Therapeutic Potential and Critical Analysis of the PCSK9 Monoclonal Antibodies Evolocumab and Alirocumab

被引:24
|
作者
White, C. Michael [1 ,2 ,3 ]
机构
[1] Univ Connecticut, Sch Pharm, Storrs, CT 06269 USA
[2] Univ Connecticut, Storrs, CT 06269 USA
[3] Hartford Hosp, Storrs, CT USA
关键词
hypercholesterolemia; familial hypercholesterolemia; PCSK9; inhibitors; evolocumab; alirocumab; ACUTE CORONARY SYNDROMES; FAMILIAL HYPERCHOLESTEROLEMIA; CARDIOVASCULAR EVENTS; CHOLESTEROL LEVELS; REDUCING LIPIDS; STATIN THERAPY; HEART-DISEASE; HIGH-RISK; SAFETY; EFFICACY;
D O I
10.1177/1060028015608487
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: To review the mechanism of action for PCSK9 monoclonal antibodies and critically evaluate the therapeutic potential of evolocumab and alirocumab in the treatment of hypercholesterolemia. Data Sources: Ovid MEDLINE search from 1980 to August 2015 using the terms PCSK9, evolocumab, and alirocumab with forward and backward citation tracking. Study Selection and Data Extraction: English-language trials and studies assessing the mechanism, efficacy, or safety of PCSK9 monoclonal antibodies were included. Data Synthesis: PCSK9 monoclonal antibodies have a potent ability to reduce low-density lipoprotein (LDL) by almost 50% in controlled trials: -47.49% (95% CI = -69.6% to -25.4%). They have an acceptable safety profile with no significant elevations in Creatine Kinase (CK) (odds ratio [OR] = 0.72; 95% CI = 0.54 to 0.96) or serious adverse events (OR = 1.01; 95% CI = 0.87 to 1.18), and preliminary evidence suggests reductions in myocardial infarction (OR = 0.49; 95% CI = 0.26 to 0.93). Although it is effective in several familial hypercholesterolemia (FH) patient types, it does not work in homozygous patients with dual allele LDL receptor negative polymorphisms or those who are homozygous for autosomal recessive hypercholesterolemia. Conclusions: Although not preferred over statins because of limited clinical trial evidence of cardiovascular event reductions, dosing convenience, and expense, PCSK9 monoclonal antibodies will have a prominent role to play in the treatment of hypercholesterolemia, especially in patients needing large LDL reductions, including patients with many types of FH.
引用
收藏
页码:1327 / 1335
页数:9
相关论文
共 50 条
  • [21] Safety of Monoclonal Antibodies Inhibiting PCSK9 in Pregnancy: Disproportionality Analysis in VigiBase®
    Noseda, Roberta
    Bedussi, Francesca
    Panchaud, Alice
    Ceschi, Alessandro
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2024, : 346 - 350
  • [22] Characterization of Autosomal Dominant Hypercholesterolemia Caused by PCSK9 Gain of Function Mutations and Its Specific Treatment With Alirocumab, a PCSK9 Monoclonal Antibody
    Hopkins, Paul N.
    Defesche, Joep
    Fouchier, Sigrid W.
    Bruckert, Eric
    Luc, Gerald
    Cariou, Bertrand
    Sjouke, Barbara
    Leren, Trond P.
    Harada-Shiba, Mariko
    Mabuchi, Hiroshi
    Rabes, Jean-Pierre
    Carrie, Alain
    van Heyningen, Charles
    Carreau, Valerie
    Farnier, Michel
    Teoh, Yee P.
    Bourbon, Mafalda
    Kawashiri, Masa-aki
    Nohara, Atsushi
    Soran, Handrean
    Marais, A. David
    Tada, Hayato
    Abifadel, Marianne
    Boileau, Catherine
    Chanu, Bernard
    Katsuda, Shoji
    Kishimoto, Ichiro
    Lambert, Gilles
    Makino, Hisashi
    Miyamoto, Yoshihiro
    Pichelin, Matthieu
    Yagi, Kunimasa
    Yamagishi, Masakazu
    Zair, Yassine
    Mellis, Scott
    Yancopoulos, George D.
    Stahl, Neil
    Mendoza, Johanna
    Du, Yunling
    Hamon, Sara
    Krempf, Michel
    Swergold, Gary D.
    CIRCULATION-CARDIOVASCULAR GENETICS, 2015, 8 (06) : 823 - 831
  • [23] EVOLOCUMAB AND ALIROCUMAB INCREASES TOTAL PCSK9 PLASMA LEVELS IN HYPOCHOLESTEROLEMIC PATIENTS: INVESTIGATION OF THE BASIC MOLECULAR MECHANISMS
    Ferri, N.
    Lupo, M. G.
    Trevisin, M.
    Zambon, S.
    Zambon, A.
    ATHEROSCLEROSIS, 2021, 331 : E4 - E4
  • [24] Is there enough evidence with evolocumab and alirocumab (antibodies to proprotein convertase substilisin-kexin type, PCSK9) on cardiovascular outcomes to use them widely?
    Doggrell, Sheila Anne
    Lynch, Kaileen Anne
    EXPERT OPINION ON BIOLOGICAL THERAPY, 2015, 15 (12) : 1671 - 1675
  • [25] PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia
    Ito, Matthew K.
    Santos, Raul D.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2017, 57 (01): : 7 - 32
  • [26] Focus on alirocumab: A PCSK9 antibody to treat hypercholesterolemia
    Devito, Fiorella
    Zito, Annapaola
    Ricci, Gabriella
    Carbonara, Rosa
    Dentamaro, Ilaria
    Cortese, Francesca
    Carbonara, Santa
    Ciccone, Marco Matteo
    PHARMACOLOGICAL RESEARCH, 2015, 102 : 168 - 175
  • [27] Efficacy and Safety of PCSK9 Monoclonal Antibodies in Patients With Diabetes
    Marouf, Bushra Hassan
    Iqbal, Zohaib
    Mohamad, Jamal Basheer
    Bashir, Bilal
    Schofield, Jonathan
    Syed, Akheel
    Kilpatrick, Eric S.
    Stefanutti, Claudia
    Soran, Handrean
    CLINICAL THERAPEUTICS, 2022, 44 (02) : 331 - 348
  • [28] PCSK9 Monoclonal Antibodies Have Come a Long Way
    Sandra Zendjebil
    Philippe Gabriel Steg
    Current Atherosclerosis Reports, 2024, 26 (12) : 721 - 732
  • [29] PCSK9 Inhibitors: What Lies Beyond Monoclonal Antibodies?
    不详
    EBIOMEDICINE, 2015, 2 (12): : 1835 - 1835
  • [30] Monoclonal antibodies against PCSK9: from bench to clinic
    Guijarro Herraiz, Carlos
    CLINICA E INVESTIGACION EN ARTERIOSCLEROSIS, 2016, 28 : 14 - 21