Positron emission tomography/computed tomography (PET/CT) with 18FFDG is widely used to assess tumor glycolytic metabolism, whereas 18FPSMA-1007 or 68GaPSMA-11 PET/CT is associated with tumor neovascularization. Notably, some lesions exhibit an intralesional “mismatch”, in which different regions within the same lesion demonstrate higher uptake of either 18FFDG or PSMA-targeted radiotracers, suggesting distinct metabolic phenotypes and possible intratumoral heterogeneity. However, few studies have explored the combined use of these tracers. To evaluate the intralesional distribution of 18FFDG and (18FPSMA-1007 or 68GaPSMA-11) in PET/CT images across malignancies using qualitative and semiquantitative parameters, aiming to investigate patterns of intralesional uptake mismatch. This retrospective cross-sectional study included patients with differentiated thyroid cancer, lung cancer, hepatocellular carcinoma, lymphoma, and multiple myeloma undergoing staging or restaging. All patients underwent both 18FFDG and 18FPSMA-1007 or 68GaPSMA-11 PET/CT within an interval. The largest soft-tissue lesion (or bone lesion with a soft-tissue component) with a maximum diameter = 4 cm was selected for analysis. PET/CT images were evaluated qualitatively and semiquantitatively. Qualitative assessment of intralesional tracer uptake differences was performed using a classification system. Intralesional PSMA distribution relative to FDG uptake was classified as peripheral (1), central (2), diffuse (3), or segmental (4). Semiquantitative parameters, including SUVmax, SUVmean, metabolic tumor volume (MTV), and total lesion metabolism (TLM; MTV × SUVmean), were measured with a PET/CT viewer plug-in for ImageJ (FIJI). MTV was defined using a fixed SUV threshold (= 2.5) for 18FFDG and uptake above the mediastinal blood pool for PSMA tracers.Eleven patients were included: 3/11 (27%) thyroid cancer, 3/11 (27%) lung cancer, 2/11 (18%) hepatocellular carcinoma, 2/11 (18%) multiple myeloma, and 1/11 (9%) lymphoma (3 males, 8 females; mean age 63.4 ± 13.8 years). Visual analysis demonstrated predominantly peripheral PSMA uptake in 5/11 patients (46%), including all thyroid cancer cases. Segmental PSMA uptake was observed in 3/11 (27%), central uptake in 2/11 (18%), and diffuse uptake in 1/11 (9%). Median (range) SUVmax, SUVmean, MTV, and TLM for PSMA and FDG were respectively: 21.5 (4.9–73) vs 14.8 (4.1–36.6) p = 0.4389; 6.22 (2.93–12.5) vs 7 (3–17.6); p = 0.9314; 81.7 (3.3–228.9) vs. 77.2 (14.9–313.5) p = 0.6665; and 519.5 (9.7–1345.3) vs 716.2 (46.8–4229.2) p = 0.5457.Intralesional uptake mismatch between FDG and PSMA is highly prevalent across neoplastic lesions from different malignancies. However, semiquantitative parameters did not differ significantly at the population level, possibly due to the limited sample size or because this phenomenon is predominantly spatial and not fully captured by global metrics. The frequent peripheral PSMA uptake pattern may reflect neovascularization surrounding relatively hypoxic or necrotic tumor cores. Segmental and central uptake patterns may suggest the coexistence of distinct tumor cell clones within the same lesion, whereas diffuse uptake may reflect more homogeneous tumor biology. Further studies integrating PET imaging with spatially correlated, multi-site tumor biopsies are warranted to clarify the biological significance of intralesional FDG/PSMA mismatch patterns across different cancers.
Portilho et al. (Sun,) studied this question.