Table 3.
124I-PU-H71 accumulates in tumors, with negligible retention in most normal organs.
| Organ | 4 hour (n=30) | 24 hour (n=30) | ||
|---|---|---|---|---|
| Mean SUV | Mean SD | Mean SUV | Mean SD | |
| Aortic blood pool | 0.5 | 0.2 | 0.2 | 0.1 |
| Appendicular skeleton* (humerus)* | 0.5 | 0.3 | 0.3 | 0.3 |
| Axial skeleton* | 1.0 | 0.3 | 0.3 | 0.3 |
| Brain | 0.1 | 0.1 | 0.1 | 0.2 |
| Kidney | 1.5 | 0.6 | 0.6 | 0.4 |
| Liver | 6.4 | 2.3 | 2.3 | 1.7 |
| Lung | 0.4 | 0.2 | 0.2 | 0.1 |
| Muscle, skeletal | 0.4 | 0.2 | 0.2 | 0.1 |
| Myocardium | 2.8 | 1.0 | 1.7 | 1.1 |
| Spleen | 2.0 | 1.2 | 0.7 | 0.4 |
| Thyroid | 2.3 | 1.3 | 1.1 | 0.9 |
| Tumors | 1.9 | 2.0 | 0.9 | 0.8 |
Note: Biodistribution and tumor uptake at 4 and 24 hours after tracer injection. Shown are study population (n=30 patients) average and standard deviation values for tracer uptake in major organs and tracer-avid tumors in terms of standardized uptake value (SUV average; see Methods). Thyroid uptake likely represents free radioiodide uptake (product of in vivo tracer metabolism); hepatic uptake likely represents tracer metabolism and hepatobiliary excretion.
Tracer uptake in humerus considered representative of compact bone/osteogenic cell tracer avidity and the spine representative of tracer uptake in bone red marrow (see Results).