Surrogate markers in antiangiogenesis clinical trials

D W Davis1, D J McConkey, J L Abbruzzese

  • 11Department of Cancer Biology, Unit 173, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA. dardavis@mdanderson.org

Insights

Novel antiangiogenic agents show promise against solid tumors but face development challenges. New surrogate markers are crucial for assessing these angiogenesis inhibitors

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Novel antiangiogenic agents are being developed as potentially more effective and less toxic alternatives to traditional cytotoxic chemotherapy for solid tumors.
  • Early clinical trials reveal the complexity of targeting angiogenesis, indicating that developing effective antiangiogenic therapies is more challenging than initially anticipated.

Purpose of the Study:

  • To review the current clinical data on the development of surrogate markers for angiogenesis inhibitors.
  • To highlight the necessity of new methods and markers for evaluating the biological activity of antiangiogenic agents.

Main Methods:

  • Review of available clinical data.
  • Analysis of studies on angiogenesis inhibitors and their surrogate markers.

Main Results:

  • The development of clinically useful antiangiogenic therapy is complex.
  • New methods and surrogate markers are essential for successful development.

Conclusions:

  • Surrogate markers are crucial for assessing the efficacy and guiding the development of novel antiangiogenic agents.
  • Further research into robust surrogate markers is needed to overcome the challenges in antiangiogenic therapy development.