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Originally published as JCO Early Release 10.1200/JCO.2009.22.3875 on August 24 2009

Journal of Clinical Oncology, Vol 27, No 29 (October 10), 2009: pp. 4865-4873
© 2009 American Society of Clinical Oncology.

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REVIEW ARTICLES

Thrombotic Events in Patients With Cancer Receiving Antiangiogenesis Agents

Maurizio Zangari, Louis M. Fink, Francesca Elice, Fenghuang Zhan, Dorothy M. Adcock, Guido J. Tricot

From the University of Utah, Division of Hematology, Blood/Marrow Transplant and Myeloma Program, Salt Lake City, UT; Nevada Cancer Institute, Laboratory Medicine, Las Vegas, NV; Esoterix, Aurora, CO; and St Bortolo Hospital, Vicenza, Italy.

Corresponding author: Maurizio Zangari, MD, 30 North 1900 East, SOM Rm 5C402, Salt Lake City, UT 84132; e-mail: maurizio.zangari{at}hsc.utah.edu.

Tumor-associated neoangiogenesis has recently become a suitable target for antineoplastic drug development. In this overview, we discuss specific drug-associated hemostatic complications, the already known pathogenetic mechanisms involved, and the effect of varying antithrombotic strategies. Multiple agents with angiogenic inhibitory capacity (thalidomide, lenalidomide, bevacizumab, sunitinib, sorafenib, and sirolimus) have obtained US Food and Drug Administration approval, and many others have entered clinical trials. Arterial and venous thromboembolism and hemorrhage have emerged as significant toxicities associated with the use of angiogenesis inhibitors. We present a detailed analysis of the literature on thrombotic complication of antiangiogenic drugs. Close attention to hemostatic complications during antiangiogenic treatment is warranted. Further studies are required to better understand the pathophysiologic mechanisms involved and to define a safe prophylactic strategy.

Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.


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G. H. Lyman and A. A. Khorana
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P. Rana and M. N. Levine
Prevention of Thrombosis in Ambulatory Patients With Cancer
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