martine
Grimaldi, David
Levrat, Albrice
Azoulay, Elie
Lemiale, Virginie
author_sort Toffart, Anne-Claire
collection PubMed
description BACKGROUND: Immune checkpoint inhibitors (ICI) have revolutionized the management of cancer. They can induce immune-related adverse events (irAE) leading to intensive care unit (ICU) admission. We aimed to describe irAEs for ICU admissions in solid cancer patients treated with ICIs. METHODS: This prospective multicenter study was conducted in France and Belgium. Adult patients with solid tumor and treated with systemic ICIs within the last 6 months, requiring non-programmed ICU admission were included. Patients admitted for microbiologically documented sepsis were excluded. Imputability of irAEs in ICU admissions was described according to the WHO-UMC classification system at ICU admission and at ICU discharge. The use of immunosuppressant treatment was reported. RESULTS: 115 patients were eligible. Solid tumor was mainly lung cancer (n = 76, 66%) and melanoma (n = 18, 16%). They were mainly treated with an anti-PD-(L)1 alone (n = 110, 96%). Main ICU admission reasons were acute respiratory failure (n = 66, 57%), colitis (n = 14, 13%), and cardiovascular disease (n = 13, 11%). ICU admission was considered “likely” associated with irAE for 48% (n = 55) of patients. Factors independently associated with irAE were a good ECOG performance status (PS) (ECOG-PS of 0 or 1 vs. ECOG-PS of 2–3, odds ratio [OR] = 6.34, 95% confidence interval [95% CI] 2.13–18.90, and OR = 3.66, 95% CI 1.33–10.03, respectively), and a history of irAE (OR = 3.28, 95% CI 1.19–9.01). Steroids were prescribed for 41/55 (75%) patients with ICU admission “likely” related to irAE. Three patients were subsequently treated with immunosuppressants. CONCLUSION: IrAEs accounted for half of ICU admissions in cancer patients receiving ICIs. They could be treated with steroids. Identifying the imputability of irAEs in ICU admissions remains a challenge. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13613-023-01122-z.
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spelling pubmed-101134022023-04-20 ICU admission for solid cancer patients treated with immune checkpoint inhibitors Toffart, Anne-Claire Meert, Anne-Pascale Wallet, Florent Gibelin, Aude Guisset, Olivier Gonzalez, Frédéric Seguin, Amélie Kouatchet, Achille Delaunay, Myriam Debieuvre, Didier Duchemann, Boris Rousseau-Bussac, Gaëlle Nyunga, Martine Grimaldi, David Levrat, Albrice Azoulay, Elie Lemiale, Virginie Ann Intensive Care Research BACKGROUND: Immune checkpoint inhibitors (ICI) have revolutionized the management of cancer. They can induce immune-related adverse events (irAE) leading to intensive care unit (ICU) admission. We aimed to describe irAEs for ICU admissions in solid cancer patients treated with ICIs. METHODS: This prospective multicenter study was conducted in France and Belgium. Adult patients with solid tumor and treated with systemic ICIs within the last 6 months, requiring non-programmed ICU admission were included. Patients admitted for microbiologically documented sepsis were excluded. Imputability of irAEs in ICU admissions was described according to the WHO-UMC classification system at ICU admission and at ICU discharge. The use of immunosuppressant treatment was reported. RESULTS: 115 patients were eligible. Solid tumor was mainly lung cancer (n = 76, 66%) and melanoma (n = 18, 16%). They were mainly treated with an anti-PD-(L)1 alone (n = 110, 96%). Main ICU admission reasons were acute respiratory failure (n = 66, 57%), colitis (n = 14, 13%), and cardiovascular disease (n = 13, 11%). ICU admission was considered “likely” associated with irAE for 48% (n = 55) of patients. Factors independently associated with irAE were a good ECOG performance status (PS) (ECOG-PS of 0 or 1 vs. ECOG-PS of 2–3, odds ratio [OR] = 6.34, 95% confidence interval [95% CI] 2.13–18.90, and OR = 3.66, 95% CI 1.33–10.03, respectively), and a history of irAE (OR = 3.28, 95% CI 1.19–9.01). Steroids were prescribed for 41/55 (75%) patients with ICU admission “likely” related to irAE. Three patients were subsequently treated with immunosuppressants. CONCLUSION: IrAEs accounted for half of ICU admissions in cancer patients receiving ICIs. They could be treated with steroids. Identifying the imputability of irAEs in ICU admissions remains a challenge. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13613-023-01122-z. Springer International Publishing 2023-04-18 /pmc/articles/PMC10113402/ /pubmed/37072645 http://dx.doi.org/10.1186/s13613-023-01122-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Toffart, Anne-Claire
Meert, Anne-Pascale
Wallet, Florent
Gibelin, Aude
Guisset, Olivier
Gonzalez, Frédéric
Seguin, Amélie
Kouatchet, Achille
Delaunay, Myriam
Debieuvre, Didier
Duchemann, Boris
Rousseau-Bussac, Gaëlle
Nyunga, Martine
Grimaldi, David
Levrat, Albrice
Azoulay, Elie
Lemiale, Virginie
ICU admission for solid cancer patients treated with immune checkpoint inhibitors
title ICU admission for solid cancer patients treated with immune checkpoint inhibitors
title_full ICU admission for solid cancer patients treated with immune checkpoint inhibitors
title_fullStr ICU admission for solid cancer patients treated with immune checkpoint inhibitors
title_full_unstemmed ICU admission for solid cancer patients treated with immune checkpoint inhibitors
title_short ICU admission for solid cancer patients treated with immune checkpoint inhibitors
title_sort icu admission for solid cancer patients treated with immune checkpoint inhibitors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113402/
https://www.ncbi.nlm.nih.gov/pubmed/37072645
http://dx.doi.org/10.1186/s13613-023-01122-z
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