Delgado Bolton Roberto C, Calapaquí Terán Adriana K, Santiago Almeida Ludmila, Paez Diana, Estrada Lobato Enrique, Brink Anita, Knoll Peter, Treglia Giorgio, Giammarile Francesco
Department of Diagnostic Imaging (Radiology) and Nuclear Medicine, University Hospital San Pedro and Centre for Biomedical Research of La Rioja (CIBIR), Logroño, L.R., Spain; Servicio Cántabro de Salud, Santander, Spain.
Servicio Cántabro de Salud, Santander, Spain; Department of Pathology, University Hospital "Marqués de Valdecilla", Santander, Spain; Instituto de Investigación Sanitaria Valdecilla (IDIVAL), Santander, Spain.
Semin Nucl Med. 2025 Sep;55(5):734-739. doi: 10.1053/j.semnuclmed.2025.05.003. Epub 2025 Jun 1.
Nuclear medicine has seen significant advancements in recent years, especially in the area of Positron Emission Tomography (PET) imaging. One of these innovations is the use of Fibroblast Activation Protein Inhibitors (FAPI) as a novel radiotracer. FAPI PET imaging has shown promising results in various malignancies, including sarcomas, which are a diverse group of cancers originating from mesenchymal cells. This review aims to explore the potential of FAPI PET imaging in the diagnosis, staging, and treatment monitoring of sarcomas. Several studies have demonstrated the potential of FAPI PET in sarcomas. Furthermore, FAPI PET imaging has shown potential in assessing treatment response, with changes in FAPI uptake correlating with treatment outcomes. However, there are challenges to be addressed. The heterogeneity of sarcomas, both inter- and intra-tumoral, may affect the uniformity of Fibroblast Activation Protein (FAP) expression and thus the effectiveness of FAPI PET imaging. In conclusion, the introduction of FAPI PET imaging represents a significant advancement in the field of nuclear medicine and oncology. As we continue to deepen our understanding of this novel imaging technique, it is hoped that FAPI PET imaging will play an increasingly important role in the fight against cancer. However, as with any new technology, further research is needed to fully understand the potential and limitations of FAPI PET imaging in the clinical setting.
近年来,核医学取得了显著进展,尤其是在正电子发射断层扫描(PET)成像领域。其中一项创新是使用成纤维细胞活化蛋白抑制剂(FAPI)作为新型放射性示踪剂。FAPI PET成像在包括肉瘤在内的各种恶性肿瘤中显示出了有前景的结果,肉瘤是一类起源于间充质细胞的多种癌症。本综述旨在探讨FAPI PET成像在肉瘤诊断、分期和治疗监测中的潜力。多项研究证明了FAPI PET在肉瘤中的潜力。此外,FAPI PET成像在评估治疗反应方面也显示出潜力,FAPI摄取的变化与治疗结果相关。然而,仍有一些挑战需要解决。肉瘤在肿瘤间和肿瘤内的异质性可能会影响成纤维细胞活化蛋白(FAP)表达的一致性,从而影响FAPI PET成像的有效性。总之,FAPI PET成像的引入代表了核医学和肿瘤学领域的一项重大进展。随着我们对这种新型成像技术的理解不断深入,希望FAPI PET成像在抗癌斗争中发挥越来越重要的作用。然而,与任何新技术一样,需要进一步研究以充分了解FAPI PET成像在临床环境中的潜力和局限性。