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      Cardiovascular Toxicity Related to Cancer Treatment: A Pragmatic Approach to the American and European Cardio‐Oncology Guidelines

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          Abstract

          The considerable progress made in the field of cancer treatment has led to a dramatic improvement in the prognosis of patients with cancer. However, toxicities resulting from these treatments represent a cost that can be harmful to short‐ and long‐term outcomes. Adverse events affecting the cardiovascular system are one of the greatest challenges in the overall management of patients with cancer, as they can compromise the success of the optimal treatment against the tumor. Such adverse events are associated not only with older chemotherapy drugs such as anthracyclines but also with many targeted therapies and immunotherapies. Recognizing this concern, several American and European governing societies in oncology and cardiology have published guidelines on the cardiovascular monitoring of patients receiving potentially cardiotoxic cancer therapies, as well as on the management of cardiovascular toxicities. However, the low level of evidence supporting these guidelines has led to numerous discrepancies, leaving clinicians without a consensus strategy to apply. A cardio‐oncology expert panel from the French Working Group of Cardio‐Oncology has undertaken an ambitious effort to analyze and harmonize the most recent American and European guidelines to propose roadmaps and decision algorithms that would be easy for clinicians to use in their daily practice. In this statement, the experts addressed the cardiovascular monitoring strategies for the cancer drugs associated with the highest risk of cardiovascular toxicities, as well as the management of such toxicities.

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          Most cited references72

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          2018 ESC/ESH Guidelines for the management of arterial hypertension

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            2016 European Guidelines on cardiovascular disease prevention in clinical practice: The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts)Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR).

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              Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: American Society of Clinical Oncology Clinical Practice Guideline

              Purpose To increase awareness, outline strategies, and offer guidance on the recommended management of immune-related adverse events in patients treated with immune checkpoint inhibitor (ICPi) therapy. Methods A multidisciplinary, multi-organizational panel of experts in medical oncology, dermatology, gastroenterology, rheumatology, pulmonology, endocrinology, urology, neurology, hematology, emergency medicine, nursing, trialist, and advocacy was convened to develop the clinical practice guideline. Guideline development involved a systematic review of the literature and an informal consensus process. The systematic review focused on guidelines, systematic reviews and meta-analyses, randomized controlled trials, and case series published from 2000 through 2017. Results The systematic review identified 204 eligible publications. Much of the evidence consisted of systematic reviews of observational data, consensus guidelines, case series, and case reports. Due to the paucity of high-quality evidence on management of immune-related adverse events, recommendations are based on expert consensus. Recommendations Recommendations for specific organ system-based toxicity diagnosis and management are presented. While management varies according to organ system affected, in general, ICPi therapy should be continued with close monitoring for grade 1 toxicities, with the exception of some neurologic, hematologic, and cardiac toxicities. ICPi therapy may be suspended for most grade 2 toxicities, with consideration of resuming when symptoms revert to grade 1 or less. Corticosteroids may be administered. Grade 3 toxicities generally warrant suspension of ICPis and the initiation of high-dose corticosteroids (prednisone 1 to 2 mg/kg/d or methylprednisolone 1 to 2 mg/kg/d). Corticosteroids should be tapered over the course of at least 4 to 6 weeks. Some refractory cases may require infliximab or other immunosuppressive therapy. In general, permanent discontinuation of ICPis is recommended with grade 4 toxicities, with the exception of endocrinopathies that have been controlled by hormone replacement. Additional information is available at www.asco.org/supportive-care-guidelines and www.asco.org/guidelineswiki .
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                Author and article information

                Contributors
                franck.thuny@gmail.com
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                05 September 2020
                15 September 2020
                : 9
                : 18 ( doiID: 10.1002/jah3.v9.18 )
                : e018403
                Affiliations
                [ 1 ] PICARO Cardio‐Oncology Program Department of Pharmacology Department of Cardiology Caen Hospital Medical School Caen‐Normandy University Caen France
                [ 2 ] Unit of Heart Failure and Valvular Heart Diseases Department of Cardiology Nord Hospital Center for CardioVascular and Nutrition Research (C2VN) University Mediterranean Center of Cardio‐Oncology (MEDI‐CO Center) Assistance Publique – Hôpitaux de Marseille Aix‐Marseille University Marseille France
                [ 3 ] Mediterranean Group of Cardio‐Oncology (gMEDICO) Marseille France
                [ 4 ] UNICO‐GRECO Cardio‐Oncology Program Department of Cardiology Saint‐Antoine Hospital Tenon Hospital Inserm 856 Assistance Publique – Hôpitaux de Paris Sorbonne University Paris France
                [ 5 ] Department of Hematology Caen Hospital Medical School Caen‐Normandy University Caen France
                [ 6 ] UNICO‐GRECO Cardio‐Oncology Program Department of Pharmacology Centre d’Investigation Clinique Paris‐Est Pitié‐Salpêtrière Hospital Assistance Publique – Hôpitaux de Paris Sorbonne University Paris France
                [ 7 ] Drug Development Department (DITEP) Gustave Roussy Paris‐Saclay University Villejuif France
                [ 8 ] Departement of Hematology Conception Hospital Assistance Publique – Hôpitaux de Marseille Aix‐Marseille University Marseille France
                [ 9 ] Departement of Hematology Paoli‐Calmettes Cancer Institute Aix‐Marseille University Marseille France
                [ 10 ] Unit of Cardio‐Oncology and Prevention European Georges Pompidou Hospital Assistance Publique – Hôpitaux de Paris Sorbonne University Paris France
                [ 11 ] Department of Cardiology Lariboisière Hospital UMR‐S 942 Assistance Publique – Hôpitaux de Paris Paris University Paris France
                Author notes
                [*] [* ] Correspondence to: Franck Thuny, MD, PhD, Unit of Heart Failure and Valvular Heart Diseases, Hôpital NORD, University Mediterranean Centre of Cardio‐Oncology Center, Chemin des Bourrely, Aix‐Marseille University, 13015 Marseille, France. E‐mail: franck.thuny@ 123456gmail.com

                [†]

                Dr Alexandre and Dr Cautela contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-0331-3307
                https://orcid.org/0000-0002-8727-7154
                Article
                JAH35466
                10.1161/JAHA.120.018403
                7727003
                32893704
                6d6a80bf-9122-4632-a9ce-c117137af83a
                © 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 07 July 2020
                : 21 July 2020
                : 23 July 2020
                Page count
                Figures: 5, Tables: 2, Pages: 33, Words: 25161
                Funding
                Funded by: Fédération Française de Cardiologie , open-funder-registry 10.13039/501100003100;
                Categories
                Special Report
                Special Report
                Custom metadata
                2.0
                15 September 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.1 mode:remove_FC converted:30.09.2020

                Cardiovascular Medicine
                cancer,cardio‐oncology,cardiotoxicity,guidelines
                Cardiovascular Medicine
                cancer, cardio‐oncology, cardiotoxicity, guidelines

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