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

Kathrin Philipp‐Abbrederis(Technical University of Munich), Ken Herrmann(Universitäts-Kinderklinik Würzburg), Stefan Knop(Universitätsklinikum Würzburg), Margret Schottelius(Technical University of Munich), Matthias Eiber(Technical University of Munich), Katharina Lückerath(Universitätsklinikum Würzburg), Elke Pietschmann(Technical University of Munich), Stefan Habringer(German Cancer Research Center), Carlos Gerngroß(Technical University of Munich), Katharina Franke(Technical University of Munich), Martina Rudelius(University of Würzburg), Andreas Schirbel(Universitätsklinikum Würzburg), Constantin Lapa(Universitätsklinikum Würzburg), Kristina Schwamborn(Munich University of Applied Sciences), Sabine Steidle(Technical University of Munich), Elena Hartmann(University of Würzburg), Andreas Rosenwald(University of Würzburg), Saskia Kropf, Ambros J. Beer(Technical University of Munich), Christian Peschel(German Cancer Research Center), Hermann Einsele(Universitätsklinikum Würzburg), Andreas K. Buck(Universitätsklinikum Würzburg), Markus Schwaiger(German Cancer Research Center), Katharina S. Götze(German Cancer Research Center), Hans‐Jürgen Wester(German Cancer Research Center), Ulrich Keller(German Cancer Research Center)
EMBO Molecular Medicine
March 3, 2015
Cited by 212Open Access
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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.


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