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Br J Cancer ; 119(8): 915-921, 2018 10.
Article in English | MEDLINE | ID: mdl-30318508

ABSTRACT

BACKGROUND: Optimal duration of anticoagulation for cancer-associated thrombosis (CAT) remains unclear. This study assessed D-dimer (DD) and high-sensitivity C-reactive protein (hs-CRP) levels after the withdrawal of anticoagulation treatment to predict the risk of venous thromboembolism (VTE) recurrence among patients with CAT. METHODS: Prospective, multicentre study to evaluate CAT with ≥3 months of anticoagulation that was subsequently discontinued. Blood samples were taken when patients stopped the anticoagulation and 21 days later to determine the DD and hs-CRP levels. All patients were followed up for 6 months to detect VTE recurrence. RESULTS: Between 2013 and 2015, 325 patients were evaluated and 114 patients were ultimately enrolled in the study. The mean age was 62 ± 14 years and nearly 40% had metastasis. Ten patients developed VTE recurrence within 6 months (8.8%, 95% confidence interval [CI]: 4.3-15.5%). The DD and hs-CRP levels after 21 days were associated with VTE recurrence. The subdistribution hazard ratios were 9.82 for hs-CRP (95% CI: 19-52) and 5.81 for DD (95% CI: 1.1-31.7). CONCLUSIONS: This study identified that hs-CRP and DD were potential biomarkers of VTE recurrence after discontinuation of anticoagulation in CAT. A risk-adapted strategy could identify low-risk patients who may benefit from discontinuation of anticoagulation.


Subject(s)
Anticoagulants/administration & dosage , C-Reactive Protein/analysis , Fibrin Fibrinogen Degradation Products/analysis , Neoplasms/pathology , Venous Thromboembolism/prevention & control , Venous Thrombosis/prevention & control , Withholding Treatment/statistics & numerical data , Anticoagulants/therapeutic use , Drug Administration Schedule , Female , Humans , Male , Middle Aged , Neoplasms/blood supply , Prospective Studies , Recurrence , Risk Assessment , Risk Factors , Secondary Prevention/methods , Venous Thromboembolism/drug therapy , Venous Thrombosis/drug therapy
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