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. Author manuscript; available in PMC: 2022 Feb 1.
Published in final edited form as: Eur J Nucl Med Mol Imaging. 2020 Aug 8;48(2):383–394. doi: 10.1007/s00259-020-04978-6

Fig. 9.

Fig. 9

Binding specificity of [89Zr]ZrDFO-Amivantamab (0.37 MBq = 2.5 μg) in vivo determined by biodistribution studies at 4 days p.i in the MDA-MB-468 xenograft model, was evaluated 4 days p.i. (a) [89Zr]ZrDFO-Amivantamab uptake in the tumor under baseline and blocking conditions with 20 mg/kg of Amivantamab, α-EGFR, or α-c-MET (n = 3 per group); (b) Comparison of tumor uptake among [89Zr]ZrDFO-Amivantamab, [89Zr]ZrDFO-α-EGFR and [89Zr]ZrDFO-α-c-MET (n = 4 per group; * p < 0.05, ** p < 0.01)