Imaging of Tumor Characteristics and Molecular Pathways With PET: Developments Over the Last Decade Toward Personalized Cancer Therapy

Int J Radiat Oncol Biol Phys. 2018 Nov 15;102(4):1165-1182. doi: 10.1016/j.ijrobp.2018.04.055. Epub 2018 May 4.

Abstract

Purpose: Improvements in personalized therapy are made possible by the advances in molecular biology that led to developments in molecular imaging, allowing highly specific in vivo imaging of biological processes. Positron emission tomography (PET) is the most specific and sensitive imaging technique for in vivo molecular targets and pathways, offering quantification and evaluation of functional properties of the targeted anatomy.

Materials and methods: This work is an integrative research review that summarizes and evaluates the accumulated current status of knowledge of recent advances in PET imaging for cancer diagnosis and treatment, concentrating on novel radiotracers and evaluating their advantages and disadvantages in cancer characterization. Medline search was conducted, limited to English publications from 2007 onward. Identified manuscripts were evaluated for most recent developments in PET imaging of cancer hypoxia, angiogenesis, proliferation, and clonogenic cancer stem cells (CSC).

Results: There is an expansion observed from purely metabolic-based PET imaging toward antibody-based PET to achieve more information on cancer characteristics to identify hypoxia, proangiogenic factors, CSC, and others. 64Cu-ATSM, for example, can be used both as a hypoxia and a CSC marker.

Conclusions: Progress in the field of functional imaging will possibly lead to more specific tumor targeting and personalized treatment, increasing tumor control and improving quality of life.

Publication types

  • Review

MeSH terms

  • Humans
  • Neoplasms / blood supply
  • Neoplasms / diagnostic imaging*
  • Neoplasms / pathology
  • Neoplasms / therapy*
  • Neovascularization, Pathologic / diagnostic imaging
  • Positron-Emission Tomography / methods*
  • Precision Medicine / methods*
  • Radioactive Tracers
  • Tumor Hypoxia

Substances

  • Radioactive Tracers