Sociedad Americana de Hirudoterapia

How I treat cancer-associated thrombosis

Research article published in ESMO open (2020)

Última actualización: June 18, 2026Revisado por: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewEnsayos clínicosMoik et al. · ESMO open, 2020

Abstract

Patients with cancer are at an increased risk of symptomatic venous thromboembolism (VTE). In addition, an increasing number of patients with incidental thromboembolic events have been recorded in clinical practice. Therapeutic anticoagulation is crucial to prevent thrombus progression and reduce risk of recurrence; however, this comes at the price of an increased bleeding risk, which necessitates a personalised approach to choose the most appropriate type of therapy. Over the last decade, low-molecular-weight heparin has been the preferred anticoagulant agent for patients with cancer-associated thrombosis due to better efficacy and similar safety profile compared with vitamin K antagonists. While direct oral anticoagulants (DOAC) have emerged as new option for treatment of VTE in a general population, only limited data have been available specifically for patients with cancer until recently. Randomised, controlled trials have now been published, establishing DOAC as an alternative for the treatment of cancer-associated thrombosis. However, the improvement in the therapeutic armamentarium is accompanied by a number of special considerations. For instance, risk of bleeding is elevated in patients with cancer-associated VTE receiving DOAC, especially in certain tumour types (eg, gastrointestinal), and no guidance exists regarding their use in patients with severe thrombocytopaenia. Furthermore, DOAC are prone to certain drug-drug interactions and their effect might be altered due to nausea and vomiting in patients receiving chemotherapy. Here, we provide guidance on how to treat cancer-associated VTE and how new evidence from randomised controlled trials can be implemented in clinical practice. There are still clinical scenarios where robust evidence is lacking and treatment recommendations are based on extrapolations from other populations or expert opinion only. Therefore, additional research in special subpopulations is needed to optimise management of patients in challenging clinical scenarios.

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

Publication typeJournal ArticleReview
Indexed MeSH termsHumansNeoplasmsThrombosis

Resumen

Peer-reviewed clinical and outcomes research relevant to medicinal leech therapy and its biology. Indexed in PubMed and verified against the NCBI record.

Por qué esto importa para la hirudoterapia

Este artículo de orientación experta "Cómo trato" revisa la gestión del tromboembolismo venoso asociado al cáncer, señalando que la heparina de bajo peso molecular ha sido el agente preferido mientras que los ensayos aleatorizados ahora establecen los anticoagulantes orales directos como una alternativa, y detalla consideraciones especiales como el riesgo de sangrado elevado (notablemente en tumores gastrointestinales), la incertidumbre en la trombocitopenia severa, las interacciones medicamentosas y la absorción afectada por las náuseas y vómitos relacionados con la quimioterapia. Para la ASH, subraya cómo las decisiones de anticoagulación son individualizadas y sensibles al sangrado en pacientes complejos, contexto relevante para comprender la biología antitrombótica que fundamenta la discusión sobre el secretoma de la sanguijuela medicinal. Es un artículo de opinión experta narrativa en lugar de investigación primaria, no aborda la hirudoterapia ni los agentes derivados de sanguijuelas, y los autores notan explícitamente que varias recomendaciones se basan en extrapolación o opinión experta donde falta evidencia robusta.

Citación

How I treat cancer-associated thrombosis.

Moik et al. · ESMO open, 2020

Contexto clínico relacionado

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

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