Semin Thromb Hemost 2012; 38(08): 768-779
DOI: 10.1055/s-0032-1328888
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Mechanisms of Thrombosis in Paraproteinemias: The Effects of Immunomodulatory Drugs

Maurizio Zangari
1   Myeloma Program, Division of Hematology, University of Utah, Salt Lake City, Utah
,
Tamara Berno
1   Myeloma Program, Division of Hematology, University of Utah, Salt Lake City, Utah
,
Fenghuang Zhan
1   Myeloma Program, Division of Hematology, University of Utah, Salt Lake City, Utah
,
Guido Tricot
2   Holden Cancer Center's Bone Marrow Transplant and Myeloma Program, University of Iowa, Iowa City, Iowa
,
Louis Fink
3   Desert Research Institute, Las Vegas, Nevada
› Institutsangaben
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Publikationsdatum:
28. Oktober 2012 (online)

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Abstract

The introduction of immunomodulatory drugs (IMiDs) has improved clinical outcome in patients with multiple myeloma (MM). However, their use has been associated with a higher risk of cardiovascular complications. The use of IMiDs with dexamethasone, chemotherapy, or in combination with erythropoietic agents enhances the risk of venous thromboembolism (VTE) up to 25%. The pathogenesis of this increased risk of VTE seen with IMiD-based combination therapy is not yet fully understood, but several mechanisms have been proposed to explain the development of this hypercoagulable state. In cancer patients, prothrombotic factors include age, chemotherapy, immobility, enhanced expression of tissue factor of malignant cells, circulating microparticles, and increased vascular endothelial growth factor (VEGF). In patients with paraproteinemias, immunoglobulin-specific mechanisms may also be involved and include hypofibrinolysis, hyperviscosity, procoagulant autoantibody production, effects of inflammatory cytokines, and acquired activated protein C resistance (APCR). In this review we will focus on IMiD-associated effects on specific thrombotic mechanisms.