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      Tales from the future—nuclear cardio-oncology, from prediction to diagnosis and monitoring

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          Abstract

          Cancer and cardiovascular diseases (CVD) often share common risk factors, and patients with CVD who develop cancer are at high risk of experiencing major adverse cardiovascular events. Additionally, cancer treatment can induce short- and long-term adverse cardiovascular events. Given the improvement in oncological patients’ prognosis, the burden in this vulnerable population is slowly shifting towards increased cardiovascular mortality. Consequently, the field of cardio-oncology is steadily expanding, prompting the need for new markers to stratify and monitor the cardiovascular risk in oncological patients before, during, and after the completion of treatment. Advanced non-invasive cardiac imaging has raised great interest in the early detection of CVD and cardiotoxicity in oncological patients. Nuclear medicine has long been a pivotal exam to robustly assess and monitor the cardiac function of patients undergoing potentially cardiotoxic chemotherapies. In addition, recent radiotracers have shown great interest in the early detection of cancer-treatment-related cardiotoxicity. In this review, we summarize the current and emerging nuclear cardiology tools that can help identify cardiotoxicity and assess the cardiovascular risk in patients undergoing cancer treatments and discuss the specific role of nuclear cardiology alongside other non-invasive imaging techniques.

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          Graphical Abstract

          Pathophysiological pathways interconnecting cancers and CVD: genetic predispositions, cardiovascular risk factors, and cancer-treatment-related cardiotoxicity. CVD in cancer patients (and corresponding nuclear cardiology tools) consist mainly of cancer-treatment-related cardiac dysfunction (explored with MUGA/ERNA), myocardial ischaemia (with nuclear MPI), and myocarditis (with 18F-FDG PET). Abbreviations: 18F-FDG, fluor-18-radiolabelled fluorodeoxyglucose; CVD, cardiovascular diseases; ERNA, equilibrium radionuclide angiography; MPI, myocardial perfusion imaging; MUGA, multigated acquisition; PET, positron emission tomography.

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          Oncology meets immunology: the cancer-immunity cycle.

          The genetic and cellular alterations that define cancer provide the immune system with the means to generate T cell responses that recognize and eradicate cancer cells. However, elimination of cancer by T cells is only one step in the Cancer-Immunity Cycle, which manages the delicate balance between the recognition of nonself and the prevention of autoimmunity. Identification of cancer cell T cell inhibitory signals, including PD-L1, has prompted the development of a new class of cancer immunotherapy that specifically hinders immune effector inhibition, reinvigorating and potentially expanding preexisting anticancer immune responses. The presence of suppressive factors in the tumor microenvironment may explain the limited activity observed with previous immune-based therapies and why these therapies may be more effective in combination with agents that target other steps of the cycle. Emerging clinical data suggest that cancer immunotherapy is likely to become a key part of the clinical management of cancer. Copyright © 2013 Elsevier Inc. All rights reserved.
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            Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging.

            The rapid technological developments of the past decade and the changes in echocardiographic practice brought about by these developments have resulted in the need for updated recommendations to the previously published guidelines for cardiac chamber quantification, which was the goal of the joint writing group assembled by the American Society of Echocardiography and the European Association of Cardiovascular Imaging. This document provides updated normal values for all four cardiac chambers, including three-dimensional echocardiography and myocardial deformation, when possible, on the basis of considerably larger numbers of normal subjects, compiled from multiple databases. In addition, this document attempts to eliminate several minor discrepancies that existed between previously published guidelines. Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2015. For permissions please email: journals.permissions@oup.com.
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              2021 ESC Guidelines on cardiovascular disease prevention in clinical practice

                Author and article information

                Contributors
                Journal
                Eur Heart J Cardiovasc Imaging
                Eur Heart J Cardiovasc Imaging
                ehjcimaging
                European Heart Journal Cardiovascular Imaging
                Oxford University Press (US )
                2047-2404
                2047-2412
                September 2023
                19 July 2023
                19 July 2023
                : 24
                : 9
                : 1129-1145
                Affiliations
                Department of Nuclear Medicine, University Hospital Zurich , Rämistrasse 100, 8091 Zurich, Switzerland
                Center for Molecular Cardiology, University of Zurich , Wagistrasse 12, 8952 Schlieren, Switzerland
                Department of Nuclear Medicine, Bichat University Hospital, AP-HP, University Diderot , 75018 Paris, France
                Nuclear Medicine, Institut de Cancérologie de Strasbourg Europe (ICANS), University Hospitals of Strasbourg , 67093 Strasbourg, France
                Molecular Imaging-DRHIM, IPHC, UMR 7178, CNRS/Unistra , 67093 Strasbourg, France
                Department of Nuclear Medicine, University Hospital Zurich , Rämistrasse 100, 8091 Zurich, Switzerland
                Kantonsspital Glarus , Burgstrasse 99, 8750 Glarus, Switzerland
                Department of Nuclear Medicine, University Hospital Zurich , Rämistrasse 100, 8091 Zurich, Switzerland
                Center for Molecular Cardiology, University of Zurich , Wagistrasse 12, 8952 Schlieren, Switzerland
                Department of Nuclear Medicine, University Hospital Zurich , Rämistrasse 100, 8091 Zurich, Switzerland
                Center for Molecular Cardiology, University of Zurich , Wagistrasse 12, 8952 Schlieren, Switzerland
                Imaging Department, Fondazione CNR/Regione Toscana Gabriele Monasterio , Via G. Moruzzi 1, 56124 Pisa, Italy
                Department of Nuclear Medicine, University Hospital Zurich , Rämistrasse 100, 8091 Zurich, Switzerland
                Department of Nuclear Medicine, University Hospital Zurich , Rämistrasse 100, 8091 Zurich, Switzerland
                Center for Molecular Cardiology, University of Zurich , Wagistrasse 12, 8952 Schlieren, Switzerland
                Department of Cardiology, University Hospital Inselspital Bern , Freiburgstrasse 18, 3010 Bern, Switzerland
                Department of Nuclear Medicine, University Hospital Zurich , Rämistrasse 100, 8091 Zurich, Switzerland
                Center for Molecular Cardiology, University of Zurich , Wagistrasse 12, 8952 Schlieren, Switzerland
                Author notes
                Corresponding author. E-mail: nidaa.mikail@ 123456gmail.com

                Conflict of interest: All authors have the following to disclose. The University Hospital of Zurich holds a research contract with GE Healthcare. C.G. has received research grants from the Novartis Foundation, Switzerland. A.M. has provided a consulting, advisory, or speaker role for Amgen, Astellas, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Gerresheimer, GSK, Janssen, Merck, MSD, Novartis, Roche, Sanofi, Servier, Takeda, and Vifor; has received research funding from Bayer, Sanofi, Gerresheimer (personal), and Merck & Cie (institutional); has intellectual property interests relating to Merck & Cie (not related to this report); has been paid to provide expert testimony for Sanofi; and has reported travel/accommodation expenses paid for by Amgen, Astellas, Boehringer Ingelheim, Janssen, Merck, Roche, Sanofi, and Servier.

                Author information
                https://orcid.org/0000-0003-4896-1428
                https://orcid.org/0000-0003-2424-3894
                https://orcid.org/0000-0003-3378-1723
                Article
                jead168
                10.1093/ehjci/jead168
                10501471
                37467476
                78a91257-4eab-484d-b15b-7060bf0f4ad3
                © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 April 2023
                : 07 July 2023
                : 26 July 2023
                Page count
                Pages: 17
                Categories
                Review
                AcademicSubjects/MED00200
                Editor's Choice
                Eurheartj/31
                Eurheartj/34
                Eurheartj/37
                Eurheartj/36

                Cardiovascular Medicine
                cardio-oncology,nuclear cardiology,pet,scintigraphy,fdg,myocardial perfusion imaging,cmr,echocardiography,ctrcd

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