The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study

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Standard

The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study. / D’souza, Maria; Nielsen, Dorte; Svane, Inge Marie; Iversen, Kasper; Rasmussen, Peter Vibe; Madelaire, Christian; Fosbøl, Emil; Køber, Lars; Gustafsson, Finn; Andersson, Charlotte; Gislason, Gunnar; Torp-pedersen, Christian; Schou, Morten.

I: European Heart Journal, Bind 42, Nr. 16, 2021, s. 1621-1631.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

D’souza, M, Nielsen, D, Svane, IM, Iversen, K, Rasmussen, PV, Madelaire, C, Fosbøl, E, Køber, L, Gustafsson, F, Andersson, C, Gislason, G, Torp-pedersen, C & Schou, M 2021, 'The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study', European Heart Journal, bind 42, nr. 16, s. 1621-1631. https://doi.org/10.1093/eurheartj/ehaa884

APA

D’souza, M., Nielsen, D., Svane, I. M., Iversen, K., Rasmussen, P. V., Madelaire, C., Fosbøl, E., Køber, L., Gustafsson, F., Andersson, C., Gislason, G., Torp-pedersen, C., & Schou, M. (2021). The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study. European Heart Journal, 42(16), 1621-1631. https://doi.org/10.1093/eurheartj/ehaa884

Vancouver

D’souza M, Nielsen D, Svane IM, Iversen K, Rasmussen PV, Madelaire C o.a. The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study. European Heart Journal. 2021;42(16):1621-1631. https://doi.org/10.1093/eurheartj/ehaa884

Author

D’souza, Maria ; Nielsen, Dorte ; Svane, Inge Marie ; Iversen, Kasper ; Rasmussen, Peter Vibe ; Madelaire, Christian ; Fosbøl, Emil ; Køber, Lars ; Gustafsson, Finn ; Andersson, Charlotte ; Gislason, Gunnar ; Torp-pedersen, Christian ; Schou, Morten. / The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study. I: European Heart Journal. 2021 ; Bind 42, Nr. 16. s. 1621-1631.

Bibtex

@article{4e735f94dff145c2a287f4af113ec319,
title = "The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study",
abstract = "AimsThe study aimed to estimate the risk of cardiac events in immune checkpoint inhibitor (ICI)-treated patients with lung cancer or malignant melanoma.Methods and resultsThe study included consecutive patients with lung cancer or malignant melanoma in 2011–17 nationwide in Denmark. The main composite outcome was cardiac events (arrhythmia, peri- or myocarditis, heart failure) or cardiovascular death. Absolute risks were estimated and the association of ICI and cardiac events was analysed in multivariable Cox models. We included 25 573 patients with lung cancer. Of these, 743 were treated with programmed cell death-1 inhibitor (PD1i) and their 1-year absolute risk of cardiac events was 9.7% [95% confidence interval (CI) 6.8–12.5]. Of the 13 568 patients with malignant melanoma, 145 had PD1i and 212 had cytotoxic T-lymphocyte-associated protein-4 inhibitor (CTLA-4i) treatment. Their 1-year risks were 6.6% (1.8–11.3) and 7.5% (3.7–11.3). The hazard rates of cardiac events were higher in patients with vs. without ICI treatment. Within 6 months from 1st ICI administration, the hazard ratios were 2.14 (95% CI 1.50–3.05) in patients with lung cancer and 4.30 (1.38–13.42) and 4.93 (2.45–9.94) in patients with malignant melanoma with PD1i and CTLA-4i, respectively. After 6 months, HRs were 2.26 (1.27–4.02) for patients with lung cancer and 3.48 (1.91–6.35) for patients with malignant melanoma and CTLA-4i.ConclusionsAmong patients with lung cancer and malignant melanoma, ICI treated had increased rates of cardiac events. The absolute risks were higher in these data compared with previous pharmacovigilance studies (e.g. 1.8% peri-/myocarditis 1-year risk).",
author = "Maria D{\textquoteright}souza and Dorte Nielsen and Svane, {Inge Marie} and Kasper Iversen and Rasmussen, {Peter Vibe} and Christian Madelaire and Emil Fosb{\o}l and Lars K{\o}ber and Finn Gustafsson and Charlotte Andersson and Gunnar Gislason and Christian Torp-pedersen and Morten Schou",
year = "2021",
doi = "10.1093/eurheartj/ehaa884",
language = "English",
volume = "42",
pages = "1621--1631",
journal = "European Heart Journal",
issn = "0195-668X",
publisher = "Oxford University Press",
number = "16",

}

RIS

TY - JOUR

T1 - The risk of cardiac events in patients receiving immune checkpoint inhibitors: a nationwide Danish study

AU - D’souza, Maria

AU - Nielsen, Dorte

AU - Svane, Inge Marie

AU - Iversen, Kasper

AU - Rasmussen, Peter Vibe

AU - Madelaire, Christian

AU - Fosbøl, Emil

AU - Køber, Lars

AU - Gustafsson, Finn

AU - Andersson, Charlotte

AU - Gislason, Gunnar

AU - Torp-pedersen, Christian

AU - Schou, Morten

PY - 2021

Y1 - 2021

N2 - AimsThe study aimed to estimate the risk of cardiac events in immune checkpoint inhibitor (ICI)-treated patients with lung cancer or malignant melanoma.Methods and resultsThe study included consecutive patients with lung cancer or malignant melanoma in 2011–17 nationwide in Denmark. The main composite outcome was cardiac events (arrhythmia, peri- or myocarditis, heart failure) or cardiovascular death. Absolute risks were estimated and the association of ICI and cardiac events was analysed in multivariable Cox models. We included 25 573 patients with lung cancer. Of these, 743 were treated with programmed cell death-1 inhibitor (PD1i) and their 1-year absolute risk of cardiac events was 9.7% [95% confidence interval (CI) 6.8–12.5]. Of the 13 568 patients with malignant melanoma, 145 had PD1i and 212 had cytotoxic T-lymphocyte-associated protein-4 inhibitor (CTLA-4i) treatment. Their 1-year risks were 6.6% (1.8–11.3) and 7.5% (3.7–11.3). The hazard rates of cardiac events were higher in patients with vs. without ICI treatment. Within 6 months from 1st ICI administration, the hazard ratios were 2.14 (95% CI 1.50–3.05) in patients with lung cancer and 4.30 (1.38–13.42) and 4.93 (2.45–9.94) in patients with malignant melanoma with PD1i and CTLA-4i, respectively. After 6 months, HRs were 2.26 (1.27–4.02) for patients with lung cancer and 3.48 (1.91–6.35) for patients with malignant melanoma and CTLA-4i.ConclusionsAmong patients with lung cancer and malignant melanoma, ICI treated had increased rates of cardiac events. The absolute risks were higher in these data compared with previous pharmacovigilance studies (e.g. 1.8% peri-/myocarditis 1-year risk).

AB - AimsThe study aimed to estimate the risk of cardiac events in immune checkpoint inhibitor (ICI)-treated patients with lung cancer or malignant melanoma.Methods and resultsThe study included consecutive patients with lung cancer or malignant melanoma in 2011–17 nationwide in Denmark. The main composite outcome was cardiac events (arrhythmia, peri- or myocarditis, heart failure) or cardiovascular death. Absolute risks were estimated and the association of ICI and cardiac events was analysed in multivariable Cox models. We included 25 573 patients with lung cancer. Of these, 743 were treated with programmed cell death-1 inhibitor (PD1i) and their 1-year absolute risk of cardiac events was 9.7% [95% confidence interval (CI) 6.8–12.5]. Of the 13 568 patients with malignant melanoma, 145 had PD1i and 212 had cytotoxic T-lymphocyte-associated protein-4 inhibitor (CTLA-4i) treatment. Their 1-year risks were 6.6% (1.8–11.3) and 7.5% (3.7–11.3). The hazard rates of cardiac events were higher in patients with vs. without ICI treatment. Within 6 months from 1st ICI administration, the hazard ratios were 2.14 (95% CI 1.50–3.05) in patients with lung cancer and 4.30 (1.38–13.42) and 4.93 (2.45–9.94) in patients with malignant melanoma with PD1i and CTLA-4i, respectively. After 6 months, HRs were 2.26 (1.27–4.02) for patients with lung cancer and 3.48 (1.91–6.35) for patients with malignant melanoma and CTLA-4i.ConclusionsAmong patients with lung cancer and malignant melanoma, ICI treated had increased rates of cardiac events. The absolute risks were higher in these data compared with previous pharmacovigilance studies (e.g. 1.8% peri-/myocarditis 1-year risk).

U2 - 10.1093/eurheartj/ehaa884

DO - 10.1093/eurheartj/ehaa884

M3 - Journal article

C2 - 33291147

VL - 42

SP - 1621

EP - 1631

JO - European Heart Journal

JF - European Heart Journal

SN - 0195-668X

IS - 16

ER -

ID: 261611536