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Evolocumab in HIV-Infected Patients With Dyslipidemia: Primary Results of the Randomized, Double-Blind BEIJERINCK Study.
Boccara, Franck; Kumar, Princy N; Caramelli, Bruno; Calmy, Alexandra; López, J Antonio G; Bray, Sarah; Cyrille, Marcoli; Rosenson, Robert S.
Afiliação
  • Boccara F; AP-HP, Hôpitaux de l'Est Parisien, Hôpital Saint-Antoine, Department of Cardiology, Sorbonne Université-INSERM UMR S_938, Centre de Recherche Saint-Antoine, Paris, France. Electronic address: franck.boccara@aphp.fr.
  • Kumar PN; Division of Infectious Diseases and Travel Medicine, Georgetown University School of Medicine, Washington, DC.
  • Caramelli B; Interdisciplinary Medicine in Cardiology Unit, InCor, University of São Paulo, São Paulo, Brazil.
  • Calmy A; HIV/AIDS Unit, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.
  • López JAG; Global Development, Amgen Inc., Thousand Oaks, California.
  • Bray S; Global Development, Amgen Inc., Thousand Oaks, California.
  • Cyrille M; Global Development, Amgen Inc., Thousand Oaks, California.
  • Rosenson RS; Cardiometabolics Unit, Mount Sinai Heart, Icahn School of Medicine at Mount Sinai, New York, New York.
J Am Coll Cardiol ; 75(20): 2570-2584, 2020 05 26.
Article em En | MEDLINE | ID: mdl-32234462
ABSTRACT

BACKGROUND:

People living with human immunodeficiency virus (PLHIV) are at increased risk of atherosclerotic cardiovascular disease (ASCVD) and are prone to statin-related adverse events from drug-drug interactions with certain antiretroviral regimens.

OBJECTIVES:

This study sought to evaluate the efficacy and safety of evolocumab in dyslipidemic PLHIV.

METHODS:

BEIJERINCK (EvolocumaB Effect on LDL-C Lowering in SubJEcts with Human Immunodeficiency VirRus and INcreased Cardiovascular RisK) is a randomized, double-blind, multinational trial comparing monthly subcutaneous evolocumab 420 mg with placebo in PLHIV with hypercholesterolemia/mixed dyslipidemia taking maximally-tolerated statin therapy. The primary endpoint was the percent change (baseline to week 24) in low-density lipoprotein cholesterol (LDL-C); secondary endpoints included achievement of LDL-C <70 mg/dl and percent change in other plasma lipid and lipoprotein levels. Treatment-emergent adverse events were also examined.

RESULTS:

A total of 464 patients were analyzed (mean age of 56.4 years, 82.5% male, mean duration with HIV of 17.4 years). ASCVD was documented in 35.6% of patients, and statin intolerance/contraindications to statin use were present in 20.7% of patients. Evolocumab reduced LDL-C by 56.9% (95% confidence interval 61.6% to 52.3%) from baseline to week 24 versus placebo. An LDL-C level of <70 mg/dl was achieved in 73.3% of patients in the evolocumab group versus 7.9% in the placebo group. Evolocumab also significantly reduced other atherogenic lipid levels, including non-high-density lipoprotein cholesterol, apolipoprotein B, and lipoprotein(a) (all p < 0.0001). Evolocumab was well tolerated, and treatment-emergent adverse events patient incidence was similar among evolocumab and placebo groups.

CONCLUSIONS:

Evolocumab was safe and significantly reduced lipid levels in dyslipidemic PLHIV on maximally-tolerated statin therapy. Evolocumab is an effective therapy for lowering atherogenic lipoproteins in PLHIV with high cardiovascular risk. (Safety, Tolerability & Efficacy on LDL-C of Evolocumab in Subjects With HIV & Hyperlipidemia/Mixed Dyslipidemia; NCT02833844).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / Inibidores de Hidroximetilglutaril-CoA Redutases / Fármacos Anti-HIV / Dislipidemias / Anticorpos Monoclonais Humanizados Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / Inibidores de Hidroximetilglutaril-CoA Redutases / Fármacos Anti-HIV / Dislipidemias / Anticorpos Monoclonais Humanizados Idioma: En Ano de publicação: 2020 Tipo de documento: Article