Cangrelor in Patients With Coronary Artery Disease Pretreated With Ticagrelor The Switching Antiplatelet (SWAP)-5 Study

被引:22
作者
Franchi, Francesco [1 ]
Ortega-Paz, Luis [1 ]
Rollini, Fabiana [1 ]
Galli, Mattia [1 ,2 ]
Been, Latonya [1 ]
Ghanem, Ghussan [1 ]
Shalhoub, Awss [1 ]
Ossi, Tiffany [1 ]
Rivas, Andrea [1 ]
Md, Xuan Zhou [1 ]
Pineda, Andres M. [1 ]
Suryadevara, Siva [1 ]
Soffer, Daniel [1 ]
Zenni, Martin M. [1 ]
Reiter, Birgit [3 ]
Jilma, Bernd [4 ]
Angiolillo, Dominick J. [1 ]
机构
[1] Univ Florida, Div Cardiol, Coll Med, Jacksonville, FL USA
[2] Maria Cecilia Hosp, GVM Care & Res, Cotignola, Italy
[3] Med Univ Vienna, Clin Inst Lab Med, Vienna, Austria
[4] Med Univ Vienna, Dept Clin Pharmacol, Vienna, Austria
关键词
cangrelor; pharmacodynamic; pharmacokinetic; platelets; switching; ticagrelor; PLATELET INHIBITION; CLOPIDOGREL; CONSENSUS; THERAPY; PRASUGREL; INTERVENTION; DEFINITIONS; TRANSITION; TRIALS;
D O I
10.1016/j.jcin.2022.10.034
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND There are no studies specifically designed to rule out a drug-drug interaction (DDI) when cangrelor is used among patients who have been pretreated with ticagrelor. OBJECTIVES This study sought to rule out a DDI among cangrelor-treated patients who have been pretreated with ticagrelor. METHODS In this prospective, randomized, double-blind, placebo-controlled, crossover, pharmacokinetic (PK) and pharmacodynamic ( PD) study, patients with coronary artery disease (N = 20) were pretreated with a 180-mg ticagrelor loading dose and after 1 hour randomized to placebo or cangrelor (bolus and infusion for 2 hours). Patients crossed over after 1 to 4 weeks of washout. PK analysis included ticagrelor plasma levels and its active metabolite. PD assessments included VerifyNow P2Y12 reaction units (PRU), light transmittance aggregometry, vasodilator-stimulated phosphoprotein, and Total Thrombus-Formation Analysis System. PK/PD assessments were performed at 7 time points. RESULTS Compared with placebo, adding cangrelor to patients pretreated with ticagrelor resulted in a significant reduction in PRU at 30 minutes and 1 hour after starting infusion. At 2 hours after stopping cangrelor/placebo infusion, PRU were low and similar in both groups (16.9 vs 12.6; mean difference: 4.3; 95% CI: similar to 28.6 to 37.3), meeting the noninferiority primary endpoint (predefined noninferiority margin 45 PRU). Consistent findings were shown with all PD assays. PK tracked PD findings with no differences between groups in plasma levels of ticagrelor and its metabolite. CONCLUSIONS Compared with placebo, the use of cangrelor in patients pretreated with ticagrelor results in enhanced platelet inhibition with no differences in PK/PD profiles after discontinuation of drug infusion indicating the absence of a DDI. (PD and PK Profiles of Switching Between Cangrelor and Ticagrelor Following Ticagrelor Pre-treatment [SWAP-5]; NCT04634162) (c) 2023 by the American College of Cardiology Foundation.
引用
收藏
页码:36 / 46
页数:11
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