Effects of Inclisiran in Patients With Atherosclerotic Cardiovascular Disease: A Pooled Analysis of the ORION-10 and ORION-11 Randomized Trials

被引:2
|
作者
Wright, R. Scott [1 ,2 ]
Ray, Kausik K. [3 ]
Landmesser, Ulf [4 ,5 ]
Koenig, Wolfgang [6 ,7 ,8 ]
Raal, Frederick J. [9 ]
Leiter, Lawrence A. [10 ]
Conde, Lorena Garcia [11 ]
Han, Jackie [12 ]
Schwartz, Gregory G. [13 ]
机构
[1] Mayo Clin, Div Pediat Cardiol, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Cardiol, 200 First St SW, Rochester, MN 55905 USA
[3] Imperial Coll London, Imperial Ctr Cardiovasc Dis Prevent, Dept Primary Care & Publ Hlth, London, England
[4] Deutsch Herzzentrum Charite, Dept Cardiol Angiol & Intens Care Med, Berlin, Germany
[5] Charite Univ Med Berlin, Berlin Inst Hlth, DZHK, Partner Site Berlin, Berlin, Germany
[6] Tech Univ Munich, Partner Site Munich Heart Alliance, Munich, Germany
[7] DZHK German Ctr Cardiovasc Res, Partner Site Munich Heart Alliance, Munich, Germany
[8] Univ Ulm, Inst Epidemiol & Med Biometry, Ulm, Germany
[9] Univ Witwatersrand, Fac Hlth Sci, Johannesburg, South Africa
[10] Univ Toronto, St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
[11] Novartis Pharm AG, Basel, Switzerland
[12] Novartis Pharmaceut, E Hanover, NJ USA
[13] Univ Colorado, Sch Med, Div Cardiol, Aurora, CO USA
关键词
CHRONIC KIDNEY-DISEASE; LDL-CHOLESTEROL; RISK; PREVALENCE; EFFICACY; THERAPY; SAFETY;
D O I
10.1016/j.mayocp.2024.03.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the efficacy, safety, and tolerability of inclisiran in participants with atherosclerotic cardiovascular disease (ASCVD) from ORION-10 and ORION-11 stratified by key patient characteristics. Patients and Methods: Participants were randomized 1:1 to receive 300 mg inclisiran sodium (284 mg inclisiran) or placebo on Days 1, 90, 270, and 450, alongside background lipid-lowering therapy. This pooled, post hoc analysis stratified participants with ASCVD by sex, age, race, kidney function, body mass index, and glycemic status. Co-primary endpoints were percentage changes in low-density lipoprotein cholesterol (LDL-C) from baseline to Day 510, and after Day 90 and up to Day 540 (time-adjusted). LDL-C goal attainment and safety were also assessed. Results: This analysis of 2975 participants included: female, n=827; Black, n=213; 75 years of age or older, n=458; obese, n=1474; diabetes, n=1182; and moderate-to-severe chronic kidney disease, n=538. Mean baseline LDL-C levels in the total ASCVD population were balanced between treatment centage changes in LDL-C from baseline were -51.5% (95% CI, -54.0 to -49.0) and -52.1% (95% CI, -53.9 to -50.4) to Day 510 and Day 540 (time-adjusted), respectively; this was consistent across subgroups. LDL-C less than 55 mg/dL at one or more visits was reached by 87.6% of participants receiving inclisiran. The inclisiran safety profile was consistent across subgroups. Conclusion: Twice-yearly inclisiran (after initial and 3-month doses) was well tolerated and provided significant, consistent LDL-C reductions for up to 18 months in participants with ASCVD independent of key patient characteristics (ORION-10; NCT03399370 and ORION-11; (c) 2024 THE AUTHORS. Published by Elsevier Inc on behalf of Mayo Foundation for Medical Education and Research. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/) <black square> Mayo Clin Proc. 2024;99(8):1222-1235
引用
收藏
页码:1222 / 1235
页数:14
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