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      The spectrum of cardiovascular complications related to immune-checkpoint inhibitor treatment : Including myocarditis and the new entity of non inflammatory left ventricular dysfunction

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          Abstract

          Background

          The full range of cardiovascular complications related to the use of Immune checkpoint inhibitors (ICI) is not fully understood. We aim to describe the spectrum of cardiovascular adverse events (cvAEs) by presenting our real-world experience of the diagnosis and management of these complications.

          Methods

          Two thousand six hundred and forty-seven (2647) patients were started on ICI treatment between 2014 and 2020. Data from 110 patients referred to the cardio-oncology service with a suspected cvAE was collected prospectively and analysed.

          Results

          Eighty-nine patients (3.4%) were confirmed to have cvAEs while on ICI therapy. Myocarditis was the most frequent event (33/89), followed by tachyarrhythmia (27/89), non-inflammatory left ventricular dysfunction (NILVD) (15/89) and pericarditis (7/89). Results from myocarditis and non-inflammatory left ventricular dysfunction cohorts were compared. Myocarditis and NILVD showed significant differences in respect toof troponin elevation, cardiac magnetic resonance abnormalities and ventricular function. Dual ICI therapy and other immune related adverse events were more frequently associated with myocarditis than NILVD. There was a significant difference in the median time from starting ICI treatment to presentation with myocarditis versus NILVD (12 vs 26 weeks p = 0.049). Through early recognition of myocarditis, prompt treatment with steroids and interruption of ICI, there were no cardiovascular in-hospital deaths. NILVD did not require steroid treatment and ICI could be restarted safely.

          Conclusions

          The full spectrum of cardiovascular complications in patients with immune checkpoint inhibitors is much broader than initially described. Myocarditis remains the most frequent cvAE related to ICI treatment. A novel type of myocardial injury was observed and defined as Atrial tachyarrhythmias and NILVD were also frequent in this cohort. NILVD has a This differs fromdifferent presentation from ICI-related myocarditis, mainly usually presenting afterby the lack of inflammatory features on CMR and biomarkers and a later presentation in time.

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          Most cited references21

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          OUP accepted manuscript

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            Cancer immunotherapy using checkpoint blockade

            The release of negative regulators of immune activation (immune checkpoints) that limit antitumor responses has resulted in unprecedented rates of long-lasting tumor responses in patients with a variety of cancers. This can be achieved by antibodies blocking the cytotoxic T lymphocyte antigen-4 (CTLA-4) or the programmed death-1 (PD-1) pathway, either alone or in combination. The main premise for inducing an immune response is the pre-existence of antitumor T cells that were limited by specific immune checkpoints. Most patients who have tumor responses maintain long lasting disease control, yet one third of patients relapse. Mechanisms of acquired resistance are currently poorly understood, but evidence points to alterations that converge on the antigen presentation and interferon gamma signaling pathways. New generation combinatorial therapies may overcome resistance mechanisms to immune checkpoint therapy.
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              2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC).

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                Author and article information

                Contributors
                m.andres@rbht.nhs.uk
                Journal
                Cardiooncology
                Cardiooncology
                Cardio-oncology
                BioMed Central (London )
                2057-3804
                24 November 2022
                24 November 2022
                2022
                : 8
                : 21
                Affiliations
                [1 ]GRID grid.420545.2, ISNI 0000 0004 0489 3985, Cardio-Oncology Service, , Royal Brompton Hospital, Guy’s and St. Thomas’ NHS Foundation Trust, ; Sydney Street, SW3 6NP London, UK
                [2 ]GRID grid.7445.2, ISNI 0000 0001 2113 8111, National Heart and Lung Institute, Imperial College London, ; London, UK
                [3 ]GRID grid.448878.f, ISNI 0000 0001 2288 8774, Department of Hospital Therapy N°1, , Sechenov University, ; Moscow, Russia
                [4 ]GRID grid.424926.f, ISNI 0000 0004 0417 0461, Royal Marsden Hospital Foundation Trust, ; London, UK
                Article
                147
                10.1186/s40959-022-00147-w
                9685864
                36424659
                904a239f-e56f-47ce-9523-5ce2df440b61
                © The Author(s) 2022

                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/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 29 July 2022
                : 7 November 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100012147, Royal Brompton and Harefield NHS Foundation Trust;
                Funded by: FundRef http://dx.doi.org/10.13039/501100001674, Fondation Leducq;
                Categories
                Research
                Custom metadata
                © The Author(s) 2022

                cancer survivorship,immunotherapy,myocarditis,cardiomyopathy

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