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Theranostics and Molecular-targeted Endo-radiotherapy: The Current Landscape and Future Directions
Aamir Nazar1,2, Sandip Basu1,2
1Professor, Radiation Medicine Centre, Bhabha Atomic Research Centre, Tata Memorial Centre Annexe, Parel.
Abstract:
Molecular theranostics has revolutionized the field of personalized medicine, specifically augmenting "precision oncology" and is now integral in the management of malignancies like differentiated thyroid carcinoma, neuroendocrine tumors, and metastatic carcinoma prostate. The potential of theranostics is huge with possible applications in a variety of tumors, including at their early stages. This article will focus on the advancements in nuclear theranostics-highlighting the expanded indications of already established radionuclide therapies like peptide receptor radionuclide therapy (PRRT), prostate specific membrane antigen radioligand therapy (PRLT), and meta-iodobenzylguanidine therapy (MIBG therapy); and also on novel radiolabeled theranostic agents targeting fibroblast activated protein (FAPI-based radiopharmaceuticals), chemokine receptor targeting agents (pentixfor/pentixather), integrins, cholecystokinin receptors and their potential applications.
Insights
Molecular theranostics enhances precision oncology for managing cancers like thyroid, neuroendocrine, and prostate tumors. Advancements include established therapies and novel agents targeting FAPI, chemokine receptors, and integrins for broader applications.
Area of Science:
- Nuclear medicine
- Oncology
- Radiopharmaceutical therapy
Background:
- Molecular theranostics is transforming personalized medicine and precision oncology.
- It is crucial in managing differentiated thyroid carcinoma, neuroendocrine tumors, and metastatic prostate cancer.
- Theranostics holds significant potential for early-stage and diverse cancer applications.
Purpose of the Study:
- To review advancements in nuclear theranostics.
- To highlight expanded indications for established therapies.
- To discuss novel radiolabeled agents and their potential.
Main Methods:
- Review of established radionuclide therapies: peptide receptor radionuclide therapy (PRRT), prostate specific membrane antigen radioligand therapy (PRLT), and meta-iodobenzylguanidine therapy (MIBG therapy).
- Exploration of novel theranostic agents targeting fibroblast activated protein (FAPI), chemokine receptors (e.g., pentixfor/pentixather), integrins, and cholecystokinin receptors.
Main Results:
- Established therapies (PRRT, PRLT, MIBG) show expanded clinical utility.
- Emerging theranostic agents targeting FAPI, chemokine receptors, integrins, and cholecystokinin receptors demonstrate promising potential.
- Nuclear theranostics offers a growing armamentarium for various malignancies.
Conclusions:
- Nuclear theranostics is a rapidly evolving field with significant clinical impact.
- Expanded indications and novel agents are broadening the scope of theranostic applications in oncology.
- Continued research promises further integration of theranostics into cancer management.
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