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Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

4800 - Systematic Literature Review and Network Meta-analysis of oral Anticoagulants for the Treatment of Venous Thromboembolism in patients with cancer

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Supportive Care and Symptom Management

Tumour Site

Presenters

Hyunkyung Park

Citation

Annals of Oncology (2018) 29 (suppl_8): viii603-viii640. 10.1093/annonc/mdy300

Authors

H. Park, J. Kim, J. Cho, J.H. Lim, M.H. Lee

Author affiliations

  • Hemato-oncology, Inha University Hospital, 22332 - Incheon/KR
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Resources

Abstract 4800

Background

Based on the current guideline, treatment options for cancer-associated thrombosis include low molecular weight heparin (LMWH), unfractionated heparin (UFH), warfarin, and fondaparinux. However, in patients who do not have cancer, direct oral anticoagulants are preferred for the treatment of VTE. In some cases, the use of LMWH is limited due to administration by the subcutaneous route. In this study, we compared the efficacy and safety of oral anticoagulants including vitamin K antagonists (VKA) and direct-acting oral anticoagulants (DOAC) for the treatment of cancer-associated VTE.

Methods

We conducted a systematic literature review to identify all eligible randomized controlled trials (RCT) by searching PubMed, Web of Science, ASH, ASCO, EHA, and ESMO databases. The relative risks (RR) of recurrent VTE (efficacy) and major bleeding (safety) were analyzed using Bayesian network meta-analysis with a fixed-effect model.

Results

Four DOACs (apixaban, dabigatran, edoxaban, rivaroxaban) were identified in five RCTs. When comparing the efficacy between VKA and DOACs, the recurrence rate of VTE was lower in the treatment with DOACs than with VKA, but not statistically significant. (apixaban: odds ratio [OR] 0.55, 95% credible intervals [CrI] 0.10-2.4; dabigatran: OR 0.76, 95% CrI 0.32-1.8; edoxaban: OR 0.49, 95% CrI 0.12-1.7; rivaroxaban OR 0.57, 95% CrI 0.19-1.7). In safety, the risk of major bleeding was relatively low in the use of DOACs compared to VKA, except for edoxaban (apixaban: OR 0.42, 95% CrI 0.058-2.2; dabigatran: OR 0.82, 95% CrI 0.25-2.7; edoxaban: OR 1.6, 95% CrI 0.38-8.4; rivaroxaban OR 0.47, 95% CrI 0.14-1.5).

Conclusions

For the treatment of VTE in cancer patients, DOAC has a favorable tendency for the efficacy and safety compared to VKA. DOACs could be one of the standard treatment options for management of VTE in cancer patients. Among DOACs, epixaban has a relatively good outcome.

Clinical trial identification

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Editorial Acknowledgement

none

Disclosure

All authors have declared no conflicts of interest.

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