Preclinical Evaluations of Therapies Combining the Vascular Targeting Agent Combretastatin A-4 Disodium Phosphate and Conventional Anticancer Therapies in the Treatment of Kaposi's Sarcoma

Authors

  • Lingyun Li From the Department of Pharmacology and Experimental Therapeutics (L. Li, D.W. Siemann) and Department of Radiation Oncology (D.W. Siemann), Shands Cancer Center, University of Florida, Gainesville, FL, USA, and the Department of Interdisciplinary Oncology and Department of Pathology (A.M. Rojiani), H. Lee Mof. tt Cancer Center and Research Institute, University of South Florida, Tampa, FL, USA
  • Amyn M. Rojiani From the Department of Pharmacology and Experimental Therapeutics (L. Li, D.W. Siemann) and Department of Radiation Oncology (D.W. Siemann), Shands Cancer Center, University of Florida, Gainesville, FL, USA, and the Department of Interdisciplinary Oncology and Department of Pathology (A.M. Rojiani), H. Lee Mof. tt Cancer Center and Research Institute, University of South Florida, Tampa, FL, USA
  • Dietmar W. Siemann From the Department of Pharmacology and Experimental Therapeutics (L. Li, D.W. Siemann) and Department of Radiation Oncology (D.W. Siemann), Shands Cancer Center, University of Florida, Gainesville, FL, USA, and the Department of Interdisciplinary Oncology and Department of Pathology (A.M. Rojiani), H. Lee Mof. tt Cancer Center and Research Institute, University of South Florida, Tampa, FL, USA

DOI:

https://doi.org/10.1080/028418602317314127

Abstract

The antitumor efficacy of the vascular targeting agent combretastatin A-4 disodium phosphate (CA4DP) was evaluated in a xenograft model of Kaposi's sarcoma (KS) grown in athymic mice. Response to CA4DP alone or in combination with localized radiation treatment or systemic chemotherapy (cisplatin or vinblastine) was assessed using a clonogenic cell survival or tumor growth delay assay. Administering increasing doses of CA4DP to tumor-bearing mice resulted in a dose-dependent increase in tumor cell kill. CA4DP also enhanced the antitumor effects of radiation and chemotherapy ~ 10-100-fold. Although single doses of CA4DP as large as 300 mg/kg failed to alter tumor growth, the same total dose, administered as 3 fractions in 5 or 9 days, resulted in significant growth delay. Such repeated CA4DP exposures also significantly increased the response of KS xenografts to cisplatin. These findings suggest that CA4DP ought to be considered as a candidate agent for therapeutic evaluation in AIDS-KS patients.

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Published

2002-01-01

How to Cite

Li, L., Rojiani, A. M., & Siemann, D. W. (2002). Preclinical Evaluations of Therapies Combining the Vascular Targeting Agent Combretastatin A-4 Disodium Phosphate and Conventional Anticancer Therapies in the Treatment of Kaposi’s Sarcoma. Acta Oncologica, 41(1), 91–97. https://doi.org/10.1080/028418602317314127