Is there enough evidence with evolocumab and alirocumab (antibodies to proprotein convertase substilisin-kexin type, PCSK9) on cardiovascular outcomes to use them widely?

被引:5
作者
Doggrell, Sheila Anne [1 ]
Lynch, Kaileen Anne [1 ]
机构
[1] Queensland Univ Technol, Brisbane, Qld 4001, Australia
关键词
alirocumab; cardiovascular events; evolocumab; LDL cholesterol; PCSK9; antibodies; safety; SUBTILISIN/KEXIN TYPE 9; MONOCLONAL-ANTIBODY; LDL-C; HYPERCHOLESTEROLEMIA; EFFICACY; STATIN; SAFETY; TOLERABILITY; MONOTHERAPY; TRIAL;
D O I
10.1517/14712598.2015.1093109
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Statins alone often do not reduce LDL cholesterol levels sufficiently to given maximum cardiovascular benefit. Thus, additional drugs are required to reduce the levels of LDL cholesterol. Monoclonal antibodies to PCSK9 have recently been shown to decrease LDL cholesterol, but it is not known whether they improve cardiovascular outcomes.Areas covered: We evaluated two clinical trials reporting cardiovascular outcomes with antibodies to PCSK9, the OSLER extension with evolocumab, and the ODYSSEY LONG TERM trial with alirocumab.Expert opinion: In OSLER and ODYSSEY LONG TERM, there were very few cardiovascular outcomes, but the trials do suggest that evolocumab and alirocumab may reduce these outcomes. However, there are also some safety concerns with both of these antibodies. Large clinical outcome trials are underway with both evolocumab and alirocumab, which will probably clarify both the safety concerns and any cardiovascular benefits with these antibodies. In our opinion, these antibodies may be suitable for use in subjects with familial hypercholesterolemia, who are uncontrolled with their present medications, provided intensive safety and cardiovascular monitoring is being undertaken. However, evolocumab and alirocumab should be used with caution in other subjects, until outcome studies in higher numbers of subjects have shown acceptable safety and cardiovascular profiles.
引用
收藏
页码:1671 / 1675
页数:5
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