Your browser doesn't support javascript.
loading
Circulating Blood Biomarkers and Risk of Venous Thromboembolism in Cancer Patients: A Systematic Review and Meta-Analysis.
Roy, Danielle Carole; Wang, Tzu-Fei; Lun, Ronda; Zahrai, Amin; Mallick, Ranjeeta; Burger, Dylan; Zitikyte, Gabriele; Hawken, Steven; Wells, Philip.
Afiliación
  • Roy DC; Faculty of Medicine, School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
  • Wang TF; Faculty of Medicine, School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
  • Lun R; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Zahrai A; The Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Mallick R; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Burger D; The Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Zitikyte G; Vascular Neurology, Stanford Healthcare, Palo Alto, California, United States.
  • Hawken S; Faculty of Medicine, School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
  • Wells P; The Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Thromb Haemost ; 2024 Jun 12.
Article en En | MEDLINE | ID: mdl-38768631
ABSTRACT

BACKGROUND:

Cancer patients have an increased risk of venous thromboembolism (VTE). Currently, the availability of highly discriminatory prediction models for VTE in cancer patients is limited. The implementation of biomarkers in prediction models might lead to refined VTE risk prediction. In this systematic review and meta-analysis, we aimed to evaluate candidate biomarkers and their association with cancer-associated VTE.

METHODS:

We searched Medline, EMBASE, and Cochrane Central for studies that evaluated biomarkers in adult cancer patients from inception to September 2022. We included studies reporting on VTE after a cancer diagnosis with biomarker measurements performed at a defined time point. Median/mean differences (for continuous measures) and odds ratios (for dichotomous measures) with 95% confidence intervals were estimated and pooled using random-effects models.

RESULTS:

We included 113 studies in the systematic review. Of these, 50 studies were included in the meta-analysis. We identified two biomarkers at cancer diagnosis (factor VIII and time to peak thrombin), three biomarkers pre-chemotherapy (D-dimer, fibrinogen, and mean platelet volume), and one biomarker preoperatively (platelet count) that had significant median or mean differences. Additionally, we found that hemoglobin <100 g/L and white blood count >11 × 109/L were significantly associated with future VTE risk only when measured at cancer diagnosis. Pre-chemotherapy neutrophil-to-lymphocyte ratio ≥3 and preoperative platelet count ≥400 × 109/L were also found to be associated with future VTE risk.

CONCLUSION:

In conclusion, this study identified nine candidate blood biomarkers that may help in optimizing VTE prediction in cancer patients that should be further explored in future studies.

Texto completo: 1 Colección: 01-internacional Idioma: En Revista: Thromb Haemost Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Idioma: En Revista: Thromb Haemost Año: 2024 Tipo del documento: Article País de afiliación: Canadá