Publication | Open Access
PET Tracer <sup>18</sup>F-Fluciclovine Can Detect Histologically Proven Bone Metastatic Lesions: A Preclinical Study in Rat Osteolytic and Osteoblastic Bone Metastasis Models
20
Citations
32
References
2017
Year
<sup>18</sup>F-Fluciclovine (<i>trans</i>-1-amino-3-<sup>18</sup>F-fluorocyclobutanecarboxylic acid; <i>anti</i>-<sup>18</sup>F-FACBC) is a positron emission tomography (PET) tracer for diagnosing cancers (e.g., prostate and breast cancer). The most frequent metastatic organ of these cancers is bone. Fluciclovine-PET can visualize bony lesions in clinical practice; however, such lesions have not been described histologically. <b>Methods:</b> We investigated the potential of <sup>14</sup>C-fluciclovine in aiding the visualization of osteolytic and osteoblastic bone metastases (with histological analyses), compared with <sup>3</sup>H-2-deoxy-2-fluoro-D-glucose (<sup>3</sup>H-FDG), <sup>3</sup>H-choline chloride (<sup>3</sup>H-choline), and <sup>99m</sup>Tc-hydroxymethylene diphosphonate (<sup>99m</sup>Tc-HMDP) by using triple-tracer autoradiography in rat breast cancer osteolytic (on day 12 ± 1 postinjection of MRMT-1) and prostate cancer osteoblastic (on day 20 ± 3 postinjection of AT6.1) metastatic models. <b>Results:</b> The distribution patterns of <sup>14</sup>C-fluciclovine, <sup>3</sup>H-FDG, and <sup>3</sup>H-choline, but not <sup>99m</sup>Tc-HMDP, were similar in both models, and the lesions where these tracers accumulated were, histologically, typical osteolytic and osteoblastic lesions. <sup>99m</sup>Tc-HMDP accumulated mostly in osteoblastic lesions. <sup>14</sup>C-fluciclovine could visualize the osteolytic lesions as early as day 6 postinjection of MRMT-1. However, differential distributions in <sup>14</sup>C-fluciclovine and <sup>3</sup>H-FDG existed, based on histological differences: low <sup>14</sup>C-fluciclovine and high <sup>3</sup>H-FDG accumulation in osteolytic lesions with inflammation. In the osteoblastic metastatic model, visualization of osteoblastic lesions with <sup>14</sup>C-fluciclovine was not clear, yet clearer than with <sup>3</sup>H-FDG. Although half of the osteoblastic lesions with <sup>14</sup>C-fluciclovine accumulation showed negligible <sup>3</sup>H-choline accumulation in comparison, they were histologically similar to lesions with marked <sup>14</sup>C-fluciclovine and <sup>3</sup>H-choline accumulation. <b>Conclusion:</b> These results suggest that fluciclovine-PET can visualize true osteolytic and osteoblastic bone metastatic lesions.
| Year | Citations | |
|---|---|---|
Page 1
Page 1