Fibroblast Activation Protein Inhibitor Theranostics in Sarcoma

Sarcomas are rare and heterogeneous cancers arising from mesenchymal tissues, presenting diagnostic and therapeutic challenges. Fibroblast activation protein (FAP), overexpressed in the tumor microenvironment of many sarcomas, has emerged as a promising theranostic target. FAP inhibitors (FAPI)-PET/CT demonstrates excellent sensitivity and specificity in detecting primary tumors, local recurrence, and distant metastases, even in low-grade sarcomas. This facilitates accurate staging and personalized treatment. Various FAPI radiotracers, including FAPI-04, FAPI-46, and FAP-2286, offer unique pharmacokinetic properties. FAPI-targeted radionuclide therapy (TRT) employs therapeutic radioisotopes to deliver targeted radiation to FAP-expressing tumor cells. Early clinical trials show promising disease control rates and manageable toxicity profiles. However, challenges remain, including FAP expression heterogeneity and the need for optimized treatment protocols. The aim of this review is to provide a comprehensive overview of the current evidence and future directions of FAPI-based theranostics in sarcoma management, highlighting its potential to improve patient outcomes.

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Publication Details

Journal
Clinical Nuclear Medicine
Published
2026-02-23
DOI
https://doi.org/10.1097/rlu.0000000000006318
Primary Topic
Peptidase Inhibition and Analysis
Type
article
Field-Weighted Citation Impact
0.00
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article

Fibroblast Activation Protein Inhibitor Theranostics in Sarcoma

Narges Jokar, Esmail Jafari, Majid Assadi, Malik Juweid et al.
Clinical Nuclear Medicine
Peptidase Inhibition and Analysis
article

Fibroblast Activation Protein Inhibitor Theranostics in Sarcoma

Narges Jokar, Esmail Jafari, Majid Assadi, Malik Juweid, Nader Shakibazad, Seyed Javad Rekabpour
article en

Abstract

Sarcomas are rare and heterogeneous cancers arising from mesenchymal tissues, presenting diagnostic and therapeutic challenges. Fibroblast activation protein (FAP), overexpressed in the tumor microenvironment of many sarcomas, has emerged as a promising theranostic target. FAP inhibitors (FAPI)-PET/CT demonstrates excellent sensitivity and specificity in detecting primary tumors, local recurrence, and distant metastases, even in low-grade sarcomas. This facilitates accurate staging and personalized treatment. Various FAPI radiotracers, including FAPI-04, FAPI-46, and FAP-2286, offer unique pharmacokinetic properties. FAPI-targeted radionuclide therapy (TRT) employs therapeutic radioisotopes to deliver targeted radiation to FAP-expressing tumor cells. Early clinical trials show promising disease control rates and manageable toxicity profiles. However, challenges remain, including FAP expression heterogeneity and the need for optimized treatment protocols. The aim of this review is to provide a comprehensive overview of the current evidence and future directions of FAPI-based theranostics in sarcoma management, highlighting its potential to improve patient outcomes.

Clinical Nuclear Medicine
University of Jordan (JO), Active Medicine (United Kingdom) (GB), Institute of Nuclear Physics (UZ), Salman Farsi University of Kazerun (IR), Bushehr University of Medical Sciences (IR)
Good health and well-being
Openalex Percentile: Top 42%
Peptidase Inhibition and Analysis
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