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Updated: Jun 26, 2025

Development of a 68Gallium-Labeled D-Peptide PET Tracer for Imaging Programmed Death-Ligand 1 Expression
Published on: February 3, 2023
The cutting edge: Promising oncology radiotracers in clinical development
Jorge D Oldan1, Martin G Pomper2, Rudolf A Werner3
1Molecular Imaging and Therapeutics, Department of Radiology, University of North Carolina, Chapel Hill, NC 27516, USA.
Abstract:
Molecular imaging moves forward with the development of new imaging agents, and among these are new radiotracers for nuclear medicine applications, particularly positron emission tomography (PET). A number of new targets are becoming accessible for use in oncologic applications. In this review, major new radiotracers in clinical development are discussed. Prominent among these is the family of fibroblast-activation protein-targeted agents that interact with the tumor microenvironment and may show superiority to 2-deoxy-2-[18F]fluoro-d-glucose in a subset of different tumor histologies. Additionally, carbonic anhydrase IX (CAIX) inhibitors are directed at clear cell renal cell carcinoma, which has long lacked an effective PET imaging agent. Those CAIX agents may also have utility in hypoxic tumors. Pentixafor, which binds to a transmembrane receptor, may similarly allow for visualization by PET of low-grade lymphomas, as well as being a second agent for multiple myeloma that opens theranostic possibilities. There are new adrenergic agents aimed at providing a PET-visible replacement to the single-photon-emitting radiotracer meta-[123I]iodobenzylguanidine (MIBG). Finally, in response to a major development in oncologic chemotherapy, there are new radiotracers targeted at assessing the suitability or use of immunotherapeutic agents. All of these and the existing evidence for their utility are discussed.
Insights
New radiotracers for positron emission tomography (PET) are advancing cancer imaging. These novel agents target the tumor microenvironment, specific cancers like renal cell carcinoma, lymphomas, and immunotherapies, offering improved diagnostic capabilities.
Area of Science:
- Nuclear medicine
- Molecular imaging
- Oncology
Background:
- Advancements in molecular imaging are driven by new imaging agents.
- Radiotracers are crucial for nuclear medicine, especially positron emission tomography (PET).
- New molecular targets are emerging for oncologic applications.
Purpose of the Study:
- To review major new radiotracers in clinical development for oncologic applications.
- To discuss the potential advantages of novel agents over current standards like 2-deoxy-2-[18F]fluoro-d-glucose (FDG).
- To highlight agents targeting the tumor microenvironment, specific cancers, and immunotherapies.
Main Methods:
- Review of clinical development of new radiotracers.
- Discussion of agents targeting fibroblast activation protein (FAP).
- Analysis of carbonic anhydrase IX (CAIX) inhibitors, Pentixafor, adrenergic agents, and immunotherapeutic agents.
Main Results:
- Fibroblast activation protein (FAP)-targeted agents show potential superiority to FDG in certain tumor types.
- Carbonic anhydrase IX (CAIX) inhibitors offer new PET imaging for clear cell renal cell carcinoma and hypoxic tumors.
- Pentixafor enables PET visualization of low-grade lymphomas and multiple myeloma, with theranostic potential.
- New adrenergic agents provide PET alternatives to meta-[123I]iodobenzylguanidine (MIBG).
- Novel radiotracers are being developed to assess immunotherapy suitability.
Conclusions:
- New radiotracers are expanding PET applications in oncology.
- Targeting the tumor microenvironment and specific cancer biomarkers enhances imaging capabilities.
- Emerging agents offer improved diagnostics and theranostics for various cancers and treatments.
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