ArticleEJNMMI research2025
A fibroblast activation protein targeted optical tracer for identifying primary and metastatic sarcoma during resection.
Article in EJNMMI research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundSarcomas represent a heterogeneous group of mesenchymal tumors that, despite accounting for only 1% of cancers worldwide, rank among the top five causes of cancer-related deaths in patients under 20 years old. Surgical resection remains the primary treatment for these malignancies, as effective systemic therapies are limited, particularly for high-grade disease. However, surgical outcomes are often compromised by incomplete resection, leading to high local and distal recurrence rates. Intraoperative molecular imaging has emerged as a promising approach to improve surgical outcomes but has been hindered by the lack of tumor-specific targeting agents. Fibroblast activation protein (FAP), selectively expressed by mesenchymal tumors and absent in healthy tissues, presents a promising target for fluorescence-guided cancer resections.
resultsWe demonstrate that 41% of human sarcomas express FAP, with expression correlating with higher histologic grade. The FAP-S0456 optical tracer specifically bound to FAP-expressing sarcomas with minimal binding to normal tissues, exhibiting excellent tumor-to-background ratios (3.8 ± 0.43). In vitro studies confirmed FAP-S0456's specificity for human FAP with a dissociation constant of approximately 10 nM. In murine xenograft models, the tracer accurately identified both primary tumors and pulmonary metastases of FAP-expressing sarcomas. Importantly, using needle confocal laser endomicroscopy, we demonstrated that FAP-S0456 enables real-time, single-cell visualization of metastatic tumor cells during surgery, including micrometastases not detected by conventional imaging.
conclusionsFAP-S0456 represents a promising molecular imaging agent for the detection and surgical removal of primary and metastatic sarcomas. Its high specificity for FAP-expressing tumor cells, favorable biodistribution profile, and ability to detect microscopic disease offer potential to improve complete surgical resection. These findings support the development of FAP-targeted fluorescence-guided surgery for sarcoma patients, which may lead to improved oncologic outcomes, particularly for those with pulmonary metastases where complete surgical clearance is critical for survival.
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