Thromb Haemost 2008; 99(06): 1040-1048
DOI: 10.1160/TH07-09-0541
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Hypercoagulability in patients with haematological neoplasia: No apparent initiation by tissue factor

Helene F. S. Negaard
1   Departments of Haematology
4   Faculty of Medicine, University of Oslo, Norway
,
Per Ole Iversen
1   Departments of Haematology
4   Faculty of Medicine, University of Oslo, Norway
,
Bjørn Østenstad
2   Oncology, and
,
Nina Iversen
3   Medical Genetics, Ullevål University Hospital Trust, Oslo, Norway
,
Pål A. Holme
5   Department of Haematology, Rikshospitalet UNiversity Hospital Trust, Oslo, Norway
,
Per Morten Sandset
1   Departments of Haematology
4   Faculty of Medicine, University of Oslo, Norway
› Institutsangaben
Financial support: The study was financially supported with grants from the Norwegian Eastern Health Authority Trust (fellowship for HFSN), Ullevål University Hospital Trust and the University of Oslo, Norway.
Weitere Informationen

Publikationsverlauf

Received 05. September 2007

Accepted after major revision 31. März 2008

Publikationsdatum:
27. November 2017 (online)

Summary

Patients with haematological malignancies carry increased risk of venous thrombosis (VT). However, the mechanisms that link these malignancies to activated coagulation have not been fully identified. Since anti-haemostatic agents are studied in clinical trials for their potential to prolong survival in cancer patients, a detailed characterisation of haemostatic markers in cancer subtypes is needed. Hence, in this study, we measured the plasma concentrations and mRNA expression in blood mononuclear cells of haemostatic parameters in 93 patients with haematological neoplasias (acute myeloid leukaemia, chronic lymphatic leukaemia, multiple myeloma, and non-Hodgkin’s lymphoma) before start and after completion of cancer therapy. At diagnosis we found activation of coagulation and fibrinolysis, especially in patients with acute myeloid leukaemia. This hypercoagulation was not associated with increased levels of tissue factor (TF) or factor VII (fVII) antigen or mRNA, or levels of activated fVII. In conclusion we found a hypercoagulable state in patients with haematological malignancy that did not seem to be initiated by TF.

 
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