Circulating and imaging markers for angiogenesis

Arvind P Pathak1, Warren E Hochfeld, Simon L Goodman

  • 1JHU ICMIC Program, The Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USA. pathak@mri.jhu.edu

Angiogenesis
|October 18, 2008
PubMed

Insights

Anti-angiogenesis therapy shows promise for inhibiting tumor growth, validated by recent successes in colon cancer. New circulating and imaging markers are needed to dynamically monitor tumor angiogenesis in vivo.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Anti-angiogenesis is a validated strategy for inhibiting tumor growth, supported by preclinical and clinical data.
  • Vascular Endothelial Growth Factor (VEGF) neutralizing antibodies have shown success in metastatic colon carcinoma patients.
  • The clinical success of anti-angiogenesis necessitates reliable surrogate markers.

Purpose of the Study:

  • To review the need for reliable markers of angiogenesis.
  • To discuss the limitations of current markers like microvessel density.
  • To explore the development of circulating and imaging markers for in vivo monitoring of angiogenesis.

Main Methods:

  • Review of preclinical and clinical data on anti-angiogenesis.
  • Analysis of the utility of microvessel density as a surrogate marker.
  • Discussion on the requirements for novel circulating and imaging markers.

Main Results:

  • Microvessel density is a static "snap-shot" and insufficient for dynamic assessment.
  • There is an acute need for non-invasive, in vivo markers of angiogenesis.
  • Circulating and imaging markers are required for repeated monitoring in diverse tumor types.

Conclusions:

  • Anti-angiogenesis is a clinically relevant cancer treatment strategy.
  • Current markers for angiogenesis lack dynamic and in vivo assessment capabilities.
  • Development of novel circulating and imaging markers is crucial for effective monitoring and management of angiogenesis in cancer.