In vivo molecular imaging of chemokine receptor CXCR4 expression in patients with advanced multiple myeloma

EMBO Mol Med. 2015 Apr;7(4):477-87. doi: 10.15252/emmm.201404698.

Abstract

CXCR4 is a G-protein-coupled receptor that mediates recruitment of blood cells toward its ligand SDF-1. In cancer, high CXCR4 expression is frequently associated with tumor dissemination and poor prognosis. We evaluated the novel CXCR4 probe [(68)Ga]Pentixafor for in vivo mapping of CXCR4 expression density in mice xenografted with human CXCR4-positive MM cell lines and patients with advanced MM by means of positron emission tomography (PET). [(68)Ga]Pentixafor PET provided images with excellent specificity and contrast. In 10 of 14 patients with advanced MM [(68)Ga]Pentixafor PET/CT scans revealed MM manifestations, whereas only nine of 14 standard [(18)F]fluorodeoxyglucose PET/CT scans were rated visually positive. Assessment of blood counts and standard CD34(+) flow cytometry did not reveal significant blood count changes associated with tracer application. Based on these highly encouraging data on clinical PET imaging of CXCR4 expression in a cohort of MM patients, we conclude that [(68)Ga]Pentixafor PET opens a broad field for clinical investigations on CXCR4 expression and for CXCR4-directed therapeutic approaches in MM and other diseases.

Keywords: CXCR4; chemokine receptor; in vivo imaging; multiple myeloma; positron emission tomography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic*
  • Heterografts
  • Humans
  • Mice
  • Mice, Inbred NOD
  • Molecular Imaging / methods*
  • Molecular Probes / pharmacology*
  • Multiple Myeloma* / metabolism
  • Multiple Myeloma* / pathology
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Transplantation
  • Positron-Emission Tomography / methods*
  • Receptors, CXCR4 / biosynthesis*

Substances

  • CXCR4 protein, human
  • Molecular Probes
  • Neoplasm Proteins
  • Receptors, CXCR4