Management of cardiac disease in cancer patients throughout oncological treatment: ESMO consensus recommendations.


Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
02 2020
Historique:
received: 23 07 2019
revised: 18 10 2019
accepted: 21 10 2019
entrez: 22 1 2020
pubmed: 22 1 2020
medline: 7 1 2021
Statut: ppublish

Résumé

Cancer and cardiovascular (CV) disease are the most prevalent diseases in the developed world. Evidence increasingly shows that these conditions are interlinked through common risk factors, coincident in an ageing population, and are connected biologically through some deleterious effects of anticancer treatment on CV health. Anticancer therapies can cause a wide spectrum of short- and long-term cardiotoxic effects. An explosion of novel cancer therapies has revolutionised this field and dramatically altered cancer prognosis. Nevertheless, these new therapies have introduced unexpected CV complications beyond heart failure. Common CV toxicities related to cancer therapy are defined, along with suggested strategies for prevention, detection and treatment. This ESMO consensus article proposes to define CV toxicities related to cancer or its therapies and provide guidance regarding prevention, screening, monitoring and treatment of CV toxicity. The majority of anticancer therapies are associated with some CV toxicity, ranging from asymptomatic and transient to more clinically significant and long-lasting cardiac events. It is critical however, that concerns about potential CV damage resulting from anticancer therapies should be weighed against the potential benefits of cancer therapy, including benefits in overall survival. CV disease in patients with cancer is complex and treatment needs to be individualised. The scope of cardio-oncology is wide and includes prevention, detection, monitoring and treatment of CV toxicity related to cancer therapy, and also ensuring the safe development of future novel cancer treatments that minimise the impact on CV health. It is anticipated that the management strategies discussed herein will be suitable for the majority of patients. Nonetheless, the clinical judgment of physicians remains extremely important; hence, when using these best clinical practices to inform treatment options and decisions, practitioners should also consider the individual circumstances of their patients on a case-by-case basis.

Identifiants

pubmed: 31959335
pii: S0923-7534(19)36080-6
doi: 10.1016/j.annonc.2019.10.023
pmc: PMC8019325
mid: NIHMS1663331
pii:
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Journal Article Practice Guideline

Langues

eng

Sous-ensembles de citation

IM

Pagination

171-190

Subventions

Organisme : NCI NIH HHS
ID : R01 CA233610
Pays : United States

Informations de copyright

Copyright © 2019 European Society for Medical Oncology. Published by Elsevier Ltd. All rights reserved.

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Auteurs

G Curigliano (G)

European Institute of Oncology IRCCS, Milan, Italy; Department of Oncology and Haematology (DIPO), University of Milan, Milan, Italy.

D Lenihan (D)

Cardiovascular Division, Cardio-Oncology Center of Excellence, Washington University Medical Center, St. Louis, USA.

M Fradley (M)

Cardio-oncology Program, Division of Cardiovascular Medicine, Morsani College of Medicine and H. Lee Moffitt Cancer Center and Research Institute, University of South Florida, Tampa, USA.

S Ganatra (S)

Cardio-Oncology Program, Lahey Medical Center, Burlington.

A Barac (A)

Cardio-Oncology Program, Medstar Heart and Vascular Institute and MedStar Georgetown Cancer Institute, Georgetown University Hospital, Washington DC, USA.

A Blaes (A)

Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, USA.

J Herrmann (J)

Mayo Clinic College of Medicine, Rochester, USA.

C Porter (C)

University of Kansas Medical Center, Lawrence, USA.

A R Lyon (AR)

Royal Brompton Hospital and Imperial College, London, UK.

P Lancellotti (P)

GIGA Cardiovascular Sciences, Acute Care Unit, Heart Failure Clinic, CHU Sart Tilman, University Hospital of Liège, Liège, Belgium.

A Patel (A)

Morsani College of Medicine, University of South Florida, Tampa, USA.

J DeCara (J)

Medicine Section of Cardiology, University of Chicago, Chicago, USA.

J Mitchell (J)

Washington University Medical Center, St. Louis, USA.

E Harrison (E)

HCA Memorial Hospital and University of South Florida, Tampa, USA.

J Moslehi (J)

Vanderbilt University School of Medicine, Nashville, USA.

R Witteles (R)

Division of Cardiovascular Medicine, Falk CVRC, Stanford University School of Medicine, Stanford, USA.

M G Calabro (MG)

Department of Anesthesia and Intensive Care, IRCCS, San Raffaele Scientific Institute, Milan, Italy.

R Orecchia (R)

European Institute of Oncology IRCCS, Milan, Italy.

E de Azambuja (E)

Institut Jules Bordet and L'Université Libre de Bruxelles, Brussels, Belgium.

J L Zamorano (JL)

University Hospital Ramon y Cajal, Madrid, Spain.

R Krone (R)

Division of Cardiology, Washington University, St. Louis, USA.

Z Iakobishvili (Z)

Clalit Health Services, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

J Carver (J)

Division of Cardiology, Abramson Cancer Center, Hospital of the University of Pennsylvania, Philadelphia, USA.

S Armenian (S)

Department of Population Sciences, City of Hope Comprehensive Cancer Center, Duarte, USA.

B Ky (B)

University of Pennsylvania School of Medicine, Philadelphia, USA.

D Cardinale (D)

Cardioncology Unit, European Institute of Oncology, IRCCS, Milan, Italy.

C M Cipolla (CM)

Cardiology Department, European Institute of Oncology, IRCCS, Milan, Italy.

S Dent (S)

Duke Cancer Institute, Duke University, Durham, USA.

K Jordan (K)

Department of Medicine V, Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg, Germany.

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