Blood Reviews
Volume 23, Issue 3 , Pages 129-135, May 2009

Does antithrombotic therapy improve survival in cancer patients?

  • Moya S. Cunningham

      Affiliations

    • Academic Unit of Clinical and Molecular Oncology, Institute of Molecular Medicine, Trinity College Dublin, Ireland
  • ,
  • Roger J.S. Preston

      Affiliations

    • Haemostasis Research Group, Institute of Molecular Medicine, Trinity Health Centre, St. James’s Hospital, Trinity College Dublin, Ireland
  • ,
  • James S. O’Donnell

      Affiliations

    • Haemostasis Research Group, Institute of Molecular Medicine, Trinity Health Centre, St. James’s Hospital, Trinity College Dublin, Ireland
    • National Centre for Hereditary Coagulation Disorders, St. James’s Hospital, James’s Street, Dublin, Ireland
    • Corresponding Author InformationCorresponding author. Address: Haemostasis Research Group, Institute of Molecular Medicine, Trinity Health Centre, St. James’s Hospital, Trinity College Dublin, Ireland. Tel.: +353 1 416 2141; fax: +353 1 410 3570.

published online 01 December 2008.

Summary 

Venous thromboembolism (VTE) is a common complication of malignancy, and is associated with significant morbidity and mortality. Anticoagulant therapy, in the form of heparin and warfarin, plays an important role in the prevention of recurrent VTE. Recent studies have demonstrated that long-term therapy with low molecular weight heparin (LMWH) is more effective than warfarin in patients with cancer. In addition, accumulating clinical evidence suggests that LMWH significantly improves overall survival in cancer patients without VTE. Intriguingly, however, this improved survival cannot simply be explained by a reduction in fatal pulmonary embolism. Furthermore, the beneficial effects persist long after the LMWH has been discontinued, suggesting that LMWH can directly influence tumour cell biology. This hypothesis is entirely plausible, given the complex feedback mechanisms that exist between tumour cells, coagulation proteases, and vascular endothelial cells. Furthermore, an accumulating body of in vitro experimental evidence suggests that both heparin and warfarin have direct antineoplastic effects. Further large randomized controlled trials will be required in order to validate these exciting preliminary data, and to define whether anticoagulant therapy may constitute a useful adjunctive therapy in the management of cancer patients without VTE.

Keywords: Warfarin, Heparin, Cancer, Venous thromboembolism

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PII: S0268-960X(08)00080-5

doi:10.1016/j.blre.2008.10.002

Blood Reviews
Volume 23, Issue 3 , Pages 129-135, May 2009