Abstract

Simple SummaryProstate cancer (PCa) is one of the most frequent malignancies diagnosed in men and its prognosis depends on the stage at diagnosis. Molecular imaging, namely PET/CT or PET/MRI using prostate-specific radiotracers, has gained increasing application in accurately evaluating PCa at staging, especially in cases of high-risk disease, and it is now also recommended by international guidelines. Radiomic analysis is an emerging research field with a high potential to offer non-invasive and longitudinal biomarkers for personalized medicine, and several applications have been described in oncology patients. In this review, we discuss the available evidence on the role of radiomic analysis in PCa imaging at staging, exploring two different hybrid imaging modalities, such as PET/CT and PET/MRI, and the whole spectrum of radiotracers involved.We performed a systematic review of the literature to provide an overview of the application of PET radiomics for the prediction of the initial staging of prostate cancer (PCa), and to discuss the additional value of radiomic features over clinical data. The most relevant databases and web sources were interrogated by using the query “prostate AND radiomic* AND PET”. English-language original articles published before July 2021 were considered. A total of 28 studies were screened for eligibility and 6 of them met the inclusion criteria and were, therefore, included for further analysis. All studies were based on human patients. The average number of patients included in the studies was 72 (range 52–101), and the average number of high-order features calculated per study was 167 (range 50–480). The radiotracers used were [68Ga]Ga-PSMA-11 (in four out of six studies), [18F]DCFPyL (one out of six studies), and [11C]Choline (one out of six studies). Considering the imaging modality, three out of six studies used a PET/CT scanner and the other half a PET/MRI tomograph. Heterogeneous results were reported regarding radiomic methods (e.g., segmentation modality) and considered features. The studies reported several predictive markers including first-, second-, and high-order features, such as “kurtosis”, “grey-level uniformity”, and “HLL wavelet mean”, respectively, as well as PET-based metabolic parameters. The strengths and weaknesses of PET radiomics in this setting of disease will be largely discussed and a critical analysis of the available data will be reported. In our review, radiomic analysis proved to add useful information for lesion detection and the prediction of tumor grading of prostatic lesions, even when they were missed at visual qualitative assessment due to their small size; furthermore, PET radiomics could play a synergistic role with the mpMRI radiomic features in lesion evaluation. The most common limitations of the studies were the small sample size, retrospective design, lack of validation on external datasets, and unavailability of univocal cut-off values for the selected radiomic features.

Highlights

  • Prostate cancer (PCa) is the most frequently diagnosed malignancy in men and the fifth leading cause of death worldwide [1,2]

  • The 5-year risk stratification in patients with primary PCa is mainly based on clinical stage, prostate-specific antigen (PSA), and Gleason Score (GS), derived from invasive biopsy samples [3]

  • Positron emission tomography (PET) combined with computed tomography (CT) or magnetic resonance imaging (MRI) can help to localize suspicious lesions in the prostate gland by using several prostate-specific radiotracers (i.e., Choline—labelled with either 18F and 11C, 18F-Fluciclovine, and prostate specific membrane antigen-prostatespecific membrane antigen (PSMA) ligands labelled with 68Ga or 18F), providing a valuable tool for the detection of cancer, and for the initial staging of disease [6,7]

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Summary

Introduction

Prostate cancer (PCa) is the most frequently diagnosed malignancy in men and the fifth leading cause of death worldwide [1,2]. In primary PCa, risk stratification at staging is crucial to determine prognosis and treatment strategies. The 5-year risk stratification in patients with primary PCa is mainly based on clinical stage, prostate-specific antigen (PSA), and Gleason Score (GS), derived from invasive biopsy samples [3]. Biopsy sampling cannot help in assessing the entire prostate gland and often it might incorrectly grade PCa, especially because of tumor downstaging. Positron emission tomography (PET) combined with computed tomography (CT) or magnetic resonance imaging (MRI) can help to localize suspicious lesions in the prostate gland by using several prostate-specific radiotracers (i.e., Choline—labelled with either 18F and 11C, 18F-Fluciclovine, and prostate specific membrane antigen-PSMA ligands labelled with 68Ga or 18F), providing a valuable tool for the detection of cancer, and for the initial staging of disease [6,7]

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