Initial results with [18F]FAPI-74 PET/CT in idiopathic pulmonary fibrosis

Mori; Y.; Kramer; V.; Novruzov; E.; Mamlins; E.; Röhrich; M.; Fernández; R.; Amaral; H.; Soza-Ried; C.; Monje; B.; Sabbagh; E.; Florenzano; M.; Giesel; F.L.; Undurraga; Å

Keywords: FAPI; Fibroblast activation protein; Fibrosis; Idiopathic pulmonary disease; PET

Abstract

Abstract: Idiopathic pulmonary fibrosis (IPF) is a chronic fibrosing interstitial lung disease with a poor prognosis. 68Ga-labeled FAP ligands exhibited highly promising results due to the crucial role of activated fibroblasts in fibrosis imaging of the lung. However, 18F-labeled FAP ligands might provide qualitatively much higher imaging results with accompanying economic benefits due to large-scale production. Thus, we sought to investigate the potential of [18F]FAPI-74 prospectively in a small patient cohort. Methods: Eight patients underwent both [18F]FAPI-74-PET/CT and HRCT scans and were then compared with a control group without any fibrosing pulmonary disease. The tracer uptake of fibrotic lung areas was analyzed in synopsis with radiological and clinical parameters. Results: We observed a positive correlation between the fibrotic active volume, the Hounsfield scale, as well as the vital and diffusing capacity of the lung. Conclusion: The initial results confirm our assumption that [18F]FAPI-74 offers a viable non-invasive assessment method for pulmonary fibrotic changes in patients with IPF.

Más información

Título según WOS: ID WOS:001130143600001 Not found in local WOS DB
Título según SCOPUS: Initial results with [18F]FAPI-74 PET/CT in idiopathic pulmonary fibrosis
Título de la Revista: European Journal of Nuclear Medicine and Molecular Imaging
Volumen: 51
Número: 6
Editorial: Springer
Fecha de publicación: 2024
Página de inicio: 1605
Página final: 1611
Idioma: English
DOI:

10.1007/s00259-023-06564-y

Notas: ISI, SCOPUS