Molecular imaging of targeted therapies with positron emission tomography: the visualization of personalized cancer

Lemonitsa H Mammatas1, Henk M W Verheul, N Harry Hendrikse

  • 1Dept of Medical Oncology VUmc Cancer Center Amsterdam, VU University Medical Center, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.

Abstract

Insights

Positron emission tomography (PET) molecular imaging with targeted anticancer drugs shows promise for personalized cancer care. This technique non-invasively quantifies drug distribution, aiding treatment and toxicity assessments.

Area of Science:

  • Oncology
  • Molecular Imaging
  • Radiochemistry

Background:

  • Molecular imaging visualizes biological processes at the molecular/cellular level, complementing anatomical imaging in oncology.
  • Positron emission tomography (PET) uses radiotracers to visualize molecular targets and drug biodistribution.
  • Current challenges include standardizing processes and clinical implementation.

Purpose of the Study:

  • To review the literature on molecular imaging with PET for personalized targeted cancer treatment strategies.
  • To highlight the potential of PET in improving cancer care through molecular insights.

Main Methods:

  • Literature review of studies utilizing PET for personalized cancer therapy.
  • Focus on radiolabelled ligands for target identification and radiolabelled drugs for biodistribution studies.
  • Analysis of PET's role in intratumoural target identification and therapy uptake visualization.

Main Results:

  • PET enables visualization of functional tumor cell behavior.
  • Radiolabelled drugs allow in vivo visualization of biodistribution and intratumoural uptake.
  • Early clinical evidence suggests PET's value in target identification and response prediction.

Conclusions:

  • Molecular imaging with PET and targeted anticancer drugs offers significant potential for personalized cancer care.
  • Non-invasive quantification of drug accumulation in tumors and normal tissues informs therapeutic and toxic effects.

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