TY - JOUR
T1 - Impact of malignancy on outcomes in European patients with atrial fibrillation
T2 - A report from the ESC-EHRA EURObservational research programme in atrial fibrillation general long-term registry
AU - Malavasi, Vincenzo L.
AU - Vitolo, Marco
AU - Proietti, Marco
AU - Diemberger, Igor
AU - Fauchier, Laurent
AU - Marin, Francisco
AU - Nabauer, Michael
AU - Potpara, T.
AU - Dan, Gheorghe Andrei
AU - Kalarus, Zbigniew
AU - Tavazzi, Luigi
AU - Maggioni, Aldo Pietro
AU - Lane, Deirdre A.
AU - Lip, Gregory Y.H.
AU - Boriani, Giuseppe
AU - the ESC-EHRA EORP-AF Long-Term General Registry Investigators
A2 - Goda, A.
A2 - Mairesse, G.
A2 - Shalganov, T.
A2 - Antoniades, L.
A2 - Taborsky, M.
A2 - Riahi, S.
A2 - Muda, P.
A2 - García Bolao, I.
A2 - Piot, O.
A2 - Etsadashvili, K.
A2 - Simantirakis, E. N.
A2 - Haim, M.
A2 - Azhari, A.
A2 - Najafian, J.
A2 - Santini, M.
A2 - Mirrakhimov, E.
A2 - Kulzida, K.
A2 - Erglis, A.
A2 - Poposka, L.
A2 - Burg, M. R.
A2 - Crijns, H. J.G.M.
A2 - Erküner, null
A2 - Atar, D.
A2 - Lenarczyk, R.
A2 - Martins Oliveira, M.
A2 - Shah, D.
A2 - Serdechnaya, E.
A2 - Zëra, E.
A2 - Jubele, K.
A2 - Kalejs, O.
N1 - Funding Information:
Since the start of EORP, the following companies have supported the programme: Abbott Vascular Int. (2011–2021), Amgen Cardiovascular (2009–2018), AstraZeneca (2014–2021), Bayer (2009–2018), Boehringer Ingelheim (2009–2019), Boston Scientific (2009–2012), The Bristol-Myers Squibb and Pfizer Alliance (2011–2016), The Alliance Daiichi Sankyo Europe GmbH and Eli Lilly and Company (2011–2017), Edwards (2016–2019), Gedeon Richter Plc. (2014–2017), Menarini Int. Op. (2009–2012), MSD-Merck & Co. (2011–2014), Novartis Pharma AG (2014–2020), ResMed (2014–2016), Sanofi (2009–2011), SERVIER (2010–2021) and Vifor (2019–2022). EORP Oversight Committee, Executive and Steering Committees (National Coordinators) of the EURObservational Research Programme (EORP)—Atrial Fibrillation General Long-Term (EORP—AFGen LT) Registry of the European Society of Cardiology (ESC). Data collection was conducted by the EORP department by Patti-Ann McNeill as Project Officer and Viviane Missiamenou as Data Manager. Overall activities were coordinated and supervised by Doctor Aldo P. Maggioni (EORP Scientific Coordinator).
Publisher Copyright:
© 2022 Stichting European Society for Clinical Investigation Journal Foundation. Published by John Wiley & Sons Ltd.
PY - 2022/7
Y1 - 2022/7
N2 - Background: The management of patients with atrial fibrillation (AF) and malignancy is challenging given the paucity of evidence supporting their appropriate clinical management. Purpose: To evaluate the outcomes of patients with active or prior malignancy in a contemporary cohort of European AF patients. Methods: Patients enrolled in the EURObservational Research Programme in AF General Long-Term Registry were categorized into 3 categories: No Malignancy (NoMal), Prior Malignancy (PriorMal) and Active Malignancy (ActiveMal). The primary outcomes were all-cause death and the composite outcome MACE. Results: A total of 10 383 patients were analysed. Of these, 9597 (92.4%) were NoMal patients, 577 (5.6%) PriorMal and 209 (2%) ActiveMal. Lack of any antithrombotic treatment was more prevalent in ActiveMal patients (12.4%) as compared to other groups (5.0% vs 6.3% for PriorMal and NoMal, p <.001). After a median follow-up of 730 days, there were 982 (9.5%) deaths and 950 (9.7%) MACE events. ActiveMal was independently associated with a higher risk for all-cause death (HR 2.90, 95% CI 2.23–3.76) and MACE (HR 1.54, 95% CI 1.03–2.31), as well as any haemorrhagic events and major bleeding (OR 2.42, 95% CI 1.49–3.91 and OR 4.18, 95% CI 2.49–7.01, respectively). Use of oral anticoagulants was not significantly associated with a higher risk for all-cause death or bleeding in ActiveMal patients. Conclusions: In a large contemporary cohort of AF patients, active malignancy was independently associated with all-cause death, MACE and haemorrhagic events. Use of anticoagulants was not associated with a higher risk of all-cause death in patients with active malignancies.
AB - Background: The management of patients with atrial fibrillation (AF) and malignancy is challenging given the paucity of evidence supporting their appropriate clinical management. Purpose: To evaluate the outcomes of patients with active or prior malignancy in a contemporary cohort of European AF patients. Methods: Patients enrolled in the EURObservational Research Programme in AF General Long-Term Registry were categorized into 3 categories: No Malignancy (NoMal), Prior Malignancy (PriorMal) and Active Malignancy (ActiveMal). The primary outcomes were all-cause death and the composite outcome MACE. Results: A total of 10 383 patients were analysed. Of these, 9597 (92.4%) were NoMal patients, 577 (5.6%) PriorMal and 209 (2%) ActiveMal. Lack of any antithrombotic treatment was more prevalent in ActiveMal patients (12.4%) as compared to other groups (5.0% vs 6.3% for PriorMal and NoMal, p <.001). After a median follow-up of 730 days, there were 982 (9.5%) deaths and 950 (9.7%) MACE events. ActiveMal was independently associated with a higher risk for all-cause death (HR 2.90, 95% CI 2.23–3.76) and MACE (HR 1.54, 95% CI 1.03–2.31), as well as any haemorrhagic events and major bleeding (OR 2.42, 95% CI 1.49–3.91 and OR 4.18, 95% CI 2.49–7.01, respectively). Use of oral anticoagulants was not significantly associated with a higher risk for all-cause death or bleeding in ActiveMal patients. Conclusions: In a large contemporary cohort of AF patients, active malignancy was independently associated with all-cause death, MACE and haemorrhagic events. Use of anticoagulants was not associated with a higher risk of all-cause death in patients with active malignancies.
KW - all-cause death
KW - atrial fibrillation
KW - cancer
KW - malignancy
KW - NOACs
KW - registry
UR - http://www.scopus.com/inward/record.url?scp=85131903509&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/35305020/
U2 - 10.1111/eci.13773
DO - 10.1111/eci.13773
M3 - Article
C2 - 35305020
AN - SCOPUS:85131903509
SN - 0014-2972
VL - 52
JO - European Journal of Clinical Investigation
JF - European Journal of Clinical Investigation
IS - 7
M1 - e13773
ER -