4.7 Article

Early detection of radiation-induced myocardial damage by [18F]AlF-NOTA-FAPI-04 PET/CT imaging

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Publisher

SPRINGER
DOI: 10.1007/s00259-022-05962-y

Keywords

Radiation-induced heart damage; Fibroblast activation protein; PET; CT

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This study demonstrates that [F-18]AlF-NOTA-FAPI-04 PET/CT imaging can noninvasively detect radiation-induced myocardial damage and has great clinical potential for early monitoring of this condition.
Purpose Retrospective analysis revealed increased [F-18]AlF-NOTA-FAPI-04 uptake in the myocardium of patients with esophageal squamous cell cancer (ESCC) treated with concurrent chemoradiotherapy (CCRT). This study investigated and verified the feasibility of [F-18]AlF-NOTA-FAPI-04 PET/CT for detecting radiation-induced myocardial damage (RIMD). Methods Myocardial FAPI uptake was analyzed before and during radiotherapy in thirteen ESCC patients treated with CCRT. In the animal study, a single dose of 50 Gy was delivered to the cardiac apex of Wistar rats (24 rats, including 16 RIMD model rats and 8 control model rats). RIMD model rats were scanned with [F-18]AlF-NOTA-FAPI-04 PET/CT weekly for 12 weeks, and left ventricular ejection fraction (LVEF) was measured by magnetic resonance imaging. Dynamic, blocking, and [F-18]FDG PET/CT studies (4 rats/group) were performed on RIMD rats at 5 weeks post-radiation, and histopathological analyses were conducted. Results Increased FAPI uptake in the myocardium was found after CCRT (1.53 +/- 0.53 vs 1.88 +/- 0.70, P = 0.015). In RIMD rats, significantly increased FAPI uptake in the damaged myocardium was observed from the 2nd week post-radiation exposure and peaked in the 5th week. Significantly more intense tracer accumulation was observed in the damaged myocardium than in the remote myocardium, as identified by decreased [F-18]FDG uptake and confirmed by autoradiography, hematoxylin-eosin, Masson's trichrome, and immunohistochemical staining. The LVEF remained unchanged at the 3rd week post-radiation exposure but was remarkably decreased compared with that in the control group at the 8th week. Conclusion Through clinical phenomena and animal experimental studies, this study indicated that [F-18]AlF-NOTA-FAPI-04 PET/CT imaging can detect RIMD noninvasively and before a decrease in LVEF, indicating the clinical potential of [F-18]AlF-NOTA-FAPI-04 as a PET/CT tracer for early monitoring of RIMD.

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