Article Synopsis

  • Study Purpose
  • : The research assessed the effectiveness of an "inclisiran first" strategy for patients with atherosclerotic cardiovascular disease who don't reach LDL-C goals, comparing this approach with usual care that only involves statins.
  • Key Findings
  • : 450 patients were randomized, showing that the "inclisiran first" approach resulted in a 60% reduction in LDL-C, compared to just 7% in usual care. It also helped a higher percentage of patients reach LDL-C targets (<70 mg/dL: 81.8% vs 22.2%).
  • Safety and Tolerability
  • : While the "inclisiran first" strategy did not lead to increased serious

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Article Abstract

Background: Most patients with atherosclerotic cardiovascular disease fail to achieve guideline-directed low-density lipoprotein cholesterol (LDL-C) goals. Twice-yearly inclisiran lowers LDL-C by ∼50% when added to statins.

Objectives: This study evaluated the effectiveness of an "inclisiran first" implementation strategy (adding inclisiran immediately upon failure to reach LDL-C <70 mg/dL despite receiving maximally tolerated statins) vs representative usual care in U.S. patients with atherosclerotic cardiovascular disease.

Methods: VICTORION-INITIATE, a prospective, pragmatically designed trial, randomized patients 1:1 to inclisiran (284 mg at days 0, 90, and 270) plus usual care (lipid management at treating physician's discretion) vs usual care alone. Primary endpoints were percentage change in LDL-C from baseline and statin discontinuation rates.

Results: We randomized 450 patients (30.9% women, 12.4% Black, 15.3% Hispanic); mean baseline LDL-C was 97.4 mg/dL. The "inclisiran first" strategy led to significantly greater reductions in LDL-C from baseline to day 330 vs usual care (60.0% vs 7.0%; P < 0.001). Statin discontinuation rates with "inclisiran first" (6.0%) were noninferior vs usual care (16.7%). More "inclisiran first" patients achieved LDL-C goals vs usual care (<70 mg/dL: 81.8% vs 22.2%; <55 mg/dL: 71.6% vs 8.9%; P < 0.001). Treatment-emergent adverse event (TEAE) and serious TEAE rates compared similarly between treatment strategies (62.8% vs 53.7% and 11.5% vs 13.4%, respectively). Injection-site TEAEs and TEAEs causing treatment withdrawal occurred more commonly with "inclisiran first" than usual care (10.3% vs 0.0% and 2.6% vs 0.0%, respectively).

Conclusions: An "inclisiran first" implementation strategy led to greater LDL-C lowering compared with usual care without discouraging statin use or raising new safety concerns. (A Randomized, Multicenter, Open-label Trial Comparing the Effectiveness of an "Inclisiran First" Implementation Strategy to Usual Care on LDL Cholesterol [LDL-C] in Patients With Atherosclerotic Cardiovascular Disease and Elevated LDL-C [≥70 mg/dL] Despite Receiving Maximally Tolerated Statin Therapy [VICTORION-INITIATE]; NCT04929249).

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http://dx.doi.org/10.1016/j.jacc.2024.03.382DOI Listing

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Article Synopsis
  • Study Purpose
  • : The research assessed the effectiveness of an "inclisiran first" strategy for patients with atherosclerotic cardiovascular disease who don't reach LDL-C goals, comparing this approach with usual care that only involves statins.
  • Key Findings
  • : 450 patients were randomized, showing that the "inclisiran first" approach resulted in a 60% reduction in LDL-C, compared to just 7% in usual care. It also helped a higher percentage of patients reach LDL-C targets (<70 mg/dL: 81.8% vs 22.2%).
  • Safety and Tolerability
  • : While the "inclisiran first" strategy did not lead to increased serious
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Correction to: Inclisiran: First Approval.

Drugs

June 2021

Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.

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Inclisiran: First Approval.

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February 2021

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

Inclisiran (Leqvio; Novartis) is a first-in-class, cholesterol-lowering small interfering RNA (siRNA) conjugated to triantennary N-acetylgalactosamine carbohydrates (GalNAc). Inclisiran received its first approval in December 2020 in the EU for use in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet. It is intended for use in combination with a statin or a statin with other lipid-lowering therapies in patients unable to reach low-density lipoprotein cholesterol goals with the maximum tolerated statin dose.

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