Estimating Bleeding Risk in Patients with Cancer-Associated Thrombosis: Evaluation of Existing Risk Scores and

Maria A de Winter1, Jannick A N Dorresteijn2, Walter Ageno3

  • 1Department of Acute Internal Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.

Thrombosis and Haemostasis
|September 20, 2021
PubMed

Insights

Existing bleeding risk scores perform poorly in cancer-associated thrombosis (CAT). A new model, "CAT-BLEED," shows promise but needs further validation for clinical use in CAT patients.

Area of Science:

  • Hematology
  • Oncology
  • Clinical Epidemiology

Background:

  • Assessing bleeding risk is crucial for managing cancer-associated thrombosis (CAT).
  • Current bleeding risk scores lack validation in CAT patients and are not recommended for clinical practice.
  • Effective risk stratification is needed to guide treatment decisions and improve patient outcomes.

Purpose of the Study:

  • To compare the predictive performance of existing venous thromboembolism (VTE) bleeding risk scores, a pragmatic cancer type classification, and a novel prediction model for clinically relevant bleeding in CAT patients.
  • To evaluate the utility of established risk scores and propose improved methods for bleeding risk estimation in this specific population.

Main Methods:

  • A posthoc analysis of the Hokusai VTE Cancer study involving 1,046 patients treated for CAT.
  • External validation of seven existing bleeding risk scores (ACCP-VTE, HAS-BLED, Hokusai, Kuijer, Martinez, RIETE, VTE-BLEED).
  • Comparison with a pragmatic classification based on cancer type and a newly derived competing risk-adjusted prediction model ('CAT-BLEED').

Main Results:

  • Existing risk scores demonstrated poor to moderate predictive performance (C-statistics: 0.50-0.57) with poor calibration.
  • The pragmatic classification and the 'CAT-BLEED' model showed moderate internal validation performance (C-statistics: 0.61 and 0.63, respectively) with good calibration.
  • 149 clinically relevant bleeding events were analyzed within 6 months post-CAT diagnosis.

Conclusions:

  • Established bleeding risk scores are inadequate for patients with cancer-associated thrombosis (CAT).
  • A pragmatic classification based on cancer type offers marginal improvement in risk prediction.
  • The novel 'CAT-BLEED' model shows potential but requires external validation and demonstration of clinical utility with various direct oral anticoagulants (DOACs).
Abstract

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