Key result
In elderly patients with cancer-related VTE, DOAC use was associated with a significantly reduced risk of death from any cause (aHR 0.65) compared with warfarin, with no difference in major bleeding.
Why the study?
Little was known about the effects of direct oral anticoagulants in patients with cancer-related venous thromboembolism.
Does DOAC therapy reduce recurrent VTE, major bleeding, and death from any cause in elderly patients with cancer-associated VTE compared to warfarin?
Cohort (n=445)
No
Does DOAC therapy reduce recurrent VTE, major bleeding, and death from any cause in elderly patients with cancer-associated VTE compared to warfarin?
Hazard Ratio: 0.65 (95% CI 0.52–0.8)
Absolute Event Rate: 17% vs 29.5%
p-value: p=0.005
In elderly patients with cancer-associated VTE, DOACs were associated with a significant reduction in all-cause mortality compared to warfarin, without increasing the risk of major bleeding or recurrent VTE.
May support DOAC preference over warfarin in elderly cancer VTE; hypothesis-generating and requires RCT confirmation.
Background Little is known about the effects of direct oral anticoagulants (DOACs) in cancer[1]related venous thromboembolism patients. Methods Data of patients with cancer-related venous thromboembolism (VTE) were retrieved from King Abdulaziz Medical City Database during 2016–2020. We excluded patients who were not using oral anticoagulants, used anticoagulants for <30 days, used 2 agents concomitantly or switched anticoagulants,were aged <65. The primary outcomes were recurrent VTE,major bleeding, and death from any cause. Results We identified 717 patients who received a diagnosis of cancer-related VTE. After the exclusion criteria were applied, 445 patients remained, 298 were used warfarin, and 147 were received NOACs. Both groups were followed up for 12±2 months. The mean age of the patients was 71 ± 8 in the DOACs group and 76 ±6 in the warfarin group (p > 0.05); 48.24% of patients in the DOAC group and 46.98% of patients in the warfaringroup were men (p > 0.05). The mean HAS-BLED score was 3.7 ± 3.8 in the NOAC group and 3.8 ± 3.9 in the warfaringroup (p > 0.05). Furthermore, among patients with cancer-related VTE, DOAC was associated with no difference in major bleeding or recurrence events (CRR = 0.91, 95% CI = 0.78–1.05; CRR = 0.63, 95% CI = 0.52–0.77, respectively), and significantly reduced death from any cause (aHR = 0.65, 95% CI = 0.52–0.80) compared with warfarin. Conclusions In elderly patients with cancer-related VTE, DOAC was associated with reduced death from any cause compared with warfarin, whereas no difference in major bleeding or recurrent VTE were observed between these treatment modalities.
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Prof. Fahad Abdullah Saleh Aleidan (2022) conducted a cohort in Cancer-associated venous thromboembolism (n=445). Direct oral anticoagulants (DOACs) vs. Warfarin was evaluated on Death from any cause (aHR 0.65, 95% CI 0.52-0.80, p=0.005). In elderly patients with cancer-related VTE, DOAC use was associated with a significantly reduced risk of death from any cause (aHR 0.65) compared with warfarin, with no difference in major bleeding.
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