Articles

The role of direct oral anticoagulants in the management of cancer-associated thrombosis

BJH - volume 10, issue 4, june 2019

A. Awada MD, PhD, J-F. Baurain MD, PhD, P. Clement MD, PhD, P. Hainaut MD, PhD, S. Holbrechts MD, PhD, K. Jochmans MD, PhD, V. Mathieux MD, PhD, J. Mebis MD, PhD, M. Strijbos MD, PhD, C. Vulsteke MD, PhD, T. Vanassche MD, PhD, P. Verhamme MD, PhD

Cancer patients are at an increased risk of venous thromboembolism (VTE). The current standard initial treatment of an acute episode of VTE in cancer patients consists of the administration of three to six months of subcutaneous low molecular weight heparin (LMWH) at a dose adjusted to the body weight. The efficacy and safety profile of LMWHs are well established, but a drawback of these agents is that they require daily subcutaneous administration. In addition, they are mainly cleared through the kidneys, and their use in patients with severe renal insufficiency may require dose reduction or monitoring of the anti-Xa activity. To address the issues with LMWH, several direct oral anticoagulants (DOAC) have been developed for the treatment of VTE. In contrast to LMWHs and vitamin K antagonist, DOACs directly interfere with thrombin or activated factor X (FXa). DOACs have now become standard treatment options in the general management of VTE, but until recently, there were no results of clinical trials specifically assessing the role of DOACs in the treatment of cancer-associated thrombosis. Recently, the Hokusai VTE cancer study and preliminary data from the Select-D trial demonstrated that DOACs are non-inferior to LMWH in preventing recurrent VTE. However, both studies also show that this comes at the cost of an increased rate of both major and clinically-relevant non-major bleeding. Especially in the subgroup of patients with gastrointestinal cancer, the benefit in VTE recurrence with the DOAC seems to be outbalanced by a significantly increased bleeding risk. Based on the available results, DOACs might represent an interesting alternative for LMWH in certain subgroups of patients, but with an important list of exceptions. It seems reasonable not to use DOACs in patients with a high bleeding risk, and especially in patients with gastrointestinal cancer, DOACs should not be the first-line choice. In summary, while LMWHs are currently the standard of care in the acute management of cancer-associated thrombosis, the advent of DOACs is welcomed for patients at a low bleeding risk who are in need of long-term anticoagulation.

(BELG J HEMATOL 2019;10(4):169–76)

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O01 INHERITED ANTITHROMBIN DEFICIENCY AND THROMBOSIS IN CHILDHOOD: DATA FROM A LARGE MULTICENTRIC COHORT

BJH - 2019, issue ?, february 2019

C. Orlando , B. De La Morena-barrio , M.e. De La Morena-barrio , V. Vicente , J. Corral , K. Jochmans MD, PhD

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P01 EVALUATION OF THE COBAS T 711 COAGULATION ANALYSER: A SINGLE CENTER EXPERIENCE

BJH - 2019, issue ?, february 2019

C. Orlando , S. Damiaens , Ö. Belce , K. Jochmans MD, PhD

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P03 PREVALENCE OF HETEROZYGOUS TYPE 2N VON WILLEBRAND DISEASE MUTATIONS IN A BELGIAN SURVEY

BJH - 2019, issue ?, february 2019

I. Vangenechten , J. Jongenotter , K. Jochmans MD, PhD, C. Orlando , A. Gothot MD, PhD, K. Vandenbosch , A. Gadisseur MD, PhD

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A-136 THE p.Arg498Cys MUTATION IN THE CYSTEINE RICH DOMAIN OF ADAMTS13 RESULTS IN A SECRETION DEFICIENCY

BJH - volume 8, issue Abstract Book BSTH, february 2017

A.-S. Schelpe , C. Orlando , C. Geeroms , I. Pareyn , N. VanDePutte , H. Deckmyn , K. Jochmans MD, PhD, S.F. De Meyer , K. VanHoorelbeke

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A-128 PREVALENCE OF HETEROZYGOUS TYPE 2N VON WILLEBRAND DISEASE MUTATIONS IN BELGIUM

BJH - volume 8, issue Abstract Book BSTH, february 2017

J. Jongenotter , I. Vangenechten , K. Jochmans MD, PhD, C. Orlando , A. Gothot MD, PhD, K. Vandenbosch , A. Gadisseur MD, PhD

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A-133 ACQUIRED HAEMOPHILIA A

BJH - volume 8, issue Abstract Book BSTH, february 2017

Y. Van der Beken , C. Orlando , K. Fostier MD, K. Jochmans MD, PhD

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