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Effect of Evolocumab on Complex Coronary Disease Requiring Revascularization.
Oyama, Kazuma; Furtado, Remo H M; Fagundes, Antonio; Zelniker, Thomas A; Tang, Minao; Kuder, Julia; Murphy, Sabina A; Hamer, Andrew; Wang, Huei; Keech, Anthony C; Giugliano, Robert P; Sabatine, Marc S; Bergmark, Brian A.
Affiliation
  • Oyama K; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA; Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Furtado RHM; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA; Hospital Israelita Albert Einsteinand Instituto do Coraçao da Faculdade de Medicina da USP, Sao Paulo, Brazil.
  • Fagundes A; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Zelniker TA; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA; Division of Cardiology, Vienna General Hospital and Medical University of Vienna, Vienna, Austria.
  • Tang M; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Kuder J; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Murphy SA; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Hamer A; Amgen, Thousand Oaks, California, USA.
  • Wang H; Amgen, Thousand Oaks, California, USA.
  • Keech AC; National Health and Medical Research Council Clinical Trials Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Giugliano RP; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Sabatine MS; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Bergmark BA; TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA. Electronic address: bbergmark@bwh.harvard.edu.
J Am Coll Cardiol ; 77(3): 259-267, 2021 01 26.
Article in En | MEDLINE | ID: mdl-33197560
ABSTRACT

OBJECTIVES:

This study sought to evaluate the ability of the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor evolocumab to reduce the risk of complex coronary atherosclerosis requiring revascularization.

BACKGROUND:

PCSK9 inhibitors induce plaque regression and reduce the risk of coronary revascularization overall.

METHODS:

FOURIER (Further Cardiovascular Outcomes Research with PCSK9 Inhibition in Subjects with Elevated Risk) was a randomized trial of the PCSK9 inhibitor evolocumab versus placebo in 27,564 patients with stable atherosclerotic cardiovascular disease on statin therapy followed for a median of 2.2 years. Clinical documentation of revascularization events was blindly reviewed to assess coronary anatomy and procedural characteristics. Complex revascularization was the composite of complex percutaneous coronary intervention (PCI) (as per previous analyses, ≥1 of multivessel PCI, ≥3 stents, ≥3 lesions treated, bifurcation PCI, or total stent length >60 mm) or coronary artery bypass grafting surgery (CABG).

RESULTS:

In this study, 1,724 patients underwent coronary revascularization, including 1,482 who underwent PCI, 296 who underwent CABG, and 54 who underwent both. Complex revascularization was performed in 632 (37%) patients. Evolocumab reduced the risk of any coronary revascularization by 22% (hazard ratio [HR] 0.78; 95% CI 0.71 to 0.86; p < 0.001), simple PCI by 22% (HR 0.78; 95% CI 0.70 to 0.88; p < 0.001), complex PCI by 33% (HR 0.67; 95% CI 0.54 to 0.84; p < 0.001), CABG by 24% (HR 0.76; 95% CI 0.60 to 0.96; p = 0.019), and complex revascularization by 29% (HR 0.71; 95% CI 0.61 to 0.84; p < 0.001). The magnitude of the risk reduction with evolocumab in complex revascularization tended to increase over time (20%, 36%, and 41% risk reductions in the first, second, and beyond second years).

CONCLUSIONS:

Adding evolocumab to statin therapy significantly reduced the risk of developing complex coronary disease requiring revascularization, including complex PCI and CABG individually. (Further Cardiovascular Outcomes Research with PCSK9 Inhibition in Subjects with Elevated Risk (FOURIER); NCT01764633.).
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Disease / Antibodies, Monoclonal, Humanized / PCSK9 Inhibitors / Anticholesteremic Agents / Myocardial Revascularization Type of study: Clinical_trials Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Am Coll Cardiol Year: 2021 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Disease / Antibodies, Monoclonal, Humanized / PCSK9 Inhibitors / Anticholesteremic Agents / Myocardial Revascularization Type of study: Clinical_trials Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Am Coll Cardiol Year: 2021 Document type: Article Affiliation country: Japón
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