#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

First clinical experience with inclisiran in Slovakia – experience with administration, management and efficacy from one center


Authors: Štefan Tóth;  Patrik Buček;  Richard David;  Matej Šajty
Authors‘ workplace: Kardiologická ambulancia, Kardiocomp s. r. o., Košice 1
Published in: AtheroRev 2024; 9(1): 27-34
Category: Reviews

Overview

Introduction: Inhibition of the cascade of proprotein convertase subtilisin kexin type 9 (PCSK9) has been shown to be an effective method of reducing LDL-C, which represents one of the most important risk factors for the development and progression of cardiovascular diseases. Inclisiran represents the first small interfering RNA (siRNA) inhibiting PCSK9, whose effectiveness in reducing LDL-C is reported in clinical studies by ± 50 %. The aim of this study was to describe the effect of inclisiran in real clinical conditions as well as the first clinical experience with administration in Slovakia. Methods: In this observational study, we indicated a total of 36 patients for inclisiran therapy within the framework of standard examinations, procedures and reimbursements from the public health insurance. Patients completed a standard lipid profile examination (LDL-C, HDL-C, TC, TG, Lp(a)) and hsCRP before submitting applications for therapy approval and then +1 month after 2 administrations of therapy. The mean change in lipid profile levels was determined for each patient who received the second dose of inclisiran. Results: A total of 31 patients, 22 patients with ACS/revaskularisation and 9 patients after stroke, were approved by health insurance companies. One patient with statin intolerance, 24 patients with the maximum statin dose and 6 patients with a reduced dose were included. From the total number of patients, we had LDL-C samples taken after 3 + 1 months from 22 patients. The average entry value of the selected parameters was: LDL-C 3.56 [3.01; 4.14] mmol/L, Lp(a) 14.28 [8.19; 21.05] mg/dL hsCRP 4.2 [2.9; 5.5] mg/dL. After 3+1 months of therapy, we recorded a decrease in LDL-C by 57.46 % [50.41; 76.82], hsCRP by 1.2 [0.5; 1.9] mg/dL, Lp(a) by 14.29 % [8.19; 21.05] mg/dL. Safety was similar to clinical studies, with mild pain at the injection site in 26 administrations and flu-like symptoms the next day in 3 administrations. Conclusion: Our first experience with inclisiran in the clinical setting showed a slightly more effective reduction in LDL-C levels compared to clinical studies, a decrease in hsCRP levels as well as Lp(a). However, the decrease in Lp(a) was not present, and there were patients with a better response to therapy, or non-responders. The safety profile was similar to the clinical studies.

Keywords:

lipoprotein(a) – inclisiran – hsCRP – LDL-C – reaching target values


Sources

Vardas P, Townsend N, Torbica A et al. European Society of Cardiology: cardiovascular disease statistics 2021. Eur Heart J 2022; 43(8): 716–799. Dostupné z DOI: <http://dx.doi.org/10.1093/eurheartj/ehab892>.

Baigent C, Blackwell L, Emberson J et al. [Cholesterol Treatment Trialists’ (CTT) Collaboration]. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet 2010; 376(9753): 1670–1681. Dostupné z DOI: <http://dx.doi.org/10.1016/S0140–6736(10)61350–5>.

Nicholls SJ, Kataoka Y, Nissen SE et al. Effect of evolocumab on coronary plaque phenotype and burden in statin-treated patients following myocardial infarction. JACC Cardiovasc Imaging 2022; 15(7): 1308–1321. Dostupné z DOI: <http://dx.doi.org/10.1016/j.jcmg.2022.03.002>.

Ray KK, Molemans B, Schoonen WM et al. [DA VINCI study]. EU-Wide cross-sectional observational study of lipid-modifying therapy use in secondary and primary care: the DA VINCI study. Eur J Prev Cardiol 2021; 28: 1279–1289. Dostupné z DOI: <http://dx.doi.org/10.1093/eurjpc/zwaa047>.

Toth S, Turek M, Pella D. Success in achieving LDL-C target values in a high-risk population in Slovakia: SlovakLipid retrospective study. Archives of Medical Science 2023. Dostupné z DOI: <https://doi.org/10.5114/aoms/170961>.

Mach F, Baigent C, Catapano AL et al. 2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk: the Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS). Eur Heart J 2020; 41(1): 111–188. Dostupné z DOI: <http://dx.doi.org/10.1093/eurheartj/ehz455>.

Mulder JW, Galema-Boers AM, van Lennep JE. First clinical experiences with inclisiran in a real-world setting. J Clin Lipidol 2023; 17(6): 818–827. Dostupné z DOI: <http://dx.doi.org/10.1016/j.jacl.2023.09.005>.

Ray KK, Stoekenbroek RM, Kallend D et al. Effect of 1 or 2 Doses of Inclisiran on Low-Density Lipoprotein Cholesterol Levels: One-Year Follow-up of the ORION-1 Randomized Clinical Trial. JAMA Cardiol 2019; 4(11): 1067–1075. Dostupné z DOI: <http://dx.doi.org/10.1001/jamacardio.2019.3502>.

Ray KK, Troquay RP, Visseren FI et al. Long-term efficacy and safety of inclisiran in patients with high cardiovascular risk and elevated LDL cholesterol (ORION-3): Results from the 4-year open-label extension of the ORION-1 trial. Lancet Diabetes Endocrinol 2023; 11: 109–119. Dostupné z DOI: <http://dx.doi.org/10.1016/S2213–8587(22)00353–9>.

Raal FJ, Kallend D, Ray KK et al. Inclisiran for the Treatment of Heterozygous Familial Hypercholesterolemia. N Engl J Med 2020; 382(16): 1520–1530. Dostupné z DOI: <http://dx.doi.org/10.1056/NEJMoa1913805>.

Ray KK, Wright RS, Kallend D et al. Two Phase 3 Trials of Inclisiran in Patients with Elevated LDL Cholesterol. N Engl J Med 2020; 382(16): 1507–1519. Dostupné z DOI: <http://dx.doi.org/10.1056/NEJMoa1912387>.

Katsiki N, Vrablik M, Banach M et al. Inclisiran, low-density lipoprotein cholesterol and lipoprotein (a). Pharmaceuticals (Basel) 2023; 16(4): 577. Dostupné z DOI: <http://dx.doi.org/10.3390/ph16040577>.

Padam P, Barton L, Wilson S et al. Lipid lowering with inclisiran: a real-world single-centre experience. Open Heart 2022; 9(2), e002184. Dostupné z DOI: <http://dx.doi.org/10.1136/openhrt-2022–002184>.

Basile C, Gargiulo P, Merlini PA et al. Efficacy and safety of inclisiran in real world practice: insights from the Cholinet registry. Eur Heart J 2023; 44(Suppl 2): ehad655–2812. Dostupné z DOI: <http://dx.doi.org/10.1093/eurheartj/ehad655.2812>.

Makhmudova U, Schatz U, Perakakis N et al. High interindividual variability in LDL-cholesterol reductions after inclisiran administration in a real-world multicenter setting in Germany. Clin Res Cardiol 2023; 112(11): 1639–1649. Dostupné z DOI: <http://dx.doi.org/10.1007/s00392–023–02247–8>.

Alonso R, Arroyo-Olivares R, Muñiz-Grijalvo O et al. Persistence with long-term PCSK9 inhibitor treatment and its effectiveness in familial hypercholesterolaemia: data from the SAFEHEART study. Eur J Prev Cardiol 2023; 30(4): 320–328. Dostupné z DOI: <http://dx.doi.org/10.1093/eurjpc/zwac277>.

Ray KK, Bruckert E, Peronne-Filardi P et al. Long-term persistence with evolocumab treatment and sustained reductions in LDL-cholesterol levels over 30 months: final results from the European observational HEYMANS study. Atherosclerosis 2023; 366: 14–21. Dostupné z DOI: <http://dx.doi.org/10.1016/j.atherosclerosis.2023.01.002>.

Sahebkar A, Simental‐Mendía LA, Guerrero‐Romero F et al. Effect of statin therapy on plasma proprotein convertase subtilisin kexin 9 (PCSK9) concentrations: a systematic review and meta‐analysis of clinical trials. Diabetes Obes Metab 2015; 17(11): 1042–1055. Dostupné z DOI: <http://dx.doi.org/10.1111/dom.12536>.

Taylor BA, Thompson PD et al. Statins and their effect on PCSK9 -impact and clinical relevance. Curr Atheroscler Rep 2016; 18(8): 46. Dostupné z DOI: <http://dx.doi.org/10.1007/s11883–016–0604–3>.

Patnaik S, Pollevick ME, Lara-Breitinger KM et al. Inter-Individual Variability in Lipid Response: A Narrative Review. Am J Med 2022; 135(12) :1427–1433.e7. Dostupné z DOI: <http://dx.doi.org/10.1016/j.amjmed.2022.06.018>.

Gayoso-Rey M, Díaz-Trastoy O, Romero-Ventosa EY et al. Effectiveness, safety, and adherence to treatment of proprotein convertase subtilisin/Kexin Type 9 inhibitors in real practice. Clin Ther 2021; 43(4): e111-e121. Dostupné z DOI: <http://dx.doi.org/10.1016/j.clinthera.2021.02.002>.

Oleaga C, Shapiro MD, Hay J et al. Hepatic sensing loop regulates PCSK9 secretion in response to inhibitory antibodies. J Am Coll Cardiol 2021; 78(14): 1437–1449. Dostupné z DOI: <http://dx.doi.org/10.1016/j.jacc.2021.07.056>.

Sabatine MS, Giugliano RP, Keech AC et al. Evolocumab and clinical outcomes in patients with cardiovascular disease. N Engl J Med 2017; 376(18): 1713–1722. Dostupné z DOI: <http://dx.doi.org/10.1056/NEJMoa1615664>.

Schwartz GG, Steg PG, Szarek M et al. Alirocumab and cardiovascular outcomes after acute coronary syndrome. N Engl J Med 2018; 379(22): 2097–2107. Dostupné z DOI: <http://dx.doi.org/10.1056/NEJMoa1801174>.

Liberopoulos E. Lipoprotein (a) reduction with proprotein convertase subtilisin/kexin type 9 inhibitors: An unsolved mystery. Eur J Prev Cardiol 2021; 28(8): 813–815. Dostupné z DOI: <http://dx.doi.org/10.1177/2047487320926777>.

Libby P, Ridker PM. Inflammation and atherosclerosis: role of C-reactive protein in risk assessment. Am J Med 2004; 116(Suppl 6A): S9-S16. Dostupné z DOI: <http://dx.doi.org/10.1016/j.amjmed.2004.02.006>.

Landmesser U, Conde LG, Wright RS et al. Effect of inclisiran on haematological and immunological biomarkers: A Pooled analysis of ORION-9,-10 and-11 trial data. Atherosclerosis 2012; 331: E37. Dostupné z DOI: <https://doi.org/10.1016/j.atherosclerosis.2021.06.106>.

Labels
Angiology Diabetology Internal medicine Cardiology General practitioner for adults
Login
Forgotten password

Enter the email address that you registered with. We will send you instructions on how to set a new password.

Login

Don‘t have an account?  Create new account

#ADS_BOTTOM_SCRIPTS#