Preclinical ImmunoPET Imaging of Thyroid-Stimulating Hormone Receptor Expression in Thyroid Cancer using

Wenhui Fu1, Ephraim E Parent1, Justyna J Gleba2

  • 1Department of Radiology, Mayo Clinic, Jacksonville, Florida 32224, United States.

PubMed

Insights

A novel Copper-64 labeled antibody ([64Cu]Cu-NOTA-TSHR-Ab) shows promise for imaging advanced thyroid cancers by targeting the thyroid-stimulating hormone receptor (TSHR). This radiotracer demonstrates high specificity and superior tumor detection compared to [18F]FDG PET imaging.

Area of Science:

  • Nuclear medicine
  • Oncology
  • Radiopharmaceutical chemistry

Background:

  • Advanced thyroid cancers are aggressive and often resistant to conventional treatments.
  • The thyroid-stimulating hormone receptor (TSHR) is a promising target due to its high expression in thyroid cancers and limited expression elsewhere.
  • Radiotheranostics offer a dual approach for imaging and therapy.

Purpose of the Study:

  • To develop and evaluate a Copper-64 labeled antibody for positron emission tomography (PET) imaging of TSHR expression in advanced thyroid cancer.
  • To assess the specificity, binding affinity, and tumor targeting capabilities of the novel radiotracer in preclinical models.
  • To compare the diagnostic performance of the novel radiotracer with established PET imaging agents.

Main Methods:

  • Radiosynthesis of human anti-TSHR recombinant antibody K1-70 labeled with Copper-64 ([64Cu]Cu-NOTA-TSHR-Ab).
  • In vitro characterization of radiotracer specificity and binding affinity using TSHR-positive and wild-type cells.
  • In vivo immunoPET imaging in mouse models bearing thyroid cancer xenografts, including biodistribution and blocking studies.
  • Comparative analysis with [18F]FDG PET imaging.

Main Results:

  • Successful radiosynthesis of [64Cu]Cu-NOTA-TSHR-Ab with high radiochemical yield and purity.
  • Demonstrated high specificity and nanomolar binding affinity for TSHR-positive cells in vitro.
  • ImmunoPET imaging revealed rapid and specific tumor targeting in TSHR-positive thyroid tumors in vivo.
  • Blocking studies confirmed reduced off-target signals, and [64Cu]Cu-NOTA-TSHR-Ab outperformed [18F]FDG in tumor detection.

Conclusions:

  • [64Cu]Cu-NOTA-TSHR-Ab is a highly promising radiotracer for PET imaging of TSHR-positive advanced thyroid cancers.
  • The radiotracer has the potential to guide and monitor TSHR-targeted therapies.
  • Further clinical evaluation is warranted for patient stratification and treatment optimization.