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Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban

Cancer‐associated venous thromboembolism (VTE) is a frequent, potentially life‐threatening event that complicates cancer management. Anticoagulants are the cornerstone of therapy for the treatment and prevention of cancer‐associated thrombosis (CAT); factor Xa–inhibiting direct oral anticoagulants (...

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Autores principales: Bauersachs, Rupert, Khorana, Alok A., Lee, Agnes Y. Y., Soff, Gerald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292665/
https://www.ncbi.nlm.nih.gov/pubmed/32548552
http://dx.doi.org/10.1002/rth2.12327
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author Bauersachs, Rupert
Khorana, Alok A.
Lee, Agnes Y. Y.
Soff, Gerald
author_facet Bauersachs, Rupert
Khorana, Alok A.
Lee, Agnes Y. Y.
Soff, Gerald
author_sort Bauersachs, Rupert
collection PubMed
description Cancer‐associated venous thromboembolism (VTE) is a frequent, potentially life‐threatening event that complicates cancer management. Anticoagulants are the cornerstone of therapy for the treatment and prevention of cancer‐associated thrombosis (CAT); factor Xa–inhibiting direct oral anticoagulants (DOACs; apixaban, edoxaban, and rivaroxaban), which have long been recommended for the treatment of VTE in patients without cancer, have been investigated in this setting. The first randomized comparisons of DOACs against low‐molecular‐weight heparin for the treatment of CAT indicated that DOACs are efficacious in this setting, with findings reflected in recent updates to published guidance on CAT treatment. However, the higher risk of bleeding events (particularly in the gastrointestinal tract) with DOACs highlights the need for appropriate patient selection. Further insights will be gained from additional studies that are ongoing or awaiting publication. The efficacy and safety of DOAC thromboprophylaxis in ambulatory patients with cancer at a high risk of VTE have also been assessed in placebo‐controlled randomized controlled trials of apixaban and rivaroxaban. Both studies showed efficacy benefits with DOACs, but both studies also showed a nonsignificant increase in major bleeding events while on treatment. This review summarizes the evidence base for rivaroxaban use in CAT, the patient profile potentially most suited to DOAC use, and ongoing controversies under investigation. We also describe ongoing studies from the CALLISTO (Cancer Associated thrombosis—expLoring soLutions for patients through Treatment and Prevention with RivarOxaban) program, which comprises several randomized clinical trials and real‐world evidence studies, including investigator‐initiated research.
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spelling pubmed-72926652020-06-15 Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban Bauersachs, Rupert Khorana, Alok A. Lee, Agnes Y. Y. Soff, Gerald Res Pract Thromb Haemost Review Articles Cancer‐associated venous thromboembolism (VTE) is a frequent, potentially life‐threatening event that complicates cancer management. Anticoagulants are the cornerstone of therapy for the treatment and prevention of cancer‐associated thrombosis (CAT); factor Xa–inhibiting direct oral anticoagulants (DOACs; apixaban, edoxaban, and rivaroxaban), which have long been recommended for the treatment of VTE in patients without cancer, have been investigated in this setting. The first randomized comparisons of DOACs against low‐molecular‐weight heparin for the treatment of CAT indicated that DOACs are efficacious in this setting, with findings reflected in recent updates to published guidance on CAT treatment. However, the higher risk of bleeding events (particularly in the gastrointestinal tract) with DOACs highlights the need for appropriate patient selection. Further insights will be gained from additional studies that are ongoing or awaiting publication. The efficacy and safety of DOAC thromboprophylaxis in ambulatory patients with cancer at a high risk of VTE have also been assessed in placebo‐controlled randomized controlled trials of apixaban and rivaroxaban. Both studies showed efficacy benefits with DOACs, but both studies also showed a nonsignificant increase in major bleeding events while on treatment. This review summarizes the evidence base for rivaroxaban use in CAT, the patient profile potentially most suited to DOAC use, and ongoing controversies under investigation. We also describe ongoing studies from the CALLISTO (Cancer Associated thrombosis—expLoring soLutions for patients through Treatment and Prevention with RivarOxaban) program, which comprises several randomized clinical trials and real‐world evidence studies, including investigator‐initiated research. John Wiley and Sons Inc. 2020-04-04 /pmc/articles/PMC7292665/ /pubmed/32548552 http://dx.doi.org/10.1002/rth2.12327 Text en © 2020 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Bauersachs, Rupert
Khorana, Alok A.
Lee, Agnes Y. Y.
Soff, Gerald
Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban
title Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban
title_full Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban
title_fullStr Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban
title_full_unstemmed Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban
title_short Cancer‐associated venous thromboembolism: Treatment and prevention with rivaroxaban
title_sort cancer‐associated venous thromboembolism: treatment and prevention with rivaroxaban
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292665/
https://www.ncbi.nlm.nih.gov/pubmed/32548552
http://dx.doi.org/10.1002/rth2.12327
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