Effect of the PCSK9 Inhibitor Evolocumab on Total Cardiovascular Events in Patients With Cardiovascular Disease: A Prespecified Analysis From the FOURIER Trial.


Journal

JAMA cardiology
ISSN: 2380-6591
Titre abrégé: JAMA Cardiol
Pays: United States
ID NLM: 101676033

Informations de publication

Date de publication:
01 07 2019
Historique:
pubmed: 23 5 2019
medline: 17 6 2020
entrez: 23 5 2019
Statut: ppublish

Résumé

The PCSK9 inhibitor evolocumab reduced low-density lipoprotein cholesterol and first cardiovascular events in the Further Cardiovascular Outcomes Research With PCSK9 Inhibition in Subjects With Elevated Risk (FOURIER) trial, but patients remain at high risk of recurrent cardiovascular events. To evaluate the effect of evolocumab on total cardiovascular events, given the importance of total number of cardiovascular events to patients, clinicians, and health economists. Secondary analysis of a randomized, double-blind clinical trial. The FOURIER trial compared evolocumab or matching placebo and followed up patients for a median of 2.2 years. The study included 27 564 patients with stable atherosclerotic disease receiving statin therapy. Data were analyzed between May 2017 and February 2019. The primary end point (PEP) was time to first cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization; the key secondary end point was time to first cardiovascular death, myocardial infarction, or stroke. In a prespecified analysis, total cardiovascular events were evaluated between treatment arms. The mean age of patients was 63 years, 69% of patients were taking high-intensity statin therapy, and the median LDL-C at baseline was 92 mg/dL (to convert to millimoles per liter, multiply by 0.0259). There were 2907 first PEP events and 4906 total PEP events during the trial. Evolocumab reduced total PEP events by 18% (incidence rate ratio [RR], 0.82; 95% CI, 0.75-0.90; P < .001) including both first events (hazard ratio, 0.85; 95% CI, 0.79-0.92; P < .001) and subsequent events (RR, 0.74; 95% CI, 0.65-0.85). There were 2192 total primary events in the evolocumab group and 2714 total events in the placebo group. For every 1000 patients treated for 3 years, evolocumab prevented 22 first PEP events and 52 total PEP events. Reductions in total events were driven by fewer total myocardial infarctions (RR, 0.74; 95% CI, 0.65-0.84; P < .001), strokes (RR, 0.77; 95% CI, 0.64-0.93; P = .007), and coronary revascularizations (RR, 0.78; 95% CI, 0.71-0.87; P < .001). The addition of the PCSK9 inhibitor evolocumab to statin therapy improved clinical outcomes, with significant reductions in total PEP events, driven by decreases in myocardial infarction, stroke, and coronary revascularization. More than double the number of events were prevented with evolocumab vs placebo as compared with the analysis of only first events. These data provide further support for the benefit of continuing aggressive lipid-lowering therapy to prevent recurrent cardiovascular events. ClinicalTrials.gov identifier: NCT01764633.

Identifiants

pubmed: 31116355
pii: 2733138
doi: 10.1001/jamacardio.2019.0886
pmc: PMC6537798
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Anticholesteremic Agents 0
PCSK9 Inhibitors 0
PCSK9 protein, human EC 3.4.21.-
evolocumab LKC0U3A8NJ

Banques de données

ClinicalTrials.gov
['NCT01764633']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

613-619

Références

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Auteurs

Sabina A Murphy (SA)

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Masschusetts.

Terje R Pedersen (TR)

Oslo University Hospital, Ullevål and Medical Faculty, University of Oslo, Oslo, Norway.

Zbigniew A Gaciong (ZA)

Department of Internal Medicine, Hypertension and Vascular Diseases, The Medical University of Warsaw, Warsaw, Poland.

Richard Ceska (R)

Center for Preventive Cardiology, 3rd Internal Medicine Clinic, University General Hospital and Charles University 1st Medical Faculty, Prague, Czech Republic.

Marat V Ezhov (MV)

National Cardiology Research Center, Moscow, Russia.

Derek L Connolly (DL)

Birmingham City and Sandwell Hospitals and the Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, England.

J Wouter Jukema (JW)

Department of Cardiology, Leiden University Medical Center, Leiden, the Netherlands.

Kalman Toth (K)

First Department of Medicine, University of Pecs, Medical School, Pecs, Hungary.

Matti J Tikkanen (MJ)

Folkhälsan Research Center, University of Helsinki, Helsinki, Finland.

Kyungah Im (K)

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Masschusetts.

Stephen D Wiviott (SD)

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Masschusetts.

Christopher E Kurtz (CE)

Amgen, Thousand Oaks, California.

Narimon Honarpour (N)

Amgen, Thousand Oaks, California.

Robert P Giugliano (RP)

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Masschusetts.

Anthony C Keech (AC)

Sydney Medical School, National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia.

Peter S Sever (PS)

Imperial College London, London, England.

Marc S Sabatine (MS)

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Masschusetts.
Deputy Editor.

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Classifications MeSH