Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Dec 28;18(1):57.
doi: 10.3390/ijms18010057.

Immuno-PET for Clinical Theranostic Approaches

Affiliations
Review

Immuno-PET for Clinical Theranostic Approaches

Clément Bailly et al. Int J Mol Sci. .

Abstract

Recent advances in molecular characterization of tumors have allowed identification of new molecular targets on tumor cells or biomarkers. In medical practice, the identification of these biomarkers slowly but surely becomes a prerequisite before any treatment decision, leading to the concept of personalized medicine. Immuno-positron emission tomography (PET) fits perfectly with this approach. Indeed, monoclonal antibodies (mAbs) labelled with radionuclides represent promising probes for theranostic approaches, offering a non-invasive solution to assess in vivo target expression and distribution. Immuno-PET can potentially provide useful information for patient risk stratification, diagnosis, selection of targeted therapies, evaluation of response to therapy, prediction of adverse effects or for titrating doses for radioimmunotherapy. This paper reviews some aspects and recent developments in labelling methods, biological targets, and clinical data of some novel PET radiopharmaceuticals.

Keywords: antibody; immuno-PET; molecular imaging.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Topic of research on Webofknowledge.com: “immuno-positron emission tomography (PET)”. This report reflects citations to source items indexed within Web of Science Core Collection.
Figure 2
Figure 2
Immuno-PET maximum-intensity-projection images recorded in five patients (one patient of each cohort, A to E) included in the optimization part of the first-in-human immuno-PET trial using anti-carcinoembryonic antigen CEA bispecific antibody and 68Ga-labelled peptide in metastatic medullary thyroid carcinoma. Arrows showed foci considered as pathologic by immuno-PET. (This research was originally published in JNM. Immuno-PET using anti-CEA bispecific antibody and 68Ga-labelled peptide in metastatic medullary thyroid carcinoma: clinical optimization of the pre-targeting parameters in a First-in Human trial. Bodet-Milin et al. J. Nucl. Med. 2016, 57, 1505–1511. © by the Society of Nuclear Medicine and Molecular Imaging, Inc., Reston, VA, USA).

Similar articles

Cited by

References

    1. Hanahan D., Weinberg R.A. Hallmarks of cancer: The next generation. Cell. 2011;144:646–674. doi: 10.1016/j.cell.2011.02.013. - DOI - PubMed
    1. Alam I.S., Arshad M.A., Nguyen Q.-D., Aboagye E.O. Radiopharmaceuticals as probes to characterize tumour tissue. Eur. J. Nucl. Med. Mol. Imaging. 2015;42:537–561. doi: 10.1007/s00259-014-2984-3. - DOI - PubMed
    1. Mellstedt H. Monoclonal antibodies in human cancer. Drugs Today. 2003;39:1–16. - PubMed
    1. Fauvel B., Yasri A. Antibodies directed against receptor tyrosine kinases: Current and future strategies to fight cancer. MAbs. 2014;6:838–851. doi: 10.4161/mabs.29089. - DOI - PMC - PubMed
    1. Medinger M., Drevs J. Receptor tyrosine kinases and anticancer therapy. Curr. Pharm. Des. 2005;11:1139–1149. doi: 10.2174/1381612053507611. - DOI - PubMed

Substances

LinkOut - more resources