Indirect Comparison of the Efficacy and Safety of Alirocumab and Evolocumab: A Systematic Review and Network Meta-Analysis.

AIMS Although alirocumab and evolocumab have both been associated with improved outcomes in patients with dyslipidemia or established atherosclerotic cardiovascular disease, data on their respective performances are scarce. This study aimed at providing an indirect comparison of the efficacy and safety of alirocumab versus evolocumab. METHODS AND RESULTS We conducted a systematic review and network meta-analysis of randomized trials comparing alirocumab or evolocumab to placebo with consistent background lipid lowering therapy up to November 2018. We estimated the relative risk and the 95% confidence intervals using fixed effect model in a frequentist pairwise and network meta-analytic approach. A total of 30 trials, enrolling 59,026 patients were included. Eligibility criteria varied significantly across trials evaluating alirocumab and evolocumab. Compared with evolocumab, alirocumab was associated with a significant reduction in all-cause death (RR: 0.80; 95%CI: 0.66-0.97) but not in cardiovascular death (RR: 0.83; 95%CI: 0.65-1.05). This study did not find any significant differences in myocardial infarction (RR: 1.15; 95%CI: 0.99-1.34), stroke (RR: 0.96; 95%CI: 0.71-1.28) or coronary revascularization (RR: 1.13; 95%CI: 0.99-1.29) between the two agents. Alirocumab was associated with a 27% increased risk of injection site reaction compared to evolocumab; however, no significant differences were found in terms of treatment discontinuations, systemic allergic reaction, neurocognitive events, ophthalmologic events, or new-onset of or worsening of pre-existing diabetes. CONCLUSION Alirocumab and evolocumab share a similar safety profile except for injection site reaction. No significant differences were observed across the efficacy endpoints, except for all-cause death, which may be related to the heterogeneity of the studied populations treated with the two drugs.

[1]  G. Rosano,et al.  An expert opinion paper on statin adherence and implementation of new lipid-lowering medications by the ESC Working Group on Cardiovascular Pharmacotherapy: Barriers to be overcome , 2020 .

[2]  P. Filardi,et al.  ESC Position Paper on statins adherence and implementation of new lipid-lowering medications: barriers to be overcome. , 2019, European heart journal. Cardiovascular pharmacotherapy.

[3]  V. Aboyans,et al.  Epidemiology, treatment patterns and outcomes in patients with coronary or lower extremity artery disease in France. , 2019, Archives of cardiovascular diseases.

[4]  A. Gotto,et al.  PCSK9 and inflammation: a review of experimental and clinical evidence. , 2019, European heart journal. Cardiovascular pharmacotherapy.

[5]  M. Sabatine,et al.  2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. , 2019, European heart journal.

[6]  H. Bays Alirocumab, Decreased Mortality, Nominal Significance, P Values, Bayesian Statistics, and the Duplicity of Multiplicity. , 2019, Circulation.

[7]  Deepak L. Bhatt,et al.  Effect of Alirocumab on Mortality After Acute Coronary Syndromes , 2019 .

[8]  S. Pocock,et al.  Efficacy and safety of alirocumab and evolocumab: a systematic review and meta-analysis of randomized controlled trials. , 2019, European heart journal.

[9]  Daniel E Forman,et al.  2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. , 2019, Journal of the American College of Cardiology.

[10]  P. Raggi,et al.  Baseline low-density lipoprotein cholesterol to predict the extent of cardiovascular benefit from lipid-lowering therapies: a review , 2018, European heart journal. Cardiovascular pharmacotherapy.

[11]  Odyssey Outcomes Investigators Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome , 2018 .

[12]  R. Giugliano,et al.  Efficacy and Safety of Further Lowering of Low-Density Lipoprotein Cholesterol in Patients Starting With Very Low Levels: A Meta-analysis , 2018, JAMA cardiology.

[13]  Jeroen J. Bax,et al.  2017 Update of ESC/EAS Task Force on practical clinical guidance for proprotein convertase subtilisin/kexin type 9 inhibition in patients with atherosclerotic cardiovascular disease or in familial hypercholesterolaemia , 2017, European heart journal.

[14]  Jennifer G. Robinson,et al.  New strategies for the development of lipid-lowering therapies to reduce cardiovascular risk , 2018, European heart journal. Cardiovascular pharmacotherapy.

[15]  Francesca N. Delling,et al.  Heart Disease and Stroke Statistics—2018 Update: A Report From the American Heart Association , 2018, Circulation.

[16]  Philip D. Harvey,et al.  No evidence of neurocognitive adverse events associated with alirocumab treatment in 3340 patients from 14 randomized Phase 2 and 3 controlled trials: a meta-analysis of individual patient data , 2017, European heart journal.

[17]  T. Wisløff,et al.  Modelling the cost-effectiveness of PCSK9 inhibitors vs. ezetimibe through LDL-C reductions in a Norwegian setting , 2017, European heart journal. Cardiovascular pharmacotherapy.

[18]  A. Keech,et al.  Clinical efficacy and safety of achieving very low LDL-cholesterol concentrations with the PCSK9 inhibitor evolocumab: a prespecified secondary analysis of the FOURIER trial , 2017, The Lancet.

[19]  A. Keech,et al.  Cognitive Function in a Randomized Trial of Evolocumab , 2017, The New England journal of medicine.

[20]  G. Norata,et al.  PCSK9 deficiency results in increased ectopic fat accumulation in experimental models and in humans , 2017, European journal of preventive cardiology.

[21]  O. Descamps,et al.  Pooled Safety Analysis of Evolocumab in Over 6000 Patients From Double-Blind and Open-Label Extension Studies , 2017, Circulation.

[22]  P. Ridker,et al.  Lipid‐Reduction Variability and Antidrug‐Antibody Formation with Bococizumab , 2017, The New England journal of medicine.

[23]  A. Keech,et al.  Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease , 2017, The New England journal of medicine.

[24]  Jennifer G. Robinson,et al.  Efficacy and Safety of Alirocumab 150 mg Every 4 Weeks in Patients With Hypercholesterolemia Not on Statin Therapy: The ODYSSEY CHOICE II Study , 2016, Journal of the American Heart Association.

[25]  G. Norata,et al.  Biology of proprotein convertase subtilisin kexin 9: beyond low-density lipoprotein cholesterol lowering. , 2016, Cardiovascular research.

[26]  E. Navarese,et al.  From proprotein convertase subtilisin/kexin type 9 to its inhibition: state-of-the-art and clinical implications. , 2016, European heart journal. Cardiovascular pharmacotherapy.

[27]  R. Dufour,et al.  Familial hypercholesterolemia: PCSK9 InsLEU genetic variant and prediabetes/diabetes risk. , 2015, Journal of clinical lipidology.

[28]  Jennifer G. Robinson,et al.  Efficacy and safety of alirocumab in reducing lipids and cardiovascular events. , 2015, The New England journal of medicine.

[29]  H. Bays,et al.  Anti-PCSK9 monotherapy for hypercholesterolemia: the MENDEL-2 randomized, controlled phase III clinical trial of evolocumab. , 2014, Journal of the American College of Cardiology.

[30]  Harald Binder,et al.  A graphical tool for locating inconsistency in network meta-analyses , 2013, BMC Medical Research Methodology.

[31]  V. Gebski,et al.  Effect of a monoclonal antibody to PCSK9 on low-density lipoprotein cholesterol levels in statin-intolerant patients: the GAUSS randomized trial. , 2012, JAMA.

[32]  S. Wasserman,et al.  Efficacy, safety, and tolerability of a monoclonal antibody to proprotein convertase subtilisin/kexin type 9 as monotherapy in patients with hypercholesterolaemia (MENDEL): a randomised, double-blind, placebo-controlled, phase 2 study , 2012, The Lancet.

[33]  J. Mckenney,et al.  Atorvastatin with or without an antibody to PCSK9 in primary hypercholesterolemia. , 2012, The New England journal of medicine.

[34]  J. Sterne,et al.  The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials , 2011, BMJ : British Medical Journal.

[35]  D. Moher,et al.  Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement , 2009, BMJ.