Key result
Rivaroxaban yields similar recurrent VTE rates in asymptomatic versus symptomatic patients.
Why the study?
An established treatment strategy for asymptomatic pulmonary embolism or deep vein thrombosis remains uncertain in Japan.
Does rivaroxaban treatment yield similar outcomes in asymptomatic versus symptomatic patients with venous thromboembolism?
Observational (n=1,016)
Yes
Does rivaroxaban treatment yield similar outcomes in asymptomatic versus symptomatic patients with venous thromboembolism?
Hazard Ratio: 0.6 (95% CI 0.22–1.62)
Absolute Event Rate: 1.8% vs 3.1%
p-value: p=0.31
Rivaroxaban demonstrates a similar safety and efficacy profile for both asymptomatic and symptomatic venous thromboembolism in a real-world Japanese cohort.
Comparable outcomes with rivaroxaban in asymptomatic versus symptomatic VTE; leaves open whether guidelines should endorse treatment in Japan.
BACKGROUND: An established treatment strategy for asymptomatic pulmonary embolism (PE) or deep vein thrombosis (DVT) remains uncertain in Japan; therefore, in this study, we clarify the characteristics and outcomes of symptomatic compared to asymptomatic patients with PE or DVT. METHODS: This prospective, multicenter sub-analysis of the J'xactly study in Japan included 1,016 patients (mean age, 68; 41% male) with venous thromboembolism (VTE) treated with rivaroxaban. RESULTS: Asymptomatic PE patients (47% of PE patients) were more likely to have active cancer and asymptomatic proximal DVT at lower severity than symptomatic PE patients, despite no differences in age, sex, or the proportion receiving intensive 30 mg/day-rivaroxaban. Patients with asymptomatic DVT (34% of DVT patients) were older, had higher rates of female sex, active cancer, and distal DVT, and received shorter, less intense rivaroxaban treatment. Incidences did not differ between asymptomatic and symptomatic PE patients for recurrent symptomatic VTE (hazard ratio [HR], 0.60; 95% confidence interval [CI], 0.22-1.62; P = 0.31) or major bleeding (HR, 0.68; 95% CI, 0.20-2.33; P = 0.58), nor between asymptomatic and symptomatic DVT patients for recurrent symptomatic VTE (HR, 0.56; 95% CI, 0.23-1.40; P = 0.21) and major bleeding (HR, 1.47; 95% CI, 0.54-3.97; P = 0.45). CONCLUSIONS: The real-world composite adverse event rate for treatment with rivaroxaban, as physician-adjusted for dose and duration, was similar for asymptomatic and symptomatic patients regardless of the presence of PE or DVT, suggesting a favorable safety profile for potential rivaroxaban treatment for asymptomatic VTE.
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Migita et al. (2023) conducted an observational in Venous thromboembolism (VTE) (n=1,016). Asymptomatic venous thromboembolism vs. Symptomatic venous thromboembolism was evaluated on Recurrence or aggravation of symptomatic VTE (PE group) (HR 0.60, 95% CI 0.22-1.62, p=0.31). In patients treated with rivaroxaban, the incidence of recurrent symptomatic VTE did not differ significantly between asymptomatic and symptomatic patients with pulmonary embolism (HR 0.60) or deep vein thrombosis (HR 0.56).
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