Reduction in Platelet Reactivity With Prasugrel 5 mg in Low-Body-Weight Patients Is Noninferior to Prasugrel 10 mg in Higher-Body-Weight Patients

被引:72
作者
Erlinge, David [1 ]
Ten Berg, Jurrien [2 ]
Foley, David [3 ]
Angiolillo, Dominick J. [4 ]
Wagner, Henrik [1 ]
Brown, Patricia B. [5 ]
Zhou, Chunmei [5 ]
Luo, Junxiang [5 ]
Jakubowski, Joseph A. [5 ]
Moser, Brian [5 ]
Small, David S. [5 ]
Bergmeijer, Thomas [2 ]
James, Stefan [6 ,7 ]
Winters, Kenneth J. [5 ]
机构
[1] Lund Univ, Dept Cardiol, S-22185 Lund, Sweden
[2] St Antonius Hosp, Dept Cardiol, Nieuwegein, Netherlands
[3] Clin Res Ctr, Dublin, Ireland
[4] Univ Florida, Coll Med, Div Cardiol, Jacksonville, FL 90034 USA
[5] Eli Lilly & Co, Indianapolis, IN 46285 USA
[6] Dept Med Sci, Uppsala, Sweden
[7] Uppsala Clin Res Ctr, Uppsala, Sweden
关键词
coronary artery disease; low body weight; platelet reactivity; prasugrel; ACUTE CORONARY SYNDROMES; TRITON-TIMI; 38; ACTIVE METABOLITE; CLOPIDOGREL; INHIBITION; EXPOSURE;
D O I
10.1016/j.jacc.2012.08.964
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objectives The aim of this study was to confirm prior modeling data suggesting that prasugrel 5 mg in low-body-weight (LBW) patients would be noninferior to prasugrel 10 mg in higher-body-weight (HBW) patients as assessed by maximal platelet aggregation (MPA). Background Prasugrel 10 mg reduced ischemic events compared with clopidogrel 75 mg but increased bleeding, particularly in LBW patients. Methods In this blinded, 3-period, crossover study in stable patients with coronary artery disease (CAD) taking aspirin, prasugrel 5 and 10 mg and clopidogrel 75 mg were administered to LBW (56.4 +/- 3.7 kg; n = 34) and HBW patients (84.7 +/- 14.9 kg; n = 38). Assays included light transmission aggregometry (LTA), VerifyNow P2Y12 (VN), and vasodilator-associated stimulated phosphoprotein (VASP) level measured predose and after each 12-day treatment. Results Median MPA by LTA for prasugrel 5 mg in LBW patients was noninferior to the 75th percentile for prasugrel 10 mg in HBW patients (primary endpoint) and mean MPA was similar, but active metabolite exposure was lowered by 38%. Within LBW patients, prasugrel 5 mg lowered MPA more than clopidogrel (least squares mean difference [95% confidence interval]: -3.7% [-6.72%, -0.69%]) and resulted in lower rates of high on-treatment platelet reactivity (HPR). Within HBW patients, prasugrel 10 mg lowered MPA more than clopidogrel (-16.9% [-22.3%, -11.5%]). Similar results were observed by VN and VASP. Prasugrel 10 mg in LBW patients was associated with more mild to moderate bleeding (mainly bruising) compared with prasugrel 5 mg and clopidogrel. Conclusions In aspirin-treated patients with CAD, prasugrel 5 mg in LBW patients reduced platelet reactivity to a similar extent as prasugrel 10 mg in HBW patients and resulted in greater platelet inhibition, lower HPR, and similar bleeding rates compared with clopidogrel. (Comparison of Prasugrel and Clopidogrel in Low Body Weight Versus Higher Body Weight With Coronary Artery Disease [FEATHER]; NCT01107925) (J Am Coll Cardiol 2012; 60: 2032-40) (C) 2012 by the American College of Cardiology Foundation
引用
收藏
页码:2032 / 2040
页数:9
相关论文
共 10 条
[1]
[Anonymous], 2012, PRAS EF EUR UN SUMM
[2]
[Anonymous], 2012, PRAS EFF PACK INS
[3]
Optimizing of thienopyridine therapy by multiple electrode platelet aggregometry in clopidogrel low responders undergoing PCI [J].
Behr, Tobias ;
Kuch, Bernhard ;
Behr, Werner ;
von Scheidt, Wolfgang .
CLINICAL RESEARCH IN CARDIOLOGY, 2011, 100 (10) :907-914
[4]
The association of cigarette smoking with enhanced platelet inhibition by clopidogrel [J].
Bliden, Kevin P. ;
DiChiara, Joseph ;
Lawal, Lookman ;
Singla, Anand ;
Antonino, Mark J. ;
Baker, Brian A. ;
Bailey, William L. ;
Tantry, Udaya S. ;
Gurbel, Paul A. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 52 (07) :531-533
[5]
Study design and rationale of a comparison of prasugrel and clopidogrel in medically managed patients with unstable angina/non-ST-segment elevation myocardial infarction: The TaRgeted platelet Inhibition to cLarify the Optimal strateGy to medicallY manage Acute Coronary Syndromes (TRILOGY ACS) trial [J].
Chin, Chee Tang ;
Roe, Matthew T. ;
Fox, Keith A. A. ;
Prabhakaran, Dorairaj ;
Marshall, Debra A. ;
Petitjean, Helene ;
Lokhnygina, Yuliya ;
Brown, Eileen ;
Armstrong, Paul W. ;
White, Harvey D. ;
Ohman, E. Magnus .
AMERICAN HEART JOURNAL, 2010, 160 (01) :16-U35
[6]
Population pharmacokinetics and pharmacodynamics of prasugrel and clopidogrel in aspirin-treated patients with stable coronary artery disease [J].
Ernest, C. Steven, II ;
Small, David S. ;
Rohatagi, Shashank ;
Salazar, Daniel E. ;
Wallentin, Lars ;
Winters, Kenneth J. ;
Wrishko, Rebecca E. .
JOURNAL OF PHARMACOKINETICS AND PHARMACODYNAMICS, 2008, 35 (06) :593-618
[7]
Increased active metabolite formation explains the greater platelet inhibition with prasugrel compared to high-dose clopidogrel [J].
Payne, Christopher D. ;
Li, Ying Grace ;
Small, David S. ;
Ernest, C. Steven, II ;
Farid, Nagy A. ;
Jakubowski, Joseph A. ;
Brandt, John T. ;
Salazar, Daniel E. ;
Winters, Kenneth J. .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2007, 50 (05) :555-562
[8]
Relationship Between Exposure to Prasugrel Active Metabolite and Clinical Outcomes in the TRITON-TIMI 38 Substudy [J].
Riesmeyer, Jeffrey S. ;
Salazar, Daniel E. ;
Weerakkody, Govinda J. ;
Ni, Lan ;
Wrishko, Rebecca E. ;
Ernest, C. Steven, II ;
Luo, Junxiang ;
Li, Ying G. ;
Small, David S. ;
Rohatagi, Shashank ;
Macias, William L. .
JOURNAL OF CLINICAL PHARMACOLOGY, 2012, 52 (06) :789-797
[9]
Prasugrel versus clopidogrel in patients with acute coronary syndromes [J].
Wiviott, Stephen D. ;
Braunwald, Eugene ;
McCabe, Carolyn H. ;
Montalescot, Gilles ;
Ruzyllo, Witold ;
Gottlieb, Shmuel ;
Neumann, Franz-Joseph ;
Ardissino, Diego ;
De Servi, Stefano ;
Murphy, Sabina A. ;
Riesmeyer, Jeffrey ;
Weerakkody, Govinda ;
Gibson, C. Michael ;
Antman, Elliott M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (20) :2001-2015
[10]
Population Pharmacokinetic Analyses to Evaluate the Influence of Intrinsic and Extrinsic Factors on Exposure of Prasugrel Active Metabolite in TRITON-TIMI 38 [J].
Wrishko, Rebecca E. ;
Ernest, C. Steven, II ;
Small, David S. ;
Li, Ying G. ;
Weerakkody, Govinda J. ;
Riesmeyer, Jeffrey R. ;
Macias, William L. ;
Rohatagi, Shashank ;
Salazar, Daniel E. ;
Antman, Elliott M. ;
Wiviott, Stephen D. ;
Braunwald, Eugene ;
Ni, Lan .
JOURNAL OF CLINICAL PHARMACOLOGY, 2009, 49 (08) :984-998