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Rivaroxaban for cancer-associated venous thromboembolism

All cancers can increase the risk of developing venous thromboembolism (VTE), and anticoagulants should be considered as an optimal treatment for patients suffering from cancer-associated VTE. However, there is still a debate about whether the new oral anticoagulant, rivaroxaban, can bring better ef...

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Autores principales: Liang, Bo, Liang, Yi, Zhao, Li-Zhi, Zhao, Yu-Xiu, Gu, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454885/
https://www.ncbi.nlm.nih.gov/pubmed/33913387
http://dx.doi.org/10.1177/00368504211012160
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author Liang, Bo
Liang, Yi
Zhao, Li-Zhi
Zhao, Yu-Xiu
Gu, Ning
author_facet Liang, Bo
Liang, Yi
Zhao, Li-Zhi
Zhao, Yu-Xiu
Gu, Ning
author_sort Liang, Bo
collection PubMed
description All cancers can increase the risk of developing venous thromboembolism (VTE), and anticoagulants should be considered as an optimal treatment for patients suffering from cancer-associated VTE. However, there is still a debate about whether the new oral anticoagulant, rivaroxaban, can bring better efficacy and safety outcomes globally. Thus, this systematic review and meta-analysis was conducted to evaluate the efficacy and safety of rivaroxaban. We searched PubMed, Cochrane Central Register of Controlled Trials, Web of Science, and China National Knowledge Infrastructure for relevant published papers before 1 September 2019, with no language restrictions. The primary outcomes are defined as the recurrence of VTE. The secondary outcomes are defined as clinically relevant non-major bleeding, adverse major bleeding events, and all-cause of death. The data were analyzed by Stata with risk ratio (RR) and 95% confidence interval (CI). Four trials encompassing 1996 patients were included. Rivaroxaban reduced recurrent VTE with no significant difference (RR = 0.68, 95% CI = 0.43–1.07). Similarly, there were no significant differences in adverse major bleeding events (RR = 0.86, 95% CI = 0.37–2.00), clinically relevant non-major bleeding (RR = 1.24, 95% CI = 0.73–2.12) and all-cause mortality (RR = 0.76, 95% CI = 0.40–1.44). In a selected study population of cancer patients with VTE, rivaroxaban is as good as other anticoagulants. Further, carefully designed randomized controlled trials should be performed to confirm these results.
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spelling pubmed-104548852023-08-26 Rivaroxaban for cancer-associated venous thromboembolism Liang, Bo Liang, Yi Zhao, Li-Zhi Zhao, Yu-Xiu Gu, Ning Sci Prog Article All cancers can increase the risk of developing venous thromboembolism (VTE), and anticoagulants should be considered as an optimal treatment for patients suffering from cancer-associated VTE. However, there is still a debate about whether the new oral anticoagulant, rivaroxaban, can bring better efficacy and safety outcomes globally. Thus, this systematic review and meta-analysis was conducted to evaluate the efficacy and safety of rivaroxaban. We searched PubMed, Cochrane Central Register of Controlled Trials, Web of Science, and China National Knowledge Infrastructure for relevant published papers before 1 September 2019, with no language restrictions. The primary outcomes are defined as the recurrence of VTE. The secondary outcomes are defined as clinically relevant non-major bleeding, adverse major bleeding events, and all-cause of death. The data were analyzed by Stata with risk ratio (RR) and 95% confidence interval (CI). Four trials encompassing 1996 patients were included. Rivaroxaban reduced recurrent VTE with no significant difference (RR = 0.68, 95% CI = 0.43–1.07). Similarly, there were no significant differences in adverse major bleeding events (RR = 0.86, 95% CI = 0.37–2.00), clinically relevant non-major bleeding (RR = 1.24, 95% CI = 0.73–2.12) and all-cause mortality (RR = 0.76, 95% CI = 0.40–1.44). In a selected study population of cancer patients with VTE, rivaroxaban is as good as other anticoagulants. Further, carefully designed randomized controlled trials should be performed to confirm these results. SAGE Publications 2021-04-29 /pmc/articles/PMC10454885/ /pubmed/33913387 http://dx.doi.org/10.1177/00368504211012160 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Article
Liang, Bo
Liang, Yi
Zhao, Li-Zhi
Zhao, Yu-Xiu
Gu, Ning
Rivaroxaban for cancer-associated venous thromboembolism
title Rivaroxaban for cancer-associated venous thromboembolism
title_full Rivaroxaban for cancer-associated venous thromboembolism
title_fullStr Rivaroxaban for cancer-associated venous thromboembolism
title_full_unstemmed Rivaroxaban for cancer-associated venous thromboembolism
title_short Rivaroxaban for cancer-associated venous thromboembolism
title_sort rivaroxaban for cancer-associated venous thromboembolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454885/
https://www.ncbi.nlm.nih.gov/pubmed/33913387
http://dx.doi.org/10.1177/00368504211012160
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