Can PSMA PET detect intratumour heterogeneity in histological PSMA expression of primary prostate cancer? Analysis of [<sup>68</sup>Ga]Ga-PSMA-11 and [<sup>18</sup>F]PSMA-1007.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 39821663.
- Also identified by DOI 10.1007/s00259-025-07078-5 and PMC identifier 12014795.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Prostate-specific membrane-antigen positron emission tomography (PSMA PET) is a promising candidate for non-invasive characterization of prostate cancer (PCa). This study evaluated whether PET with tracers [<sup>68</sup>Ga]Ga-PSMA-11 or [<sup>18</sup>F]PSMA-1007 is capable to depict intratumour heterogeneity of histological PSMA expression. Thirty-five patients with biopsy-proven primary PCa without evidence of metastatic disease nor prior interventions were prospectively enrolled. All patients underwent PSMA PET combined with computer tomography (CT) with either [<sup>68</sup>Ga]Ga-PSMA-11 (cohort I, 20 patients) or [<sup>18</sup>F]PSMA-1007 (cohort II, 15 patients) followed by radical prostatectomy. Specimens were scanned by ex-vivo CT and histologically prepared. On digitized whole-mount prostate sections, PCa areas with different morphologies were manually defined and H-Score of immunohistochemical PSMA expression was calculated with assistance by artificial intelligence (AI). PCa areas with similar H-Score were unified in segmentation on ex-vivo CT. After co-registration on PSMA PET-CT, Spearman's coefficients of PSMA expression to mean and maximum standardized uptake value (SUV<sub>mean</sub> and SUV<sub>max</sub>) were calculated. Furthermore, the agreement of the co-registered tumour areas to gross tumour volume (GTV) in PSMA PET was analysed. Thirty-two patients were included in the final analysis. For histological PCa areas, immunohistochemical PSMA expression correlated significantly to SUV<sub>mean</sub> and SUV<sub>max</sub> (p < 0.001, p = 0.001). An approximate linear correlation between H-Score and SUV<sub>mean</sub> / SUV<sub>max</sub> was found for tumour areas larger than 400 μm² in histology (p < 0.001). Tumour areas with strong PSMA expression showed a significantly larger overlap to GTV in PSMA PET after co-registration than tumour areas with very low PSMA expression (p < 0.01). No significant differences were found between the two tracer cohorts (p = 0.72). PSMA PET with both [<sup>68</sup>Ga]Ga-PSMA-11 or [<sup>18</sup>F]PSMA-1007 is able to detect changes in histological PSMA expression within PCa lesions allowing biologically targeted radiotherapy.
Medical subject headings
- Prostatic Neoplasms
- Glutamate Carboxypeptidase II
- Antigens, Surface
- Oligopeptides
- Edetic Acid
- Niacinamide
- Positron Emission Tomography Computed Tomography
- Glycine
- Gene Expression Regulation, Neoplastic
- Positron-Emission Tomography