Thromb Haemost 2009; 101(04): 762-769
DOI: 10.1160/TH08-09-0563
New Technologies, Diagnostic Tools and Drugs
Schattauer GmbH

Treatment of venous thromboembolism in patients with cancer: Subgroup analysis of the Matisse clinical trials

Frederiek F. van Doormaal
1   Academic Medical Center, Amsterdam, The Netherlands
,
Gary E. Raskob
2   University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA
,
Bruce L. Davidson
3   University of Washington School of Medicine, Seattle, Washington, USA
,
Hervé Decousus
4   Hospital de Bellevue, St-Etienne, France
,
Alexander Gallus
5   Flinders Medical Center, Adelaide, South Australia, Australia
,
Anthie W. A. Lensing
6   Academic Medical Center, Amsterdam, The Netherlands
,
Franco Piovella
7   U.O. Malattie Tromboemboliche, IRCCS Policlinico San Matteo, Pavia, Italy
,
Martin H. Prins
8   University Hospital of Maastricht, Maastricht, The Netherlands
,
Harry R. Büller
9   Academic Medical Center, Amsterdam, The Netherlands
› Author Affiliations
Further Information

Publication History

Received: 02 September 2008

Accepted after major revision: 27 March 2008

Publication Date:
23 November 2017 (online)

Summary

In the initial treatment of venous thromboembolism (VTE) fondaparinux, a pentasaccharide, is a good alternative to heparin. Whether this is also true for cancer patients is unknown. We performed two post-hoc analyses of two randomized studies to compare efficacy, safety and overall survival of fondaparinux to standard initial (low-molecular-weight) heparin (LMWH) treatment in cancer patients with venous thromboembolism. Two hundred thirty-seven cancer patients with deep venous thrombosis (DVT) were initially treated with fondaparinux or enoxaparin. Two hundred forty cancer patients with pulmonary embolism (PE) received fondaparinux or unfractionated heparin. The initial treatment was followed by vitamin K antagonists. In DVT patients, the three-month recurrence rate was 5.4% in the enoxaparin recipients compared to 12.7% in those treated with fondaparinux [absolute difference 7.3%, 95% CI 0.1, 14.5]. A recurrence was observed in 8.9% of the PE patients treated with fondaparinux compared to 17.2% in the unfractionated heparin recipients [absolute difference –8.3, 95% CI –16.7, 0.1]. In both studies no difference in bleeding and overall survival was observed. Regarding overall survival and bleeding fondaparinux is comparable to enoxaparin and unfractionated heparin in cancer patients. No significant differences in recurrent VTE were observed when comparing fondaparinux with unfractionated or LMWH. Because of study limitations these results should be considered hypothesis-generating.

 
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