Sociedad Americana de Hirudoterapia

Cancer-associated venous thromboembolism: Treatment and prevention with rivaroxaban.

Review published in Research and practice in thrombosis and haemostasis (2020)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Narrative reviewEnsayos clínicosDesarrollo de fármacosBauersachs et al. · Research and practice in thrombosis and haemostasis, 2020

Abstract

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.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleReview

Resumen

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...

Por qué esto importa para la hirudoterapia

Esta revisión resume la base de evidencia para el uso de rivaroxabán, un anticoagulante oral directo, en el tratamiento y la prevención del tromboembolismo venoso (TEV) asociado a cáncer. Si bien el manejo más amplio de la trombosis está tangencialmente relacionado con los objetivos terapéuticos de los anticoagulantes derivados de sanguijuelas, este resumen se enfoca exclusivamente en anticoagulantes orales directos y en heparina de bajo peso molecular. No hay mención de sanguijuelas, hirudoterapia ni medicamentos basados en hirudina como la bivalirudina. En consecuencia, el artículo no tiene relevancia directa para el dominio específico de la terapia con sanguijuelas y el secretoma de la sanguijuela de la American Society of Hirudotherapy.

Citación

Cancer-associated venous thromboembolism: Treatment and prevention with rivaroxaban.

Bauersachs et al. · Research and practice in thrombosis and haemostasis, 2020

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: 18 de junio de 2026

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.