Why the study?
Do investigational target-specific oral anticoagulants improve clinical benefit and minimize bleeding risks in patients requiring treatment and prevention of venous thromboembolism?
Do investigational target-specific oral anticoagulants improve clinical benefit and minimize bleeding risks in patients requiring treatment and prevention of venous thromboembolism?
This systematic review highlights edoxaban as a promising investigational target-specific oral anticoagulant for VTE management, though direct comparisons and solutions to existing TSOAC limitations are still lacking.
Edoxaban warrants priority evaluation in VTE development; extends TSOAC data but leaves head-to-head comparisons open.
Anticoagulation therapy is often indicated for the treatment and prevention of venous thromboembolism (VTE). Despite advances in anticoagulant management with parenteral anticoagulants and vitamin K antagonists, limitations to their use still exists, leading to investigation of alternative anticoagulants such as factor Xa inhibitors and direct thrombin inhibitors. To date, 3 target-specific oral anticoagulants (TSOACs) are Food and Drug Administration approved; several other agents are currently in development to optimize VTE management and minimize bleeding risks. The objective of this systematic review article is to provide clinicians an overview of the clinical evidence on the investigational TSOACs for the treatment and prevention of VTE. Of the agents in development, edoxaban holds the most promise due to robust data supporting its clinical benefit with a similar bleeding risk to currently approved agents. Clinicians should understand the TSOACs under investigation, since differences in pharmacokinetics and pharmacodynamics may influence clinical decision making and agent selection for management of VTE. Currently, no direct comparisons between TSOACs have been conducted. Agents under investigation have yet to overcome the major limitations of the currently existing TSOACs. Further studies are necessary to clarify which TSOAC agent is best for management of VTE in clinical practice.
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Devabhakthuni et al. (2015) studied this question.
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