Abstract
This position statement from the Heart Failure Association of the European Society of Cardiology Cardio-Oncology Study Group in collaboration with the International Cardio-Oncology Society presents practical, easy-to-use and evidence-based risk stratification tools for oncologists, haemato-oncologists and cardiologists to use in their clinical practice to risk stratify oncology patients prior to receiving cancer therapies known to cause heart failure or other serious cardiovascular toxicities. Baseline risk stratification proformas are presented for oncology patients prior to receiving the following cancer therapies: anthracycline chemotherapy, HER2-targeted therapies such as trastuzumab, vascular endothelial growth factor inhibitors, second and third generation multi-targeted kinase inhibitors for chronic myeloid leukaemia targeting BCR-ABL, multiple myeloma therapies (proteasome inhibitors and immunomodulatory drugs), RAF and MEK inhibitors or androgen deprivation therapies. Applying these risk stratification proformas will allow clinicians to stratify cancer patients into low, medium, high and very high risk of cardiovascular complications prior to starting treatment, with the aim of improving personalised approaches to minimise the risk of cardiovascular toxicity from cancer therapies.
Original language | English (US) |
---|---|
Pages (from-to) | 1945-1960 |
Number of pages | 16 |
Journal | European Journal of Heart Failure |
Volume | 22 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2020 |
Keywords
- Cardio-oncology
- Cardiotoxicity
- Heart failure
- Risk factors
- Risk prediction
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
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Baseline cardiovascular risk assessment in cancer patients scheduled to receive cardiotoxic cancer therapies : a position statement and new risk assessment tools from the Cardio-Oncology Study Group of the Heart Failure Association of the European Society of Cardiology in collaboration with the International Cardio-Oncology Society. / Lyon, Alexander R.; Dent, Susan; Stanway, Susannah et al.
In: European Journal of Heart Failure, Vol. 22, No. 11, 11.2020, p. 1945-1960.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Baseline cardiovascular risk assessment in cancer patients scheduled to receive cardiotoxic cancer therapies
T2 - a position statement and new risk assessment tools from the Cardio-Oncology Study Group of the Heart Failure Association of the European Society of Cardiology in collaboration with the International Cardio-Oncology Society
AU - Lyon, Alexander R.
AU - Dent, Susan
AU - Stanway, Susannah
AU - Earl, Helena
AU - Brezden-Masley, Christine
AU - Cohen-Solal, Alain
AU - Tocchetti, Carlo G.
AU - Moslehi, Javid J.
AU - Groarke, John D.
AU - Bergler-Klein, Jutta
AU - Khoo, Vincent
AU - Tan, Li Ling
AU - Anker, Markus S.
AU - von Haehling, Stephan
AU - Maack, Christoph
AU - Pudil, Radek
AU - Barac, Ana
AU - Thavendiranathan, Paaladinesh
AU - Ky, Bonnie
AU - Neilan, Tomas G.
AU - Belenkov, Yury
AU - Rosen, Stuart D.
AU - Iakobishvili, Zaza
AU - Sverdlov, Aaron L.
AU - Hajjar, Ludhmila A.
AU - Macedo, Ariane V.S.
AU - Manisty, Charlotte
AU - Ciardiello, Fortunato
AU - Farmakis, Dimitrios
AU - de Boer, Rudolf A.
AU - Skouri, Hadi
AU - Suter, Thomas M.
AU - Cardinale, Daniela
AU - Witteles, Ronald M.
AU - Fradley, Michael G.
AU - Herrmann, Joerg
AU - Cornell, Robert F.
AU - Wechelaker, Ashutosh
AU - Mauro, Michael J.
AU - Milojkovic, Dragana
AU - de Lavallade, Hugues
AU - Ruschitzka, Frank
AU - Coats, Andrew J.S.
AU - Seferovic, Petar M.
AU - Chioncel, Ovidiu
AU - Thum, Thomas
AU - Bauersachs, Johann
AU - Andres, M. Sol
AU - Wright, David J.
AU - López-Fernández, Teresa
AU - Plummer, Chris
AU - Lenihan, Daniel
N1 - Funding Information: A.R.L. is supported by the Fondation Leducq Network of Excellence in Cardio-Oncology. C.G.T. is supported by the grant ‘Ricerca di Ateneo Federico II 2017’. A.L.S. is supported by the Heart Foundation of Australia Future Leader Fellowship (Award ID 101918). J.M. is supported by R01 HL141466. R.A.d.B. is supported by the European Research Council (ERC CoG 818715, SECRETE-HF), and furthermore by the Netherlands Heart Foundation (CVON DOSIS, grant 2014-40, CVON SHE-PREDICTS-HF, grant 2017-21; CVON RED-CVD, grant 2017-11; and CVON PREDICT2, grant 2018-30); and the Innovational Research Incentives Scheme program of the Netherlands Organization for Scientific Research (NWO VIDI, grant 917.13.350). C.M. is supported by the German Research Foundation (DFG; SFB-894, TRR-219; Ma 2528/7-1) and the German Ministry of Education and Research (BMBF; 01EO1504). Funding Information: A.R.L. has received speaker, advisory board or consultancy fees and/or research grants from Pfizer, Novartis, Servier, Amgen, Takeda, Roche, Janssens‐Cilag Ltd, Clinigen Group, Eli Lily, Eisai, Bristol‐Myers Squibb, Ferring Pharmaceuticals and Boehringer Ingelheim. S.D. has received speaker, advisory board or research funding from Novartis, Eli Lilly, Genetech and Pfizer. S.S. has received speaker, advisory board or consultancy fees from Roche, Clinigen and Eli Lilly. H.E. has received grants from Roche and Sanofi‐Aventis, and advisory board or speaker fees from Daiichi‐Sankyo, AstraZeneca, INTAS Pharmaceuticals, Pfizer, Amgen and Prime Oncology. A.C.S. has received speaker, advisory board or consultancy fees and/or research grants from Novartis, Servier, Amgen, Abbott, Vifor, AstraZeneca, MSD, Roche, Takeda and Bristol‐Myers Squibb. J.M. has served as a consultant for Novartis, Pfizer, Bristol‐Myers Squibb, Takeda, Pharmacyclics, Regeneron, Myokardia, Audentes Pharmaceuticals, AstraZeneca, Deciphera, Ipsen, and Intrexon and has received grant funding from Pfizer and Bristol‐Myers Squibb. J.D.G. receives research funding from Amgen. T.G.N. has received speaker, advisory board or consultancy fees from Parexel, Intrinsic Imaging, Bristol‐Myers Squibb, H3 Biomedicine, Aprea Therapeutics. A.L.S. has received speaker fees, advisory board and/or research grants from Bayer, Biotronik, Novartis and Vifor. B.K. has received consultancy fees from Bristol‐Myers Squibb. C.G.T. received speaking fees from Alere. H.S. received honoraria for presentations from Servier, Novartis, AstraZeneca, Abbott and Boehringer Ingelheim. C.M. has received speak fees from Pfizer. R.F.C. has received advisory board or consultancy fees from Karyopharm Therapeutics, Takeda and Janssen. V.K. has participated in advisory boards, conferences and educational meetings for Accuray, Astellas, Bayer, Janssen and Boston Scientific. T.L.F. has received speaker fees from Janssen, Amgen, Servier, Daiichi‐Sankyo, MSD, and Philips. A.B. serves on DSMB for CTI Biopharma and has received honoraria from Bristol‐Myers Squibb. P.T. has received speaker fees from Boehringer Ingelheim, Takeda, Amgen. M.S.A. has received personal fees from Servier. D.F. has received consultation fees, speaker honoraria and/or travel grants from Abbott, Boehringer Ingelheim, Daiichi‐Sankyo, Menarini, Novartis, Pfizer, Roche and Servier. C.M. has received speaker, advisory board or consultancy fees from Servier, Amgen, Boehringer Ingelheim, Astra, Novartis, Bayer, Berlin Chemie, Bristol‐Myers Squibb, Daiichi‐Sankyo, Pfizer. S.D.R. has received speaker and advisory board consultancy fees from Servier, Novartis and Clinigen Group. M.G.F. has received advisory board fees from Novartis and research funding from Medtronic. Z.I. has received advisory board or speaker fees from Novartis, AstraZeneca, Boehringer Ingelheim, Pfizer, Bayer, Eli Lilly. T.T. is founder and shareholder of Cardior Pharmaceuticals, served in an advisory board of Novo Nordisk and received honoraria from Amicus Therapeutics and Sanofi‐Genzyme. J.B. has received speaker, advisory board or consultancy fees and/or research grants from Novartis, Vifor, Bayer, Servier, Abiomed, Boehringer Ingelheim, Daiichi‐Sankyo, AstraZeneca, CVRx, BMS, Pfizer, MSD, Abbott, Medtronic and Zoll not related to this manuscript. C.P. has received travel expenses and honoraria for speaking at educational meetings or advisory boards from Amgen, Bayer, Celgene, Ferring, Incyte, Novartis, Pfizer and Roche. Conflict of interest: Funding Information: A.R.L. is supported by the Fondation Leducq Network of Excellence in Cardio‐Oncology. C.G.T. is supported by the grant ‘Ricerca di Ateneo Federico II 2017’. A.L.S. is supported by the Heart Foundation of Australia Future Leader Fellowship (Award ID 101918). J.M. is supported by R01 HL141466. R.A.d.B. is supported by the European Research Council (ERC CoG 818715, SECRETE‐HF), and furthermore by the Netherlands Heart Foundation (CVON DOSIS, grant 2014‐40, CVON SHE‐PREDICTS‐HF, grant 2017‐21; CVON RED‐CVD, grant 2017‐11; and CVON PREDICT2, grant 2018‐30); and the Innovational Research Incentives Scheme program of the Netherlands Organization for Scientific Research (NWO VIDI, grant 917.13.350). C.M. is supported by the German Research Foundation (DFG; SFB‐894, TRR‐219; Ma 2528/7‐1) and the German Ministry of Education and Research (BMBF; 01EO1504). M.S.A. has received research support from the German Cardiovascular Research Center. Publisher Copyright: © 2020 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
PY - 2020/11
Y1 - 2020/11
N2 - This position statement from the Heart Failure Association of the European Society of Cardiology Cardio-Oncology Study Group in collaboration with the International Cardio-Oncology Society presents practical, easy-to-use and evidence-based risk stratification tools for oncologists, haemato-oncologists and cardiologists to use in their clinical practice to risk stratify oncology patients prior to receiving cancer therapies known to cause heart failure or other serious cardiovascular toxicities. Baseline risk stratification proformas are presented for oncology patients prior to receiving the following cancer therapies: anthracycline chemotherapy, HER2-targeted therapies such as trastuzumab, vascular endothelial growth factor inhibitors, second and third generation multi-targeted kinase inhibitors for chronic myeloid leukaemia targeting BCR-ABL, multiple myeloma therapies (proteasome inhibitors and immunomodulatory drugs), RAF and MEK inhibitors or androgen deprivation therapies. Applying these risk stratification proformas will allow clinicians to stratify cancer patients into low, medium, high and very high risk of cardiovascular complications prior to starting treatment, with the aim of improving personalised approaches to minimise the risk of cardiovascular toxicity from cancer therapies.
AB - This position statement from the Heart Failure Association of the European Society of Cardiology Cardio-Oncology Study Group in collaboration with the International Cardio-Oncology Society presents practical, easy-to-use and evidence-based risk stratification tools for oncologists, haemato-oncologists and cardiologists to use in their clinical practice to risk stratify oncology patients prior to receiving cancer therapies known to cause heart failure or other serious cardiovascular toxicities. Baseline risk stratification proformas are presented for oncology patients prior to receiving the following cancer therapies: anthracycline chemotherapy, HER2-targeted therapies such as trastuzumab, vascular endothelial growth factor inhibitors, second and third generation multi-targeted kinase inhibitors for chronic myeloid leukaemia targeting BCR-ABL, multiple myeloma therapies (proteasome inhibitors and immunomodulatory drugs), RAF and MEK inhibitors or androgen deprivation therapies. Applying these risk stratification proformas will allow clinicians to stratify cancer patients into low, medium, high and very high risk of cardiovascular complications prior to starting treatment, with the aim of improving personalised approaches to minimise the risk of cardiovascular toxicity from cancer therapies.
KW - Cardio-oncology
KW - Cardiotoxicity
KW - Heart failure
KW - Risk factors
KW - Risk prediction
UR - http://www.scopus.com/inward/record.url?scp=85089099624&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85089099624&partnerID=8YFLogxK
U2 - 10.1002/ejhf.1920
DO - 10.1002/ejhf.1920
M3 - Article
C2 - 32463967
AN - SCOPUS:85089099624
SN - 1388-9842
VL - 22
SP - 1945
EP - 1960
JO - European Journal of Heart Failure
JF - European Journal of Heart Failure
IS - 11
ER -