Cangrelor With and Without Glycoprotein IIb/IIIa Inhibitors in Patients Undergoing Percutaneous Coronary Intervention

Cangrelor, an intravenous, reversible P2Y12 antagonist, is approved for use in patients undergoing percutaneous coronary intervention (PCI). This study sought to evaluate the efficacy and safety of cangrelor compared with clopidogrel in subgroups that did and did not receive glycoprotein IIb/IIIa in...

Full description

Saved in:
Bibliographic Details
Published inJournal of the American College of Cardiology Vol. 69; no. 2; pp. 176 - 185
Main Authors Vaduganathan, Muthiah, Deliargyris, Efthymios N., Price, Matthew J., Menozzi, Alberto, Álvarez, Carlos Alejandro, Dick, Ronald, Cross, David, Thompson, Peter, Altenberger, Johann, Godinho, Antonio, Precoma, Dalton, Carvalho, Antônio, Chapidze, Gulnara, Heuer, Hubertus, Genth-Zotz, Sabine, Moebius-Winkler, Sven, Buerke, Michael, Hoffmann, Stefan, Moellmann, Helge, Katus, Hugo, Klauss, Volker, Hiremath, Shirish, Sethi, Kamal, Dudek, Dariusz, Gasior, Zbigniew, Kornacewicz-Jach, Zdzislawa, Ostrowski, Jakub, Tendera, Michal, Zmudka, Krzysztof, Kosmider, Maciej, Melgares, Rafael, Goicolea, Francisco, Niederman, Alan, Negus, Brian, Paulowski, John, Pollack, Charles, Spriggs, Douglas, Chavez, Ivan, Waksman, Ron, Henderson, Joseph, Pacifico, Luigi, Andreou, Costa, Batchelor, Wayne, Wang, John, Winters, Rex, Jenkins, Stephen, Cannon, Louis, Westerhausen, Don, McLaurin, Brent, Shroff, Adhir, Pow, Thomas, O'Shaughnessy, Charles, Shaikh, Saeed R., Lawrence, Mark, Pocovi, Antonio, Londero, Hugo, Airton, José, Jorgova, Julia, Rifai, Nizar, Klimsa, Zdenek, Branny, Marian, Jain, Rajesh, Baum, Svetlana, Kosmachova, Elena, Markov, Valentin, Chernov, Sergey, Cha, Kwang-Soo, Youn, Tae Jin, Hur, Seung-Ho, Pyun, Wook-Bum, Choe, Hyunmin, Jeong, Myung-Ho, Figueras, Jaume, Chamnarnphol, Noppadol, Lui, Charles, Breall, Jeffrey, Istfan, Pierre, Sklar, Joel, Lundstrom, Robert, Brilakis, Emmanouil, Quealy, Kathleen, Mann, J. Tift, Khabeishvili, George, Behrens, Steffen, Dissmann, Martin, Franz, Wolfgang, Mugge, Andreas, Poerner, Tudor, Richardt, Gert, Bramucci, Ezio, Dubaniewicz, Witold, Trebacz, Jaroslaw, Witkowski, Adam, Dovgalevsky, Yakov, Kaewsuwanna, Pinij, Jafar, Zubair, Lipsitt, Michael, Martinez-Arraras, Joaquin, Siegel, Craig, Tauth, Jeffrey
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 17.01.2017
Elsevier Limited
Subjects
Online AccessGet full text
ISSN0735-1097
1558-3597
1558-3597
DOI10.1016/j.jacc.2016.10.055

Cover

More Information
Summary:Cangrelor, an intravenous, reversible P2Y12 antagonist, is approved for use in patients undergoing percutaneous coronary intervention (PCI). This study sought to evaluate the efficacy and safety of cangrelor compared with clopidogrel in subgroups that did and did not receive glycoprotein IIb/IIIa inhibitors (GPIs). This pooled, patient-level analysis of the 3 CHAMPION (Cangrelor versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition) trials analyzed all randomized patients who underwent PCI and received the study drug (n = 24,902). Only bailout/rescue GPI use was permitted, except in CHAMPION PCI, in which routine or bailout/rescue GPI use was at the site investigator’s discretion. The primary efficacy endpoint was the composite of all-cause mortality, myocardial infarction, ischemia-driven revascularization, or stent thrombosis at 48 h after randomization. Overall, 3,173 patients (12.7%) received a GPI, most commonly eptifibatide (69.4%). Despite variation in indications for GPIs, baseline characteristics were well balanced between the cangrelor and clopidogrel arms in subsets receiving and not receiving GPIs. Rates of the primary composite endpoint were lower with cangrelor compared with clopidogrel in patients who did (4.9% vs. 6.5%; odds ratio [OR]: 0.74; 95% confidence interval [CI]: 0.55 to 1.01) or did not receive a GPI (3.6% vs. 4.4%; OR: 0.82; 95% CI: 0.72 to 0.94; Pint = 0.55). Cangrelor did not increase the primary safety endpoint, GUSTO-defined severe/life-threatening bleeding, in patients who did (0.4% vs. 0.5%; OR: 0.71; 95% CI: 0.25 to 1.99) or did not receive GPIs (0.2% vs. 0.1%; OR: 1.56; 95% CI: 0.80 to 3.04; Pint = 0.21). GPI use was associated with increased risk of bleeding in both treatment arms. Cangrelor’s efficacy in reducing ischemic complications in patients undergoing PCI was maintained irrespective of GPI administration. GPI use was associated with substantially higher bleeding rates, regardless of the randomization to cangrelor or clopidogrel. (A Clinical Trial to Demonstrate the Efficacy of Cangrelor [PCI]: NCT00305162; Cangrelor Versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition [PLATFORM]: NCT00385138; A Clinical Trial Comparing Cangrelor to Clopidogrel Standard Therapy in Subjects Who Require Percutaneous Coronary Intervention [PCI] [CHAMPION PHOENIX] [CHAMPION]: NCT01156571) [Display omitted]
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Feature-1
content type line 23
ObjectType-Undefined-3
ISSN:0735-1097
1558-3597
1558-3597
DOI:10.1016/j.jacc.2016.10.055