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Cardiovascular events after the initiation of immune checkpoint inhibitors
We sought to clarify the incidence of major adverse cardiac events (MACE) after the initiation of immune checkpoint inhibitors (ICIs). We analyzed the JMDC Claims Database between 2005 and 2021. The study included 2972 patients with no history of cardiovascular disease and a prescription for an ICI....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220239/ https://www.ncbi.nlm.nih.gov/pubmed/37251893 http://dx.doi.org/10.1016/j.heliyon.2023.e16373 |
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author | Suzuki, Yuta Kaneko, Hidehiro Tamura, Yuichi Okada, Akira Fujiu, Katsuhito Michihata, Nobuaki Takeda, Norifumi Jo, Taisuke Morita, Hiroyuki Node, Koichi Yasunaga, Hideo Komuro, Issei |
author_facet | Suzuki, Yuta Kaneko, Hidehiro Tamura, Yuichi Okada, Akira Fujiu, Katsuhito Michihata, Nobuaki Takeda, Norifumi Jo, Taisuke Morita, Hiroyuki Node, Koichi Yasunaga, Hideo Komuro, Issei |
author_sort | Suzuki, Yuta |
collection | PubMed |
description | We sought to clarify the incidence of major adverse cardiac events (MACE) after the initiation of immune checkpoint inhibitors (ICIs). We analyzed the JMDC Claims Database between 2005 and 2021. The study included 2972 patients with no history of cardiovascular disease and a prescription for an ICI. The primary outcome was the incidence of MACE, including myocarditis, pericarditis, Takotsubo cardiomyopathy, atrio-ventricular block, heart failure, myocardial infarction, and stroke. The median age of study participants was 59 (Q1-Q3 53–65) years, and 2163 participants (72.8%) were male. Lung cancer was the most common cancer site (n = 1603). Among ICIs, programmed cell death-1 (PD-1) was most frequently used, and a combination ICI treatment was conducted in 110 patients (3.7%). During a mean follow-up of 358 ± 327 days, 419 MACE events were recorded. The incidence rate of myocarditis, pericarditis, Takotsubo cardiomyopathy, atrio-ventricular block, heart failure, myocardial infarction, and stroke was 3.4, 142.3, 10.3, 17.2, 1191.2, 55.2, and 278.5 per 10,000 person-years, respectively. The incidence of cardiovascular events was higher within 180 days after the initial prescription of ICI. The continuation rate of ICI after MACE was 38.4%. In conclusion, our analysis of a nationwide epidemiological dataset demonstrated the incidence of MACE after the initiation of ICI treatment. The incidence of heart failure was higher than expected, and the continuation rate of ICI treatment after MACE was low. Our results indicated the importance of monitoring and prevention of cardiovascular events in cancer patients requiring ICI treatment. |
format | Online Article Text |
id | pubmed-10220239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102202392023-05-28 Cardiovascular events after the initiation of immune checkpoint inhibitors Suzuki, Yuta Kaneko, Hidehiro Tamura, Yuichi Okada, Akira Fujiu, Katsuhito Michihata, Nobuaki Takeda, Norifumi Jo, Taisuke Morita, Hiroyuki Node, Koichi Yasunaga, Hideo Komuro, Issei Heliyon Research Article We sought to clarify the incidence of major adverse cardiac events (MACE) after the initiation of immune checkpoint inhibitors (ICIs). We analyzed the JMDC Claims Database between 2005 and 2021. The study included 2972 patients with no history of cardiovascular disease and a prescription for an ICI. The primary outcome was the incidence of MACE, including myocarditis, pericarditis, Takotsubo cardiomyopathy, atrio-ventricular block, heart failure, myocardial infarction, and stroke. The median age of study participants was 59 (Q1-Q3 53–65) years, and 2163 participants (72.8%) were male. Lung cancer was the most common cancer site (n = 1603). Among ICIs, programmed cell death-1 (PD-1) was most frequently used, and a combination ICI treatment was conducted in 110 patients (3.7%). During a mean follow-up of 358 ± 327 days, 419 MACE events were recorded. The incidence rate of myocarditis, pericarditis, Takotsubo cardiomyopathy, atrio-ventricular block, heart failure, myocardial infarction, and stroke was 3.4, 142.3, 10.3, 17.2, 1191.2, 55.2, and 278.5 per 10,000 person-years, respectively. The incidence of cardiovascular events was higher within 180 days after the initial prescription of ICI. The continuation rate of ICI after MACE was 38.4%. In conclusion, our analysis of a nationwide epidemiological dataset demonstrated the incidence of MACE after the initiation of ICI treatment. The incidence of heart failure was higher than expected, and the continuation rate of ICI treatment after MACE was low. Our results indicated the importance of monitoring and prevention of cardiovascular events in cancer patients requiring ICI treatment. Elsevier 2023-05-18 /pmc/articles/PMC10220239/ /pubmed/37251893 http://dx.doi.org/10.1016/j.heliyon.2023.e16373 Text en © 2023 The Authors. Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Suzuki, Yuta Kaneko, Hidehiro Tamura, Yuichi Okada, Akira Fujiu, Katsuhito Michihata, Nobuaki Takeda, Norifumi Jo, Taisuke Morita, Hiroyuki Node, Koichi Yasunaga, Hideo Komuro, Issei Cardiovascular events after the initiation of immune checkpoint inhibitors |
title | Cardiovascular events after the initiation of immune checkpoint inhibitors |
title_full | Cardiovascular events after the initiation of immune checkpoint inhibitors |
title_fullStr | Cardiovascular events after the initiation of immune checkpoint inhibitors |
title_full_unstemmed | Cardiovascular events after the initiation of immune checkpoint inhibitors |
title_short | Cardiovascular events after the initiation of immune checkpoint inhibitors |
title_sort | cardiovascular events after the initiation of immune checkpoint inhibitors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220239/ https://www.ncbi.nlm.nih.gov/pubmed/37251893 http://dx.doi.org/10.1016/j.heliyon.2023.e16373 |
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