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

材料科学 放射化学 癌症研究 化学 医学
作者
Helena Lanzafame,Christoph E. Heilig,Eva Wardelmann,Mélanie Desaulniers,Kim M. Pabst,Ilektra Antonia Mavroeidi,Ina Pretzell,Pedro Fragoso Costa,Michael Nader,Stephan Leyser,Martin Schüler,Sebastian Bauer,Jens T. Siveke,Leila Kamkar,Simon Kreutzfeldt,Stefan Fröhling,Sebastian Mühl,Ken Herrmann,Wolfgang P. Fendler,Rainer Hamacher
出处
期刊:The Journal of Nuclear Medicine [Society of Nuclear Medicine]
卷期号:: jnumed.125.269572-jnumed.125.269572
标识
DOI:10.2967/jnumed.125.269572
摘要

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. Methods: 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 90Y-labeled fibroblast activation protein inhibitor (FAPI)-46 RPT because of the high uptake observed in 68Ga-FAPI-46 PET/CT scans. Results: 90Y-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. Conclusion: 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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