YINGLONG: A Multicenter, Prospective, Non-Interventional Study Evaluating the Safety and Tolerability of Ticagrelor in Chinese Patients with Acute Coronary Syndrome

Xin Du, Yang Zheng, Ping Yang, Shuren Ma, Zaixin Yu, Xi Su, Junbo Ge, Maria Leonsson-Zachrisson, Xianhong Wang, Jing Sun, Lu Bai, Chang-Sheng Ma, YINGLONG study investigators, Xin Du, Yang Zheng, Ping Yang, Shuren Ma, Zaixin Yu, Xi Su, Junbo Ge, Maria Leonsson-Zachrisson, Xianhong Wang, Jing Sun, Lu Bai, Chang-Sheng Ma, YINGLONG study investigators

Abstract

Introduction: Ticagrelor is an oral, reversible, direct-acting P2Y12 receptor inhibitor approved for the prevention of cardiovascular events in acute coronary syndrome (ACS). In China, drug intensive monitoring regulations for new drugs require additional safety data post-approval.

Methods: YINGLONG, a single-arm, phase-IV, 1-year, non-interventional study, described the safety of ticagrelor 90 mg twice daily in Chinese patients (≥ 18 years) with ACS treated with ≥ 1 dose of ticagrelor. Primary outcomes were the incidence of adverse events (AEs), in particular, PLATelet inhibition and patient Outcomes (PLATO)-defined bleeding AEs, and other serious AEs during the 1-year follow-up. Key secondary outcomes were the incidence of major cardiovascular events.

Results: Patients (n = 1041, median age 61.0 years) had started ticagrelor and had post-dose data. Median duration of ticagrelor treatment was 357 days; 577 patients (55.4%) completed 1-year ticagrelor treatment; 973 patients (93.5%) completed 1-year follow-up. Overall, 38.7% of patients reported an AE during treatment. The most common AEs were dyspnea (n = 37, 3.6%), petechiae (n = 30, 2.9%), and chest discomfort (n = 28, 2.7%). Serious AEs, excluding bleeding, were reported in 9.8% of patients during treatment. Incidence of PLATO-defined major bleeding events was 1.1% (n = 11). Of the 21 deaths that occurred during the study (8 post-treatment), 1 was a fatal bleed. Major cardiovascular events were reported in 37 patients (3.6%).

Conclusions: Ticagrelor was well tolerated with a low rate of PLATO-defined major bleeding events in Chinese ACS patients. Safety results were consistent with the known ticagrelor profile.

Trial registration: ClinicalTrials.gov identifier, NCT02430493.

Funding: AstraZeneca Investment (China) Co., Ltd.

Keywords: Acute coronary syndrome; Bleeding; Cardiology; Chinese patients; Safety; Ticagrelor.

Figures

Fig. 1
Fig. 1
Patient disposition. *Three patients who discontinued ticagrelor before providing informed consent are excluded. AE adverse event, CABG coronary artery bypass grafting
Fig. 2
Fig. 2
Kaplan–Meier plot of time to first major cardiovascular event during the study. CV cardiovascular

References

    1. National Center for Cardiovascular Diseases, China. Report on cardiovascular diseases in China 2017 [in Chinese]. . Accessed 21 Jun 2018.
    1. Kolansky DM. Acute coronary syndromes: morbidity, mortality, and pharmacoeconomic burden. Am J Manag Care. 2009;15(2 suppl):S36–S41.
    1. Ruff CT, Braunwald E. The evolving epidemiology of acute coronary syndromes. Nat Rev Cardiol. 2011;8(3):140–147. doi: 10.1038/nrcardio.2010.199.
    1. Gao R, Patel A, Gao W, CPACS Investigators et al. Prospective observational study of acute coronary syndromes in China: practice patterns and outcomes. Heart. 2008;94(5):554–560. doi: 10.1136/hrt.2007.119750.
    1. Huo Y, Han Y, Ge J, et al. Two-year outcomes post discharge in Chinese patients with acute coronary syndrome: findings from the EPICOR Asia study. J Am Coll Cardiol. 2016;67(13):505. doi: 10.1016/S0735-1097(16)30506-X.
    1. Hao Y, Liu J, Liu J, et al. Rationale and design of the Improving Care for Cardiovascular Disease in China (CCC) project: a national effort to prompt quality enhancement for acute coronary syndrome. Am Heart J. 2016;179:107–115. doi: 10.1016/j.ahj.2016.06.005.
    1. Husted S, van Giezen JJ. Ticagrelor: the first reversibly binding oral P2Y12 receptor antagonist. Cardiovasc Ther. 2009;27(4):259–274. doi: 10.1111/j.1755-5922.2009.00096.x.
    1. Highlights of US prescribing information (BRILINTA®). 2018. . Accessed 1 Jan 2019.
    1. van Giezen JJ, Nilsson L, Berntsson P, et al. Ticagrelor binds to human P2Y12 independently from ADP but antagonizes ADP-induced receptor signaling and platelet aggregation. J Thromb Haemost. 2009;7(9):1556–1565. doi: 10.1111/j.1538-7836.2009.03527.x.
    1. Storey RF, Husted S, Harrington RA, et al. Inhibition of platelet aggregation by AZD6140, a reversible oral P2Y12 receptor antagonist, compared with clopidogrel in patients with acute coronary syndromes. J Am Coll Cardiol. 2007;50(19):1852–1856. doi: 10.1016/j.jacc.2007.07.058.
    1. Armstrong D, Summers C, Ewart L, Nylander S, Sidaway JE, van Giezen JJ. Characterization of the adenosine pharmacology of ticagrelor reveals therapeutically relevant inhibition of equilibrative nucleoside transporter 1. J Cardiovasc Pharmacol Ther. 2014;19(2):209–219. doi: 10.1177/1074248413511693.
    1. Highlights of China prescribing information (BRILINTA®). 2017. . Accessed 1 Jan 2019.
    1. Valgimigli M, Bueno H, Byrne RA, et al. 2017 ESC focused update on dual antiplatelet therapy in coronary artery disease developed in collaboration with EACTS. Kardiol Pol. 2017;75(12):1217–1299.
    1. Chinese Society of Cardiology and Chinese College of Cardiovascular Physicians 2016 China percutaneous coronary intervention guidelines. Chin J Cardiol. 2016;2016(44):382–400.
    1. Chinese Society of Cardiology 2016 Non–ST-segment elevation acute coronary syndrome diagnosis and treatment guidelines. Chin J Cardiol. 2017;45:359–376.
    1. Wallentin L, Becker RC, Budaj A, et al. Ticagrelor versus clopidogrel in patients with acute coronary syndromes. N Engl J Med. 2009;361(11):1045–1057. doi: 10.1056/NEJMoa0904327.
    1. Kang HJ, Clare RM, Gao R, PLATO Investigators et al. Ticagrelor versus clopidogrel in Asian patients with acute coronary syndrome: a retrospective analysis from the Platelet Inhibition and Patient Outcomes (PLATO) Trial. Am Heart J. 2015;169(6):899–905.e1. doi: 10.1016/j.ahj.2015.03.015.
    1. Gao R, Wu Y, Liu H, DAYU study investigators et al. Safety and incidence of cardiovascular events in Chinese patients with acute coronary syndrome treated with ticagrelor: the 12-month, phase IV, multicenter, single-arm DAYU study. Cardiovasc Drugs Ther. 2018;32(1):47–56. doi: 10.1007/s10557-018-6772-3.
    1. Bi Y, Gao R, Patel A, CPACS Investigators et al. Evidence-based medication use among Chinese patients with acute coronary syndromes at the time of hospital discharge and 1 year after hospitalization: results from the Clinical Pathways for Acute Coronary Syndromes in China (CPACS) study. Am Heart J. 2009;157(3):509–16.e1. doi: 10.1016/j.ahj.2008.09.026.
    1. Goto S, Huang CH, Park SJ, Emanuelsson H, Kimura T. Ticagrelor vs. clopidogrel in Japanese, Korean and Taiwanese patients with acute coronary syndrome—randomized, double-blind, phase III PHILO study. Circ J. 2015;79(11):2452–2460. doi: 10.1253/circj.CJ-15-0112.
    1. Guo YM, Zhao ZC, Zhang L, Li HZ, Li Z, Sun HL. CYP2C19 polymorphisms in acute coronary syndrome patients undergoing clopidogrel therapy in Zhengzhou population. Genet Mol Res. 2016;15(2).
    1. Tam CC, Kwok J, Wong A, et al. Genotyping-guided approach versus the conventional approach in selection of oral P2Y12 receptor blockers in Chinese patients suffering from acute coronary syndrome. J Int Med Res. 2017;45(1):134–146. doi: 10.1177/0300060516677190.
    1. Xie X, Ma Y-T, Yang Y-N, et al. CYP2C19 phenotype, stent thrombosis, myocardial infarction, and mortality in patients with coronary stent placement in a Chinese population. PLoS ONE. 2013;8(3):e59344. doi: 10.1371/journal.pone.0059344.
    1. Ma TK, Lam YY, Tan VP, Yan BP. Variability in response to clopidogrel: how important are pharmacogenetics and drug interactions? Br J Clin Pharmacol. 2011;72(4):697–706. doi: 10.1111/j.1365-2125.2011.03949.x.

Source: PubMed

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