Skip to main content
. 2024 Aug 26;14(14):5371–5387. doi: 10.7150/thno.100091

Table 3.

Absorbed doses in MPC tumor allografts and animal survival after treatment with lutetium‑177- and copper‑67-labeled TATE variants

TATE variant RN A m DT, Tumor PFS # OS Animals
[MBq/nmol] [Gy] [days] [days] n (per exp.)
Control/vehicle - - - 3.40 15.2 8 (3, 3, 2)
DOTA 177Lu 39.6 ± 0.09 41.1 ± 3.65 18.7 28.4 5 (5)
22.6 ± 1.42 22.0 ± 1.11 11.3 22.7 6 (3, 3)
NODAGA 67Cu 40.3 ± 0.76 9.51 ± 0.95 8.06 21.0 6 (4, 2)
24.6 ± 0.67 7.82 ± 0.79 7.42 16.9 5 (3, 2)
NODAGA-cLAB4 67Cu 41.5 ± 0.56 40.2 ± 3.09 16.6 27.3 6 (3, 3)
21.5 ± 0.54 34.6 ± 2.73 13.9 25.2 5 (2, 1, 2)

Each animal received an initial activity dose of 50 MBq; (Am) molar activity at treatment start; (DT, Tumor) mean absorbed dose in tumors; (n) number of animals per group and per independent experiment; (OS) overall survival defined as < 10‑fold change in tumor volume and (PFS) progression-free survival defined as < 2‑fold change in tumor volume compared to treatment start; (RN) radionuclide; Am, ID, and DT presented as means ± standard error, PFS and OS presented as medians; Pearson correlation coefficient (rp) and significance of linear relationships with DT: r = 0.96, p < 0.01, # r = 0.98, p < 0.001