Direct Oral Anticoagulants and Cancer-related Venous Thromboembolism: Insights from an Updated Meta-Analysis

被引:0
作者
Omidi, Fatemeh [1 ]
Sadeghi, Soheila [2 ]
Rahmannia, Maryam [3 ]
Bonjar, Amir Hashem Shahidi [3 ]
Berger, Nathan A. [4 ]
Nasiri, Mohammad Javad [3 ]
机构
[1] Shahid Beheshti Univ Med Sci, Imam Hossein Hosp, Dept Cardiol, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Imam Hossein Hosp, Dept Internal Med, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Sch Med, Dept Internal Med, Tehran, Iran
[4] Case Western Reserve Univ, Case Comprehens Canc Ctr, Dept Oncol, Cleveland, OH 44106 USA
关键词
Direct oral anticoagulants; thromboprophylaxis; cancer-associated venous thromboembolism; meta-analysis; DISEASE;
D O I
10.2174/0115733947322285241004075557
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Cancer-associated venous thromboembolism (VTE) presents a complex clinical challenge, with the need to balance effective anticoagulation against the risk of bleeding. Direct oral anticoagulants (DOACs) offer convenience but their efficacy and safety in this context remain debated. This systematic review and meta-analysis endeavor to evaluate the effectiveness and safety of DOACs in managing VTE associated with cancer. The findings offer essential perspectives to guide clinical decision-making. Methods We performed an exhaustive search across electronic databases such, as PubMed, EMBASE, and the Cochrane CENTRAL, spanning from their inception to December 15, 2023. Only English-published articles evaluating the effectiveness and safety of DOACs in managing cancer-associated VTE were considered. Evaluation criteria encompassed recurrent VTE, major bleeding (MB), clinically significant non-major bleeding (CSNMB), and clinically relevant bleeding (CRB). Statistical analyses were conducted utilizing Comprehensive Meta-Analysis software. Results From the 1195 records, 8 studies with 3913 patients were included. DOACs demonstrated a significant reduction in recurrent VTE risk (OR: 0.73, CI 95%: 0.57-0.93, p =0.01) compared to traditional anticoagulants. However, there was a marginal increase in MB risk (OR: 1.24, CI 95%: 0.90-1.69, p =0.17) with DOACs, though not statistically significant. Notably, DOACs were associated with a higher risk of CRNMB (OR: 1.64, CI 95%: 1.24-2.17, p <0.001) and CRB (OR: 1.22, CI 95%: 1.00-1.52, p =0.04). No publication bias was observed. Gastrointestinal cancer, Rivaroxaban/apixaban use, switching from dalteparin, improved physical function with DOACs, specific tumor sites, and older age subgroups were predictors for bleeding complications in cancer patients on anticoagulant therapy. Conclusion This meta-analysis provides evidence supporting the efficacy of DOACs in reducing VTE recurrence in cancer patients. However, the increased risk of bleeding complications warrants careful consideration in personalized treatment decisions. Ongoing research is necessary to refine therapeutic strategies in this complex clinical landscape.
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