Proprotein convertase subtilisin kexin type 9 inhibitors: update from clinical trials to real-world experience

被引:11
作者
Farnier, Michel [1 ]
机构
[1] Lipid Clin, Point Med, Dijon, France
关键词
cardiovascular prevention; LDL-cholesterol; monoclonal antibodies; proprotein convertase subtilisin kexin type 9 inhibitors; EVOLOCUMAB AMG 145; HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; LIPOPROTEIN CHOLESTEROL LEVELS; PCSK9; INHIBITION; CARDIOVASCULAR-DISEASE; MONOCLONAL-ANTIBODY; LDL CHOLESTEROL; JAPANESE PATIENTS; STATIN THERAPY; HEART-DISEASE;
D O I
10.1097/MOL.0000000000000356
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose of review After the approval of alirocumab and evolocumab, the first two monoclonal antibodies (mAbs) targeting proprotein convertase subtilisin kexin type 9 (PCSK9), this review provides an update on recent PCSK9 inhibitors data and describes recommendations for the use before the results of the ongoing cardiovascular endpoint trials. Recent findings New studies and complementary analysis of phase III trials have consistently shown that alirocumab and evolocumab are highly effective in reducing LDL-cholesterol and to some extent lipoprotein (a). Some preliminary findings coming from exploratory and post-hoc analyses of the longer-term safety phase III trials and meta-analyses suggest that these mAbs can decrease the incidence of cardiovascular events. Whether or not mAbs targeting PCSK9 definitively reduce the incidence of cardiovascular events without safety concerns shall be demonstrated with the ongoing cardiovascular outcome trials. Waiting these outcome trials and given the high cost of these mAbs, groups of experts have proposed as priorities groups of patients with familial hypercholesterolemia and with atherosclerotic cardiovascular disease who have substantially elevated LDL-cholesterol on maximally tolerated statin/ezetimibe therapy. Summary Before the results of large cardiovascular outcome trials, PCSK9 inhibitors should be only used in some categories of patients with familial hypercholesterolemia and/or with atherosclerotic cardiovascular disease.
引用
收藏
页码:597 / 604
页数:8
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