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Direct oral anticoagulant for the prevention of thrombosis in ambulatory patients with cancer: A systematic review and meta-analysis.

Publication ,  Journal Article
Li, A; Kuderer, NM; Garcia, DA; Khorana, AA; Wells, PS; Carrier, M; Lyman, GH
Published in: J Thromb Haemost
December 2019

BACKGROUND: It is unclear if direct oral anticoagulant (DOAC) is efficacious and safe for prophylaxis of venous thromboembolism (VTE) in ambulatory patients with cancer. METHODS: We performed a systematic review using EMBASE, MEDLINE, and CENTRAL. Inclusion criteria included adult ambulatory patients with cancer, prophylactic use of DOAC, and randomized controlled trials. Exclusion criteria included pediatric patients, inpatient or postoperative setting, therapeutic indication of DOAC, or non-phase III randomized controlled trial. Two authors screened/reviewed articles and abstracted the data. Meta-analysis was performed using random-effects model. Efficacy outcome included overall and symptomatic VTE incidence during the first 6 months. Safety outcomes included major bleeding and clinically relevant non-major bleeding (CRNMB) incidence during the on-treatment period. Subgroup analysis was performed for intermediate- and high-risk Khorana score. RESULTS: A total of 202 records were identified and 28 full-text articles were assessed. Two studies with 1415 participants were included for meta-analysis. For DOAC vs placebo, the relative risks for overall and symptomatic VTE incidence by 6 months were 0.56 (0.35-0.89) and 0.58 (0.29-1.13), respectively. The relative risks for major bleeding and CRNMB while on-treatment were 1.96 (0.80-4.82) and 1.28 (0.74-2.20), respectively. Patients with high-risk Khorana score (3+) derived the largest absolute risk reduction of VTE. CONCLUSIONS: Low-dose DOAC reduces the rate of overall VTE in higher risk cancer patients starting systemic chemotherapy. It may reduce the rate of symptomatic VTE but increase the likelihood of bleeding.

Duke Scholars

Published In

J Thromb Haemost

DOI

EISSN

1538-7836

Publication Date

December 2019

Volume

17

Issue

12

Start / End Page

2141 / 2151

Location

England

Related Subject Headings

  • Venous Thrombosis
  • Venous Thromboembolism
  • Treatment Outcome
  • Risk Factors
  • Risk Assessment
  • Neoplasms
  • Incidence
  • Humans
  • Hemorrhage
  • Factor Xa Inhibitors
 

Citation

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Li, A., Kuderer, N. M., Garcia, D. A., Khorana, A. A., Wells, P. S., Carrier, M., & Lyman, G. H. (2019). Direct oral anticoagulant for the prevention of thrombosis in ambulatory patients with cancer: A systematic review and meta-analysis. J Thromb Haemost, 17(12), 2141–2151. https://doi.org/10.1111/jth.14613
Li, Ang, Nicole M. Kuderer, David A. Garcia, Alok A. Khorana, Philip S. Wells, Marc Carrier, and Gary H. Lyman. “Direct oral anticoagulant for the prevention of thrombosis in ambulatory patients with cancer: A systematic review and meta-analysis.J Thromb Haemost 17, no. 12 (December 2019): 2141–51. https://doi.org/10.1111/jth.14613.
Li A, Kuderer NM, Garcia DA, Khorana AA, Wells PS, Carrier M, et al. Direct oral anticoagulant for the prevention of thrombosis in ambulatory patients with cancer: A systematic review and meta-analysis. J Thromb Haemost. 2019 Dec;17(12):2141–51.
Li, Ang, et al. “Direct oral anticoagulant for the prevention of thrombosis in ambulatory patients with cancer: A systematic review and meta-analysis.J Thromb Haemost, vol. 17, no. 12, Dec. 2019, pp. 2141–51. Pubmed, doi:10.1111/jth.14613.
Li A, Kuderer NM, Garcia DA, Khorana AA, Wells PS, Carrier M, Lyman GH. Direct oral anticoagulant for the prevention of thrombosis in ambulatory patients with cancer: A systematic review and meta-analysis. J Thromb Haemost. 2019 Dec;17(12):2141–2151.
Journal cover image

Published In

J Thromb Haemost

DOI

EISSN

1538-7836

Publication Date

December 2019

Volume

17

Issue

12

Start / End Page

2141 / 2151

Location

England

Related Subject Headings

  • Venous Thrombosis
  • Venous Thromboembolism
  • Treatment Outcome
  • Risk Factors
  • Risk Assessment
  • Neoplasms
  • Incidence
  • Humans
  • Hemorrhage
  • Factor Xa Inhibitors