Clinical outcomes following catheter-related venous thrombo-embolism among children with acute lymphoblastic leukemia
Multicenter study published in Thrombosis research (2026)
Resumen
Venous thrombo-embolism (VTE) occurs in 10-15% of pediatric patients with acute lymphoblastic leukemia (ALL), yet the optimal duration of anticoagulation remains unclear. In this retrospective multi-center cohort study, we reported the clinical outcomes of pediatric patients treated for ALL with a history of central venous catheter (CVC)-related VTE and compared outcomes based on duration of anticoagulation. Patients aged 1-21 years old with newly-diagnosed ALL (2010-2023), receiving asparaginase-containing chemotherapy, experiencing a radiologically-proven CVC-related VTE requiring medical intervention, were included. Cumulative incidence and 95% confidence interval (CI) were estimated for VTE progression/recurrence and clinically relevant bleeding. Cox proportional hazard models were performed to compare clinical outcomes based on anticoagulation duration, categorized as a) asparaginase-based (following a 6-week course of anticoagulation, until the end of asparaginase' expected effects or earlier) or extended (later than asparaginase's expected effects), and b) before vs. after CVC removal. We included 106 patients (median age: 10 years, 59% male). Overall, 22 patients sustained a VTE progression/recurrence (cumulative incidence: 22%, 95% CI: 14-30%). Most progression/recurrences occurred while patients were still on anticoagulation, at a median of 54 days after index VTE. Duration of anticoagulation was not associated with VTE progression/recurrence (extended vs. asparaginase-based: HR = 1.49, 95%CI: 0.60-3.69, p = 0.392; after vs. before CVC removal: HR = 1.36, 95% CI: 0.49-3.74, p = 0.552). Clinically relevant bleeding occurred in 11/106 patients (cumulative incidence: 12%, 95% CI: 6-19%) and was not associated with anticoagulation duration. In summary, VTE progression/recurrence was common in pediatric patients with ALL. Further investigation into alternative approaches to reduce VTE progression/recurrence is warranted.
Resumen tomado de PubMed (NCBI) para el registro citado, en el idioma original. La versión de referencia es la de la publicación original.
El resumen se deja sin traducir para conservar la redacción original de los autores.
Síntesis
In a retrospective cohort of 106 children with acute lymphoblastic leukemia and catheter-related venous thromboembolism, progression or recurrence affected 22% and clinically relevant bleeding 12%, with neither outcome associated with anticoagulation duration.
Por qué esto importa para la hirudoterapia
Esta cohorte multicéntrica retrospectiva de 106 niños (edades de 1-21) con leucemia linfoblástica aguda y tromboembolismo venoso relacionado con el catéter venoso central encontró que el 22% presentó progresión o recurrencia de VTE y el 12% presentó sangrado clínicamente relevante, sin diferencias significativas según la duración de la anticoagulación (basada en asparaginasa vs. extendida; antes vs. después de la extracción del catéter). Su relevancia para ASH es contextual: demuestra que la estrategia óptima de anticoagulación para los coágulos asociados a catéter sigue sin resolverse incluso con agentes farmacéuticos modernos, enmarcando la necesidad insatisfecha más amplia que motiva el interés en mecanismos antitrombóticos alternativos y derivados de sanguijuelas. Advertencia honesta: se trata de una cohorte observacional oncológica pediátrica de anticoagulantes convencionales; no estudia sanguijuelas, no hace ninguna afirmación sobre la hirudoterapia y, dado que la hirudoterapia no está indicada en esta población propensa a trombocitopenia y con riesgo de sangrado, no debe enmarcarse como un respaldo a la terapia con sanguijuelas aquí.
Citación
Clinical outcomes following catheter-related venous thrombo-embolism among children with acute lymphoblastic leukemia.
Pelland-Marcotte MC et al. · Thrombosis research, 2026
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Añadido a la biblioteca ASH: 28 de mayo de 2026 · Última actualización del sitio: 18 de junio de 2026