Molecular imaging and theranostic approaches in pheochromocytoma and paraganglioma

David Taïeb1, Karel Pacak2

  • 1Department of Nuclear Medicine, La Timone University Hospital, CERIMED, Aix-Marseille University, 264, rue Saint-Pierre, 13385, Marseille, France. david.taieb@ap-hm.fr.

Cell and Tissue Research
|February 17, 2018
PubMed

Insights

Neural crest-derived tumors like pheochromocytomas and paragangliomas (PPGLs) are well-suited for radiopharmaceutical imaging. Theranostics using somatostatin agents offer a promising new treatment for metastatic PPGLs.

Area of Science:

  • Oncology
  • Nuclear Medicine
  • Endocrinology

Background:

  • Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors originating from neural crest cells.
  • These tumors often overexpress specific molecular targets, making them amenable to targeted therapies.
  • Current treatment for metastatic PPGLs remains challenging, necessitating novel therapeutic strategies.

Purpose of the Study:

  • To explore the potential of radiopharmaceuticals for imaging PPGLs.
  • To evaluate the evolving role of somatostatin-based theranostics in managing metastatic PPGLs.

Main Methods:

  • Review of current literature on PPGLs, their molecular targets, and imaging techniques.
  • Analysis of emerging theranostic approaches utilizing somatostatin receptor agonists and antagonists.

Main Results:

  • PPGLs exhibit overexpression of targets suitable for radiopharmaceutical detection.
  • Theranostic strategies employing somatostatin agonists and antagonists are demonstrating significant advancements.
  • These agents show promise for both diagnosis and targeted therapy in PPGL patients.

Conclusions:

  • PPGLs are prime candidates for advanced imaging and theranostic interventions.
  • Somatostatin-based theranostics represent a significant progression in the therapeutic armamentarium for metastatic PPGLs.
  • Further research and clinical application of these targeted approaches are warranted.