Effectiveness and Safety of Rivaroxaban in Patients With Cancer-Associated Venous Thrombosis
Research article published in Journal of the National Comprehensive Cancer Network : JNCCN (2018)
Abstract
Background: Although not designated as guideline-recommended first-line anticoagulation therapy, patients are receiving rivaroxaban for the treatment and secondary prevention of cancer-associated venous thrombosis (CAT). We sought to estimate the cumulative incidence of recurrent venous thromboembolism (VTE), major bleeding, and mortality/hospice care in patients with CAT treated with outpatient rivaroxaban in routine practice. Methods: Using US MarketScan claims data from January 2012 through June 2015, we identified adults with active cancer (using SEER program coding) who had ≥1 primary hospitalization or emergency department discharge diagnosis code for VTE (index event) and received rivaroxaban as their first outpatient anticoagulant within 30 days of the index VTE. Patients were required to have ≥180 days of continuous medical/prescription benefits prior to the index VTE. Patients with a previous claim for VTE, atrial fibrillation, or valvular disease or receiving anticoagulation during the baseline period were excluded. We estimated the cumulative incidence with 95% CIs of recurrent VTE, major bleeding, and mortality or need for hospice care at 180 days, assuming competing risks. Results: A total of 949 patients with active cancer were initiated on rivaroxaban following their index VTE. Time from active cancer diagnosis to index CAT was ≤90 days for 27% of patients, 91 to 180 days for 19%, and >180 days for 54%. The mean [SD] age of patients was 62.5 [12.8] years, 43.6% had pulmonary embolism, and metastatic disease was present in 42.6%. During follow-up, there were 37 cases of recurrent VTE, 22 cases of major bleeding (17 gastrointestinal, 3 intracranial, 1 genitourinary, and 1 other bleed), and 105 deaths/hospice claims. The cumulative incidence estimate was 4.0% (95% CI, 2.8%-5.4%) for recurrent VTE, 2.7% (95% CI, 1.7%-4.0%) for major bleeding, and 11.3% (95% CI, 9.2%-13.6%) for mortality/hospice care. Conclusions: Event rates observed in this rivaroxaban-treated cohort were overall consistent with previous studies of patients with rivaroxaban- and warfarin-managed CAT.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Peer-reviewed research on anticoagulant and antithrombotic agents relevant to leech-derived compounds and thrombosis management. Indexed in PubMed and verified against the NCBI record.
Por qué esto importa para la hirudoterapia
Utilizando datos de reclamaciones de US MarketScan, este estudio de cohorte del mundo real siguió a 949 pacientes con cáncer que iniciaron rivaroxabán ambulatorio (un inhibidor del Factor Xa) después de una tromboembolia venosa, estimando incidencias acumulativas a 180 días del 4.0% para VTE recurrente, 2.7% para hemorragia mayor y 11.3% para mortalidad o atención de hospicio, tasas que los autores encontraron ampliamente consistentes con cohortes previas manejadas con rivaroxabán y warfarin. Para la hirudoterapia, esto proporciona antecedentes sobre el desempeño de un anticoagulante sintético oral en la atención de rutina de la trombosis asociada al cáncer, el panorama clínico en el que se posicionan conceptualmente los antitrombóticos derivados de sanguijuelas. Advertencia: se trata de una cohorte retrospectiva de reclamaciones administrativas (sujeta a limitaciones de codificación y confusión por indicación) de un inhibidor sintético del Factor Xa, no un ensayo aleatorizado y no un estudio de ninguna molécula derivada de sanguijuelas, por lo que constituye únicamente evidencia contextual.
Citación
Effectiveness and Safety of Rivaroxaban in Patients With Cancer-Associated Venous Thrombosis.
Kohn et al. · Journal of the National Comprehensive Cancer Network : JNCCN, 2018
Contexto clínico relacionado
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Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: June 18, 2026