<sup>90</sup>Y-FAPI-46 Theranostics Leads to Near-Complete Metabolic Response in 3 Patients with Solitary Fibrous Tumors

Solitary fibrous tumor (SFT) is a rare soft-tissue sarcoma with limited treatment options, especially in advanced or metastatic cases. Fibroblast activation protein α (FAPα) is overexpressed in certain sarcomas, including SFTs, making it a promising target for diagnostics and radiopharmaceutical therapy (RPT). We present the cases of 3 patients with metastatic SFTs who, after exhausting standard treatments, underwent molecular profiling and showed elevated FAPα expression. <b>Methods:</b> Messenger RNA and protein expression of FAPα were examined in biopsy samples from 3 patients participating in the Molecularly Aided Stratification for Tumor Eradication Research program, a multicenter observational study focused on biology-driven stratification of adults with advanced cancer. Messenger RNA expression levels were quantified as transcripts per million, with RNA extraction, sequencing, and data processing performed using established protocols. Protein expression was assessed and stained with FAPα immunohistochemistry using a recombinant anti-FAPα antibody. Following the recommendation of the molecular tumor board, these patients received <sup>90</sup>Y-labeled fibroblast activation protein inhibitor (FAPI)-46 RPT because of the high uptake observed in <sup>68</sup>Ga-FAPI-46 PET/CT scans. <b>Results:</b> <sup>90</sup>Y-FAPI-46 RPT led to substantial clinical benefits, including metabolic resolution and symptom relief, with disease control confirmed using RECIST and PERCIST. Treatment was well-tolerated, with only minor adverse events observed. <b>Conclusion:</b> Our findings underscore the utility of FAPα screening as a predictive biomarker and the potential of FAP-targeted RPT as a viable treatment for advanced SFT.

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Publication Details

Journal
Journal of Nuclear Medicine
Published
2025-07-24
DOI
https://doi.org/10.2967/jnumed.125.269572
Citations
8
Primary Topic
Peptidase Inhibition and Analysis
Type
article
Field-Weighted Citation Impact
8.36
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article

90Y-FAPI-46 Theranostics Leads to Near-Complete Metabolic Response in 3 Patients with Solitary Fibrous Tumors

Stefan Fröhling, Ken Herrmann, Christoph E. Heilig, Pedro Fragoso Costa et al.
8 citations
Journal of Nuclear Medicine
Peptidase Inhibition and Analysis
8.36
article

90Y-FAPI-46 Theranostics Leads to Near-Complete Metabolic Response in 3 Patients with Solitary Fibrous Tumors

Stefan Fröhling, Ken Herrmann, Christoph E. Heilig, Pedro Fragoso Costa, Sebastian Bauer, Martin Schüler, Eva Wardelmann, Simon Kreutzfeldt, Kim M. Pabst, Ilektra Antonia Mavroeidi, Wolfgang P. Fendler, Helena Lanzafame, Mélanie Desaulniers, Sebastian Mühl, Jens Thomas Siveke, Rainer Hamacher, Michael Nader, Ina Pretzell, Stephan Leyser, Leila Kamkar
article en
8 citations

Abstract

Solitary fibrous tumor (SFT) is a rare soft-tissue sarcoma with limited treatment options, especially in advanced or metastatic cases. Fibroblast activation protein α (FAPα) is overexpressed in certain sarcomas, including SFTs, making it a promising target for diagnostics and radiopharmaceutical therapy (RPT). We present the cases of 3 patients with metastatic SFTs who, after exhausting standard treatments, underwent molecular profiling and showed elevated FAPα expression. <b>Methods:</b> Messenger RNA and protein expression of FAPα were examined in biopsy samples from 3 patients participating in the Molecularly Aided Stratification for Tumor Eradication Research program, a multicenter observational study focused on biology-driven stratification of adults with advanced cancer. Messenger RNA expression levels were quantified as transcripts per million, with RNA extraction, sequencing, and data processing performed using established protocols. Protein expression was assessed and stained with FAPα immunohistochemistry using a recombinant anti-FAPα antibody. Following the recommendation of the molecular tumor board, these patients received <sup>90</sup>Y-labeled fibroblast activation protein inhibitor (FAPI)-46 RPT because of the high uptake observed in <sup>68</sup>Ga-FAPI-46 PET/CT scans. <b>Results:</b> <sup>90</sup>Y-FAPI-46 RPT led to substantial clinical benefits, including metabolic resolution and symptom relief, with disease control confirmed using RECIST and PERCIST. Treatment was well-tolerated, with only minor adverse events observed. <b>Conclusion:</b> Our findings underscore the utility of FAPα screening as a predictive biomarker and the potential of FAP-targeted RPT as a viable treatment for advanced SFT.

Journal of Nuclear MedicineVol. 66(9)
Université de Sherbrooke (CA), German Cancer Research Center (DE), Heidelberg University (DE), University of Münster (DE), West Cancer Center (US), National Center for Tumor Diseases (DE), Essen University Hospital (DE), Deutsches Konsortium für Translationale Krebsforschung (DE)
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Openalex Percentile: Top 2%
Peptidase Inhibition and Analysis
8.36
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