Les nouveaux anticoagulants en 2024: développement des inhibiteurs du facteur XI et du XIa

被引:0
|
作者
Bentounes, Nun K. [1 ,2 ]
Melicine, Sophie [1 ,2 ]
Martin, Anne-Celine [1 ,3 ]
Smadja, David M. [1 ,2 ,4 ]
Gendron, Nicolas [1 ,2 ,4 ]
机构
[1] Univ Paris Cite, Innovat Therapies Haemostasis, INSERM, F-75006 Paris, France
[2] Ctr Univ Paris Cite APHP CUP, AP HP, Serv Hematol, 20 Rue Leblanc, F-75015 Paris, France
[3] Ctr Univ Paris Cite APHP CUP, AP HP, Serv Cardiol, 20 Rue Leblanc, F-75015 Paris, France
[4] INNOVTE, F CRIN, St Etienne, France
关键词
FXI/XIa inhibitor; anticoagulants; thromboembolic venous disease; atrial fibrillation; thrombus; haemostasis; DIRECT ORAL ANTICOAGULANTS; ASHKENAZI JEWS; VENOUS THROMBOEMBOLISM; REDUCED INCIDENCE; DEFICIENCY; THROMBOSIS; MUTATIONS; OUTCOMES; PHASE-2;
D O I
10.1684/abc.2024.1865
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Thrombosis remains one of the leading causes of death in the world. The history of anticoagulation has evolved considerably from non-specific drugs ( i.e. , heparins and vitamin K antagonists, VKA) to agents that directly target specific coagulation factors ( i.e. , argatroban, fondaparinux and direct oral anticoagulants, DOAC). Since the last decade, DOAC are widely used in clinical practice because of their ease to use, their favorable pharmacological profile and the fact that they do not require monitoring. However, despite having a better safety profile than vitamin K antagonist, their bleeding risk is not negligible. New anticoagulants targeting the contact phase of coagulation are currently being developed and could make it possible to prevent the risk of thrombosis without impairing hemostasis. Epidemiological and preclinical data on FXI deficiency make FXI a promising therapeutic target. The aim of this review is to summarize the results of the various clinical trials available that focus on FXI/FXIa inhibition, and to highlight the challenges that this new therapeutic class of anticoagulants will face.
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页码:9 / 23
页数:15
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