International Journal of Radiation Oncology * Biology * Physics
Volume 64, Issue 1 , Pages 33-37, 1 January 2006

ZD6474, an inhibitor of VEGFR and EGFR tyrosine kinase activity in combination with radiotherapy

  • Barbara Frederick, Ph.D.

      Affiliations

    • Department of Radiation Oncology, University of Colorado Health Sciences Center, Aurora, CO
  • ,
  • Dan Gustafson, Ph.D.

      Affiliations

    • Department of Pharmacology, University of Colorado Health Sciences Center, Aurora, CO
  • ,
  • Cataldo Bianco, M.D.

      Affiliations

    • Dipartimento di Oncologia, dei Trapianti e delle Nuove Technologie in Medicina, Universita di Pisa, Pisa, Italy
  • ,
  • Fortunato Ciardiello, M.D.

      Affiliations

    • Department of Molecular and Clinical Endocrinology, Universita degli Studi di Napoli Federico II, Naples, Italy
  • ,
  • Isaiah Dimery, Ph.D.

      Affiliations

    • AstraZeneca, Wilmington, DE
  • ,
  • David Raben, M.D.

      Affiliations

    • Department of Radiation Oncology, University of Colorado Health Sciences Center, Aurora, CO
    • Corresponding Author InformationReprint requests to: David Raben, M.D., Department of Radiation Oncology, University of Colorado Health Sciences Center, Anschutz Cancer Pavillion, 1665 N. Ursula St., Suite 1032, F796, Aurora, CO 80010-0510. Tel: (720) 848-0116; Fax: (720) 848-0222

Received 22 March 2005; received in revised form 4 May 2005; accepted 6 May 2005.

Radiation enhances both epithelial growth factor receptor (EGFR) and vascular endothelial growth factor (VEGF) expression, which are a part of key pathways for tumor progression. Some tumors may not respond well to EGFR inhibitors alone or may develop resistance to EGFR inhibitors. Therefore, drug therapy targeted to VEGF receptors and EGFRs, when combined with radiotherapy (RT), may improve tumor control and provide wider applicability. This article focuses on ZD6474, an inhibitor of EGFR and VEGF receptor signaling in combination with RT. We discuss preclinical and clinical studies with RT and inhibitors of VEGF or EGFR signaling first. We then address issues associated with ZD6474 pharmacokinetic dosing, and scheduling when combined with RT. We also discuss ZD6474 in the context of anti-EGFR therapy resistance. Dual inhibition of EGFR and VEGF receptor signaling pathways shows promise in enhancing RT efficacy.

Keywords:  Tyrosine kinase inhibitor , Vascular endothelial growth factor receptor , Radiotherapy , Angiogenesis

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PII: S0360-3016(05)00962-4

doi:10.1016/j.ijrobp.2005.05.050

International Journal of Radiation Oncology * Biology * Physics
Volume 64, Issue 1 , Pages 33-37, 1 January 2006