Why the study?
Do direct oral anticoagulants (DOACs) prevent recurrent venous thromboembolism and effectively treat acute symptomatic venous thromboembolism compared to standard therapy?
Do direct oral anticoagulants (DOACs) prevent recurrent venous thromboembolism and effectively treat acute symptomatic venous thromboembolism compared to standard therapy?
DOACs are noninferior to standard therapy for the treatment and secondary prevention of venous thromboembolism, offering a similar or improved safety profile regarding major bleeding.
Trial design differences among DOAC VTE studies limit direct comparisons; leaves open optimal agent selection.
Direct oral anticoagulants (DOACs) have been compared with standard therapy in large phase III studies to assess their safety and efficacy in the treatment of deep vein thrombosis and/or pulmonary embolism and in the secondary prevention of recurrent venous thromboembolism. Although the mean population age and the gross inclusion and exclusion criteria were similar across these studies, they differed in other aspects such as overall study design and acute treatment strategies. The 4 DOACs examined in phase III trials (apixaban, edoxaban, rivaroxaban, and dabigatran) showed noninferiority compared with standard therapy for the treatment of deep vein thrombosis and/or pulmonary embolism and for the prevention of recurrent venous thromboembolism. Furthermore, these DOACs exhibited a similar safety profile to standard therapy, with the risk of major bleeding significantly reduced in some of these studies. Rivaroxaban and apixaban were tested as a single-drug approach, whereas in the dabigatran and edoxaban studies, initial bridging with parenteral agents was employed. The purpose of this review is to compare the phase III studies of DOACs in this indication, to highlight the differences, and to discuss a series of clinically relevant issues, including the management of key patient subgroups (eg, fragile patients, those with cancer or renal impairment), extended treatment, use of comedications, heparin pretreatment versus a single-drug approach, and the bleeding profiles of the DOACs.
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Granziera et al. (2015) studied this question.
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