Application of Artificial Intelligence in Oncologic Molecular PET-Imaging: A Narrative Review on Beyond [18F]F-FDG TracersPart II. [18F]F-FLT, [18F]F-FET, [11C]C-MET and Other Less-Commonly Used Radiotracers

R Eisazadeh, M Shahbazi-Akbari, SA Mirshahvalad, C Pirich (Co-author), M Beheshti* (Last author)

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

3 Citations (Web of Science)

Abstract

Following the previous part of the narrative review on artificial intelligence (AI) applications in positron emission tomography (PET) using tracers rather than F-18-fluorodeoxyglucose ([F-18]F-FDG), in this part we review the impact of PET-derived radiomics data on the diagnostic performance of other PET radiotracers, F-18-O-(2-fluoroethyl)-L-tyrosine ([F-18]F-FET), F-18-Fluorothymidine ([F-18]F-FLT) and C-11-Methionine ([C-11]C-MET). [F-18]F-FET-PET, using an artificial amino acid taken up into upregulated tumoral cells, showed potential in lesion detection and tumor characterization, especially with its ability to reflect glioma heterogeneity. [F-18]F-FET-PET-derived textural features appeared to have the potential to reveal considerable information for accurate delineation for guiding biopsy and treatment, differentiate between low-grade and high-grade glioma and related wild-type genotypes, and distinguish pseudoprogression from true progression. In addition, models built using clinical parameters and [F-18]F-FET-PET-derived radiomics features showed acceptable results for survival stratification of glioblastoma patients. [F-18]F-FLT-PET-based characteristics also showed potential in evaluating glioma patients, correlating with Ki-67 and patient prognosis. AI-based PET-volumetry using this radiotracer as a proliferation marker also revealed promising preliminary results in terms of guide-targeting bone marrow-preserving adaptive radiation therapy. Similar to [F-18]F-FET, the other amino acid tracer which reflects cellular proliferation, [C-11]C-MET, has also shown acceptable performance in predicting tumor grade, distinguishing brain tumor recurrence from radiation necrosis, and treatment monitoring by PET-derived radiomics models. In addition, PET-derived radiomics features of various radiotracers such as [F-18]F-DOPA, [F-18]F-FACBC, [F-18]F-NaF, [Ga-68]Ga-CXCR-4 and [F-18]F-FMISO may also provide useful information for tumor characterization and predict of disease outcome. In conclusion, AI using tracers beyond [F-18]F-FDG could improve the diagnostic performance of PET-imaging for specific indications and help clinicians in their daily routine by providing features that are often not detectable by the naked eye.
Original languageEnglish
Pages (from-to)293-301
Number of pages9
JournalSEMINARS IN NUCLEAR MEDICINE
Volume54
Issue number2
DOIs
Publication statusPublished - Mar 2024

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