Why the study?
Guidelines caution using direct oral anticoagulants in cancer patients due to drug-drug interactions with antineoplastic therapies, but the clinical impact of these interactions on venous thromboembolism recurrence and bleeding has not been studied in clinical trials.
Do drug-drug interactions between apixaban or rivaroxaban and antineoplastic therapy increase venous thromboembolism recurrence and bleeding in cancer patients?
Cohort
Do drug-drug interactions between apixaban or rivaroxaban and antineoplastic therapy increase venous thromboembolism recurrence and bleeding in cancer patients?
In a small retrospective cohort, the presence of drug-drug interactions between direct oral anticoagulants and antineoplastic therapy did not definitively confirm a higher risk of bleeding or VTE recurrence.
Answers are grounded in this paper and cite their sources.
The clinical impact of DOAC-antineoplastic DDIs remains unclear in cancer-associated VTE; this retrospective analysis leaves open questions for prospective trials.
INTRODUCTION: Venous thromboembolism is a common complication among cancer patients with an estimated risk of 20%. American Society of Clinical Oncology guidelines recommend direct oral anticoagulants for long-term anticoagulation but caution the use of direct oral anticoagulants because of drug-drug interactions with antineoplastic therapies. The clinical impact of these drug-drug interactions is yet to be studied in clinical trials. This study aims to evaluate the effect of the drug-drug interactions on venous thromboembolism recurrence and bleeding. METHODS: This is a retrospective cohort study that included cancer patients with venous thromboembolism receiving apixaban or rivaroxaban with antineoplastic therapy. The impact of the drug-drug interaction was determined by its effect on the rates of venous thromboembolism recurrence and bleeding in patients with a drug-drug interaction compared to patients with no drug-drug interaction. RESULTS: The primary composite endpoint of venous thromboembolism recurrence and bleeding events occurred in 65% versus 62% of patients in drug-drug interaction and non-drug-drug interaction groups accordingly. There was a higher rate of venous thromboembolism recurrence and minor bleeding events with anti-mitotic microtubule inhibitors and a higher rate of minor bleeding events with hormonal therapy and alkylating agents. Among the drug-drug interaction group, there were no major bleeding events reported with mild drug-drug interactions when compared to moderate-to-severe drug-drug interactions. There was no difference in time to venous thromboembolism recurrence between rivaroxaban and apixaban. CONCLUSION: Due to small sample size, our study results could not confirm a higher risk of bleeding or venous thromboembolism recurrence with the drug-drug interactions. Further prospective study is warranted, but clinicians should be aware of these drug-drug interactions and identify them using available literature.
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Yassine et al. (2020) conducted a cohort in Venous thromboembolism in cancer patients. Drug-drug interaction between DOACs and antineoplastic therapy vs. No drug-drug interaction was evaluated on Composite endpoint of venous thromboembolism recurrence and bleeding events.
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