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Vascular Disrupting Agents in Clinical Development

Overview
Journal Br J Cancer
Specialty Oncology
Date 2007 Mar 22
PMID 17375046
Citations 76
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Abstract

Growth of human tumours depends on the supply of oxygen and nutrients via the surrounding vasculature. Therefore tumour vasculature is an attractive target for anticancer therapy. Apart from angiogenesis inhibitors that compromise the formation of new blood vessels, a second class of specific anticancer drugs has been developed. These so-called vascular disrupting agents (VDAs) target the established tumour vasculature and cause an acute and pronounced shutdown of blood vessels resulting in an almost complete stop of blood flow, ultimately leading to selective tumour necrosis. As a number of VDAs are now being tested in clinical studies, we will discuss their mechanism of action and the results obtained in preclinical studies. Also data from clinical studies will be reviewed and some considerations with regard to the future development are given.

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References
1.
Chaplin D, Dougherty G . Tumour vasculature as a target for cancer therapy. Br J Cancer. 1999; 80 Suppl 1:57-64. View

2.
Tozer G, Prise V, Wilson J, Locke R, Vojnovic B, Stratford M . Combretastatin A-4 phosphate as a tumor vascular-targeting agent: early effects in tumors and normal tissues. Cancer Res. 1999; 59(7):1626-34. View

3.
Siemann D, Bibby M, Dark G, Dicker A, Eskens F, Horsman M . Differentiation and definition of vascular-targeted therapies. Clin Cancer Res. 2005; 11(2 Pt 1):416-20. View

4.
Bilenker J, Flaherty K, Rosen M, Davis L, Gallagher M, Stevenson J . Phase I trial of combretastatin a-4 phosphate with carboplatin. Clin Cancer Res. 2005; 11(4):1527-33. DOI: 10.1158/1078-0432.CCR-04-1434. View

5.
de Jonge M, van der Gaast A, Planting A, van Doorn L, Lems A, Boot I . Phase I and pharmacokinetic study of the dolastatin 10 analogue TZT-1027, given on days 1 and 8 of a 3-week cycle in patients with advanced solid tumors. Clin Cancer Res. 2005; 11(10):3806-13. DOI: 10.1158/1078-0432.CCR-04-1937. View